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Isolation Identification and Analysis of Phytoconstituents

This document provides information on the extraction and identification of several phytoconstituents including curcumin, artemisin, atropine, citral, menthol, caffeine, and reserpine. For each constituent, it describes the biological source, extraction method, and thin layer chromatography method for identification and analysis.

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Murugan M
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412 views30 pages

Isolation Identification and Analysis of Phytoconstituents

This document provides information on the extraction and identification of several phytoconstituents including curcumin, artemisin, atropine, citral, menthol, caffeine, and reserpine. For each constituent, it describes the biological source, extraction method, and thin layer chromatography method for identification and analysis.

Uploaded by

Murugan M
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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ISOLATION

IDENTIFICATION AND
ANALYSIS OF PHYTOCONSTITUENTS
DR.U.SRINIVASA,
PROFESSOR AND HEAD,
SRINIVAS COLLLEGE OF PHARMACY,
MANGALORE – 574143
EMAIL
[email protected], [email protected],
[email protected]
CURCUMIN
 Curcumin or Curcuminoids are the diaryl hepnoid
compounds obtained from the dried rhizomes of
Turmeric, Curcuma longa, Family – Zingiberaceae

 Curcumin is the major colouring principle. It is a


mixture of curcumin, monodesmethoxycurcumin and
bisdesmethoxycurcumin
 It as an orange yellow, crystalline powder

 Insoluble in water and ether, but soluble in alcohol

 It is used as wound healing, ant-inflammatory, anti arthritic


and antimicrobial activities

 Used against peptic ulcer


EXTRACTION AND ISOLATION
 Curcumin can be obtained by different processes

 Turmeric powder is extracted with alcohol in Soxhlet


extractor. Alcoholic extract is concentrated under reduced
pressure and dried.

 In another method , Turmeric powder is extracted with is first


extracted with hexane followed by acetone.

 The acetone extract is concentrated and dried to yield


curcumin. It is recrystallized from hot ethanol to yield orange
red needles.
Identification and Analysis
T.L.C Method
Sample preparation – Dissolved 1mg of Curcumin in 1ml
of methanol
Stationary phase - Silica gel –G
Standard sample - Curcumin
Detecting agent – Observed under U.V light at 366nm
Mobile phase – Chloroform - Ethanol - Glacial acetic acid
(94:5:1)
RF Value – Curcumin – 0.79
ARTEMISIN
 Synonym – Santonica

 Biological source – Artemisin is a sesquiterpenoid


lactone , obtained from the unexpanded flower- heads of
Artemisia annua

 Family - Compositae

 Medicinal use – Antimalarial drug

 White crystalline powder, soluble in organic solvents


EXTRACTION AND ISOLATION

 The leaves are air dried, coarsely powdered and extracted


with petroleum ether (40-60).

 The extract is concentrated ,dried and re-dissolved in


chloroform. Add acetonitrile to precipitate sugars and
waxes.

 Filter and collect the filtrate. Evaporate to dryness to yield


residue
 The chromatographic fractionation of the concentrate on
silica gel by eluting with Chloroform- ethyl acetate yields the
fraction of artemisin

 The fractions containing artemesin could be crystallised from


cyclohexane or 50% Ethanol
Identification and Analysis

T.L.C Method
Sample preparation – Dissolved 1mg of Artemisin in 1ml
of Chloroform
Stationary phase - Silica gel –G
Standard sample - Artemisin
Detecting agent – p- dimethylaminobenzaldehyde and heat at
80C to produce color
Mobile phase – Petroleum ether - Ethyl acetate (1:2)
RF Value – Compare with standard Artemisin
ATROPINE
 Atropine is a tropane alkaloid obtained from Atropa
belladonna ,Datura stramonium and Hyoscyamus niger

 Family – Solanaceae

 Used as Antispasmodic, Mydriatic etc


EXTRACTION AND ISOLATION
 Take weighed quantity of coarse powder and moisten with
sodium carbonate solution.

 Extract the blended mixture in petroleum ether. Filter the


petroleum ether extract

 Extract the filtrate with aqueous acetic acid ( alkaloids


extracted in aqueous layer)

 Extract the aqueous fraction with solvent ether and


separate both fraction. Discard solvent ether fraction
 Aqueous (Acidic fraction) made alkaline with sodium
carbonate solution to obtain precipitates of tropane
alkaloids. Filter the precipitate and dry to obtain residue.
 Dissolve the residue in diethyl ether .Filter and
concentrate the filtrate. Atropine crystals will be
separated out.
 Filter the crystals and dissolve in alcohol containing
sodium hydroxide solution ( Hyocyamine is converted to
atropine)
 Recrystallize the atropine sulphate from acetone.
Separate the crystals of atropine.
Identification and Analysis

 Chemical test –

 Vitalin –morin test -

 Take small quantity of the solid atropine and add 2 drops of


Con.nitric acid in an evaporating dish and evaporated to
dryness on water bath. Then dissolve the residue in 1ml of
acetone. Add few drops of freshly prepared alcoholic
potassium hydroxide solution.

 Violet colouration takes place due to tropane nucleus


T.L.C Method
Sample preparation – Dissolved 1mg of Atropine in 1ml
of Chloroform
Stationary phase - Silica gel –G
Standard sample - Atropine
Detecting agent – Drangendroffs reagent to produce
yellow orange Color spots
Mobile phase – Toluene - Ethyl acetate – Diethyl amine
(70:20:10)
RF Value – Compare with standard Atropine (0.70)
CITRAL
 Biological sources –

 Citral is a monoterpene aldehyde found in variety of sources


like lemon grass, lemon and orange peels etc

 Cymbopogon fleuosus ( Lemon grass) , Graminae . 75-85%


of citral present in the drug

 Citral obtained from a natural source is a mixture of two


geometric isomers geranial and neral
 Properties

 Geranial and Neral both are light oily liquids with lemon
odour

 Citral is practically insoluble in water but miscible with


alcohol, ether, benzyl benzoate etc
EXTRACTION AND ISOLATION
 The fresh plant material is hydro- distilled to obtain lemon
grass oil.
 Purification by Fractional crystallization
 To the total oil, first Sodium sulphite is added, the citral get
converted into its sulphite salt
 The salt crystallizes out of the solution
 The crystals are filtered and washed with ether or chloroform
 The product is then subjected to sodium carbonate treatment
to recover citral
Identification and Analysis

T.L.C Method
Sample preparation – Dissolved 1mg of Citral in 1ml
of methanol
Stationary phase - Silica gel –G
Standard sample - Citral
Detecting agent – 2,4,dinitrophenyl hydrazine reagent to
produce Yellow to orange Color spots
Mobile phase – Pure Chloroform
RF Value – 0.51
MENTHOL
 Biological source –
 Menthol is a monoterpene alcohol obtained from different variety of
mint oils or peppermint oils
 Biological source – It consists of the fresh flowering tops of Mentha
piperita, Mentha officinalis
 Family- Labiatate
 Granular substance or crystalline with peppermint taste and odour,
freely soluble in alcohol, chloroform, ether, petroleum ether
EXTRACTION AND ISOLATION
 Take the accurately weighed quantity of coarse powder of
Mentha piperita parts just before flowering .
 Extract the peppermint oil by water distillation method.
 Separate the oil and allow cooling. Crystals of (-) menthol
will separate out.
 Collect the crystals by centrifugation.
 Re- Crystallize menthol from acetone or any other low
boiling point solvent
Identification and Analysis

T.L.C Method
Sample preparation – Dissolved 1mg of menthol in 1ml
of methanol
Stationary phase - Silica gel –G
Standard sample - Menthol
Detecting agent – 1% vanillin – sulphuric acid reagent and heat
the plate 110 0C for 10 minutes
Mobile phase – Pure Chloroform
RF Value – 0.48-0.62
CAFFEINE
 Caffeine is a purine alkaloid obtained from Tea leaves,
Coffee seeds, cocoa, and other species
 Biological source -It consists of dried leaves of plant known
as Thea sinensis
 Family – Theaceae
 It is chemically 1,3,7, trimethyl xanthine. It is isolated from
tea and coffee seeds during decaffeination process.
 Tea leaves contains 1-4% of caffeine and coffee contains 1-
2% of caffeine
 It is white powder or white ,glistering needles, odour less,
bitter in taste, Soluble in hot water.
 Caffeine is a CNS stimulant and Diuretic
EXTRACTION AND ISOLATION
 The powder tea leaves is extracted with boiling water
and the aqueous extract is filtered while hot.

 The warm extract is treated with lead acetate to


precipitate tannins and filtered.

 The filtrate is treated with excess of dilute sulphuric


acid to precipitate lead in the form of lead sulphate.
 Filter and collect the filtrate

 The filtrate is boiled with Activated charcoal to remove


colouring matter, if any and filtered to remove charcoal

 The filtered decolourized solution is extracted with


chloroform successively .

 Combined the chloroform extracts evaporate on water


bath to yield caffeine (white powder)

 It is recrystallized with alcohol


Identification and Analysis
 Chemical test –

 Murexide test – To the caffeine add hydrochloric acid


and potassium chlorate, heated to dryness. A purple
colour is obtained by exposing the residue to vapours of
dilute ammonia.

 Thin layer chromatography (TLC)


T.L.C Method
Sample preparation – Dissolved 1mg of caffeine in 1ml
of methanol or chloroform
Stationary phase - Silica gel –G
Standard sample - Caffeine
Mobile phase – Ethyl acetate: methanol : acetic acid
(80:10:10)
Detecting agent – Expose to vapors of iodine
RF Value – 0.41
RESERPINE
 Biological source – Reserpine is an indole alkaloid
obtained from the roots of Rauwolfia serpentina
 Family – Apocyanaceae
 It is a white or pale buff to slightly yellow, odourless,
crystalline powder
 It is soluble in alcohol, acetone and chloroform.
 Reserpine is an antihypertensive and antipsychotic
agent
EXTRACTION AND ISOLATION
 Rauwolfia root powder is exhaustively extracted with 90%
alcohol by percolation
 The alcoholic extract is concentrated and dried under
reduced pressure below 60c to yield Rauwolfia dry
extract.
 Rauwolfia dry extract is extracted with Ether-chloroform-
90%alcohol (20:8:2.5)
 Collect the extract and add little dilute ammonia with
intermittent shaking. Add water and allow the drug to
settle after vigorous shaking.
 Filter off the solution and extract the residue with 4
volumes of 0.5N Ammonium sulphate in separating
funnel. Combine all the extracts.
 The extract is made alkaline with dilute ammonia to
liberate alkaloid. Finally it is extracted with chloroform.
 Collect the chloroform extract , concentrate and
evaporate on water bath to yield total rauwolfia
alkaloids.(30 different components)
 Residue is subjected to column chromatographic
fraction for the separation of reserpine
Identification and Analysis
T.L.C Method
Sample preparation – Dissolved 1mg of Reserpine in 1ml
of methanol or chloroform
Standard sample - Reserpine
Stationary phase - Silica gel – G
Mobile phase – Chloroform: acetone :diethyl amine
(50:40:10)
Detecting agent – Dragendroffs reagent
RF Value – 0.72

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