GYMNEMA SYLVESTRE R. Br: A COMPREHENSIVE REVIEW ON PHYTOCHEMICAL AND ANALYTICAL STUDYHTML Full Text
GYMNEMA SYLVESTRE R. Br: A COMPREHENSIVE REVIEW ON PHYTOCHEMICAL AND ANALYTICAL STUDY
E. R. Prajval, K. Girija*, K. Lakshman and Vinutha Bhat
Department of Pharmacognosy, PES College of Pharmacy, Bangalore - 560050, Karnataka, India.
ABSTRACT: Gymnema sylvestre R.Br is a valuable herb extensively used in the Ayurvedic and indigenous medicinal system, belonging to the family Ascelpiadaceae. It has property of abolishing the taste of sugar and hence given name gurmar (sugar destroying). This plant has also found application in pharmaceuticals; whole plant is rich in secondary metabolites, which impart medicinal uses to the plant. The view of phytochemistry gives scope for enhancement of the quality and quantity of the bioactive secondary metabolites occurring in the plant. The present review is an attempt to highlight the various phytochemical reports on Gymnema sylvestre.
Gurmar, Gymnemic acids Gymnema sylvestre, Ascelpiadaceae
INTRODUCTION: During the last two decades, the changes in modern life style and unhealthy food habits have resulted in obesity and diabetes in large sector of the population. In order to cater the needs of such people, the market is flooded with many synthetic antidiabetic medicines. However, the long term use of these drugs has resulted in many toxic side effects. Natural products and plant-based drugs are gaining importance as a source of antidiabetics due to growing concern over the use of synthetic chemicals 1. A considerable amount of work has been done to study the potentials of herbal medicines. Modern science has accepted the potential of plant kingdom as a source of new biodynamic constituents. The laborious research work that has been carried out in many research institutes in different parts of the world has brought into lime light the merits and qualities of various herbal medicine.
One such medicine with a good antidiabetic activity is Gymnema sylvestre R.Br. It is a valuable herb from the family Asclepiadaceae. It is a woody climber has a past history of usage about 2000 years in India for the treatment of “Madhumeha” 2, 3, 4. The word Gymnema is derived from a Hindu word “Gurmar” meaning destroyer of sugar and it is believed to be chewing of the leaves neutralizes the excess of body sugar level 5. The plant species is also known to be as Miracle fruit 6.
Botanical Classification: 10
Kingdom : Plantae
Division : Magnoliophyta
Class : Magnoliopsida
Order : Gentinales
Family : Asclepiadaceae
Genus : Gymnema
Species : G. sylvestre
Synonym: 7, 8, 9
English : Periploca of the woods
Hindi : Gurmar
Kannada : Kadhasige
Sanskrit : Meshashringi
Tamil : Shirukurum kaay
Telugu : Gurmaar Buuti
Bengali : Mera-singi
Guajarati : Dhuleti
Malayalam : Cakkarakkolli
Marathi : Kavali
Oriya : Gudmari
Habitat: It is found in various deciduous forest of India and common in Deccan peninsula.
FIG. 1: GYMNEMA SYLVESTRE R.Br
Ethno Medicinal Uses: 11, 12, 13
- Gymnema has played an important role in Ayurvedic medicine for centuries. Its use has been confined primarily to the management of diabetes mellitus and similar hypo / hyperglycemic conditions.
- According to the Ayurvedic Pharmacopoeia of India; both the dried leaf and root of gymnema, depending on dosage form and formulation, are also used in the treatment of svasa (bronchial asthma), kapha (cough), kustha (leprosy and other skin diseases), and vrana (wounds), among other conditions.
- Charak Samhita describes sylvestre, removes bad odor from breast milk. It is aperitive. This plant is useful as purgative and in eye troubles. The leaf extract and flower is beneficial for eyes. Bark is given in the diseases caused by vitiated kapha (phlegm). The root bark is useful in piles.
- Sushruta describes sylvestre, as a destroyer of madhumeha (glycosuria) and other urinary disease.
Phytochemical Study: Peter EM et al., in 1965 isolated nonacosane, hentriacontane, and tritriacontane by vapor phase chromatography from a hydrocarbon fraction of G. sylvestre leaves. The cyclic alcohol, conduritol A, rather than the previously reported viburnitol, was also isolated from these leaves. The molecular weight determination of conduritol A tetraacetate by mass spectrometry has been determined 14.
Joseph ES et al., in 1967 examined the leaves of G. sylvestre for the presence of alkaloids through the establishment of quaternary and nonquaternary nitrogenous fractions. The plant bases choline, betaine and adenine were isolated and identified in a combined yield of 0.04%. The amino acids leucine, isoleucine, valine, alanine and γ-amino-η-butyric acid were also identified 15.
Kurihara Y et al., in 1969 carried out structural elucidation in order to elucidate the relationship between the structures of various gymnemic acids and the abilities to suppress sweetness, the anti sweet activities of different gymnemic acid components were compared in this study. A new method was devised to isolate gymnemic acid A1 for preparative purpose. Gymnemic acid A1 was converted into A2 and finally into A3 by alkaline hydrolysis. Anti sweet activity of A1was greatly decreased to A2 where A3 didn’t show any activity 16.
Walter stocklin et al., in 1969 reported the major component, gymnemic acid A1, which possesses the antisweet property, has been shown to be a D-glucuronide of a new hexahydroxytriterpene. On the basis of physical and chemical data the structure of the new triterpene was established 17.
Joseph ES et al., in 19870 isolated genins G, K, N and gymnestrogenin with the aid of selective enzyme system and shown to be in the aglycones of gymnemic acids A-D, respectively. Genin G was found to be an acylated derivative of gymnemagenin containing formic, acetic, isovaleric and tiglic acids, while genin K differed from G by the absence of acetic acid reidue. Genin N was observed to be gymnestrogenin tiglate. The sugar moieties of acids A and B are not acylated, while those of acids C and D are indicated to be esterified with ferulic acid 18.
Isolation of crystalline gymnemagenin and gymnestrogenin from the leaves of G. sylvestre, together with preparation of various derivatives of the two aglcones, was described by Joseph ES et al., in 1971 19.
Morihiko et al., in 1989 isolated two major active components of gymnemic acids in pure state. Their chemical structures were established as D-glucuronide of 3β, 16β, 21β, 22β, 23, 28-hexahydroxyolean-12-ene which is esterified with tiglic acid or 2-methylbutyric acid at 21-C hydroxyl group, respectively. The antisweet activity of these compounds was discussed in relation to their structures 20.
Yoshisuke T et al., in 1989 reported structure of gymnemagenin, the sapogenin of antisweet principle of Gymnema was firmly established as 3β, 16β, 21β, 22α, 23, 28-hexahydroxy-olean l2-ene by the x-ray analysis of the 3β, 23; 21β, 23α-di-O-isopropylidene derivative. On the basis of this deacylgymnemic acid was elucidated as the 3-O-β-glucuronide by comparisions of 13C-NMR spectra 21.
Kazuko Y et al., in 1991 reported the leaves of G. sylvestre were extracted with 50% aqueous ethanol and the extract was successively chromatographed on an amberlite XAD-2 and tyopearl HW-40 columns to give fractions I-V. Fraction I and II were further separated by ordinary phase SiO2 and RP-HPLC on an ODS column to give five new saponins gymnema saponins I-V. Their structures were elucidated by spectroscopic studies 22.
Kazuko Y et al., in 1992 isolated seven new dammarane type saponins, named gymnemasides I-VII from the leaves of G. sylvestre, together with the previously known dammarane-type saponins, gypenoside XXVIII, XXXVII, LV, LX11 and LXIII. Their structures were characterized by spectral data and chemical transformations 23.
Liu HM et al., in 1992 isolated five antisweet principles, gymnemic acid III, IV, V, VIII, and IX, in pure states from the hot water extract of leaves of G. sylvestre The structures of gymnemic acid VIII and IX were elucidated as 3'-O-β-D-arabino-2-hexulopyranosyl gymnemic acid III and IV, respectively 24.
Kazuko Y et al., in 1992 isolated five oleanane-type triterpenoid saponins, gymnemic acids VIII-XII as antisweet principles from the leaves of G. sylvestre and characterized as glucosideuronic acid derivatives of gymnemagenin acylated with acetyl, tigloyl and 2-methylbutyroyl moieties 25.
Kazuko Y et al., in 1993 isolated four new saponins, gymnemic acids XV-XVIII, as anti sweet substances. The structures were elucidated by spectral and chemical studies. Gymnemic acids XV - XVIII, are 21- O- 2- methylbutyryl- 22- O-2 methylcrotonoyl, 16-22-O-bis-2- methylcrotonoyl, 21-O-benzyol, and 28-O-benzoyl gymnemagenin 3-O-gluculonides, respectively 26.
Niranjan PS et al., in 1996 isolated four new tritepenoid saponins, gymnemasins A, B, C and D, from the leaves of G. sylvestre, were identified as 3-O-[β-D-glucopyranosyl(1→3)-β-D-glucuronopy-ranosyl]- 22- O-tigloyl-gymnemanol, 3- O- [β-D-glucopyranosyl(1→3)- β- D- glucuronopyranosyl]-gymnemanol, 3- O- β-Dglucuronopyranosyl- 22-O-tigloyl gymnemanol and 3- O- β- D-glucuro-nopyranosyl - gymnemanol, respectively. The aglycone, gymnemanol, which is a new compound, was characterized as 3β, 16 β, 22α, 23, 28-pentahydroxyolean-12-ene 27.
Wen CY et al., in 2000 isolated six oleanane-type saponins, along with two known triterpene saponins, were isolated from the leaves of G. sylvestre. The structures of the oleanane triterpene glycosides were characterized on the basis of hydrolysis and spectral evidence, including 1D- and 2D-NMR (TOCSY, ROESY, HMQC and HMBC) and FABMS analyses 28.
Wencai Y et al., in 2001 isolated three new oleanane-type triterpene glycosides (1-3), along with the sodium salt of alternoside II, from an ethanol extract of the leaves of G. sylvestre. The structures of these new saponins were identified and structure elucidation was accomplished by interpretation of NMR (DQF-COSY, HMQC, and HMBC) results, FABMS, and hydrolysis 29.
Shu LP et al., in 2005 isolated novel oleanane type triterpenic acid from the leaves of G. sylvestre. The structure was characterized as 3β, 16β, 22β, 28-tetrahydroxy- olean-12-en-30-oic acid on the basis of spectral evidence, including 1D- and 2D-NMR (HMQC, HMBC, 1H-1H COSY and NOESY) 30.
Balaram M et al., in 2006 reported the glycone part of the flavonoid triglycoside, kaempferol 3-O-β-D-glucopyranosyl-(1→4)- α- L- rhamnopyranosyl-(1→6)-β- D- galactopyranoside, has been synthesized with good yield and stereoselectivity using N-iodosuccinimide and HClO4–silica promoted glycosylations of thioglycoside donors 31.
The chemical constituents from the stem of G. sylvestre were extracted by percolation with ethanol, part of n-butanol extract was isolated and purified by macroporous adsorptive resins, silica gel column chromatography, sephadex gel column chromatography and recrystallization. Zhen HS et al., in 2008 isolated eight compounds and were identified as Conduritol A, 1-Heptadecanol, Stigmasterol glucoside, 1-Quercitol, 1-Octadecanol, Potassium nitrate, Lupeol cinnamate, Stigmasterol 32.
Zhu XM et al., in 2008 isolated Gymnemoside-W1 and W2, together with seven known compounds from the leaves of G. sylvestre. By means of spectral and chemical analysis, the structures of the new compounds were elucidated as 16 beta-hydroxyl olean-12-en-3-O-[beta-D-glucopyranosyl (1-->6)-beta-D-glucopyranosyl]- 28- O- beta- D-glucopyranoside and 16 beta, 21 beta, 28- tri-hydroxyl-olean-12-ene-3-O-glucoronopyranoside 33.
Dr. Farzana et al., in 2010 carried out isolation and characterization of gymnemic acid from indigenous G. sylvestre leaves. Four different methods of extraction were employed to obtain the maximum yield. The method where the defatted leaves were extracted under continuous hot extraction in Soxhlet apparatus with 95% ethanol gave the maximum yield of gymnemic acid (6.15% m.f.b.). The yield was minimum in aqueous extraction method (1.66% m.f.b.) Gymnemic acid was purified by preparative chromatographic method in two solvent systems. Its circular Thin Layer Chromatography (TLC) also resulted in to a single concentric ring. Gymnemic acid was hydrolyzed by two methods to confirm its glycosidic nature. The presence of stigmasterol, β-amyrin, β-amyrin acetate and lupeol was indicated when the reference samples of these compounds were run on the same chromatoplate 34.
Krishna BR et al., in 2012 isolated Gymnemic acid from G. slyestre leaves by soxhlet using different solvents like petroleum ether, benzene, methanol and HPTLC analysis showed 30% purity with methanol 35.
Volatile components of flowers of G. sylvestre were extracted by water vapor distilling, and the 55 components were separated and 33 components were identified, accounting for 88.73% of all quantity. The principal volatile components were found to be Phytol, Pentacosane, 10-Heneicosene (c,t), 3-Eicosene, (E) -and 2-Methyl-Z-2-docosane, this study was done by Quiu Q et al., in 2013 provided scientific basis for chemical component research of flowers of G. sylvestre 36.
Liu Y et al., in 2014 isolated seven compounds from G. sylvestre and their structures were elucidated as conduritol A, stigmasterol, lupeol, stigmasterol-3-O-β-D-glucoside, the sodium salt of 22α- hydroxy- longispinogenin- 3- O- β- D-glucopyranosyl-(1→3)-β- D-glu-curono-pyranosyl-28-O-α-L-rhamnopyranoside, oleanolic acid-3-O-β-D-glucopyranosyl-(1→6)- β- D- glucopyranoside, and the sodium salt of 22α-hydroxy-longispinogenin 3- O- β-D-glucuronopyranosyl-28-O-α-L-rhamnopyranoside, on the basis of MS and spectroscopic analysis (1D and 2D NMR), as well as chemical methods 37.
Vishwa raj lal et al., in 2015 isolated and characterized the Gymnemic acid, from five ecotypes of G. sylvestre leaves with different solvent systems like petroleum ether, benzene, and methanol. The defatted leaves were extracted under continuous hot extraction in Soxhlet apparatus with 90% methanol gave the maximum yield of gymnemic acid (42%) in the ecotype collected from Ranchi. Gymnemic acid was purified by preparative chromatographic methods 38.
Srinivasan K et al., in 2016 determined the chemical composition of ethanolic extract of G. sylvestre through Gas Chromatography-Mass Spectrometry technique. GC - MS analysis of leaf extracts revealed the existence of Terpenes, alcohols, fatty acids, amine and sterols. The highest % Peak area is hexadecanoic acid, α-Santoline alcohol, recorded the next highest % peak area of 9.05. Major of the compounds belongs to terpeneoid group, namely 6-Octen-1-ol, 3, 7-dimethyl, Isophytol, Squalene, Nerolidol, β-Amyrin and Cedrene-V6 which constitutes 30.7% of the peak area. The presence of α-Tocopherol-β-D-mannoside and Vitamin E also identified through this study 39.
Analytical Study: The molecular masses of gymnemic acid homologues were determined by Toshiaki et al., in 1991 with high-performance liquid chromatography combined with atmospheric pressure ionization mass spectrometry. A mixture of gymnemic acids was chromatographed on an octadecyl silica column eluted with an aqueous methanol solution containing ammonium acetate, and directly introduced into an atmospheric pressure ionization mass spectrometer. Quasimolecular ions of gymnemic acids were detected as ammonium adduct ions. Molecular masses of thirteen different gymnemic acids and five compounds not containing glucuronic acid in their molecules were evaluated. Three pairs of geometrical isomers of gymnemic acids were found 40.
Puratchimani V et al., in 2004 carried out a simple and reproducible HPTLC for the determination gymnestrogenin from G. sylvestre was developed on silica gel 60F254 by using CHCl3:MeOH (9:1) and scanned using densitometric scanner in UV reflectance photomode at 293 nm. The linearity was observed in the range of 4 – 10 μg. The gymnestrogenin content of 1.11% in test sample w/w was observed in test sample. The average percentage recovery value of 99.1 ± 0.27 was obtained 41.
Sai Kishore S et al., in 2008 carried out a comparison study for estimation of gymnemic acids by HPLC and gravimetry method for various extracts of G. sylvestre was an Isocratic, reversed phase HPLC procedure has been adopted by using a mixture of acetonitrile (23%) and 0.1% orthophosphoric acid as mobile phase, C18 column as stationary phase and UV detector. HPLC method shows high resolution, accuracy and reproducibility than gravimetry estimation of Gymnemic acids in G. sylvestre 42.
A reproducible and reliable HPTLC method for the indirect determination of gymnemic acids as gymnemagenin in G. sylvestre plant has been reported by Trivedi PD et al., in 2008 Post-derivatzation method was used for quantification of gymnemagenin. Linearity was observed in the range of 180 - 1440 ng/spot. Percentage recovery was found to be 98.4 ± 1.0% 43.
Trivedi PD et al., in 2011 developed a liquid chromatographic method for the determination of gymnemagenin in leaves of G. sylvestre. Gymnemagenin was obtained after acidic hydrolysis followed by basic hydrolysis of the sample and extraction into ethyl acetate. Analyte separation and quantification were achieved by isocratic reversed-phase liquid chromatography and UV detection at 220 nm. The method involves the use of an RP-18e Lichrocart reversed-phase column (5 μm, 75 × 4 mm id) and a binary isocratic mobile-phase profile. Linearity was observed in the range of 9.18 to 720 μg ml-1 with correlation coefficient of 0.998. Relative standard deviation of linearity of the method was found to be 0.015% 44.
A novel attempt has been made by Killedar SG et al., in 2012 to study the various parameters for the development of G. sylvestre leaf extracts for injectable dosage forms. Ethanolic and water extracts of G. sylvestre were obtained by decoction and filtered through whatman paper-1. Stability and solubility were studied after drying the extracts in a vaccum dryer. Phytochemical screening and TLC study was carried out. Injections of different strength of dried extracts were made using normal saline and sterilized by autoclaving, where dried extracts showed 39 ºC and 65% relative humidity. Liquid extracts showed presence if triterpenoids, sugars, proteins. Gymnemic acid was found to be major constituent it was confirmed by TLC by comparing with standards 45.
Dinesh KP et al., in 2012 subjected methanol extracts of the leaves to TLC, FTIR, GC-MS analysis. TLC analysis with CH3OH:CHCl3 solvent revealed 6 fractions with Rf values of 0.23, 0.35, 0.45, 0.59, 0.69 and 0.85. FTIR spectroscopic investigation gave characteristic peak values with various functional compounds such as alcohols, phenols, alkanes, alkynes, alkyl halides, aldehydes, carboxylic acids and aromatics. GC-MS analysis gave a spectrum of compounds with 10 major peaks, most of which are bioactive compounds which may act as good antimicrobial, antiviral, antioxidant and anti-inflammatory agents 46.
In the present study attempts were done by Manika N et al., in 2012 to identify the efficient extraction procedure including solvent selection and methods, stability assessment in terms of drying as well as storage and changes occurring during annual cycle using an important analytical marker gymne-magenin. The yield of the marker was found to be highest in acid–base hydrolysis extract (1.17%). Among different drying methods adopted, gymnemagenin content was high in shade dried leaves (1.15%) while it was significantly low in sun dried material (0.54%). Estimate of yield and enriched gymnemagenin (1.01 - 1.23%) indicated that summer (April - July) is the ideal time to harvest G. sylvestre 47.
Tahira anjum et al., in 2013 studied leaves of G. sylvestre is used by peoples of Vidisha district for treatment of diabetes. The active compound of this plant is a group of acids termed as gymnemic acid. Gymnemic acids have antidiabetic, antisweetner and anti inflammatory activities. The phyto-constituents of G. sylvestre were isolated and their chemistry and structures were studied and elucidated. The result of investigation was helpful for the correct botanical identification of plant and also different sources of medicine and pharmaceutical industry 48.
Sachin EP et al., in 2014 developed a new, rapid, accurate, robust, and precise HPTLC method for concurrent quantitative determination of gymnemagenin and β-sitosterol in herbal formulation with densitometric detection. Chromatographic separation was achieved on Merck aluminum HPTLC plates precoated with silica gel 60 F254. The optimized solvent system consisted of toluene: ethyl acetate: methanol (6.5:2.5:1.4 v/v/v) were the solvent system used. Developed plates were derivatized with 5% sulphuric acid reagent followed by heating at 110ºC for 4 min in a preheated oven and scanned at 423 nm in reflectance absorbance mode. The retention factor for gymnemagenin and β-sitosterol was found to be 0.27 ± 0.02 and 0.78 ± 0.02, respectively. The proposed densitometric method was validated according to ICH Q2 (R1) guidelines. Results were found to be linear over a range of 100 - 1200 ng band−1 and 200 - 1200 ng band−1 for gymnemagenin and β-sitosterol, respectively 49.
Kusum D et al., in 2014 developed and validated a simple precise and rapid HPLC method for the quantification of gymnemic acid as deacyl gymnemic acids in G. sylvestre extract and formulations. The analysis was performed by a reverse phase chromatography on a phenomenex C18 Column with isocratic elution of acetonitrile buffer (23:77 v/v) at a flow rate of 2.0 ml/min. The linearity was found to be 50 - 800 μg/ml with correlation coefficient of 0.9998 50.
Pawan KS et al., in 2015 reported the quality control and assurance of parameters were carried out as per authenticated standard guideline to assess the quality and comparative screening of three gurmar butti leaves samples. The physicochemical data showed that the drug samples contained foreign matter (0.24%, 0.28%, 0.12%), moisture (4.24%, 4.98%, 5.20%) and ash contained (9.78%, 9.96%, 9.71%), acid in-soluble ash (1.81%, 2.04%, 1.61%), soluble extract in water (26.43%, 26.57%, 26.73%) and in alcohol (12.75%, 12.94%, 12.98%). HPTLC studies of aqueous and alcohol extracts showed various spots at 366 nm (UV region) using selected suitable solvent system of mobile phase. The quality control results revealed the absence of microbial load, Heavy metal (ppm) and Aflatoxins (ppm) contamination from the drug samples 51.
A validated (HPLC-DAD) method was developed by Tushar D et al., in 2015 for identification and quantification of bioactive principle gymnemagenin in a gradient elution mode using solvent mixture composing of acetonitrile (A), potassium dihydrogen orthophosphate (B) both solvent (A and B) containing orthophosphoric acid (0.05%, v/v). Results revealed significant differences for gymnemagenin content amongst the accessions evaluated. These accessions could be used in breeding programs for development of cultivars with optimum levels of gymnemagenin, which in turn may promote the cultivation of this high value medicinal crop 52.
Subashini MS et al., in 2015 performed different phytochemical test, TLC analysis, solubility study, total phenol content, flavonoid content and antimicrobial study in the present investigation. Fingerprint analysis and quantitative analysis of quercetin were also performed through HPTLC method in the G. sylvestre extract. Solubility in water and alcohol, moisture content and gymnemic acid content were found to be 86.36%, 88.24%, 4.20% and 26.24% w/w. Total phenol and flavonoid content were found to be 0.80% and 1.90%. Microbiological assay was also performed 53.
CONCLUSION: According to literature survey the plant has extremely large medicinal, Immemorial, Ethno botanical, traditional uses and economic uses in different systems of Medicine throughout the world. The active principles of the plant are present in very complex mixture which created limitation in their isolation. There has been a rapid development in the isolation and characterization techniques. But a view into past methods is worthful in understanding the properties of compounds present and makes future works easy, less time consuming and use of modern improved techniques. The wide varieties of compounds isolated from this plant need to research in depth to establish their profile. This paper gives detail information of some isolation and analytical procedures to provide better scope for performing the further investigation in the plant.
ACKNOWLEDGEMENT: Authors are thankful to the Director, Principal and Management of PES College of Pharmacy, Hanumanthanagar, BSK I Stage, Bengaluru - 560050, Karnataka for their encouragement and support.
CONFLICTS OF INTEREST: Nil
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How to cite this article:
Prajval ER, Girija K, Lakshman K and Bhat V: Gymnema sylvestre R. BR: A comprehensive review on phytochemical and analytical study. Int J Pharmacognosy 2018; 5(5): 270-77:.doi link: http://dx.doi. org/10.13040/IJPSR.0975-8232.IJP.5(5).270-77.
This Journal licensed under a Creative Commons Attribution-Non-commercial-Share Alike 3.0 Unported License.
E. R. Prajval, K. Girija*, K. Lakshman and V. Bhat
Department of Pharmacognosy, PES College of Pharmacy, Bangalore, Karnataka, India.
04 December, 2017
19 January, 2018
13 February, 2018
01 May, 2018