Chandigarh University Assignment-3 Subject-Phamacognosy Subject Code-255 Submitted by - Ishika Chakraborty UID NO - 18BPH1032 B.Pharmacy - 4 SEM

You might also like

Download as docx, pdf, or txt
Download as docx, pdf, or txt
You are on page 1of 20

Chandigarh University

Assignment-3
Subject- phamacognosy

Subject code-255

Submitted by- Ishika Chakraborty

UID NO- 18BPH1032

B.PHARMACY- 4TH SEM

REFRENCE- PHARMACONOSY, C.K KOKATE,


NIRALI PRAKASHAN (54TH EDITION)
Write biological source, chemical constituents and
uses of following crude drugs:

a)Benzoin
b)Guggul

1)Benzoin-

Common name-

SUMATRA BENZOIN
 
 
Synonyms
 
Gum Benjamin; Benzoinum; Benzoin; Luban (Hindi).
 
Biological Source
 
Sumatra Benzoin is obtained from the incised stem
of Styrax benzoin  Dryander and  Styrax parallelo-
neurus  Perkins.,  belonging to family Styraceae. It
contains about 25% of total balsamic acids,
calculated as cinnamic acid
 
Geographical Source
 
The trees are found in Sumatra, Malacca, Malaya,
Java, and Borneo.
 
Collection
 
The plants are medium-sized trees. Sumatra Benzoin
is a pathological resin which is formed by making
incision and by attack of fungi. In Sumatra the seeds
are sown in rice fields. The rice plants provide
protection to benzoin plants during first year. After
harvesting of the rice crop the trees are allowed to
grow. When they are 7 years old, three triangular
wounds are made in a vertical row. Tapping consists
of making in each trunk three lines of incisions
which are gradually lengthened. The first triangular
wounds are made in a vertical row about 40 cm
apart, the bark between the wounds being then
scraped smooth. The first secretion is very sticky
and is rejected. After making further cuts, each
about 4 cm above the preceding ones, a harder
secretion is obtained. Further incisions are made at
three-monthly intervals, and the secretion becomes
crystalline. About 6 weeks after each fresh tapping
the product is scraped off, the outer layer (finest
quality) being kept separate from the next layer
(intermediate quality). About 2 weeks later the strip
is scraped again, giving a lower quality darker in
colour and containing fragments of bark. Fresh
incisions are then made, and the above process is
repeated. Second exudation is milky white and is
used for medicinal purpose. The stem is incised four
times during one year. AH types of exudations are
sent to industry for further processing. A single tree
yields about 10 kg of resin per year and is
completely exhausted by the 19th year of its life.

          Styrax benzoin

Characteristics
 
Sumatra benzoin occurs in brittle masses consisting
of opaque, whitish, or reddish tears embedded in a
translucent, reddish-brown or greyish-brown,
resinous matrix. Odour, agreeable and balsamic,
taste, slightly acrid. Siamese benzoin occurs in tears
or in blocks. The tears are of variable size and
flattened; they are yellowish-brown or reddish-brown
externally, but milky-white and opaque internally.
The block form consists of small tears embedded in
a glassy, reddish-brown, resinous matrix. It has a
vanilla-like odour and a balsamic taste.
 
When heated, benzoin evolves white fumes of
cinnamic and benzoic acids which readily condense
on a cool surface as a crystalline sublimate.
 
Chemical Constituents
 
Sumatra Benzoin consists of free balsamic acid
(cinnamic and benzoic acids) (25%) and their esters.
The amount of cinnamic acid is usually double that
of benzoic acid. It also contains triterpenic acids like
siaresinolic acid (19-hydroxy-oleanolic acid) and
sumaresinolic acid (6-hydroxy-oleanolic acid); traces
of vanillin, phenylpropyl cinnamate, cinnamyl
cinnamate, and phenylethylene.
 
 
Uses
 
Sumatra Benzoin possesses expectorant, antiseptic,
carminative, stimulant, and diuretic properties. It is
used in cosmetic lotions, perfumery and to prepare
Compound Benzoin. It forms an ingredient of
inhalations in the treatment of catarrh of upper
respiratory tract in the form of Compound Benzoin
Tincture. Benzoin is used as an external antiseptic
and protective, and is one of the main ingredients of
Friar’s Balsam. It is also used to fix the odour of
incenses, skin-soaps, perfumes and other cosmetics
and for fixing the taste of certain pharmaceutical
preparations. Benzoin retards rancification of fats
and is used for this purpose in the official
benzoinated lard, also used in food, drinks and in
incense.
 
Allied Drug
 
Palembang benzoin,  an interior variety produced in
Sumatra  is collected from isolated trees from which
the resin has not been stripped for some time. It is
very light in weight and breaking with an irregular
porous fracture. It consists of reddish-brown resin,
with only a few very small tears embedded in
it. Palembang benzoin is used as a source of natural
benzoic acid.

2) Guggul –

GUGGUL
 
 
Synonyms
 
Gumgugul, Salai-gogil.
 
Biological Source
 
Guggal is a gumresin obtained by incision of the bark
of Commiphora mukul  (H. and S.) Engl., belonging to
family  Burseraceae.
 
Geographical Source
 
The tree is a small, thorny plant distributed throughout
India.
 
Collection
 
Guggal tree is a small thorny tree 4 to 6 feet tall branches
slightly ascending. It is sometimes planted in hedges. The
tree remains without any foliage for most of the year. It has
ash-coloured bark, and comes off in rough flakes, exposing
the innerbark, which also peels off. The tree exudes a
yellowish resin called gum guggul or guggulu that has a
balsamic odor. Each plant yields about one kilogram of the
product, which is collected in cold season.
 
Characteristics
 
Guggal occurs as viscid, brown tears; or in fragment pieces,
mixed with stem, piece of bark; golden yellow to brown in
colour. With water it forms a milk emulsion. It has a
balsamic odour and taste is bitter, aromatic.
                       Commiphora mukul

Chemical Constituents
 
Guggal contains gum (32%), essential oil (1.45%), sterols
(guggulsterols I to VI, β-sitosterol, cholesterol, Z- and E-
guggulsterone), sugars (sucrose, fructose), amino acids, α-
camphorene, cembrene, allylcembrol, flavonoids (quercetin
and its glycosides), ellagic acid, myricyl alcohol, aliphatic
tetrols, etc.
 
 
Uses
 
Guggal significantly lowers serum triglycerides and
cholesterol as well as LDL and VLDL cholesterols (the bad
cholesterols). At the same time, it raises levels of HDL
cholesterol (the good cholesterol), inhibits platelet
aggregation, and may increase thermogenesis through
stimulation of the thyroid, potentially resulting in weight
loss. Also gum is astringent, aritirheumatic, antiseptic,
expectorant, aphrodisiac, demulcent, and emmenagogue.
The resin is used in the form of a lotion for indolent ulcers
and as a gargle in teeth disorders, tonsillitis, pharyngitis,
and ulcerated throat.
 
Marketed Products
 
It is one of the ingredients of the preparations known as
Arogyavardhini Gutika (Dabur) and Abana, Diabecon, Diakof
(Himalaya Drug Company).
2)What are tannis? list the drugs contanning tannis
with their pharmacognostic information.

Tannins (or tannoids) are a class


of astringent, polyphenolic biomolecules that bind to
and precipitate proteins and various other organic
compounds including amino acids and alkaloids.
The term tannin (from Anglo-Norman tanner, from Medieval
Latin tannāre, from tannum, oak bark) refers to the use of
oak and other bark in tanning animal hides into leather. By
extension, the term tannin is widely applied to any
large polyphenolic compound containing
sufficient hydroxyls and other suitable groups (such
as carboxyls) to form strong complexes with
various macromolecules.
The tannin compounds are widely distributed in many
species of plants, where they play a role in protection
from predation (including as pesticides) and might help in
regulating plant growth.[1] The astringency from the tannins
is what causes the dry and puckery feeling in the mouth
following the consumption of unripened fruit, red wine or
tea.[2] Likewise, the destruction or modification of tannins
with time plays an important role when determining
harvesting times.
Tannins have molecular weights ranging from 500 to over
3,000[3] (gallic acid esters) and up to 20,000
(proanthocyanidins).

Drugs used in tannis-


Pseudo tannin Source(s)
Gallic acid Rhubarb
Tea, acacia,
Flavan-3-ols
catechu, cocoa,
(Catechins)
guarana
Nux-vomica,
Chlorogenic acid coffee, mat

Uses-
Tannins are an important ingredient in the process of
tanning leather. Tanbark from oak, mimosa, chestnut
and quebracho tree has traditionally been the primary
source of tannery tannin, though inorganic tanning
agents are also in use today and account for 90% of the
world's leather production. Tannins produce different colors
with ferric chloride (either blue, blue black, or green to
greenish-black) according to the type of tannin. Iron gall
ink is produced by treating a solution of tannins with iron(II)
sulfate. Tannin is a component in a type of
industrial particleboard adhesive developed jointly by the
Tanzania Industrial Research and Development Organization
and Forintek Labs Canada.  Pinus radiata tannins has been
investigated for the production of wood adhesives.
Condensed tannins, e.g., quebracho tannin, and Hydrolyzable
tannins, e.g., chestnut tannin, appear to be able to
substitute a high proportion of synthetic phenol in phenol-
formaldehyde resins for wood particleboard.[citation needed]
Tannins can be used for production of anti-corrosive primer,
sold under brand-name "Nox Primer" for treatment of rusted
steel surfaces prior to painting, rust converter to transform
oxidized steel into a smooth sealed surface and rust
inhibitorThe use of resins made of tannins has been
investigated to remove mercury and methylmercury from
solution. Immobilized tannins have been tested to
recover uranium from seawater.

3) Write biological source ,chemical constituents and uses


of following cride drugs :

a) Wool fat
b) Bees wax

Wool fat-
LANOLIN
 
 
Synonyms
 
Wool fat; Oesipos; Agnin; Alapurin; Anhydrous lanolin; Adeps
lanae; Laniol.
 
Biological Source
 
Lanolin is the fat-like purified secretion of the sebaceous
glands which is deposited into the wool fibres of sheep, Ovis
aries  Linn., belonging to family Bovidae.
 
Preparation
 
Wool is cut and washed with a soap or alkali. An emulsion of
wool fat, called as wool grease, takes place in water. Raw
lanolin is separated by cracking the emulsion with sulphuric
acid. Wool grease floats on the upper layer and fatty acids
are dissolved in the lower layer. Lanolin is purified by
treating with sodium peroxide and bleaching with reagents.
 
Characteristics
 
Lanolin is a yellowish white, tenacious, unctuous mass;
odour is slight and characteristic. Practically, it is insoluble
in water, but soluble in chloroform or ether with the
separation of the water. It melts in between 34 and 40°C. On
heating it forms two layers in the beginning, continuous
heating removes water. Lanolin is not saponified by an
aqueous alkali. However, saponification takes place with
alcoholic solution of alkali.
 
Anhydrous lanolin is a yellowish tenacious, semisolid fat
with slight odour. Practically it is insoluble in water but
mixes with about twice its weight of water without
separation. It is sparingly soluble in cold, more in hot
alcohol, freely soluble in benzene, chloroform, ether, carbon
disulphide, acetone, and petroleum ether.
 
Chemical Constituents
 
Lanolin is a complex mixture of esters and polyesters of 33
high molecular weight alcohols, and 36 fatty acids. The
alcohols are of three types; aliphatic alcohols, steroid
alcohols, and triterpenoid alcohols. The acids are also of
three types: saturated nonhydroxylated acids, unsaturated
nonhydroxylated acids, and hydroxylated acids. Liquid
lanolin is rich in low molecular weight, branched aliphatic
acids, and alcohols, whereas waxy lanolin is rich in high
molecular weight, straight-chain acids, and alcohols.
 
The chief constituents of lanolin are cholesterol, iso-
cholesterol, unsaturated monohydric alcohols of the formula
C H OH, both free and combined with lanoceric (C H O ),
27 45 30 60 4

lanopalmitic (C H O ), carnaubic, and other fatty acids.


16 22 3

Lanolin also contains esters of oleic and myristic acids,


aliphatic alcohols, such as cetyl, ceryl and carnaubyl
alcohols, lanosterol, and agnosterol.
 

 
Identification Tests
 
Dissolve 0.5 g of lanolin in chloroform, and to it add 1 ml of
acetic anhydride and two drops of sulphuric acid. A deep
green colour is produced, indicating the presence of
cholesterol.
 
Uses
 
Lanolin is used as an emollient, as water absorbable
ointment base in many skin creams and cosmetic and for
hoof dressing. Wool fat is readily absorbed through skin and
helps in increasing the absorption of active ingredients
incorporated in the ointment. However, it may act as an
allergenic contactant in hypersensitive persons.

BEESWAX-
 
 
Synonyms
 
White beeswax, yellow beeswax, cera alba, and cera flava.
 
Biological Source
 
Beeswax is the purified wax obtained from honeycomb of
hive bee, Apis mellifera Linn and other species of Apis,
belonging to family Apidae.
 
Geographical Source
 
It is mainly found in Jamaica, Egypt, Africa, India, France,
Italy, California etc.
 
Preparation
 
The worker bee secretes the wax due to the ability of
maintaining a high temperature and the wax is secreted in
the last four segments of abdomen on the ventral surface.
Just below the sterna it has a smooth layer of cells form the
chitinous area that secretes the wax. The chitinous area has
small pores through, which the wax exudes out. The wax is
passed to the front leg and later to the mouth; in the mouth
it gets mixed with the saliva, which is then built on the
comb. This wax forms a capping on the honey cells. Wax
forms about 1/8th part of the honeycomb. After removal of
honey, honeycomb or the capping is melted in boiling water.
On cooling the melted wax gets solidified and floats on the
surface of water while the impurities settle below and honey
leftovers get dissolved in water. The pure wax is then
poured into earthen vessels wiped with damp cloth and the
wax so obtained is yellow beeswax.
 
White beeswax is obtained from yellow beeswax. The yellow
beeswax is runned on a thin stream of spinning wet drum,
from which long ribbon like strips are scrapped off. The
ribbon strips are placed on cloth in thin layers, rotated from
time to time and bleached in sunlight till the outer layer
becomes white. White beeswax is obtained by treating
yellow beeswax chemically with potassium permanganate,
chromic acid or chlorine or charcoal.
 
Characterisitics
 
Yellow wax or Cera flava is yellowish to greyish brown
coloured solid, with agreeable, honey-like odour and a faint,
characteristic taste. When cold, it is somewhat brittle and
when broken, shows presence of a dull, granular,
noncrystalline fracture. Yellow wax is insoluble in water and
sparingly soluble in cold alcohol. It is completely soluble in
chloroform, ether, and in fixed or volatile oils, partly soluble
in cold benzene or in carbon disulphide and completely
soluble in these liquids at about 30°C.
 
White wax is less unctuous to the touch; it is yellow, soft,
and ductile at 35°C and fusible at 65°C. A yellowish-white
solid, somewhat translucent in thin layers. It has a faint,
characteristic odour which is free from rancidity and
tasteless. It is insoluble in water, soluble in chloroform,
ether, fixed oil, and volatile oils (hot turpentine oil) and
sparingly soluble in alcohol. It is not affected by the acids at
ordinary temperatures, but is converted into a black mass
when boiled with concentrated sulphuric acid.
 
Chemical Constituents
 
Beeswax contains myricin, which is melissyl palmitate;
melting point 64°C, free cerotic acid (C H O ), myricyl alcohol
26 52 2

(C H OH) is liberated when myricyl palmitate is saponified.


30 61

Melissic acid, some unsaturated acids of the oleic series,


ceryl alcohol, and 12 to 13% higher hydrocarbons are
present.
 
Uses-
 
Beeswax is used in the preparation of ointments, plaster,
and polishes.
 
Adulterants
 
Beeswax is adulterated by solid paraffin, ceresin, carnauba
wax, or other fats and waxes of animal or mineral origin.
Spermaceti and lard render wax softer and less cohesive, of
a smoother and less granular fracture and different odour
when heated. The melting point and specific gravity are
lowered by tallow, suet, lard, and especially by paraffin.
Ceresin, a principle obtained from ozokerite is also
employed as an adulterant. In yellow wax the iodine value is
also of use as a test for detection of adulterants but in white
wax the bleaching process has altered the bodies which
absorb the iodine.
 
Marketed Products
 
It is one of the ingredients of the preparations known as
Saaf Organic Eraser Body Oil and Jatyadi tail (Dabur).

You might also like