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Researchers:
Ilustre, Mary Ella Mae E. Lagos, Krizza Joy M.
Inosanto, Sarah Mae O. Lavalle, Jane Jobeth D.
Javier, Julie Anne R. Limpiado, Kathleen Gay E.
Jore, Kathleen Anne G. Traya, Jent Carl T.
Pharmacy 4A – Group 4
AUGUST 19, 2017
UNIVERSITY OF SAN AGUSTIN
COLLEGE OF HEALTH AND ALLIED MEDICAL PROFESSIONS
RESEARCH PROPOSAL DEFENSE
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UNIVERSITY OF SAN AGUSTIN
COLLEGE OF HEALTH AND ALLIED MEDICAL PROFESSIONS
RESEARCH PROPOSAL DEFENSE
Reference:
Polyalthia longifolia Sonn: an Ancient
Remedy to Explore for Novel
Therapeutic Agents
Subramanion L Jothy1, Yee Siew
Choong1, Dharmaraj Saravanan2,
Subramanian Deivanai3, Lachimanan
Yoga Latha1, Soundararajan
Vijayarathna1, Sreenivasan
Sasidharan1*
UNIVERSITY OF SAN AGUSTIN
COLLEGE OF HEALTH AND ALLIED MEDICAL PROFESSIONS
RESEARCH PROPOSAL DEFENSE
Reference:
Polyalthia longifolia Sonn: an Ancient Remedy to
Explore for Novel Therapeutic Agents
Subramanion L Jothy1, Yee Siew Choong1, Dharmaraj
Saravanan2, Subramanian Deivanai3, Lachimanan Yoga
Latha1, Soundararajan Vijayarathna1, Sreenivasan
Sasidharan1*
UNIVERSITY OF SAN AGUSTIN
COLLEGE OF HEALTH AND ALLIED MEDICAL PROFESSIONS
RESEARCH PROPOSAL DEFENSE
Phytochem
Bioassay monitored isolation work on the
methanol extract of leaves and berries lead to
three new clerodane diterpene from this plant;
methyl-16-oxo-cleroda-3,13(14)E-dien-15-oate, Reference:
3β,16α-dihydroxy-cleroda-4(18), 13(14)Z-dien-
15,16-olide, and solidagonal acid [29]. Later, two Polyalthia longifolia Sonn:
other clerodane diterpenes were obtained from an Ancient Remedy to
leaves and these were 3α,16 α-dihydroxycleroda- Explore for Novel
4(18),13(14)Z-dien-15,16-olide and 3β,16 α- Therapeutic Agents
dihydroxycleroda-4(18),13(14)Z-dien-15,16-olide Subramanion L Jothy1, Yee
[30]. Siew Choong1, Dharmaraj
Saravanan2, Subramanian
The dimeric clerodane diterpene has also been Deivanai3, Lachimanan Yoga
isolated and two examples of this bisclerodane Latha1, Soundararajan
compound are Longimide A and Longimide B Vijayarathna1, Sreenivasan
(Figure 4). These compounds were isolated Sasidharan1*
together with a cycloartane triterpene. The
triterpene was named longitriol [31].
UNIVERSITY OF SAN AGUSTIN
COLLEGE OF HEALTH AND ALLIED MEDICAL PROFESSIONS
RESEARCH PROPOSAL DEFENSE
S aureus + E. coli
Washing Rationale
Plant Collection: Fresh samples of leaves, stem bark and fruit of P. longifolia
were collected. All the collected plant parts were washed thrice with tap
water and twice with distilled water to remove the adhering salts and other
associated animals.
Reference:
Sunita et al., World J Pharm Sci 2016; 4(6): 495-501
Antimalarial activity of Polyalthia longifolia (False Ashoka) against chloroquine sensitive Plasmodium falciparum 3D7 strain
Plant collection
Healthy disease free, mature fresh plant leaf sample were collected.
Fresh leaves were washed thoroughly 2-3 times with running tap water and
once with sterile water, shade-dried without any contamination.
Reference: PHYTOCHEMICAL ANALYSIS AND ANTIMICROBIAL ACTIVITY OF POLYALTHIA LONGIFOLIA
M. THENMOZHI * AND RAJESHWARI SIVARAJ
UNIVERSITY OF SAN AGUSTIN
COLLEGE OF HEALTH AND ALLIED MEDICAL PROFESSIONS
RESEARCH PROPOSAL DEFENSE
SOLVENT EXTRACTION
Solvent Extraction
Solvent extracts
The leaves powder (10g) was extracted with solvents of
different polarities (methanol, ethanol, ethyl acetate, petroleum ether
and acetone) by cold maceration for 24h.The extracts were filtered
through Whatman No.1 filter paper. The extracts were concentrated
to dryness using rotary flask evaporator under reduced pressure.
ETHANOL RATIONALE
Reference:
PHYTOCHEMICAL
ANALYSIS AND
ANTIMICROBIAL
ACTIVITY OF
POLYALTHIA
LONGIFOLIA
M. THENMOZHI * AND
RAJESHWARI SIVARAJ
UNIVERSITY OF SAN AGUSTIN
COLLEGE OF HEALTH AND ALLIED MEDICAL PROFESSIONS
RESEARCH PROPOSAL DEFENSE
Sample preparation
The leaves were air-dried and powdered. The extract of sample was
prepared by soaking 10g of dried powdered sample in 100ml of
Ethanol for 12 h in an orbital shaker. The extracts were filtered
using Whatman filter No.1. The ethanol was then removed under
reduced pressure at 400C to obtain the dry extract.
Antibacterial Screening
Antibacterial screening
An invitro antimicrobial screening was carried out using
Mueller Hinton Agar (MHA) (Oxoid, England) by Agar well
diffusion method according to Perez et al (1990). The plates were
allowed to stand for one hour for pre-diffusion of the extract into
the medium (Esimone et al., 1998).
Phytochemical Screening And Antibacterial Activity Of Polyalthia Longifolia Crude
Extracts
* D. Uzama, M.B. David, R. Ahmadu and S.A. Thomas
UNIVERSITY OF SAN AGUSTIN
COLLEGE OF HEALTH AND ALLIED MEDICAL PROFESSIONS
RESEARCH PROPOSAL DEFENSE
Antibacterial Activity
MIC
Determination of minimum inhibitory concentration (MIC)
The minimum inhibitory concentration is the least extract
concentration which inhibited the growth of the test organisms.
The minimum inhibitory concentration was determined by
incorporating various concentrations of solutions of extract in
Muller Hinton agar(200 to 0.4mg).A loop full of standard test
bacterial broth culture was used to streak plates. The plates of
bacteria were incubated at 37oC for 24h. A positive control
containing only the growth medium and extract was also set up.
The MIC was regarded as the lowest concentration of the extract
that did not permit any visible growth of the organism.
MIC RESULT