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International Journal of Scientific and Innovative Research 2015 3 (1) P-ISSN 2347-2189, E - ISSN 2347-4971
International Journal of Scientific and Innovative Research 2015 3 (1) P-ISSN 2347-2189, E - ISSN 2347-4971
International Journal of Scientific and Innovative Research 2015 3 (1) P-ISSN 2347-2189, E - ISSN 2347-4971
EDITOR-IN-CHIEF
FORMER
DIRECTOR (RESEARCH)
SKY I NSTITUTE, KURSI ROAD, L UCKNOW, U.P, INDIA
FORMER JOINT DIRECTOR, C OUNCIL OF SCIENCE & TECHNOLOGY, UP, LUCKNOW
(DEPARTMENT OF SCIENCE AND TECHNOLOGY, UP GOVERNMENT), I NDIA
PROFESSOR, INTERNATIONAL INSTITUTE OF HERBAL MEDICINE (IIHM), LUCKNOW , U.P., INDIA
E-MAIL ID : editorijsir02@gmail.com, MOBILE-: 9794849800
Assistant Prof.
Deptt. of Education,
Rama P.G. College,
Chinhat, Lucknow,
Uttar Pradesh
Assistant Prof.
National Institute of
Fashion Technology,
Raebareli,
Uttar Pradesh
Research Scholar,
Sai Nath University,
Ranchi,
Jharkhand
Scientist,
Sky Institute
Lucknow
Uttar Pradesh
ADVISORY BOARD
Prof.(Dr.)S. P. Ojha
Prof.(Dr.)V.K. Srivastava
Former Prof & Head, Deptt. of Community Medicine
Director,
National Institute of Fashion Technology, Raebareli, Uttar Pradesh
Prof.(Dr.)N.S. Verma
Prof.(Dr.)A.K. Tripathi
Prof & Ex- Head, Deptt of Biochemistry, Former Pro- Vice Chancellor,
Former Dean, Faculty of Science, University of Lucknow, Lucknow, U.P.
Prof.(Dr.)C.M. Pandey
Former Prof & Head, Deptt. of Chemistry, Ex- Dean Faculty of Science,
University of Lucknow, Lucknow, Uttar Pradesh
Dr. S.Sinha
Prof.(Dr.) V.K.Tondon
Dr. K.Raman
Dr. P.K.Agarwal
Editor in Chief, Natural Product Communication,
Natural Product Inc 7963, Anderson Park Lane West Terville, OH, USA
Dr. R.K.Singh,
Former Director,
R. M. L. Institute of Medical Sciences, Lucknow and Prof. & Head,
Deptt. of Radiotherapy, K. G. Medical University, Lucknow, Uttar
Pradesh
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163
EDITORIAL BOARD
Prof.(Dr.) Y.B. Tripathi
Dr. K.K.Verma
Prof. & Head , Deptt. of Biochemistry, Shri Guru Ram RaiInstitute of Medical &
Health Sciences, Dehradun, Uttarakhand & Former Prof. & Head, Department of
Biochemistry, K. G. Medical University , Lucknow, U.P.
Dr. S.K.Tiwari
Lucknow Associate Prof. & Coordinator, Deptt. of Applied Physics, School for
Physical Sciences, Babasaheb Bhimrao Ambedkar University, Lucknow, U.P.
Prof. & Head, Deptt. of Oral & Maxillofacial Surgery, Faculty of Dental Sciences,
K. G. Medical University, Lucknow, Uttar Pradesh
Dr.A.K.Pandey
Dr.S.K.Pandey
Dr. C.M.K.Tripathi
Former Deputy Director & Head, Division of Fermentation Technology, CSIRCentral Drug Research Institute , Lucknow, Uttar Pradesh
Dr.G. N. Pandey
Asst. Prof., Deptt. of Physical Education, Dr. R.M.L. Avadh University, Faizabad,
Uttar Pradesh
Prof.(Dr.) L. Pandey
Prof.(Dr.) J.P.N.Rai
Prof.& Head, Deptt. of Environmental Sciences, G.B. Pant University of Agr. &
Technology, Pant Nagar, Uttarakhand
Prof. & Head, Deptt. of Biochemistry, Banaras Hindu University, Varanasi, U.P.
Asstt . Prof. , Deptt. of Electrical Engg., Institute of Engg. & Technology, Sitapur
Road, Lucknow, Uttar Pradesh
Prof. V.P.Sharma
Former Deputy Director & Head , Aquatic Toxicology Division, CSIR- Indian
Institute of Toxicology Research, Lucknow, Uttar Pradesh
Prof.(Dr.) S. M. Natu
Prof., Deptt. of Pathalogy,K.G. Medical University, Lucknow, Uttar Pradesh
Prof. , Deptt. of Civil Engg., Institute of Engg. & Technology, Sitapur Road ,
Lucknow, Uttar Pradesh
Prof.(Dr.)V.K. Sharma,
Prof.(Dr.)Anil Gaur
Prof., Deptt. of Biotechnology & Genetic Engg., G.B. Pant University of Agr. &
Technology, Pant Nagar, Uttarakhand
164
Faizabad, U. P.
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165
national and international conferences. He has actively participated in national and international conferences,
symposia and workshops and presented research papers and chaired scientific / technical sessions. He is
life member and fellow of many scientific societies such as National Academy of Sciences India , Society
of Toxicology of India, Indian Academy of Neurosciences, Bioved Research Society India, International
Society for Herbal Medicine (ISHM), Society of Biological Sciences and Rural Development, India. He has
been member of several scientific expert committees/ advisory committees to evaluate scientific research
proposals. Dr. Pandey has been actively associated with various universities and institutions in India as
examiner for conducting graduate, post graduate and doctoral level examinations in disciplines like chemical
sciences, pharmaceutical sciences, biochemical sciences, biotechnology and allied areas and member of
Board of Studies for the academic development in the department. He has been approved research supervisor
for guiding research in chemistry, biotechnology and related areas from various universities of India leading
to PhD Degree. In view of his vast research and administrative experience and broad R & D vision, Dr.
Pandey has been associated with International Journal of Scientific & Innovative Research (IJSIR) as
Editor-in-Chief.
166
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Mohit Bajpai
Chairman
Sky Institute
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167
CONTENTS
PAGE
AKANKSHA SRIVASTAVA, RAM NIWAS, VINEETA SINGH, AMREEN KHAN, C.K.M. TRIPATHI
12
VIBHA SINGH
17
27
46
51
55
61
72
80
91
R. SRIVASTAVA, D.C.RUPAINWAR
108
119
125
131
134
SHUKLA S.P., SACHAN R., DWIVEDI L., SHARMA K. J., YADAV V.P., SINGH N.B.
168
152
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ABSTRACT
Cholesterol oxidase, a bi-functional FAD-containing microbial enzyme belongs to the family
oxidoreductases which catalyzes the oxidation of cholesterol into 4-cholesten-3-one. In recent
time, cholesterol oxidase has received great attention due to its wider use in clinical
(determination of serum cholesterol) laboratories practice and in the bio- catalysis for the
production of a number of steroids. Cholesterol oxidase (COD) has been shown to possess
potent insecticidal activity, besides its use to track cell cholesterol. Moreover, this enzyme is
also implicated in the manifestation of some of the diseases of bacterial (tuberculosis), viral
(HIV) and non-viral prion origin (Alzheimers). These applications and disease mechanisms
have promoted the need of screening, isolation and characterization of newer microbes from
diverse habitats as a source of COD to learn more about its structural and functional aspects.
In this review, we discuss microbial sources of COD, its structure and important biochemical
properties besides its broad range of biological functions and applications.
Keywords: Cholesterol, Steroids, Bio-catalysis, Microorganisms, Biosensors
INTRODUCTION
The enzyme Cholesterol oxidase (COD)
(cholesterol: oxygen oxidoreductase, EC 1.1.3.6)
catalyzes the oxidation of cholesterol to 4cholesten-3-one in the presence of O2[1]. COD
has wide applications in clinical, pharmaceuticals,
food and agricultural industries which has
considerably increased the demand of this
enzyme. Various microorganisms are reported
to produce COD with specific properties.
Cholesterol oxidases are used to determine
cholesterol concentration in food and blood
serum by coupling of the enzyme with peroxidase
[2,3]
in the production of precursors for chemical
synthesis of steroid hormones, degradation of
dietary cholesterol in foods [4] and as biological
control agent [5].
COD is a monomeric bi-functional flavin
adenine dinucleotide (FAD) containing enzyme
which belongs to the oxidoreductases family and
acts on the CH-OH group of donor with oxygen
as an acceptor. COD catalyzes the oxidation of
3 -hydroxoysteroids and the isomerization of
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the enzyme. It belongs to the glucose-methanolcholine (GMC) oxidoreductase family and has
been found mostly in actinomycetes such as
Streptomyces sp. The structural and mutational
analysis of Streptomyces sp. (class-I enzyme)
has revealed that His447 and Glu361 residues
are implicated in the activity for the oxidation and
isomerization steps[34] and reported comparison
of amino acid sequences from class-I enzymes
eg. Streptomyces sp., Rhodococcus sp. and
Mycobacterium sp. These sequences contain a
consensus sequence for FAD binding, Gly-XGly-X-X-Gly, in the N-terminal region of the
COD[35].
The class-I enzyme possesses the
characteristic nucleotide-binding fold (Rossmann
-pleated sheet
fold) consisting of a
-helices and the motif
sandwiched between
needed for binding the cofactor. The
diphosphate group of the cofactor is positioned
closely to the N terminus of the first -helix of
the protein where the conserved GXGXG glycine
residues are located [29].
Class-II cholesterol oxidase
SUBSTRATE SPECIFICITY
M.Wt.
Optimum
Optimum
(kDa)
pH
Temp (C)
Arthrobacter simplex
57
7.5
50
63
7.5-8.5
40-50
Brevibacterium
sterolicum
55
7.5
50
Bordetella sp.
55
7.0
50
Burkholderia cepaca
ST-200
60
6.8-8.0
60
Corynebacterium
cholesterolicum
57
7.0-7.5
40-42
Chromobacterium sp.
DS-1
58
7.0-7.5
65
Enterobacter sp.
58
7.0
Nocardia
rhodochrous
Schizophyllum
commune
Streptomyces fradiae
7.0
Substrate Specificity
5.0
60
7.0
70
58
6.5-7.0
45-50
Streptomyces sp.
55
7.0
Streptomyces sp.
62
7.5
37
CholesteroO-Stigmasterol,
Dehydroepiandrosterone,
Ergosterol, Pregnenolone,
-Sitosterol, and
-Cholestanol.
&KROHVWHURO-Stigmasterol,
Dehydroepiandrosterone,
Ergosterol, Pregnenolone,
-Sitosterol, and
-Cholestanol.
55
7.2
Streptoverticillium
cholesterolieum
56
7.0-7.5
-Proteobacterium
58
6.5
Pseudomonas
sp.COX629
56
7.0
&KROHVWHURO-Stigmastero
(UJRVWHURODQG-Cholestanol.
&KROHVWHURO-Stigmasterol,
Dehydroepiandrosterone,
Ergosterol, Pregnenolone,
-6LWRVWHURO-Cholestanol and
Epicholesterol.
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HgCl2
[8]
[54]
HgCl2 and
AgNO3
[24]
Hg2+and Ag+
[8]
[22]
HgCl2 and
AgNO3
[55]
[22]
Hg2+andAg+
50
50
60
[20]
[11]
Streptomyces parvus
60
References
30
53
Pseudomonas sp.
strain ST-200
Inhibitors
[23]
[42]
[21]
[56]
Ba++, Mn++,
Hg++
[18]
Pb++, Ag++,
Hg++ and Zn++
[19]
[67]
&KROHVWHURO-Stigmasterol and
-6LWRVWHURO-Cholestanol
[45]
Fe2+, Zn2+ and
Hg2+
[21]
[58]
APPLICATIONS
OXIDASES
OF
CHOLESTEROL
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
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13.
14.
15.
16.
17.
18.
19.
20.
Ye D, Lei J, Li W, Ge F, Wu K, Xu W, Yong B.
Purification and characterization of extracellular
cholesterol oxidase from Enterobacter sp. World
J Microbiol Biotechnol 2008; 24: 2227-2233.
21.
Lee SY, Rhee HI, Tae WC, Shin JC, Park BK.
Purification and characterization of cholesterol
oxidase from Pseudomonas sp. and taxonomic
study of the strain. Appl Microbiol Biotechnol 1989;
31: 542-546
22.
23.
24.
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26.
27.
28.
29.
30.
31.
32.
33.
34.
35.
36.
38.
39.
40.
41.
42.
43.
46.
47.
Okada M, Matsui H, Ito Y, Fujiwara A, Inano K. Lowdensity lipoprotein cholesterol can be chemically
measured: A new superior method. J Lab Clin Med
1998; 132: 195-201.
48.
49.
10
51.
52.
53.
54.
55.
56.
57.
58.
59.
60.
61.
62.
64.
65.
66.
67.
68.
69.
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70.
71.
72.
73.
74.
75.
76.
77.
11
ABSTRACT
There are approximately 500000 plant species occurring worldwide. The World Health
Organization (WHO) estimates that 4 billion people (80% of the Worlds population) use herbal
medicines for some aspect of primary healthcare. These evidences contribute to support and
quantify the importance of screening natural plants. In India 2500 plants and 100 species of
plants used as regular source of medicine .In developed countries 25% of the medical drugs
are based on plants and their derivatives. In Indian traditional systems of medicine (Ayurveda)
it is known as sahachara, baana, kurantaka, kuranta, koranda, korandaka, shairiya and pitasaireyaka. This is a plant of miraculous nature. It has wide range of medicinal properties
which can be used for welfare of human being without any side effects. It has its traditional use
and well documented to use in modern medicine too.
Keywords: Vajradanti, Anti-inflammatory, Antidontalgic
INTRODUCTION
There are approximately 500000 plant
species occurring worldwide. The World Health
Organization (WHO) estimates that 4 billion
people (80% of the Worlds population) use
herbal medicines for some aspect of primary
healthcare. These evidences contribute to
support and quantify the importance of screening
natural plants. In India 2500 plants and 100
species of plants used as regular source of
medicine. In developed countries 25% of the
medical drugs are based on plants and their
derivatives. In Indian traditional systems of
medicine (Ayurveda) vajradanti is known as
sahachara, baana, kurantaka, kuranta, koranda,
korandaka, shairiya and pita-saireyaka. In folk
medicine it is known as piyaabaasaa, jhinti and
katsaraiya. Vajradanti is plant of Ramayan Kal .
It was found near Pampa lake . It is known as
Kurant, and pita Saireyaka in Sanskrit and
vajradanti in Hindi and Baleria prointis in
English. It belongs to family Acanthaecae and
occurs in hotter part of India . Barleria prionitis
L. (Family Acanthaceae; commonly known as
Vajradanti) is an annual shrub, 13 feet high,
found throughout Africa, India, Sri Lanka and
tropical Asia.
12
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8.
9.
10.
11.
12.
13.
14.
15.
16.
17.
18.
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Athar
Ata,
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Bosch,DrewJ.Harwank and Grant E. Pinwinski.
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ABSTRACT
Helium has varied applications in biomedicine. The research studies with hyperpolarized
helium-3 (3He) and xenon-129 (129Xe ) magnetic resonance imaging ( MRI ) have been found
useful in developing non-radiation based and sensitive approaches for chronic obstructive
pulmonary disease ( COPD ). The applications of atmospheric pressure plasmas ( APPs ) in
biomedicine are becoming better treatment protocols for various chronic diseases as the
research studies have shown their potential in bacterial sterilization, blood coagulation and
wound healing, dermatology and cancer treatment. It is interesting to emphasize that the
atmospheric pressure helium plasma jet driven by pulsed dc voltage has been utilized to treat
human lung cancer cells in vitro. This plasma device may serve as a valuable tool for reactive
oxygen species (ROS) promoting cancer therapy, a boon for cancer patients. Helium based
low temperature atmospheric pressure plasma has been found to break Amyloidfibrils into
smaller units in vitro and can be used as plasma based therapy of neurodegenerative diseases
such as Alzheimer and Parkinsons. Attempts have been made to present the biomedical
applications of helium and its utility in health and diseases. However, multidisciplinary scientific
studies on the interaction of helium based low temperature atmospheric pressure plasma on
the sub cellular and molecular levels in disease conditions could be useful in strengthening
its application in biomedicine to address the health challenges for ailing humanity.
Keywords : Helium, Hyperpolarized helium-3 (3He) and Xenon-129 (129Xe ) Magnetic Resonance
Imaging (MRI), Atmospheric Pressure Plasmas (AAPs), Chronic Obstructive Pulmonary Disease
(COPD), Cancer, Alzheimer, Parkinsons
INTRODUCTION
The unexpected prolonged exposure of
human beings to large number toxic chemicals
and xenobiotics present in the environment and
unhealthy life styles have become the major
cause of the complex diseases crippling the
human subjects in the world. This has also
resulted in multi -drug resistance problems in
the society .In the present situation, clinicians
and biomedical scientists throughout the world
are in search of developing suitable diagnostic
tool for the diseases .Radio- diagnosis has
emerged as more accurate diagnostic technique
for disease diagnosis at early stage and
measuring the clinical conditions of the diseased
people during treatment. X-ray and CT scan
commonly employed by clinicians in diagnosing
the diseases have been found to produce
harmful effects on the patients as they produce
radiations harming the body thereby making the
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18
CHEMISTRY OF HELIUM
It has been found that helium is the second
lightest and second most abundant gas in the
universe (hydrogen being one). Since no
helium compounds are known, this family of
gases was once thought to be inert. In the year
1962, scientists could be able to prepare first
noble gas compound with xenon. Helium occurs
in un-combined form. It is believed that it must
be extracted from the atmosphere by
liquefaction of air or separated from deposits
of natural gas. Research studies have predicted
that some of the terrestrial helium is the product
of the alpha decay of radioactive isotopes
beneath the crust. Helium is said to be the only
element which cannot be converted to a solid
by cooling.
Chemists have found that helium possess
lowest melting point of any element. It is widely
used in cryogenic research because its boiling
point is close to absolute zero. Helium has been
found to be a vital element in the study of super
conductivity. Research studies have revealed
that liquid helium can be used in obtaining
temperatures of a few micro kelvins by the
adiabatic demagnetization of copper nuclei.[ 3]
Helium is known to be only liquid which could
not be solidified by lowering the temperature
and remains in liquid down to absolute zero at
ordinary pressure. It has ability to solidify by
increasing the pressure while solid 3He and
4
He can be changed in volume in volume (more
than 30 percent) by applying pressure. The
specific heat of helium gas is high sand the
density of helium vapor at normal boiling point
is also very high with vapour expanding greatly
when heated at room temperature. Although
helium has weak chemical reactivity to combine
with other elements, scientific studies have been
carried towards
preparation of helium
difluoride. [4] Further, scientists have also
investigated on molecular ions of helium like
He+ and He++. Seven isotopes of helium are
known: Liquid helium (He-4) exists in two forms:
He-4I and He-4II, with sharp transition point at
2.174K. He-4I (above this temperature) is a
normal liquid, but He-4II (below it) is unlike any
other known substance. It expands on cooling,
its conductivity for heat is enormous, and neither
its heat conduction nor viscosity obeys normal
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rules.[5,6]
BIOMEDICAL APPLICATIONS
The very low boiling and melting points of
noble gases make them useful as cryogenic
refrigerants. Among these noble gases, helium
has been found varied applications in health
care. Liquid helium, which boils at 4.2K (268.95C; -452.11F) has been found useful for
supercond-ucting magnets which are needed in
Nuclear Resonance Imaging and Nuclear
Magnetic Resonance. The use of liquid helium
in Magnetic Resonance Imaging (MRI) is
continuously increasing in medical field because
of the utility of MRI in diagnosis of complex
diseases by medical profession. Magnetic
resonance imaging (MRI), nuclear magnetic
resonance imaging (NMRI) or magnetic
resonance tomography (MRT), is a medical
imaging technique used in radiology to
investigate the anatomy and physiology of the
body in both health and disease . MRI scanners
use strong magnetic fields and radio waves to
form images of the body. The technique is used
in hospitals for medical diagnosis, staging of
disease and for follow- up without exposure to
ionizing radiation.
Atmospheric pressure plasmas (APPs)
based on helium have been developed as new
tools in the biomedicine and have proved their
effectiveness in biomedical applications such as
treatment of living cells, sterilization, blood
coagulation, wound healing and air purification[2].
Low temperature plasmas have potential to
produce reactive oxygen species (ROS) and
reactive nitrogen species (RNS) having diverse
biological implications such as ROS effects on
cell membrane : per oxidation of lipids, oxidation
of proteins, DNA strands and RNS effects on
biological cells : cell signalling. The applications
of helium based MRI and low temperature
atmospheric pressure plasmas in chronic
complex diseases such as chronic obstructive
disease (COPD), cancer, neurodegenerative
diseases etc. are discussed in this review article.
Pulmonary Diseases
Complex respiratory disorders like chronic
obstructive pulmonary disease (COPD)
characterized by persistent airflow limitation that
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22
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Kaushik SS, Cleveland ZI, Cofer GP et al. Diffusionweighted hyperpolarized 129Xe MRI in healthy
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Woods JC, Yablonskiy DA, Choong CK et al. Longrange diffusion of hyperpolarized 3He in explanted
normal and emphysematous human lungs via
magnetization tagging. J Appl Physiol 2005;
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enhances cutaneous delivery of epidermal growth
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Kim, J. Y., Lee, D.-H., Ballato, J., Cao, W. & Kim, S.O. Reactive oxygen species Controllable nonthermal helium plasmas for evaluation of plasmid
DNA strand breaks. Appl. Phys. Lett. 101, 224101
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92.
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ABSTRACT
The use of lasers in medicine and biology has demonstrated its interest through innovative
advanced technologies such as laser microdissection and /or photoablation which at different
levels of expression enable understanding of the physiological mechanisms in the evolution of
a disease. Lasers have achieved a prominent position in medical application and offer unique
advantages for medical diagnosis, therapeutic treatments and internal surgeries in most
medical disciplines including dermatology, dentistry, neurosurgery, eye surgery, cancer surgery,
urology, gastroenterology etc. because of their ability to deliver high precision treatments,
whilst remaining minimally invasive. Thus Laser- based therapies and diagnostic methods
represent an area of huge future potential.Research efforts andcontinuous improvements over
recent years have resulted in excimer lasers becoming the tool of choice for many applications
in medical sciences.Excimer lasers, which are pulsed gas lasers operating with a special
mixture of noble gases and halogens, emit laser radiation in the UV and VUV spectra, at
discrete wavelengths between 351 nm and 157 nm, have shown promise in dermatology,
angioplasty, bilary laser lithotripsy, ophthalmology and orthopedics. The principal advantage
of excimer lasers is that they are capable of producing a very small, precise spot at a very low
(UV) wavelength. Excimer lasers are excellent for removing excess material through laser ablation
due to the fact that they are able to precisely destroy material with little to no thermal buildup.In
the present review, applications of excimer lasers in biomedical sciences particularly in
dermatology,ophthalmology, angioplasty, orthopaedics, lithotripsy,dentistry, medical implants
have been presented and recent studies carried out have been reviewed.Laser-associated
micro dissection offers a rapid, precise method of isolating and removing targeted cells or
groups of cells from complex biological tissues which may be helpful in understanding
physiological mechanisms on the level of a specific cell population and even on the level of
the single cell in disease conditions. Multidisciplinary research studies on the interaction of
laser with biological tissue at molecular level using biotechnological tools will enhace the
therapeutic potential of laser technology in diagnosis and treatment of chronic complex
diseases especially cancer , genetic disorders, neurogegenerative disorders ,
multidrugresistence tuberculosis , autoimmune diseases , HIV etc. and it may also be useful
in designing new and innovative strategies in drug delivery and image-guided surgery.
Keywords: Excimer Lasers, Laser-tissue Interaction, Bio-medical Applications: Dermatology,
Ophthamology, Angioplasty, Lithotripsy, Orthopaedics, Dentistry, Biomedical Implants/ Materials/
Devices
INTRODUCTION
Laser : Light Amplified Stimulated Emission
Radiation, unlike a standard light beam, is a
source of monochromatic, coherent and
unidirectional light. Over the past 50 years,
scientific research and innovations made
revolution in laser and led to the development
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30
Dermatology
The use of eximer laser in dermatology has
been considered more effective as compared
to
conventional
phototherapy
and
photochemotherapy because of the lower
cumulative UV-dose involved, the shorter time
frame required for treatment and the option of
targeting individual lesions without affecting the
surrounding healthy skin.Grema and Raulin
have reviewed the application of eximer laser in
various skin diseases such as psoriasis vulgaris,
vitiligo and atopic eczema and it has been found
very useful in these skin diseases. The eximer
laser has also been found effective in case
studies ranging from post-operative
hypopigmentation to acne vulgaris and from
alopecia areata to parapsoriasis en plaque.[6]UVB
phototherapy has been found effective for the
treatment of psoriasis. It has been observed that
for patients with localized plaque-type lesions,
308-nm excimer laser phototherapy offers rapidly
delivered, targeted, high UVB doses, while
sparing adjacent healthy skin.Studies have been
conducted to compare the advantages and
disadvantages of the 308-nm xenon chloride
(XeCI)UVB excimer laser with non targeted
broadband UVB (BB-UVB), narrowband UVB (NBUVB), and psoralen plus UVA (PUVA)
phototherapies and it has been proposed that
excimer laser exclusively treats diseased skin
with better response rates, split-body trials
revealed no differences.[7] Narrowband UVB (311
nm) phototherapy is a well-established, widely
used and highly efficient treatment for psoriasis
which is a chronic, genetically determined
inflammatory disease, characterized by an
immunomediated pathogenesis, but a big
disadvantage of this therapy is that large areas
of unaffected skin are also irradiated along with
the psoriatic lesions. Keeping in view of this
disadvantage studies have been conducted to
evaluate a 308-nm excimer laser and a 308-nm
excimer lamp in comparison with 311-nm
narrowband UVB in the treatment of patch
psoriasis by using two different dose-increase
schemes and the results of the study revealed
that both 308-nm light sources can clear patch
psoriasis in a similar manner to standard
phototherapy, with the advantage of the ability
to treat exclusively the affected skin and with a
reduced cumulative dose, thus perhaps
www.ijsir.co.in
40
2.
3.
4.
5.
6.
7.
8.
9.
10.
13.
14.
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16.
17.
18.
19.
20.
21.
22.
23.
24.
25.
27.
28.
29.
30.
Joseph
G Morelli,
Abdul-Ghani Kibbi,
James Boll and Oon Tian Tan . 193 nm Excimer
Laser Selective Ablation of In Vivo Guinea Pig
Epidermis
.Journal
of
Investigative
Dermatology (1988) 91, 532535; doi:10.1111/
1523-1747.ep12476881]
36.
37.
41
39.
40.
41.
42.
43
44
45
48
49
42
50
51
52.
53.
54.
57.
58.
59.
60.
61.
75.
76.
77.
78.
79.
70.
80.
81.
82.
83.
84.
85.
63.
64.
65.
66.
67.
68.
71.
72.
73.
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43
87.
88.
Andreas B. Imhoff,
The use of lasers in
orthopaedic surgery. Operative Techniques in
Orthopaedics, July 1995 , Volume 5, Issue 3,
Pages 192203
99.
89.
90.
91.
92.
93.
94.
95.
96.
97.
44
101. Felix
Sima, Emanuel
Axente, Carmen
Ristoscu,Ion N. Mihailescu , , Taras V.
Kononenko, Ilya A. Nagovitsin , Galina
Chudinova,Vitaly I. Konov, Marcela Socol, Ionut
Enculescu,Livia E. Simaand Stefana M. Petrescu
.Tailoring immobilization of immunoglobulin by
excimer laser for biosensor applications. Journal
of Biomedical Materials Research Part AVolume
96A, Issue 2, pages 384394, February 2011
102. Waugh, David and Lawrence, Jonathan (2011).
The enhancement of biomimetic apatite coatings
by means of KrF excimer laser surface treatment
of nylon 6,6. Lasers in Engineering, 21 (1&2).
pp. 95-114
103. Zaret, M.M., Breinin, G.M., Schmidt, H., Ripps, H.,
Siegel, I.M. and Solon, L.R. (1961) Science, 134,
1525-1526.
http://dx.doi.org/10.1126/
science.134.3489.1525
104. Avedisian, C.T., Cavicchi, R.E., McEuen, P.L. and
Zhou, X. (2009) Annals of the New York Academy
of Sciences, 1161, 62-73. http://dx.doi.org/10.1111/
j.1749-6632.2009.04090.x
105. Legres, L.G., Chamot, C., Varna, M. and Janin, A.
(2014) The Laser Technology: New Trends in
Biology and Medicine. Journal of Modern Physics,
5,
267-279.
http://dx.doi.org/10.4236/
jmp.2014.55037
106. Moo-Young, G.A. (1985) Western Journal of
Medicine, 143, 745-750
107. Anderson, R.R. (2013) Journal of Investigative
Dermatology, 133, E21-E23.
108. Herd, R. (1996) JAMA Dermatology, 132, 12621262. http://dx.doi.org/10.1001/archderm.
www.ijsir.co.in
www.ijsir.co.in
45
ACKNOWLEDGEMENT
Authors are highly grateful to the Head,
Department of Zoology, University of Lucknow,
Lucknow , India and officials of Forest Research
Institute, Kanpur for providing necessary space
for experiment.
REFERENCES
1.
2.
3.
4.
5.
6.
7.
8.
9.
CONCLUSION
The different life stages and even the shed
cuticle of larvae of Dermestes species are
important tools in estimation of post-mortem
interval [40]. This species of beetle is dominant
from mid to late decay stages of decomposition
and is forensically important [38]. The succession
pattern of insects was stage specific so in medico
legal cases the post-mortem interval is possible
even in badly decomposed body [ 41]. As the PMI
is based on the lifecycle and behaviour of
necrophagous insects, this study may help as
an important tool for estimation of the postmortem interval (PMI) in forensic science.
48
www.ijsir.co.in
Ontario. 1996;
24. Vanlaerhoven, S. L., and Anderson G. S. Insect
succession on buried carrion in two
biogeoclimatic zones of British Columbia.
Journal of Forensic Sciences. 1999; 44, 3141.
25. Early M. and Goff M.L. Arthropod succession
patterns in exposed carrion on the island of O
ahu, Hawaiian Islands, USA. J.Med. Entomol.,
1986; 23, 520-531.
26. Hoermann C., Ruther J.,Reibe S.,Madea
B.,Ayasse M.,The importance of carcass
volatiles as attractants for the hide beetle
Dermestes maculatus forensic science
international 2011;212,173-179.
27. Jones T.M., McNamara K. B., Colvin PGR,
Featherston R, Elgar MA. Mating frequency,
fecundity and fertilization success in the hide
beetle, Dermestesmaculatus. Journal of Insect
Behavior2006; 19, 357-371.
28. Taylor, T.A. Observation on the biology and
habits of dermestes maculates De Geer-a dried
fish pest in Nigeria.Nigerian Agric. J. 1964;1,
12-17.
29. Haines CP, Rees DP. Dermestes spp. A Field
Guide to the Types of Insects and Mites Infesting
Cured Fish (1989);.http://www.fao.org/docrep/
003/t0146e/T0146E04.htm (28 September
2009.
30. Osuji, F.N. Some aspects of the biology of
dermestesmaculatusDe
Geer
(Coleoptera:dermestidae) in dried fish.J.Stored
prod. Res. 1975; 11, 25-31.
31. Cloud JA, Collison CH. Comparison of various
poultry house litter components for hide beetle
(Dermestesmaculatus DeGeer)
larval
development in the laboratory. Poultry Science
1986; 65, 1911-1914.
32. Kulshrestha P, Satpathy DK. Use of beetles in
forensic entomology. Forensic Science
International2001; 120, 15-17.
33. Carvalho, L.M.L., Thyssen P.J., Linhares, A.X.
and Palhares F.A.B. A checklist of arthropods
associated with pig carrion and human corpses
in southeastern Brazil. Memorias do
InstitutoOswaldo Cruz. 2000; 95, 135-138.
34. Archer MS. Elgar MA. Cannibalism and delayed
pupation
in
hide
beetles, Dermestesmaculatus DeGeer
49
50
www.ijsir.co.in
ABSTRACT
Blow flies (family-Calliphoridae) and flesh flies (family-Sarcophagidae) are amongst the first
wave of insects which arrive on a corpse for feeding and breeding purposes. Development
rates of these flies are frequently used to determine post-mortem interval (PMI) in forensic
entomological investigations. The rate of larval growth is directly affected by environmental
conditions such as photoperiod and ambient temperature. In the flesh fly, Sarcophaga dux,
short-day photoperiods and low temperature induce pupal diapause. Diapause is a form of
dormancy in insects which confer survival during unfavourable environmental conditions. Distinct
genetic traits and endocrinological factors are found responsible for the induction and regulation
of diapauses in different insect species. The life stage at which the insect exhibits diapause is
also species specific. Present study investigates the incidence of diapause in the laboratory
reared populations of S. dux and define further the factors responsible for induction and
termination of pupal diapause in flesh flies.
Keywords: Forensic entomology, Post-mortem interval, Flesh fly, S. dux, Diapause
INTRODUCTION
Adverse winter conditions in the temperate
regions have channelled the evolution of a pupal
diapause in flesh flies of the genus Sarcophaga.
Diapause in Sarcophaga is generally found in
the young phanerocephalic pupa, it is the pupal
stage in which adult development has not been
initiated [1]. Various studies have been conducted
on the incidence of diapause in the genus
Sarcophaga [1-8]. Effect of cold temperature and
short photoperiod on pupal diapause induction
in S. argyrostoma was studied by many workers
[3,7]
, whereas in S. bullata larval photoperiod was
not shown to influence diapause. Denlinger
revealed the importance of photoperiod received
by developing embryos within the uterus of the
ovoviviparous females in the S.crassipalpis. [5, 6]
If the larvae are exposed to a short photophase
at 250 C, the pupae will not enter diapauses [5,6].
In various groups of S.crassipalpis males enter
diapause at a higher rate than females,
experiments revealed a similar pattern in the
other species of Sarcophaga [1]. In the Pieris napi,
Pararge aegeria and P. c-album a higher
tendency of males to enter diapause is also
found[9].
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12 : 12
25C
540
12 : 12
20C
240
16 : 8
17C
225
100
16 : 8
15C
192
100
52
2-
3-
4-
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6-
7-
8-
9-
20-
21-
22-
23-
24-
25-
54
www.ijsir.co.in
ABSTRACT
This paper proposes two different current control based controllers for a shunt active power
filter system. A shunt active power filter system has been designed, built to work under balanced;
unbalanced and distorted supply conditions to meet IEEE 519 recommended harmonic
standards. The shunt active filter is mainly controlled by two different control schemes i.e.
constant instantaneous power and sinusoidal current control based controller to act as a
harmonic isolator between the supply and load. This paper discusses about both the current
controllers.
Keywords: Active power filter (APF), Constant instantaneous power control strategy, Sinusoidal
current control strategy, Harmonic compensation, IEEE 519.
INTRODUCTION
Nonlinear loads produce the harmonics into
the power system and these harmonics create a
lot of disadvantages in the system. Supply gets
distorted and unbalanced when application of
unbalanced and nonlinear loads increases.
These currents pollute the supply point of the
utility. Therefore, it is very important to
compensate unbalance, harmonic and reactive
component of the load currents. Whereas when
supply is unbalanced and distorted, these
problems worsen the system. [13] By the
application of shunt active power filters can
eliminate harmonic, reactive and unbalanced
currents, improve the power supply performance
and the stability of system. Today, the soft
computing techniques are used broadly for
optimization of the system applied or in control
system. Some of them are such as adaptive tabu
search[48] used for finding the optimized values
of the controllers variables,[412] optimization of
active power filter using GA, [912] power loss
minimization using particle swarm optimization,[13]
neural network control [1418] applied in both
machinery and filter devices.
In this paper, two different control
techniques i.e. constant instantaneous power
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Figure 2: Control block diagram of the shunt active filter using constant instantaneous power
control strategy
Figure 3: Shunt active filter model using constant instantaneous power control strategy
Figure 4: Control diagram of the shunt active filter controller using sinusoidal current control strategy
Figure 5: Shunt active filter model using Sinusoidal current control strategy
CONCLUSIONS
REFERENCES
1.
58
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14.
15.
16.
17.
18.
19.
20.
21.
22.
4.
5.
6.
7.
8.
9.
10.
11.
www.ijsir.co.in
59
24.
60
25.
26.
IEEE
Recommended
Practices
and
Requirements for Harmonic Control in Electrical
Power Systems, IEEE Standard 5191992, 1992.
27.
www.ijsir.co.in
Figure 1: Schematic diagram of 180 domain (d) domain-wall (dw) structure. The arrows indicate the electric
polarization. The electric polarization has a spiral orientation as one move from one domain to the adjacent
domain.
-1
Figure 2: Schematic energy level diagrams of spins (I= 3/2) in a one - dimensional chain. W0 , W0 , W0 are the
,
-, -
-3/2 levels respectively for the case where one spin
transition probabilities of 3/2
undergoing an upward transition while the other spin undergoes downward transition (usually called flip-flop
1
0
-1
1
0
-1
term). W2 , W2 , W2 represent simultaneous upward (or down ward) flip of the pair of spins. W1 , W1 , W1
represent the single spin transition probability for the spin pairs and counted twice for each pair of spins.
www.ijsir.co.in
63
n1/ 2 ( x , t )
=
t
1
n ( x , t ) n1/ 2 ( x a , t ) W01
N 3/ 2
1
n ( x, t ) n3/ 2 ( x + a , t ) W21
N 3/ 2
1
n ( x , t ) n3/ 2 ( x a , t ) W21
N 3/ 2
+
+
+
+
+
n1/ 2 ( x , t )
=
t
1
N
1
N
1
N
1
N
1
N
1
N
1
N
1
N
n 1/ 2 ( x , t ) n1/ 2 ( x + a , t ) W00
n 1/ 2 ( x , t ) n1/ 2 ( x a , t ) W00
n3/ 2 ( x , t ) n3/ 2 ( x + a , t ) W21
1
n ( x , t ) n3/ 2 ( x + a , t ) W01
N 1/ 2
1
n ( x , t ) n1/ 2 ( x + a , t ) W01
N 3/ 2
1
n ( x , t ) n1/ 2 ( x a , t ) W00
N 1/ 2
1
n ( x , t ) n1/ 2 ( x + a , t ) W00
N 1/ 2
1
n ( x , t ) n1/ 2 ( x + a , t ) W21
N 1/ 2
1
n ( x , t ) n1/ 2 ( x a , t ) W21
N 1/ 2
1
n ( x , t ) n1/ 2 ( x + a , t ) W20
N 1/ 2
1
n ( x , t ) n1/ 2 ( x a , t ) W20
N 1/ 2
+
+
+
+
+
+
n 3/ 2 ( x , t )
=
t
+
+
+
+
1
n ( x a , t ) n1/ 2 ( x , t ) W00
N 1/ 2
1
n ( x , t ) n 1/ 2 ( x a , t ) W00
N 1/ 2
1
n ( x , t ) n1/ 2 ( x + a , t ) W01
N 3/ 2
1
n ( x , t ) n1/ 2 ( x a , t ) W01
N 3/ 2
1
n ( x , t )n1/ 2 ( x + a , t ) W20
N 1/ 2
1
n ( x , t ) n1/ 2 ( x a , t ) W20
N 1/ 2
1
n ( x , t ) n1/ 2 ( x a , t ) W20
N 1/ 2
1
n ( x , t ) n1/ 2 ( x + a , t ) W21
N 1/ 2
1
n ( x , t ) n 1/ 2 ( x a , t ) W21
N 1/ 2
+
+
1
n ( x , t ) n1/ 2 ( x + a , t ) W00
N 1/ 2
1
n ( x , t ) n1/ 2 ( x + a , t ) W00
N 1/ 2
1
n ( x , t ) n 3/ 2 ( x a , t ) W01
N 1/ 2
1
n ( x , t ) n 3/ 2 ( x + a , t ) W01
N 1/ 2
1
n ( x , t ) n 1/ 2 ( x + a , t ) W20
N 1/ 2
1
n ( x , t ) n1/ 2 ( x a , t ) W20
N 1/ 2
1
n ( x , t ) n1/ 2 ( x a , t ) W20
N 1/ 2
1
n ( x , t ) n 3/ 2 ( x + a , t ) W21
N 3/ 2
1
n ( x, t ) n 3/ 2 ( x a , t ) W21
N 3/ 2
1
n ( x , t )n1/ 2 ( x + a , t ) W01
N 3/ 2
1
n ( x , t )n 1/ 2 ( x a , t ) W01
N 3/ 2
1
n ( x , t )n 3/ 2 ( x + a , t ) W21
N 3/ 2
1
n ( x , t )n 3/ 2 ( x a , t ) W21
N 3/ 2
n1/ 2 ( x , t )n 3/ 2 ( x + a , t ) W01
n 1/ 2 ( x , t )n 3/ 2 ( x a , t ) W01
n 1/ 2 ( x , t )n1/ 2 ( x + a , t ) W21
n 1/ 2 ( x , t )n1/ 2 ( x a , t ) W21
N+1 =
n3/2- n1/2
N0 =
n+1/2 n-1/2
N-1 =
n-1/2 n-3/2
a)
W 0
W 0 (x, x+a)
(for i = 1, 0, -1)
i
W 2
W 2 (x, x+a)
W 0(x , x-
W 2 (x, x-
a)
As adjacent neighbors have identical
interactions, we can rewrite Eq. (1) as
N +1
( x, t ) =
t
2 N +1 ( x , t ) 2 N +1 ( x + a , t ) 2 N +1 ( x a , t )
+ ' N 0 ( x, t ) + ' N 0 ( x + a, t )
+ ' N 0 (x a, t )
N 0
( x, t ) = N +1 ( x , t ) + N +1 ( x + a , t ) + N +1 ( x a , t )
t
2 ' N 0 ( x, t ) 2 ' N 0 ( x + a , t ) 2 ' N 0 ( x a , t )
+ " N 1 ( x , t ) + " N 1 ( x + a , t ) + " N 1 ( x a , t )
N 1
( x , t ) = ' N 0 ( x , t ) + ' N 0 ( x + a , t ) + ' N 0 ( x a , t )
t
- 2 " N 1 ( x , t ) 2 " N 1 ( x + a , t ) - 2 " N 1 ( x a , t )
Eq. (2)
where
Eq. (1)
64
W1 W1
= 2W11 + 0 + 2 ,
2
2
W0 W0
' = 2W10 + 0 + 2 ,
2
2
W 1 W 1
" = 2W1 1 + 0 + 2 ,
2
2
W21 W01
4
W 0 W00
'= 2
4
W 1 W0 1
"= 2
4
Eq. (3)
Where
a1 = + 2
a2 = '+2 '
D1 = a 2
D2 = ' a 2
D3 = ' ' a 2
{ N-1(x, t)},
Eq. (4)
With
k1 = 3 N+1(x, 0) + N-1(x, 0) +2N0(x, 0)
k2 = N+1(x, 0) + N-1(x, 0) +2 N0(x, 0)
k3 = N+1(x, 0) + 3N-1(x, 0) +2N0(x, 0)
where
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65
1
9b
[k
Z 0" = -
1
8b
[k
3s Z +1 2 sZ 0 sZ 1
s Z +1 2 sZ 0 sZ 1
2 A02
a 2W00
0
, W00 = W0 = 2 (1 3 cos2 )
b=
16
h
Z -1" = -
1
9b
[k
s Z +1 2 sZ 0 3sZ 1
Eq. (5)
Where
2 A02
a 2W00
0
, W00 = W0 = 2 (1 3 cos2 )
b=
16
h
s being the Laplace variable.
The set of Eq. (5) can be solved for different
initial and boundary conditions. For an easy
comparison of the results with the generally
performed pulsed NMR relaxation measurements
or devising new experiments and also to study
the domain-wall effects, we consider the following
situations.
An intense radio frequency pulse is applied
to the sample at a frequency that would be equal
to the central line frequency in a crystal of same
material. We make a crude assumption to begin
with that it causes a fraction a of spins flip from
the lower state I = 1/2 to the higher state I = -1/2
and the population differences become
N0(x, 0) = -2 ,
N-1 (x, 0) = ,
N+1 (x, 0) =
Eq. (6)
e-2W1t
N0(0, t) =
[e-2W1t + e-2W2t]
Eq. (7)
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transition m = 3/2
+1/2 respectively. It should be noted in deciding
the location of the origin, i.e. x = 0, that the NMR
of nuclei lying inside the wall would not be usually
observable due to structural disorders. So, x =
0 would correspond to the region near the wall.
At present we are assuming that the wall
thickness is negligible.
Using the above boundary conditions, Eq.
(5) were solved to yield
N-1(x, t)
N0(x, t)
Eq. (9)
Where
2
C11 = C21 = 1 1 C31
18
18
4 ( k1 2 k 2 + k 3 )
12
18
1
+
22 12
22 12 18
= 1
18
( k1 4 k 2 + k 3 ) + ( k 1 4 k 2 + k 3 )
4
4
2
1
2
2 2
C12 = C22 = 1 1 C32 = 1 1 2 2 2
18
18 2 1
12
C =
C13 = C23 = 1
18 33
2 2
18
1 1 1 1 2
+ 1
18 18
2 12
22
C
C14 = C24 = 1
18 34
Eq. (8)
Where
22
= 1
18
18
(k 2k2 + k3 )
18
4 1
2
2
2
2
2 1
2 1
2
1
( k1 4 k 2 + k 3 )
4
18
22
2 2
C35 = 1 2 2 1 2
C15 = C25 = 1
18
18 2 1
2
2 2 18
C16 = C26 = 1 2 C36 = 1 2 1 1 2
18
18 18 2 22
k1 k 3
k k3
k k2
k k2
, C27 = 1
, C18 = 1
, C28 = 3
,
4
4
4
4
k 4k 2 + k 3
C38 = 1
4
C17 =
k1 2k 2 + k 3 12
1
s
4
18
18
a3 =
2
2
22 12
1
+ 18 s + 2W + 18 1
1
k 4k2 + k 3
+ 1
s + 2W1 s + 2W2
4s
a4 =
18
22 12
k1 4 k 2 + k 3
4s
s + 2W2
k1 4 k 2 + k 3
k 1 2 k 2 + k 3 12
1
4s
4s
18
2
2
1
1
+
+
18 s + 2W1 18 s + 2W2
x1
72 b 2 t
1 ( x , t ) = erfc
2 ( x , t ) =
e 2W1t
- -2W1 x1
x1 1
72 b
e
erfc 2W1t +
72 b 2 t
x 1
-2W1
x1 1
72 b
erfc 2W1t +
+ e
72 b 2 t
67
- -2W2 x1
72 b
e
erfc 2W2 t +
3 ( x, t ) = e 2W2t
x1
2
-2W2
72 b
2W2 t +
+
e
erfc
x 2
1
4 ( x , t ) = erfc
72 b 2 t
5 ( x , t ) =
6 ( x , t ) =
x1 1
72 b 2 t
x1 1
72 b 2 t
- -2W1 x 2
x 2 1
72 b
e
erfc 2W1t +
72 b 2 t
x 2
-2W1
x 2 1
72 b
erfc 2W1t +
+ e
72 b 2 t
e 2W1t
e 2W2t
- -2W2 x 2
x 2 1
72 b
e
erfc 2W2 t +
72 b 2 t
x 2
-2W2
x 2 1
72 b
erfc 2W2 t +
+e
72 b 2 t
7 ( x , t ) = erfc x
2 1
9b 2 t
Eq. (11)
Eq. (10)
Where i =1, 0 or 1 and L is the thickness
of the domain. In our treatment domain-wall
thickness has been ignored. For clarity and ready
reference the symbols and useful expressions
have been kept same as taken in the Ref.[19, 43]
RESULTS AND DISCUSSION
The time dependence of the population
differences N+1(t), N-1(t) and N0(t) as given by
Eq.(9) and (10) were evaluated numerically
using 32 point Gaussian quadrature [Abramowitz
1972] for different values of the ratios W1/W00
taking W2/W1 = 1 and various values of L/a by
Shukla et al. [43] and Pandey et al. [34] .The
necessary computer programs were developed
68
Eq. (12)
The numerical calculations were performed
by utilizing trapezoidal rule for integration over
the angles
( 0 to 1800 ) and
(0 to 3600 )
and using the 32 - point Gaussian Quadrature
program employed for single crystal calculations
described in the previous section as a
subroutine. The computer program was
developed in house in BASIC.
It was observed that the time dependence
of N0(t) is non-exponential. An attempt was made
to get an empirical relation representing this time
Eq. (13)
69
4.
5.
6.
7.
8.
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9.
10.
11.
12.
13.
14.
15.
16.
17.
18.
19.
20.
21.
22.
23.
24.
25.
26.
27.
28.
29.
30.
31.
32.
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33.
34.
35.
36.
37.
38.
39.
40.
41.
42.
43.
44.
45.
46.
47.
48.
49.
50.
51.
52.
53.
54.
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ABSTRACT
Water distribution system is an integral part of present society. It includes the features like
Collection and Storage, Transportation, Treatment, Distribution .Water distribution systems
can be classified according to the source of water that they use, like Surface Water Distribution
Systems, Groundwater Distribution Systems, Regional Rural Water Distribution Systems, and
Purchased Water Distribution Systems. There are many piping systems through which water
is distributed. Few main piping systems are listed as Transmission Lines, In-plant Piping Systems,
Distribution Mains, and Service Lines. There are various types of layouts for water distribution
network, suiting to different types of populations, communities and terrains. They can be
classified as Serial Network, Branched Network, and Looped Network. The design aspect of
water distribution system is an important area to tackle with. The designer decides about a
particular type of design depending upon the various controlling factors, the various options
are listed as System-Wide Master Planning, Transmission Main Design, Sub-division Design,
Rehabilitation and Strengthening .There are many methods for optimization of water distribution
networks. All methods of optimization are not fully successful but have some drawbacks too.
The designer must take into notice the various limitations/drawbacks before deciding a particular
type of optimization method. There are certain myths about the optimization methods which
are listed as Optimization models do not provide solutions to practical problems, Solutions
obtained by optimization approaches do not give better solution that those obtained using
traditional approaches, Optimization approaches are too difficult to use in practice, Practicing
engineers are not comfortable with optimization approaches Optimization methods are not
well suited for strengthening and expansion of existing looped water distribution network .Even
though mankind has known transportation of water through rivers, canals, streams etc. for
many centuries, the transportation of water through pipelines and its distribution through
networks is of recent origin. Even though developed nations have piped water supply, developing
nations also have started providing water through pipe networks. Even consumers in remote
villages have started getting water, if not in their residences, at least near to it. Thus, water
distribution networks have been a part of modern living.
Keywords: Water, Distribution, Network, Optimization, Loop, Method, Solution, Pipe, Series,
Link, Rural, Urban, Flow, Reliability, Design, Flexibility, Cost, Performance.
INTRODUCTION
Water distribution system is an integral part
of present society and civilization. The system
supplies water for different uses such as
domestic, public, commercial, industrial and fire
fighting purposes. Presently,water distribution
system includes the following features
1. Collection and Storage:Collection and
storage include construction of dams, ponds,
lakes, reservoirs, wells, bawlis etc.
72
Fig. 1
processed water.
2. Ground Water Distribution Systems
Water distribution systems for small
population can use ground water as source, if
sufficient quantity of ground water of good quality
is available (Fig.2). [1]
R: Reservoir
D: Distribution network
If the system is large and the terrain is
uneven, the services of booster pumps are,
generally, availed to tackle the problem.
Although, the consumers within a community are
close to one another, the communities
themselves are spread wide apart and the
source is also far away. It is usually not possible
to provide mains of enough capacity to provide
fire requirements.
3.Purchased Water Distribution Systems
Fig. 2
W: Well
D: Distribution network
WF: Well Field
However, as the population grows and water
consumption exceeds, additional source of water
becomes a necessity. Sometimes, water can be
used directly without any treatment but treatment
is necessary to remove hardness and other
impurities. If the ground water is available at
several locations, wells can be spaced around
to avoid the need of large transmission mains.
However, if large quantity of water is available in
one area, water from all wells in this area, termed
as well field, is collected and treated at one
location. This reduces operating costs and
allows a better control on water quality but
requires large transmission mains.
2. Regional Rural Water Distribution
Systems
When ground water is scarce or of poor
quality, several rural communities in a region are
grouped together and are served through a
system that is termed a Regional Rural Water
Distribution System (Fig. 3). [1]
Fig. 4
Fig. 3
Fig. 5
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S: Source
T: Treatment plant
P: Pump
R: Reservoir
D: Distribution network
RW: Raw Water
TW: Treated Water
They are usually long, large in diameter
(>400 mm) and carry large quantities of water.
They carry water from one point to another; have
few side connections except when they supply
water to bulk consumers or service reservoirs.
Fig. 7
Fig. 8
Fig. 6
S: Source
A, B, C, E, F: Nodes
D: Sink
G: Node/Sink
75
selected direction.
Pipes in distribution networks may be of cast
iron, steel, concrete, asbestos, cement or PVC.
Pipes may be un-lined or lined with cement
mortar.
Valves are provided in water distribution
networks to
(a) Control flow.
(b) Shut off pipelines during repairs or
replacements.
(c) Drain
(d) Reduce
(e) Maintain
(f)
in
selected direction.
air
from
pipelines
at higher
During filling.
(f)
DESIGN PROBLEMS
The design of water distribution system is
classified into four types of design problems
1. System Wide Master Planning
Master planning of system to determine the
general layout of water distribution system, like
locations, sizing and construction schedule of
major elements over a period that may be as
long as 10 years. The pipe diameters are large
(>400 mm) and are mainly controlled by future
demand of domestic and industrial nature. Since
the construction will be in stages, modification
in pipe sizes is permitted at the time of installation,
taking into consideration the latest data
regarding water demands.
2. Transmission Main Design
Using the master plan as a guideline, the
design of transmission mains is finalized.
The design has better idea of the temporary
demands, routes along which the pipes will be
laid, and the field data regarding different lengths
and levels. Since the pipe sizes are large, fire
flows are usually satisfied. However, the behavior
of an element during peak flows must be
considered.
3. Sub - division Design
Considering different sub-divisions, such as
residential, industrial and commercial and the
corresponding demands, the sizes of pipes within
the sub-division are decided. The transmission
main network should be studied deeply and the
pressure obtained at junction points, connecting
a sub-division to the transmission main system,
should be used in the design of pipes in the subdivision. Pipe sizes are controlled by
simultaneous peak flow without any interruption
77
REFERENCES
1.
2.
3.
4.
5.
6.
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79
ABSTRACT
Corruption today is the greatest enemy of good governance and causing harm to democracy
and development. People in India must bow their heads in shame as they are living in a country
where every organ, activity and functions are conducted with corrupt practices. Whatever the
number of institutions we create, they themselves become other dens of corruption. It seems
that good governance and corruption cannot co-exist. If it cannot which is that element
supporting such corrupt practices? The Answer is SECRECY. Secrecy in Government is the
most important cause of corruption, inefficiency and irresponsiveness and an enemy to good
governance. The purpose of this study to create the awareness in people about RTI. RTI has
enabled people to participate in the process of development which has resulted in education
of corruption and established an open and participatory governance system. Hence, in effect,
RTI Reflects and promotes the social income interest of every citizen, particularly the poor,
who are receiving the benefits of development as per their entitlements. RTI is potential tool
which indicated with a view to expediting the process of human development.
Keywords: Right to information, Good governance
INTRODUCTION
Right to information (RTI) is harnessed as
a tool for promoting participatory development,
strengthening democratic governance and
facilitating effective delivery of socio-economic
services. In the knowledge society, in which we
live today, acquisition of information and new
knowledge and its application have intense and
pervasive impact on processes of taking
informed decisions, resulting in overall
productivity gains. The Constitution of India has
guaranteed (u/s 19) the freedom of expression
and speech. Even then, a citizen had no legal
right to know about the details of public policies
and expenditures. And, therefore, it was not
possible for a common man to observe and
scrutinize the public actions with a view to
developing an understanding about the outcome
of public activities and/or providing feedback for
rectifying the deficiencies in policy planning and
the execution of programs.Despite planned
efforts of six decades, over one-third of the total
population is illiterate, poor and un-healthy. In
order to rectify the deficiencies in the
80
ELEMENTS
OF
GOOD
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2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
http://www.iitbbs.ac.in/pdf/RTI-ACT.pdf
CONCLUSION
Right to know, as a tool to access public
held information, has significant bearing on good
governance,
development
and
the
implementation of flagship programs for
alleviation of poverty. Indias economy in the last
three years has grown at unprecedented high
rate of about 8 per cent per annum, which also
coincides with RTI induced good governance.
This is unprecedented in Indias history of
development. A common man, like an elected
Member of Parliament (MP), is empowered to
seek accountability of the Government in terms
accepted policies and approved budgetary
expenditures. The Central and the State
Information Commissions have played a critical
role in enforcing the provisions of the Act as well
as educating the information seekers and
providers. Without their statutory interventions,
including use of penal provisions against the
public authorities, the benefits of RTI could not
have been reaped by the citizens and the society.
The implementation of the law on right to know
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87
ABSTRACT
Badminton is still an amateur game, but the level of commitment shows in terms in number of
hours of training by the subjects. The study suggests a professional attitude to the game at
this level. The information obtained from this study provides a platform for further research.
The pressure and personality rate in the term of competitive exposure time and training time
should be determined. Despite the limitations of this study the results provide a useful insight
into the nature, site and variables. It was an intensive attempt to excessively examine such
variables.
Keywords: Stress, Personality, Traits, Sports
INTRODUCTION
In modern era, games and sports hold a
prominent place in life. Millions of people
participate in sporting activities and spend billions
of rupees or dollars annually on sports related
activities and equipment. The impact of sports
on modem society has made it clear that sports
are a very legitimate field of academic study.
Modem thinkers in education now a days
emphasize that the best individual is one, who is
physically fit, mentally sound and sharp,
emotionally balanced and socially well adjusted.
In modern time, competition in sports needs
psychological preparation of term or individual
players. It is important as teaching the different
skills of a game on scientific lines. It is said that
modern warfare is not fought and won with
psychological strategies, similar is the case with
modern sports. Sports psychology suggests that
teams prepared not to play the game but also to
win the game. Most of the coaches agree that
physical characteristics, skills and training of the
players are extremely important but they also
indicate that good mental preparation for
competition is a necessary component for
success.
88
players.
Psychological variables are the most
important contributing factors for better
performance in all sports and games, including
Badminton. The game of Badminton requires
considerable amount of mental alertness and
mastery of skill.
Badminton is one of the most sports in the
world. It is an enjoyable, social sport that can be
played from childhood to old age, either at a
recreational level or as a competitive sport.
Badminton is an individual non contact sport
requiring jump, lunges quick changes in direction
and rapid movements from wide variety of
postural position. At high level its demands quick
reactions speed coordination and a relative good
physical condition. While basic techniques are
easy to learn, a lot of skill and training is
demanded to reach high level of play. In
tournament there is typically more than one game
a day-often, a player may participate in singles,
doubles and mixed doubles competitions, which
can result in many hours of badminton
concentrated on only a few days. Extended play
sometimes results in mental tiredness, which are
relatively common in badminton.
Badminton is one of the fastest and most
strenuous games that can be played. Singles is
particularly exhausting not only because of the
amount of court space that has to be covered in
a split second but shots have to be taken low
and high at full stretch. It is this never-ending
use of stomach muscle. The running directly
backwards twice is as hard as running forward
and the constantly needed change in direction
of movement that causes the body to serge for
a rest.
The aim of present study was to compare
stress and personality traits between boys of
sports college, sports hostel and stadium
trainees Badminton players. The Badminton
player must be stress free. The team which is
persistent usually comes out on top. There is
no substitute for practice. It takes all players
working together to become successful.
Personality of a player in other words how a
player reacts to a given situation is very
important in a competitive situation.
Development of good personality helps the
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LIMITATIONS
Questionnaire research has its limitations.
As such bias if any pertaining to the subject be
considered as a limitation of the study.
The tests were administered at different
points considering the availability of the subjects,
their mood states which might have had
influenced their response pattern on a particular
scale/instrument. This was another limitation
imposed on the investigation inadvertently.
Certain factors like diet, rest, sleep etc. were
beyond the control of the investigation and were
considered as limitations of the study.
As the subjects come from different socioeconomic groups, their dietary habits, life style,
routine of study and play were different which
were considered as limitations of the study.
No special motivation technique was used
during the test, therefore the difference that may
have occurred in performance due to lack of
motivation was recorded as the limitation of the
study.
3.
4.
5.
6.
7.
HYPOTHESIS
It was hypothesized that there will be
significant difference between college and
university men and women cricket players on all
the seven selected psychological variables using
total sample.
FINDINGS
The ultimate goal of research in physical
education will help coaches and physical
educators to train their athletes and player based
on new concept to improve their performance in
competitions. A unique aspect of the work is that
it includes recommendations for the practical use
of research findings. Sports psychology is one
of the very important factors to improve
performance in competitions. The present study
will provide the following significant contribution
on the above concept to the field of physical
education and sports:The study may determine the effect of
personality and stress on performance of
Badminton Players. The results of the study may
reveal the Psychological status of Sports
College, sports hostel and stadium trainees
90
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*Address
for
ABSTRACT
In this study, adsorption of methylene blue (MB) dye onto clean rice husks (CRH) and acidmodified CRH was investigated with respect to the contact time, MB concentrations, acid
concentrations and acid types used in the acid modification processes. The results indicate that
the acid modification process reduces the MB sorption efficiency from 98% for CRH to 67% for
NRH (nitric acid treated rice husk), 59% for HRH (hydrochloric acid treated rice husk) and 55%
for SRH (sulfuric acid treated rice husk). In order to investigate the adsorption mechanisms,
four kinetic models, i.e., pseudo-first-order, pseudo-second-order, Elovich and intra-particle
diffusion models were fit to the experimental results. The characteristic parameters and correlation
coefficients for each kinetic model were determined. The fits of the kinetic results from the
kinetic equations were compared with the experimental data. The results indicate that the acid
modification process changes the MB adsorption mechanism. Langmuir, Freundlich, Temkin,
Redlich-Peterson (RP), and Langmuir-Freundlich (LF) isotherm models were also employed to
analyze the equilibrium data, and the correlations of the experimental data to the isotherms was
examined. The LF isotherm was found to best represent the data for MB adsorption onto CRH.
The separation factor revealed the favorable nature of the isotherm to the MB-CRH system.
Keywords: Methylene Blue , Rice Husks, Waste Water, Isotherm Models, Kinetics
INTRODUCTION
Many industries, such as the cosmetics,
leather, carpet, dye manufacturing and textile
finishing industries, use dyes to color their
products. They also consume a lot of clean
water, which becomes colored wastewater,
poured into the environment where trade
wastewater measures are not in place [1,2] . The
effluents of these industries can cause local
environmental problems by significantly affecting
photosynthetic activity in aquatic life because of
the reduced light penetration. The effluents may
also be toxic to some forms of aquatic life
because of the presence of metals, chlorides,
etc., in them [3,4] In addition, introducing dye
compounds into the aquatic environment is
aesthetically displeasing. Because of these
negative impacts, there is a need to develop decolorization methods that are effective and
suitable for industrial use. Currently, the major
methods for dye and color removal involve
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(1)
(3)
(4)
(5)
(6)
(7)
93
exp (-
qt)
(8)
ln( t + to) 1/
(ln to)
(9)
ln (
)+1/
ln t
(10)
94
(11)
(12)
(13)
(14)
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(15)
(16)
(17)
95
Fig. 2- Comparison between the measured and modeled time profiles and comparison of kinetic
models in predicting qt for the adsorption of MB onto CRHs modified by various acid concentrations.
96
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[63]
and
decreased
. It was observed that
as the acid concentration increased (Table
1).This suggests that the adsorption surface of
the absorbents was affected such that the
available adsorption sites lessened as the acid
concentration increased. The simulations using
the intra-particle diffusion
Fig 4- Comparison between the measured and modeled time profiles and comparison of kinetic
models in predicting qt for the adsorption of MB onto various pretreated rice husks.
98
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MB onto CRH did not follow the pseudo-firstorder sorption rate expression of Lagergren at
high initial MB concentrations.
The pseudo-second-order kinetic constants
for adsorption of MB onto CRH are shown in
Table 3. The correlation coefficients for the
pseudo-second-order kinetic model were close
to 1.0 for all cases. In addition, the experimental
data and the simulations using the pseudosecond-order kinetic equation for the adsorption
of MB onto CRH are shown in Fig. 6b. By
comparing
Figs. 6a and 6b, it is obvious that for the
entire adsorption period the pseudo-secondorder model fits the experimental data better than
the pseudo-first-order model. This indicates that
the sorption mechanism for CRH is
chemisorption, involving covalent forces through
sharing or exchange of electrons between
sorbent and sorbate [64] .Fig. 6b also shows that
the calculated q values increased with increasing
concentration of MB, presumably due to the
enhanced mass transfer of MB molecules to the
surface of CRH. This observation suggests that
Fig.6- Comparison between the measured and modeled time profi les and comparison of kinetic
models in predicting qt for the adsorption of MB onto CRH at different initial MB concentrations.
100
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[66]
Tables
Table 1- KINETIC PARAMETERS OF THE REMOVAL OF MB FROM AQUEOUS SOLUTION BY THE
CRHS MODIFIED BY VARIOUS ACID CONCENTRATIONS
Acidconc. Pseuodo firstorder
K1 qe
k2
qe
Elovich equation
Intraparticle diffusion
kid
r2
r2
qe
r2
Elovich equation
r2
Intraparticle diffusion
kid
r2
Table 3- KINETIC PARAMETERS FOR THE EFFECTS OF INITIAL DYE CONCENTRATIONS ON SORPTION
OF MB ONTO CRH
102
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2.
3.
4.
7.
REFERENCES
1
10
6.
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12
13
14
15
16
28
29
30
31
32
17
33
18
34
19
35
36
37
38
39
40
20
21
22
23
24
25
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76 : 332340.
41
42
43
44
45
46
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57
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59
60
61
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48
49
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50
63
51
64
52
65
53
66
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*Address for Correspondence: Aashish Tiwari, Research Scholar, Sai Nath University, Ranchi .India
Email ID: aashishtiwaribu@gmail.com
ABSTRACT
In this study, we investigated the relationship between indoor and outdoor concentrations of airborne actinomycetes, fungal spores, and Bacterial Species. Different types of indoor environments
(Two different Canteen area, Institutes auditorium, laboratory, Shopping Mall) and their outdoor
environments (Institutes Outer Building area) were investigated in terms of bio-aerosol contamination. A total of 120 Sample were investigated in Indian Institute of Toxicology Research, Lucknow.
The single-stage / Bio-stage sampler was used for viable bio-aerosol sampling. During the sampling,
indoor and outdoor temperature, relative humidity, and CO2 concentration were measured. Total
bacteria counts (TBC) and fungi concentrations varied on a large scale within and between the
sampling site groups (10103 CFU/m3). The highest TBC levels were measured in Humid less Indoor
area, while the highest mold levels were measured in Canteen, Auditorium. Micrococcus spp., Staphylococcus auricularis, and Bacillus spp. were predominant bacteria species and Penicillium spp.,
Aspergillus spp., and Cladosporium spp. were the most observed mould genera detected in the
samples. Indoor-to-outdoor ratios of the observed fungi counts were calculated as approximately
around one, and for bacteria counts these ratios were higher than one. There was no statistical
difference between indoor and outdoor mould levels, while a significant difference was found between indoor and outdoor bacteria levels (p < 0.001). A significant correlation between indoor CO2
and bio-aerosols indicates insufficient ventilation.
Keywords: Contamination, Indoor Air; Bacteria, Outdoor; Aspergillum; Bio-aerosols; Conventional
methods; Microorganisms
INTRODUCTION
A variety of contaminants responsible for
adverse health effects may be found in indoor
air. Since the beginning of the areas, airborne
biological agents have attracted increased attention due to their diverse immunological activity and widespread occurrence indoors. Fungi
are commonly present in indoor environments
and cause of many diseases. Fungi and bacteria isolated from Canteen with moisture problems
have shown both cytotoxic and immunotoxic
characteristics . Many fungal species of Penicillium, Aspergillus, Alternaria and Cladosporium
have been shown to trigger rhinitis, asthma and
dermatitis. The major pathway of acquisition is
inhalation of airborne fungal spores small
enough in diameter to reach the deeper airways.
108
The sources from which fungi and bacteria derive may have importance in their health effects.
It has been established that most people spend
over 90% of their lives indoors, offices, canteen
for lunch / break-fast where they are exposed to
some indoor environmental factors such as bioaerosols which could influence their health and
physical condition. This has contributed to the
growing interest in indoor microbial studies in
recent years [1-5]. The ubiquitous nature of microorganisms in the atmosphere has contributed
to the biological contamination of indoor environments, which is mostly caused by bacteria,
moulds and yeast. They can be dangerous as
pathogenic living cells but they can also secrete
some substances harmful to health. These are
different kinds of toxic airborne metabolism prodwww.ijsir.co.in
itself to building materials and producing microbial products and ultimately causing adverse
health effects. Air sampling of microorganisms
is a popular method of conducting microbial examinations, as it allows a direct toxicological
evaluation. These results can be related to a
concentration expressed in colony forming units
per cubic meter. Sometimes information might
even be available on a particle which allows for
an estimation of how deep those particles may
penetrate into the lungs of a human being.
Micro-organisms are generally not equally
distributed in indoor air. They mostly occur in
clouds and are often overlooked in air measurements, especially if the microbial damage is hidden by paneling, walls, etc. Another reason for
false-negative results obtained by air measurements is that fungal spores are not released during all the stages of its growth. In this case, other
techniques are helpful, for example, the sampling of household dust, the sedimentation
method or direct sampling from surfaces. The
differentiation of bacteria is performed by a biochemical method as a rule, whereas in most
cases the differentiation of molds is done microscopically, especially when the forms of spores
need to be detected.
On many occasions, the growth behavior
and patterns on different nutrient agars also
have to be evaluated. Non-sporulation species
have to be triggered to produce spores, otherwise sterile mycelium will result, which means
they cannot be named by genera or even species. Methods of genetic fingerprinting are still
in their early stages and only available for some
genera or species. In the meantime enzymatic
tests have become available to decide between
mold growth and normal quantities on building
surfaces. Searching for hidden mold growth can
be a very difficult task. An example of this is if
adverse health effects like the fungal syndrome
is observed. The fungal syndrome is characterized by the occurrence of unspecific symptoms.
The analysis of microbial volatile organic compounds or even the use of specially trained
sniffer dogs are some of the methods used to
detect hidden mold growth. However, these methods have not been scientifically evaluated [22] .
The extermination of microorganisms is of110
ten carried out, but this procedure is not sufficient because non-viable spores for example,
keep their allergenic potential. The acuteness
of the rehabilitation procedures is normally considered according to the extent of the microbial
damage. Adverse health effects are supposed
to be linked with microbial growth in indoor areas and are mostly related with mold growth.
Allergies is a predominant condition which has
to be mentioned, followed by toxic alveolitis and
reactions like (allergic) bronchitis, chronic obstructive pulmonary disease, as well as the aggravation of asthma. Infections by molds and
bacteria are very rare, but persons with immunodeficiency are especially susceptible to fungal infections. It has been found that spores of
fungi contain fungal toxins (mycotoxins), which
are well known from food contaminations. It has
however not been confirmed whether these mycotoxins show toxic effects if fungal spores are
inhaled.
On the whole, the dose relationship between the concentration of microbial particles
already mentioned and the adverse health effects described, is not very well established.
When sanitary effects are observed, the susceptibility of the individual is very often crucial.
The result of this is that guidelines concerning
microbial products in indoor areas are sparse
and mostly not scientifically sound. In non-industrial indoor environments, the most important
source of airborne bacteria is the presence of
human. Specific activities like talking, sneezing,
coughing, walking, washing and toilet flushing
can generate airborne biological particulate
matter. In addition food stuffs, house plants and
flower pots, house dust, pets and their bedding,
textiles, carpets, wood material and furniture
stuffing, occasionally release spores of Alternaria, Aspergillus, Botrytis, Cladosporium, Penicillium, Scopulariopsis into the air. Although indoor
environments are considered to be protected,
they can become contaminated with particles that
present different and sometimes more serious
risks when their concentrations exceed recommended maximum limits than those related to
outdoor exposures. Human beings build the
home to be protected in the environment.
Indoor air pollution can be as much more
worse than that of outdoor air, it can cause a
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utes is often not possible, whereas air concentrations usually vary widely over time. Nevertheless, counting culturable microorganisms is potentially a very sensitive technique, allowing the
identification of many different species. Traditional culture methods have proven to be of limited use for quantitative assessment of exposure.
Culture-based techniques thus usually provide
qualitative rather than quantitative data. The
former can, however, be important in risk assessment, as not all fungal and bacterial species
pose the same hazard. Furthermore, a qualitative comparison of indoor and outdoor micro biota
(in samples collected at the same time) may provide important information about potential indoor
sources of contamination. More extensive reviews of techniques for sampling and culturing
microorganisms are available. The Sample is
collected from Bio stage Sampler, at a flow rate
of 28.3 liter / minute. There were collected 50
liters of air with Bio stage sampler by using for
two minutes. The instruments were placed one
meter above the floor and in two meter distance
in every sampling in various times.
cation. Grams staining is used for the identification and especially for classification of bacteria in their gram positive, or gram negative bacteria. For the slide preparation a drop of stain
were put on the clean slide then picked-up a
small tuff of fungus. Then gently teased the tuff
to separated the hyphae by cool needle and mix
with the Lacto phenol cotton blue stain properly
for Fungi.
Data recorded for the concentration of microbes, bacteria and fungi in Indoor and Outdoor area
Sr. no.
Sample area
Morning
session
(10:00-12:00pm)
After
lunch(2:30pm)
Morning session
(10:00-12:00pm)
After
lunch(2:30pm)
Canteen
1
sample -1
Canteen
sample-2
Canteen
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89
84
102
27
52
101
25
59
113
Canteen
3
sample-3
81
106
38
43
Canteen
sample- 4
76
99
26
44
41
58
34
52
33
59
37
65
41
67
45
87
Office sample5
1
Office sample-
2
Office sample-
3
Office sample-
34
62
34
54
Canteen
sample-5
41
71
31
62
Canteen
10
sample-6
23
37
27
56
11
Canteen
sample-7
31
59
68
105
12
Canteen
sample-8
32
56
42
85
63
Canteen
13
sample-9
24
43
35
14
Canteen
sample-10
23
52
31
51
24
46
23
67
20
48
32
85
22
54
34
87
Office sample 15
6
Office sample-
16
7
Office sample-
17
8
Office sample-
114
18
16
29
23
42
19
Office sample10
21
43
27
49
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Average
65
85
55
90
Minimum
16
29
23
42
Maximum
89
106
68
105
91
95
40
66
sample-2
98
100
31
63
Average
93
97
35
64
Minimum
91
95
31
63
Maximum
98
100
40
66
Auditorium
20
sample-1
Auditorium
21
Sample area
Bacterial concentration(Colony/plate)
(Outdoorsample)
Morning session
(10:00-12:00pm)
After
lunch(2:30pm)
Morning session
After
(10:00-12:00pm)
lunch(2:30pm)
Outdoor- 1
37
41
57
59
Outdoor-2
67
56
65
79
Outdoor-3
65
54
74
94
Outdoor-4
46
67
67
82
Outdoor- 5
70
88
78
92
Outdoor-6
64
89
64
85
Outdoor-7
56
76
85
97
Outdoor-8
74
92
Outdoor-9
54
61
64
67
10
Outdoor-10
65
72
53
68
Average
60
70
80
90
Minimum
37
41
53
59
Maximum
74
92
85
97
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76
87
115
In this study, an attempt was made to determine the composition and variability of airborne
fungal spores in a comprehensive manner by
synchronous use of non-viable and viable sampling method. The study was of a kind that first
volumetrically assessed the cultivable airborne
fungal spore in the region and determined its
relationship with the meteorological factors.
bacteria after
spp. etc. were found during sampling. The ascospores and basidiospores that constitute a significant part of the airborne fungi were recorded
only by the non-viable sampling. The ratio of total airborne fungal spores to cultivable mold was
obtained in the range of 0.19 to 4.16. The spores
of Ascomycetes and Basidiomycetes members
are visible in light microscope, but they are unable to grow in laboratory culture media. For this
reason, decrease in concentration of cultivable
mold compared to total fungal spores is generally anticipated while analyzed by light microscopy.
CONCLUSION
This study clearly indicates that there is
significant assessment of the indoor and outdoor
airborne bacteria and fungi. Airborne fungal and
bacterial concentrations in auditorium, offices,
canteen were lower than in the other facilities of
the outdoor area of building.
A large range of different bacteria including
Actinomycetes, mesophilic bacteria, Mycobacteria, gram-negative bacteria, and thermopile bacteria were present in canteen, which is specific
for indoor air quality. The moisture damage affects diversity of microbial concentration. In the
moisture-damaged building, the microbial diversity was higher in canteen, offices and other indoor area. The measurements of airborne microbial concentrations during four consecutive
months showed the variation of microbial levels
due to climatic conditions.
The results showed that the average fungal concentration was 80 CFU/m3, similarly the
average concentration of bacteria was 60 CFU/
m3 which was lower than the fungi concentration
in outdoor area and in indoor area the average
fungal concentration is 90 CFU/m3 in comparison to bacterial concentration is 65 CFU/m3.So
the result is the concentration of fungi is higher
than the bacteria in indoor and outdoor area.
54:48796.
3.
4.
5.
6.
7.
8.
9.
10.
11. Jones A, Harrison M. The effects of meteorological factors on atmospheric bioaerosol concentrationsa review. Sci Total Environ 2004;
326:15180.
12.
13.
Abdel Hameed A, Khoder M. Suspended particulates and bioaerosols emitted from an agricultural non-point source. J Environ Monit
2001;3:2069
14.
Griffin, 2007 Griffin, D.W., 2007. Atmospheric movement of microorganisms in clouds of desert dust
and implications for human health. Clin. Microbiol.
Rev., 20: 459-77.
REFERENCES
1.
15.
2.
16.
Heldman DR. Factors influencing airborne contamination of foods: a review. J. Food Sci 1974;
www.ijsir.co.in
117
Beggs CB. The Airborne Transmission of Infection in Hospital Buildings: Fact or Fiction? Indoor
Built Environ 2003;12:9-18.
18.
118
20.
21.
www.ijsir.co.in
ABSTRACT
Prediction and modeling of T-cell epitopes of Nipah virus antigenic proteins nucleocapsid,
phosphoprotein, matrix, fusion, glycoprotein, L protein, W protein, V protein and C protein
followed by the binding simulation studies of predicted highest binding scorers with their
corresponding MHC class I alleles were done in this study. ProPred1 tool was used to predict
the promiscuous MHC class I epitopes of viral proteins. 3D structures of epitopes were built
with the help of PEPstr server. Molecular dynamics simulation studies were performed through
the NAMD graphical user interface embedded in visual molecular dynamics. Epitopes IRTIAAYPL
and NPTAVPFTL of Matrix Protein and W-protein have lowest binding energy and highest
score with HLA-B*2705 and HLA-B*5101 MHC class I allele, respectively. These predicted
peptides are highly potential to induce T-cell-mediated immune response and are expected to
be useful in designing epitope-based vaccines against Nipah virus.
Keywords: Nipah virus, Encephalitis, ribavirin, Immunoinformatics, Nucleocapsid,
Phosphoprotein, Matrix, Fusion, Gycoprotein, L protein, W protein, V protein and C protein,
T-cell epitopes, Peptide- or Epitope-based Vaccine, NCBI, ProPred I, Histocompatibility Complex
(MHC) Molecules, Molecular docking.
INTRODUCTION
Nipah virus (NiV), of the family
Paramyxoviridae [1, 2] and the genus Henipavirus,
is a zoonotic virus that causes outbreaks of fatal
encephalitis in humans [3]. The human Nipah
virus (NiV) infection was first recognized in a
large outbreak of 276 reported cases in
peninsular Malaysia and Singapore from
September 1998 through May 1999[4, 5, 6, 7, 8]. The
virus was first isolated from a patient from Sungai
Nipah village in Malaysia and the name Nipah
was first introduced according to the name of
that village. It was also identified in India for the
first time in 2001 and second time in 2007.
Unfortunately, eleven outbreaks have already
occurred in Bangladesh since the first detection
of NiV in 2001, with high mortality rate an
estimated 80% in an average and 100% in some
cases [9]. The most alarming fact is that almost
every year in winter (December to March), the
deadly NiV strikes in the north and western
regions of Bangladesh. Infection with Nipah virus
is associated with encephalitis (inflammation of
the brain). After exposure and an incubation
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period of 5 to 14 days, illness presents with 314 days of fever and headache, followed by
drowsiness, disorientation and mental confusion
[10]
. These signs and symptoms can progress to
coma within 24-48 hours. Some patients have a
respiratory illness during the early part of their
infections, and half of the patients showing
severe neurological signs showed also
pulmonary signs.
During the first NiV outbreak, the virus
infected both pigs and humans, in addition to a
small number of cats, dogs and horses [5, 11]. NiV
possesses a negative-sense, non-segmented
RNA genome that is 18246 nt (Malaysian isolate)
or 18252 nt (Bangladesh isolate) in length [12]. In
Bangladesh, 135 probable or confirmed cases
of NiV infection in humans were identified from
2001 to 2008; 98 (73%) were fatal [7]. There is
no effective treatment and vaccine for Nipah
virus disease, but ribavarin may mitigate the
symptoms of nausea, vomiting, and convulsions.
Vaccination is the most effective of all the
medical interventions to save human and animal
119
Accession
No
ACT32611
Length of
amino acids
532
Phosphoprotein
ACT32612
709
Matrix
ACT32613
352
Fusion
ACT32614
546
Glycoprotein
ACT32615
602
L-Protein
ACT32616
2244
W-protein
449
V-protein
YP_007188
592
NP_112023
456
C-protein
NP_112024
166
120
modeling
of
T-cell
Start
position
474
446
474
168
624
85
201
293
192
125
45
247
45
2087
1567
1564
1537
316
186
186
66
316
40
116
0
Epitope
Allele
SLLNLRSRL
KREMSISSL
SLLNLRSRL
DRETDLVHL
EPYGAAVQL
IRTIAAYPL
IAFNLLVYL
FQKNLCFSL
KQTELSLDL
AQITAGVAL
ILSAFNTVI
RIIGVGEVL
ILSAFNTVI
VLLQAGLKL
TMVDLLSDL
GRHTMVDLL
DPELFALYL
KEEPPQKRL
NPTAVPFTL
NPTAVPFTL
DGDVERRNL
KEEPPQKRL
FCSAPVENL
PDMDLLQAL
MMASILLTL
HLA-A*0201
HLA-B*2705
HLA-A2
HLA-B*2705
HLA-B*5101
HLA-B*2705
HLA-A*0201
HLA-B*2705
HLA-B*2705
HLA-B*2705
HLA-A*0201
HLA-B*2705
HLA-A2
HLA-A2
HLA-A*0201
HLA-B*2705
HLA-B*5101
HLA-B*2705
HLA-B*5101
HLA-B*2705
HLA-B*5101
HLA-B*2705
HLA-B*2705
HLA-B*2705
HLA-B*2705
ProPred
score
3729.239
6000.000
5968.882
2000.000
572.000
6000.000
4702.218
3000
9000
2000
2489.047
2000
3901.211
3475.964
3804.077
30000.000
1522.664
3000.000
880.000
2000
520
2000
3000.000
2000
2000
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Allele
Crystal Structure
(PDB ID)
HLA-A2
1AKJ
HLA-A*0201
1AKJ
HLA-B*2705
1HSA
HLA-B*5101
1E27
Molecular docking
AutoDock 4.2[25, 26] has been used for In-silico
docking of peptides and alleles structure.
Gasteiger charges were added to the ligand and
maximum six numbers of active torsion are given
to the lead compound using AutoDock tool (http:/
/autodock.scripps.edu/resources/adt). Kollaman
charges and salvation term were added to the
protein structure using AutoDock tool. The Grid
for docking calculation was centered to cover
the protein-binding site residues and
accommodate ligand to move freely. During the
docking procedure, a Lamarckian genetic
algorithm (LGA) was used for exible peptide and
rigid protein docking calculation. Docking
parameters were as follows: 30 docking trials,
population size of 150, maximum number of
energy evaluation ranges of 250,000, maximum
number of generations is 27,000, mutation rate
of 0.02, cross-over rate of 0.8, other docking
parameters were set to the softwares default
values.
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Phosphoprotein
Matrix
Fusion
Glycoprotein
L protein
W protein
V protein
C protein
Epitope
SLLNLRSRL
KREMSISSL
SLLNLRSRL
DRETDLVHL
EPYGAAVQL
IRTIAAYPL
IAFNLLVYL
FQKNLCFSL
KQTELSLDL
AQITAGVAL
ILSAFNTVI
RIIGVGEVL
ILSAFNTVI
VLLQAGLKL
TMVDLLSDL
GRHTMVDLL
DPELFALYL
KEEPPQKRL
NPTAVPFTL
NPTAVPFTL
DGDVERRNL
KEEPPQKRL
FCSAPVENL
PDMDLLQAL
MMASILLTL
Allele
HLA*0201
HLA-B*2705
HLA-A2
HLA-B*2705
HLA-B*5101
HLA-B*2705
HLA-A*0201
HLA-B*2705
HLA-B*2705
HLA-B*2705
HLA-A*0201
HLA-B*2705
HLA-A2
HLA-A2
HLA-A*0201
HLA-B*2705
HLA-B*5101
HLA-B*2705
HLA-B*5101
HLA-B*2705
HLA-B*5101
HLA-B*2705
HLA-B*2705
HLA-B*2705
HLA-B*2705
BE
-0.57
-0.72
-1.45
0.01
-2.96
-4.03
-1.88
0.36
2.99
-0.61
-2.28
1.1
-0.86
-1.41
-0.23
0.65
-2.92
1.7
-4.14
-2.53
3.05
-0.11
-2.51
1.86
-1.54
IME
-11.61
-12.05
-12.49
-10.73
-11.02
-12.68
-11.42
-10.38
-8.04
-8.37
-11.22
-8.44
-9.81
-11.26
-10.08
-9.49
-12.17
-9.64
-11.3
-9.69
-7.99
-11.45
-10.87
-7.98
-11.38
IE
-6.7
-5.25
-4.94
-6.03
-6.84
-6.47
-4.85
-4.64
-4.27
-3.82
-6.9
-3.43
-4.73
-6.49
-6.47
-6.91
-8.04
-6.1
-7.46
-4.23
-4.52
-3.99
-7.44
-5.07
-3.75
TorE
11.04
11.34
11.04
10.74
8.05
8.65
9.55
10.74
11.04
7.76
8.95
9.55
8.95
9.84
9.84
10.14
9.25
11.34
7.16
7.16
11.04
11.34
8.35
9.84
9.84
VdwE
-10.74
-9.77
-11.75
-10.69
-10.79
10.74
-10.82
-9.12
-7.74
-8.32
-11.71
-7.99
-9.23
-9.53
-10.65
-8.65
-10.74
-7.44
-10.76
-8.89
-7.44
-9.43
-6.23
-6.28
-11.43
EE
-0.87
-2.29
-0.74
-0.04
-2.23
-1.94
-0.6
-1.26
-0.3
-0.04
0.49
-0.45
-0.58
-1.73
0.57
0.84
-1.43
-2.2
-0.54
-0.8
-0.55
-2.02
0.45
-1.7
0.15
BE: Binding Energy; IME: Intermolecular Energy; IE: Internal Energy; TorE: Torsional Energy;
VdwE:Vdw-lbDesolv Energy; EE: Electrostatic Energy.
Fig. 2: Docked W protein peptide NPTAVPFTLHLA-B*5101 allele (PDB Id: 1E27) complex
Fig. 1: Docked Matrix protein peptide IRTIAAYPL
- HLA-B*2705 allele complex depicting position
of amino acids along with the formation of two
Hydrogen bonds(shows as dotted line) with GLY1
and LYS243 residues of Protein 1HSA
122
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
Tang H., Liu X.S., Fang Y.Z., Pan L., Zhang Z.W. et
al. The epitopes of foot and mouth disease. Asian
J. Anim. Vet. Adv. 2012a; 7: 1261-1265.
123
16.
17.
18.
19.
Tang H., Liu X.S., Fang Y.Z., Pan L., Zhang Z.W. et
al. Advances in studies on vaccines of foot-andmouth disease. Asian J. Anim. Vet. Adv. 2012; 7:
1245-1254.
20.
21.
124
23.
24.
25.
26.
27.
28.
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ABSTRACT
Today the environmental degradation is a matter of great concern before human society. Both
developing as well as developed countries are facing severe environmental problems. In the
developmental process man has been ruthlessly exploiting natural resources and polluting
natural environment. The major problem of our present world is environmental degradation.
To combat this problem, we need environmentally sensitive and aware people. The present
investigation was conducted to find information about the level of environmental awareness
of B.Ed students in Dehradun district of Uttarakhand (India). It was found that their level of
environmental awareness was remarkable high.
Keywords: Environmental Awareness, Degradation, Pollution, Uttarakhand
INTRODUCTION
According to the Universal encyclopedia, the
sum total of all conditions, agencies and influences,
which affect the development, growth, life and
death of an organism, species or race is called
environment. Duglass and Roman Holland opined
that environment is a word which describe, in the
aggregate, all of the external forces, influences and
conditions which affect the life, nature, behavior
and the growth, development and maturation of
living organism. Indeed environment covers all the
outside factors that have acted have been acting
on the living being in general and humans in
particular since they began life.
The environment for man is its surroundings
on the earth. In the known universe, the earth is
only planet that is gifted with life by the Absolute. It
is mans supreme duty and responsibility to protect
the environment. Man cannot afford to ignore
environmental degradation. It is a matter of survival
or suicide. The United Nations conference on
environment and development held in Rio De
Janerio in 1992, known as Earth Summit brought
the issue of rapid environmental degradation and
climate change to the center stage and highlighted
the reasons for this and called upon the world
community to take immediate suitable steps. Same
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2.
3.
Significance
Level
Nonsignificant at
0.05 level
Sr. No.
Statistics
Value
Sample Size
300
Range
51
Mean
43.76
Median
43.84
Mode
43.23
Quartile Deviation
2.39
P10
37.70
P90
47.80
SD
3.74
10
Skewness
-1.08
11
Kurtosis
0.2366
Significance
Level
Nonsignificant
at 0.05 level
128
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Significance
Level
Non
significant
at 0.05 level
2.
3.
4.
5.
6.
Rural
male
Rural
female
129
13.
8.
9.
11.
130
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ABSTRACT
The primitive man fought against the forces and creatures of nature to protect him. The man in
the Stone Age struggled for security by taking shelter in a cave. Gradually, security was
strengthened by the formation of groups within which, all its members shared the common
risks. With the passage of time, forms of security changed to meet particular needs. Man
derived security from the possession of land and livestock. It was agricultural economy in
India, which gave rise to the system of joint family which was the main and often the sole form
of security in sickness and old age. It also assured the basic education to the children. The
principal function of life insurance is to protect against the financial consequences resulting
from the loss of human lives and to provide a systematic method of accumulating a fund for
educating children, meeting financial emergencies and finding old age security and other
benefits including tax saving and other welfare measures. Life insurance has a socially and
economically stabilizing influence.
Keywords: Insurance, Agricultural Economy, Financial Sickness
LIFE INSURANCE AND ITS PROVISION OF INBUILD SECURITY
The urge for protection led to the invention
of insurance. Life insurance policies are the
instruments of social security for the welfare of
individuals. In todays uncertain world it has
earned paramount importance and is one of the
basic necessities of life. With the arrival of human
life on Earth, the problem of want or poverty has
haunted human beings, in some or the other
form; and they always made efforts to secure
relief from it. The quest for security and freedom
from want and distress has been the unfailing
urge of man through ages. Thus, right from the
cave age till date, the story of evolution of
mankind is in fact a saga of continuous search
for security. Though centuries have passed but
these problems remained the same, in context
to the changes in economic and social
circumstances.
EVOLUTION OF LIFE INSURANCE AND
SEARCH FOR SECURITY
The primitive man fought against the forces
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http://en.wikipedia.org/wiki/Insurance
2.
http://www.economywatch.com/indianeconomy/
india-insurance-sector.html
3.
4.
5.
133
*SHUKLA S.P.1, SACHAN R.1, DWIVEDI L.2, SHARMA K.J.2, YADAV V.P.3, SINGH N.B.1
Institute of Engineering and Technology, Lucknow, India, 2Research Scholar, Sai Nath University,
Ranchi, India, 3Central Pollution Control Board, Delhi, India
ABSTRACT
This paper presents air quality data interpretation and air quality index (AQI) prevailing in 13
districts of Uttar Pradesh during period of 2001 to 2009. The mathematical function for calculating
sub-indices is based on IND-AQI and USEPA. A maximum operator calculation mode is used to
determine the overall AQI. The air pollutants included in the AQI are SO2, NO2, SPM, PM10,
PM2.5, NH3, CO, C6H6, O3, Pb, Hg, Ni, As and benzopyrene. The data show that air quality is worst
in winter months because of SPM, PM10 and PM2.5. Air Quality generally improves in monsoon
months because of washout of air pollutants with rainfall. Maximum AQI variation is found in
Ghaziabad, Agra and Firozabad whereas minimum AQI variation is found in Anpara, Gajraula
and Jhansi.
INTRODUCTION
Air pollution has emerged as a major challenge,
particularly in urban areas. The problem
becomes more complex due to the multiplicity
and complexity of the air polluting source mix
(e.g., industries, automobiles, generators,
domestic fuel burning, road side dusts,
construction activities, etc.) [1]. A human need air
for respiration. An adult at rest breathes 16
respirations per minute- approximately 5 m3/h
(lungs volume 4-6 L), with harder work the rate
is 3-6 times more (15-30 m3/h). Poor air can have
adverse impact on our quality of life and can
damage the fabric of building and sensitive flora
and fauna. Air pollution is the accumulation of
hazardous substances into the atmosphere that
danger human life and other living matter [2].
Outdoor PM air pollution is estimated to be
responsible for about 3% of adult
cardiopulmonary disease mortality, about 5% of
trachea, bronchus and lung cancer mortality, and
about 1% of mortality in children from acute
respiratory infection in urban areas worldwide.
This amounts to about 0.80 million (1.2%)
premature deaths and 6.4 million (0.5%) lost life
years [3]. The World Health Organization reports
that in 2012 around 7 million people died - one
in eight of total global deaths as a result of air
134
135
Index
Descriptor Categories
Health Effects
0-50
Good
51-100
moderate
Unusually
sensitive
people
may
experience
respiratory symptoms
101-150
151-200
Unhealthy
201-300
Very Unhealthy
significant
increase
in
respiratory
symptoms,
respiratory
symptoms
301-500
Hazardous
S.
No.
1.
2.
3.
136
[13]
4.
5.
6.
7.
8.
9.
10.
11.
12.
Particulate
Matter
(Size <2.5 m)
or PM2.5, g/m3
Ozone
(O3),
g/m3
Lead
(Pb),
3
g/m
Carbon
Monoxide
(CO),
mg/m3
Ammonia
(NH3), g/m3
Benzene
(C6H6), g/m3
Benzo(a)Pyrene
(BaP)
particulate
phase
only,
3
ng/m
Arsenic (As),
ng/m3
Nickel
(Ni),
3
ng/m
Annual
40
40
24 Hours
60
60
8 Hours
1Hour
Annual
24 Hours
8 Hours
100
180
0.50
1.0
02
100
180
0.50
1.0
02
1Hour
04
04
Annual
24 Hours
100
400
100
400
Annual
05
05
Annual
01
01
Annual
06
06
Annual
20
20
Study Area
Study area for the calculation of AQI is Uttar
Pradesh where ambient air quality is monitored
in 13 districts. Uttar Pradesh is situated between
24N-30N and 77E-84E with a population of
200 million people. The state is spread over a
total area of 243,286 km 2. Three dominant
seasons, summer (March-June), monsoon (JulyOctober) and winter (November-February) are
observed in the study area with maximum
temperature in summer (more than 45C) and
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S.
Districts
No.
1
Agra
Location of
Land Use
Monitoring Station
Pattern
Tajmahal
Sensitive
Monitoring Days
Monitoring
Agency
Sunday,
Monday, CPCB
Tuesday,
Wednesday,
Thursday, Saturday
Regional Office Bodla
Residential
Monday, Thursday
UPPCB
Nunhai
Industrial
Tuesday, Friday
UPPCB
DIC Nunhai
Sensitive
Wednesday,
CPCB
Saturday
Allahabad
Anpara
Firozabad
Gajraula
Itmad-ud-daulah
Sensitive
Tuesday, Friday
CPCB
Rambagh
Sensitive
Monday, Thursday
CPCB
Square Crossing
Residential
Monday, Thursday
UPPCB
Residential
Monday,Thursday
UPPCB
Anpara Colony
Industrial
Tuesday, Thursday
UPPCB
Renusagar Colony
Industrial
Monday,Wednesday
UPPCB
CDGI
Industrial
Tuesday, Friday
UPPCB
Tilak Nagar
Residential
Wednesday,Saturday
UPPCB
Raza Ka Tal
Residential
Monday, Thursday
UPPCB
Indira Chowk
Residential
Friday, Sunday
UPPCB
Industrial
Tuesday, Friday
UPPCB
Industrial
Tuesday, Friday
UPPCB
Bulandshahar Road
Industrial
Monday, Thursday
UPPCB
Jail Chauraha
Residential
Tuesday, Thursday
UPPCB
Veeranga Nagar
Residential
Saturday, Tuesday
UPPCB
Fazalganj
Industrial
Saturday,Wednesday
UPPCB
Jajmau
Industrial
Tuesday, Friday
UPPCB
Deputy Ka Parao
Residential
Tuesday, Friday
UPPCB
Dabauli
Residential
Monday, Thursday
UPPCB
Vikas Nagar
Residential
Monday,
Jhansi
Kanpur
Tuesday, CPCB
Thursday, Friday
Kidwai Nagar
138
Residential
Monday, Thursday
UPPCB
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10
Khurja
Lucknow
CGCRI
Industrial
Sunday, Thursday
UPPCB
Ahirpara
Residential
Tuesday, Saturday
UPPCB
Talkatora
Industrial
Monday, Thursday
UPPCB
Mahanagar
Residential
Tuesday, Thursday
UPPCB
Kapoor
Hotel Residential
UPPCB
Hazratganj
Commercial
Chandganj
Residential
Monday,Wednesday
Aminabad
Residential
Tuesday,Wednesday, UPPCB
UPPCB
Friday
11
12
13
Meerut
Noida
Varanasi
Begum Bridge
Residential
Tuesday, Friday
UPPCB
Residential
Wednesday, Friday
UPPCB
R.O. UPPB
Residential
Tuesday, Thursday
UPPCB
GEE-PEE
Industrial
Monday, Thursday
UPPCB
Regional Office
Residential
Monday, Thursday
UPPCB
Shivpuri
Residential
Friday, Tuesday
Sigra
Residential
Tuesday, Friday
Computation of AQI
To calculate AQI, first step is the calculation
of sub-indices (I 1 , I 2 ,.I- n ) for n pollutant
variables (X1, X2, .. Xn) and is carried out using
sub-indices functions that are based on air
quality standards and health effect. Each subindex value represents a relationship between
pollutant concentrations and health effect.
Mathematically
Ii= f (Xi),
i = 1, 2..n
Ip =
I HI I LO
(C P BPLO ) + I LO
BPHI BPLO
UPPCB
or equal to Cp
IHI = the air pollution index value corresponding
to BPHI of the pollutant p
ILO = the air pollution index value corresponding
to BPLO of pollutant p
In the second step, aggregation of sub-indices Ii
is used with mathematical function to calculate
overall index (I).
I = F (I1, I2In)
In second step aggregation function F may
be summation or multiplication operation or
maximum operator. In this study, maximum
operator system has been adopted as follows:
Where,
139
140
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www.ijsir.co.in
141
400
320
320
280
280
240
240
400
360
320
320
280
280
240
240
D
EC
JA
N
Months
N
O
V
0
O
CT
SE
P
40
A
U
G
40
JU
L
80
JU
N
80
SE
P
O
C
T
N
O
V
D
EC
120
JU
L
AU
G
120
JU
N
160
FE
B
M
AR
A
PR
M
A
Y
160
A
PR
200
M
A
Y
200
FE
B
AQI
360
JA
N
Months
400
400
320
320
280
280
240
240
AQI
360
200
200
160
160
120
120
80
80
40
40
S
E
P
O
C
T
N
O
V
D
E
C
JU
L
A
U
G
A
P
R
M
A
Y
FE
B
M
A
R
D
EC
N
O
V
O
CT
SE
P
A
U
G
JU
L
JU
N
M
A
Y
A
PR
M
A
R
FE
B
Months
JA
N
JU
N
AQI
M
A
R
400
AQI
D
EC
SE
P
O
C
T
N
O
V
D
E
C
Months
Months
142
N
O
V
0
O
C
T
SE
P
40
A
U
G
40
JU
N
80
A
PR
80
JA
N
120
JU
L
AU
G
120
JU
N
160
FE
B
M
AR
A
PR
M
AY
160
M
A
Y
200
FE
B
200
M
A
R
AQI
360
JA
N
AQI
Months
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400
280
280
240
240
0
D
EC
SE
P
JA
N
0
N
O
V
40
O
CT
40
JU
L
80
A
U
G
80
JU
N
120
M
A
Y
120
A
PR
160
FE
B
160
Months
Months
400
400
320
280
280
240
240
D
EC
N
O
V
O
CT
SE
P
JU
L
A
U
G
JU
N
JA
N
D
EC
N
O
V
0
O
CT
0
SE
P
40
JU
L
40
A
U
G
80
JU
N
80
M
A
Y
120
A
PR
120
FE
B
160
M
A
R
160
A
PR
200
M
A
Y
200
FE
B
AQI
320
JA
N
Months
Months
400
400
360
320
280
280
240
240
Months
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D
EC
N
O
V
O
CT
SE
P
JU
L
A
U
G
A
PR
D
EC
N
O
V
0
O
C
T
0
SE
P
40
A
U
G
40
JU
L
80
JU
N
80
M
A
Y
120
A
PR
120
FE
B
160
JA
N
160
M
A
Y
200
FE
B
200
M
A
R
AQI
320
JA
N
360
JU
N
AQI
360
M
A
R
360
AQI
SE
P
O
C
T
N
O
V
D
E
C
200
JU
L
AU
G
200
FE
B
M
AR
AP
R
M
AY
AQI
320
M
A
R
360
320
JA
N
AQI
360
JU
N
Months
143
400
360
320
280
280
240
240
Months
320
280
280
240
240
D
EC
N
O
V
O
CT
D
EC
N
O
V
O
CT
SE
P
A
U
G
JU
L
JU
N
JA
N
D
EC
0
N
O
V
0
O
CT
40
SE
P
40
JU
L
80
A
U
G
80
JU
N
120
M
A
Y
120
A
PR
160
FE
B
160
M
A
Y
200
A
PR
200
FE
B
AQI
320
M
A
R
360
M
A
R
JA
N
Months
Months
400
400
320
280
280
240
240
D
EC
N
O
V
O
C
T
SE
P
A
U
G
JU
L
M
A
Y
D
EC
N
O
V
O
C
T
0
SE
P
0
JU
L
40
A
U
G
40
JU
N
80
M
A
Y
80
A
PR
120
FE
B
120
M
A
R
160
JA
N
160
A
PR
200
M
A
R
200
JA
N
AQI
320
Months
360
FE
B
360
JU
N
AQI
SE
P
400
360
AQI
A
U
G
Months
400
144
JU
L
JA
N
D
EC
O
CT
N
O
V
0
SE
P
0
JU
L
40
A
U
G
40
JU
N
80
M
A
Y
80
A
PR
120
FE
B
120
M
A
R
160
JA
N
160
JU
N
200
A
PR
200
M
A
Y
AQI
320
FE
B
360
AQI
Months
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280
280
240
240
Months
320
280
280
240
240
D
EC
N
O
V
O
C
T
SE
P
N
O
V
D
EC
D
EC
SE
P
O
C
T
JU
L
A
U
G
N
O
V
Months
JU
N
JA
N
D
EC
O
C
T
0
N
O
V
0
SE
P
40
JU
L
40
A
U
G
80
JU
N
80
A
PR
120
M
A
Y
120
FE
B
160
M
A
R
160
A
PR
200
M
A
Y
200
FE
B
AQI
320
JA
N
360
M
A
R
360
Months
400
320
280
280
240
240
Months
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SE
P
O
CT
JU
L
A
U
G
A
PR
D
EC
N
O
V
SE
P
0
O
CT
0
A
U
G
40
JU
L
40
JU
N
80
A
PR
80
M
A
Y
120
M
A
R
120
FE
B
160
JA
N
160
FE
B
200
JA
N
AQI
320
200
360
M
A
Y
360
M
A
R
400
JU
N
AQI
JU
L
Months
400
400
AQI
A
U
G
JA
N
D
EC
0
O
CT
0
N
O
V
40
SE
P
40
JU
L
80
A
U
G
80
JU
N
120
M
A
Y
120
A
PR
160
FE
B
160
JU
N
200
A
PR
200
FE
B
AQI
320
M
A
R
360
320
JA
N
AQI
360
M
A
Y
M
A
R
400
Months
145
280
280
240
240
D
EC
D
EC
SE
P
O
C
T
N
O
V
320
280
280
240
240
Months
SE
P
O
CT
JU
L
A
U
G
JU
N
JA
N
D
EC
N
O
V
0
O
C
T
0
SE
P
40
JU
L
40
A
U
G
80
JU
N
80
M
A
Y
120
A
PR
120
FE
B
160
M
A
R
160
A
PR
200
M
A
Y
200
FE
B
AQI
320
JA
N
Months
400
400
320
320
280
280
240
240
Months
D
EC
N
O
V
SE
P
O
C
T
JU
L
A
U
G
A
PR
M
A
Y
D
EC
O
C
T
N
O
V
0
SE
P
0
JU
L
40
A
U
G
40
JU
N
80
M
A
Y
80
A
PR
120
FE
B
120
M
A
R
160
JA
N
160
FE
B
200
M
A
R
200
JA
N
AQI
360
JU
N
AQI
360
M
A
R
360
AQI
JU
L
Months
400
400
146
N
O
V
Months
A
U
G
JA
N
D
EC
0
N
O
V
0
O
C
T
40
SE
P
40
JU
L
80
A
U
G
80
JU
N
120
M
A
Y
120
A
PR
160
FE
B
160
JU
N
200
A
PR
200
FE
B
AQI
320
M
A
R
360
320
JA
N
AQI
360
M
A
Y
M
A
R
400
Months
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280
280
240
240
Months
Figure 1: Monthly variation of AQI at Lucknow during 2001-09
D
EC
N
O
V
SE
P
O
CT
JU
L
A
U
G
JA
N
D
EC
0
O
C
T
0
N
O
V
40
SE
P
40
JU
L
80
A
U
G
80
JU
N
120
M
A
Y
120
A
PR
160
FE
B
160
JU
N
200
M
A
Y
200
FE
B
AQI
320
M
A
R
360
320
JA
N
AQI
360
A
PR
M
A
R
400
Months
Overall at all 13 districts of Uttar Pradesh, AQI value decreases from July to October and lies in
good to moderate category due to rain whereas AQI value increases from November to February
and lies in unhealthy for senstive people category to unhealthy category in most of the cities as
calm condition prevails in these months compared to other months. AQI values from March to June
are indicating unhealthy for senstive people category to unhealthy category due to dust storms.
Maximum monthly AQI vaiation is found in Ghaziabad, Agra, Firozabad. Minimum AQI variation is
found in Anpara, Gajraula, Jhansi.
Seasonal variation of AQI
Figure 2 shows seasonal variation of AQI at all five monitoring stations of Lucknow city based on
available data for the period 2001 to 2009.
Talkatora Lucknow, 2001
320
320
320
280
280
280
240
240
240
200
AQI
360
200
200
160
160
160
120
120
120
80
80
80
40
40
40
WINTER
SUMMER
MONSOON
0
WINTER
Seasons
360
SUMMER
WINTER
MONSOON
360
360
320
280
280
280
240
240
240
AQI
320
AQI
320
200
200
200
160
160
160
120
120
120
80
80
80
40
40
40
WINTER
SUMMER
Seasons
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MONSOON
MONSOON
400
400
SUMMER
Seasons
Seasons
400
AQI
360
AQI
AQI
400
400
400
0
WINTER
SUMMER
Seasons
MONSOON
WINTER
SUMMER
MONSOON
Seasons
147
400
400
360
320
320
320
280
280
280
240
240
240
200
AQI
360
200
160
160
120
120
120
80
80
80
40
40
40
0
WINTER
SUMMER
MONSOON
0
WINTER
Seasons
MONSOON
WINTER
400
320
320
280
280
280
240
240
240
AQI
320
AQI
360
200
200
200
160
160
160
120
120
120
80
80
80
40
40
40
WINTER
SUMMER
MONSOON
WINTER
Seasons
SUMMER
MONSOON
WINTER
Seasons
400
320
320
320
280
280
280
240
240
240
AQI
360
AQI
360
200
160
160
120
120
120
80
80
80
40
40
40
SUMMER
MONSOON
WINTER
Seasons
SUMMER
WINTER
MONSOON
Seasons
400
320
320
320
280
280
280
240
240
240
AQI
360
AQI
360
200
200
160
160
120
120
120
80
80
80
40
40
40
SUMMER
148
MONSOON
200
160
Seasons
MONSOON
400
400
SUMMER
Seasons
360
WINTER
200
160
WINTER
MONSOON
400
360
200
SUMMER
Seasons
400
MONSOON
400
SUMMER
Seasons
360
360
AQI
SUMMER
Seasons
400
AQI
200
160
AQI
AQI
AQI
360
0
WINTER
SUMMER
Seasons
MONSOON
WINTER
SUMMER
MONSOON
Seasons
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400
320
320
280
280
280
240
240
240
360
AQI
200
200
160
160
120
120
80
80
WINTER
SUMMER
160
120
80
40
MONSOON
WINTER
Seasons
SUMMER
MONSOON
0
WINTER
Seasons
360
320
320
320
280
280
280
240
240
240
AQI
360
AQI
360
200
200
160
160
120
120
120
80
80
80
40
40
40
0
SUMMER
WINTER
MONSOON
MONSOON
WINTER
Seasons
Seasons
360
360
280
280
240
240
240
AQI
320
280
AQI
320
200
160
160
120
120
120
80
80
80
40
40
40
WINTER
SUMMER
WINTER
SUMMER
WINTER
MONSOON
400
360
360
280
240
240
240
AQI
320
280
AQI
320
280
200
160
160
120
120
120
80
80
80
40
40
40
0
SUMMER
Seasons
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MONSOON
WINTER
SUMMER
Seasons
MONSOON
200
160
WINTER
MONSOON
400
320
200
SUMMER
Seasons
Seasons
400
360
MONSOON
Seasons
200
160
MONSOON
400
320
200
SUMMER
Seasons
400
400
360
SUMMER
200
160
WINTER
MONSOON
400
SUMMER
Seasons
400
400
AQI
200
40
AQI
320
40
AQI
400
360
AQI
AQI
0
WINTER
SUMMER
MONSOON
Seasons
149
400
360
320
320
280
280
240
240
AQI
AQI
360
200
200
160
160
120
120
80
80
40
40
WINTER
SUMMER
WINTER
MONSOON
Seasons
SUMMER
MONSOON
Seasons
During period of 2001-09, maximum variation of AQI in Lucknow city is found during 2002 at
Talkatora, whereas in Kanpur city it is observed during 2005 at Vikas Nagar. The metrological condition
and turbulence in the atmosphere are the primary factors affecting pollutant distribution, dispersion
pattern and seasonal variations. The air quality generally improves in Monsoon. During Monsoon
frequent rain washes down the air borne particulates and gaseous pollutants.
Annual variation of AQI
Annual variation of AQI at all 13 districts of Uttar Pradesh having monitoring stations based on
available data for the period 2001 to 2009 has been observed. In Lucknow city, during 2005-09 there
is a little variation in AQI at all the locations (Figure 3), whereas during 2001-04, AQI value is low and
AQI value increases after 2004.
800
800
800
720
720
640
640
640
560
560
560
480
480
400
480
AQI
AQI
AQI
Aminabad Lucknow
720
400
320
320
240
240
160
160
80
80
400
320
240
160
80
Year
Y2006
Y2007
Y2009
Year
800
Year
800
Mahanagar Lucknow
Talkatora Lucknow
720
640
560
560
480
480
Year
Y
20
09
Y
20
08
Y
20
07
Y
20
06
Y
20
09
Y
20
08
Y
20
07
Y
20
06
0
Y
20
04
80
0
Y
20
05
160
80
Y
20
02
240
160
Y
20
01
320
240
Y
20
05
400
320
Y
20
04
400
Y
20
02
AQI
640
Y
20
01
720
AQI
Y2008
Y
20
08
Y2005
Y
20
09
Y
20
07
Y2009
Y
20
06
Y2008
Y
20
05
Y2007
Y
20
04
Y2006
Y
20
02
Y2005
Y
20
01
Year
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5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
15.
16.
CONCLUSION
AQI has been calculated for the 13 districts
of U.P. for knowing the status of air pollution with
its effect on human health. While comparing all
12 pollutants, it was observed that the
concentration of SPM and PM10 are higher than
the prescribed standards and concentration of
SO2 and NO2 is lower than NAAQS. The air quality
worsens in winter month and also during summer
month. The summer month are characterized by
dust winds resulting high SPM. The AQI generally
improves in monsoon period due to rain, good
to moderate. The SPM and PM10 have been
responsible pollutant for the index. The air quality
is giving the holistic view of air pollution levels
as clearly exceeded the high air pollution
category and has been crossed severe pollution
category at many places.
REFERENCES
1.
2.
3.
4.
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151
ABSTRACT
The Indian education system should adopt value based education at all levels The value oriented
educational program should not be led only during the further level, but should be carried on
further up to the level of higher education too, as it is form there that the nations political
leaders, bureaucrats and army personal would emerge. Values based education therefore is a
part of the educational programs, which cannot be shelved or done away with. It has to be a
part of life, life is a constant education, and the process of living is a process of learning. India
is badly in need of value based education and teaching system, which inculcates among the
young students values that they need to imbibe and embalm within them. Values based education
imparts social, moral integrity, character, spirituality and many more. It builds the qualities of
humanity strength and honesty in a person they become better citizens of a country. People
with high ethical values will never cheat others. People are taught to co-operate with each
other. They make their life happier and works hard to make others happy. A child learns a lot
from the people around him, if the social environment is not good, then it becomes very difficult
for him to display ethics and values in his behavior.
KEYWORDS: Value, Education, Development
INTRODUCTION
Value is a dynamic term used in different
aspects. Indian Philosophy has used it in sense
of state free from pleasure and pain 1 . In
Psychology the term Value is generally employed
to designate a dominant interest motive or broad
evaluative attitude. Psychologist in the sense of
Psychic energy. Sociologists in the sense of use
of time energy and money for certain ends. Value
has been defined variously by different
Educationist but on the whole it is interpreted to
be either a set of feeling or an action. Values
are define as, Socially approved derires and
goals that are internalized through the process
of conditioning, Learning or socialization and
these become subjective preferences, standards
and aspirations.
NEED AND IMPORTANCE
All port is right when he says ordinarily
attitude should be employed when the disposition
is bound to an object or value. Values are
generally long term standards or principles that
used to judge the worth of an idea or action2.
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2.
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REFERENCES:
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7.
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EDITORIAL POLICY
The criteria for publication are originality high scientific quality and interest to a multidisciplinary
audience. Papers not sufficiently substantiated by experimental detail will not be published. Any
technical queries will be referred back to the author although the Editors reserve the right to make
alterations in the text without altering the technical content. Manuscripts submitted under multiple
authorships are reviewed on the assumption that all listed authors concur with the submission and
that a copy of the final manuscript has been approved by all authors. If accepted, the manuscripts
shall not be published elsewhere in the same form in either the same or another language without
the consent of the Editors.
International Journal of Scientific and Innovative Research insists on ethical practices in both human
and animal experimentation. Evidence for approval by a institutional Ethics Committee (for both
human as well as animal studies) must be supplied by the authors on demand. Animal experimental
procedure should be on humane as possible and the details of anesthetics and analgesics used
should be clearly stated. The ethical standards of experiments must be in accordance with the
guidelines provided by the CPCSEA (animal) and ICMR (human). The journal will not consider any
paper which is ethically unacceptable. A statement on ethics committee permission must be included
in all research articles under the Materials and Methods section. Authors must be careful when they
reproduce text, tables and illustrations from other sources. Plagiarism will be viewed seriously. All
accepted papers are subject to editorial changes. All rights are reserved to editor-in-chief, International
Journal of Scientific & Innovative Research (IJSIR). IJSIR will be published bi-annually in the month of
July (January-June issue) and January (July-December issue) every year.
IJSIR would take much care in making your article published without much delay with your kind cooperation.
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INSTRUCTION TO AUTHORS
The International Journal of Scientific and Innovative Research is a bi-annually published online
/ offline Journal which publishes innovative research papers, reviews, mini-reviews, short
communications and notes dealing with all branches of science, technology and engineering, health
and agriculture. All manuscripts are subject to rapid peer review. Those of high quality (not previously
published and not consideration for publication in another journal) will be published without delay.
MANUSCRIPT FORMAT
The preferred format of all manuscript is MS Word or RTF. Illustrations (figures) and images
must be inserted in the manuscript at the position they should appear when published.
PREPARATION OF MANUSCRIPTS
RESEARCH PAPER
The language of the journal is English. Each manuscript should be typed double-spaced on A4
(8.5" x 11") paper size with 1 inch margins. It should be arranged in the following order: Title, Abstract,
Keywords, Introduction, Materials and Methods, Results, Conclusion, Acknowledgement, References.
Title Page
Title page should contain title of the paper in bold face, title case (font size 14), names of the
authors in normal face, upper case (font size 12) followed by the address in normal face lower case.
The author to whom all correspondence be addressed should be denoted by an asterisk mark. The
title should be as short as possible and precisely indicate the nature of the work in the communication.
Names of the authors should appear as initials followed by surnames. At the bottom left corner of the
title page, please mention *Address For correspondence and provide a functional e-mail address.
Address of the corresponding author to whom all correspondence may be sent should be given only
if is different from the address already given under authors names.
Abstract
Should start on a new page after the title page and should be typed in single-space to distinguish
it from the Introduction. Abstracts should briefly reflect all aspects of the study, as most databases list
mainly abstracts.
Key-words
Provide four to six appropriate key words after abstract.
Introduction
Shall start immediately after the abstract, as the next paragraph, but should be typed in doublespace. The Introduction should lead the reader to the importance of the study; tie-up published
literature with the aims of the study and clearly states the rationale behind the investigation.
Materials and Methods
Shall start as a continuation to introduction on the same page. All important materials used
along with their source shall be mentioned. The main methods used shall be briefly described, citing
references. Trivial details may be avoided. New methods or substantially modified methods may be
described in sufficient detail. The statistical method and the level of significance chosen shall be
clearly stated. IJSIR prefers to publish work that has been subjected to an appropriate statistical test
at one level of significance.
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Results
All findings presented in tabular or graphical form shall be described in this section. The data
should be statistically analyzed and the level or significance stated. Data that is not statistically
significant need only to be mentioned in the text no illustration is necessary. All tables and figures
must have a title or caption and legend to make them self-explanatory. Results section shall start
after materials and methods section on the same page.
Discussion
This section should follow results, deal with the interpretation of result, convey how they help
increase current understanding of the problem and should be logical. Unsupported hypothesis should
be avoided. The Discussion should state the possibilities the results uncover that need to be further
explored. There is no need to include another title such as Conclusions at the end of Discussion.
Results and discussion of results can also be combined under one section, Results and Discussion.
Acknowledgements
Should be given after the text and not in the form of foot-notes.
References
Should be numbered consecutively in the order in which they are first mentioned in the text (not
in alphabetic order). Identify references in text, tables and legends by Arabic numerals in superscript
in square brackets. References cited only in tables or figure legends should be numbered in
accordance with the sequence established by the first identification in the text of the particular table
or figure.
Journal Articles
Singh N., Verma P., Pandey B.R., Gilca M. Role of Withania somnifera in Prevention and Treatment
of Cancer: An Overview. International Journal of Pharmaceutical Sciences and Drug Research. 2011;
3(4): 274-279.
A Book
Singh N, Gilca M. Herbal Medicine Science embraces tradition a new insight into the ancient
Ayurveda. Edn 1, Lambert Academic Publishing (Germany), 2010, pp. 115-116.
A chapter in a Book
Nadkarni KM, Indian Materia Medica. Edn 3, Vol. I, Popular Prakashan, Mumbai, 2000, pp. 242-246.
A Report
World Health Organization. The World Health Report 2004: changing history.
Geneva: WHO; 2004.
Conference Proceedings
Stock A, Signal Trasduction in Bacheria. In the Proceedings of the 2004 Markey Scholars
Conference. 2004, pp. 80-89.
A Thesis
Strunk, JL. The extraction of mercury from sediment and the geochemical partitioning of mercury
in sediments from Lake Superior, M.S. thesis, Michigan State Univ. East Lansing, Ml, 1991
Illustrations
Tables Should be typed on separate sheets of paper and should not preferably contain any
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157
molecular structures. Only MS word table format should be used for preparing tables. Tables should
show lines separating columns but not those separating rows except for the top row that shows
column captions. Tables should be numbered consecutively in Arabic numerals and bear a brief title
in capital letters normal face. Tables should not be very large that they run more than one A4 sized
page.
Figures
Should be on separate pages but not inserted within the text. Figures should be numbered
consecutively in Arabic numerals and bear a brief title in lower case bold face letters below the figure.
Graphs and bar graphs should preferably be prepared using Microsoft Excel and submitted as Excel
graph pasted in MS Word.
Abbreviations, Units Etc
Authors should follow internationally agreed rules especially those adopted by the IUPAC-IUB
Commission on Biochemical Nomenclature (CBN). The journal will essentially follow the rules defined
in the IUPAC Manual of symbols and terminology for physico-chemical quantities and units.
Short Communications
The journal publishes exciting findings, preliminary data or studies that did not yield enough
information to make a full paper as short communications. These have the same format requirements
as full papers but are only up to 10 pages in length in total. Short Communications should not have
subtitles such as Introduction, Materials and Methods, Results and Discussion all these have to be
must into the running text. Short Communications preferably should have only 3-4 illustrations.
Review Articles
Should be about 15-30 pages long, contain up-to-date information, comprehensively cover
relevant literature and preferably be written by scientists who have in -depth knowledge on the topic.
All format requirements are same as those applicable to full papers. Review articles need not be
divided into section such as materials and methods and results and discussions, but should definitely
have an abstract and introduction if necessary.
Submission of Manuscript
All manuscripts (must be in English and in MS Word format) and should be submitted via our
online system or through e-mail editorijsir02@gmail.com, as an attachment for quick evaluation.
Manuscript Charges
There is no charge for the processing of papers but author(s) of each accepted paper is required
to pay a publication charge of Rs. 2,000 for Indian authors and US $ 125 for foreign authors before
the accepted paper is published.
Copyright and Permissions
Submission is a representation that the manuscript has not been published previously and is
not under consideration for publication elsewhere. Authors would be required to sign a form (to be
supplied by the Editor) transferring copyright before the manuscript can be published. By submitting
a manuscript to the editor or publisher you are deemed to have granted permission to publish the
manuscript.
Ethical Matters
Authors using experimental animals and human subjects in their investigation must seek approval
from the appropriate Ethical Committee. The method section must include a statement to prove that
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the investigation was approved and that informed consent was obtained.
Galley Proofs
Proofs will sent via e-mail as an Acrobat PDF (Portable Document Format) file. Acrobat Reader will
be required in order to read the PDF.
Manuscript Submission Process:
1.
2.
Download Cover letter -fill the necessary fields and scan it and send to our email address
along with manuscript or Upload through Online Manuscript submission option.
3.
4.
Download Copy Right Form and Sign it (by the corresponding/main author) and send
its scanned copy only to Email ID editorijsir02@gmail.com.
(Without this signed undertaking your paper would not get
displayed.)
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159
COVER LETTER
Date
Place
From
(Name and Address of the corresponding author)
To,
Editor-in-Chief
International Journal of Scientific and Innovative Research (IJSIR)
Sir,
Ref:
Title
Type
Subject
Branch
In reference to the above title, I as a corresponding author submit the manuscript for
publication in International Journal of Scientific and Innovative Research. I undertake that
animal study (if any) was taken after the prior approval of country/institutional ethical committee.
This manuscript has not been published or considered for publication by any other journal or
elsewhere. Kindly consider the manuscript for publication in your journal.
Thank you
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Individual Subscription
Institutional Subscription
Note: Subscriber should submit the subscription form to email ID: editorijsir02@gmail.com
Subscribers Name: (It includes first name, last name and professional credential (if any)
NAME .......................................................................................
INSTITUTIOANAL/ INDIVIDUAL ADDRESS ..................................
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SIGNATURE
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UNDERTAKING*
I _____________________________________________________________ (corresponding
author), working as __________________ (Designation), in __________________(Department/
Affiliation),
do
hereby
submit
the
manuscript
No.
_____
entitled:
I / We declare that this is an original research work and is not previously published or presented
elsewhere in any language and is also not in consideration in any other journal simultaneously.
I /we, all authors of the above manuscript are agree that the content of this manuscript will not
be copyrighted, submitted, or published elsewhere (including the internet), and is also not plagiarized
from any language.
I/We also solemnly affirm that not any brand name of drug/product/manufacturer was included
in this manuscript to avoid legal hindrance and I / We will responsible to face any dispute, pointed out
by anyone in future.
Signature
Affiliation
1.____________________________________
________________
__________________
2.____________________________________
________________
__________________
3.____________________________________
________________
__________________
*This undertaking must be submitted along with submission of the manuscript in IJSIR.
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