PHYTOCHEMICAL ANALYSIS OF LEAF EXTRACTS OF WATTAKAKA VOLUBILIS LINN. (STAPF) BY GC-MS METHOD
HTML Full TextPHYTOCHEMICAL ANALYSIS OF LEAF EXTRACTS OF WATTAKAKA VOLUBILIS LINN. (STAPF) BY GC-MS METHOD
Karuppusamy Sridhara Vishnusithan and Malaiyandi Kamaraj*
P.G. and Research Department of Botany, Jamal Mohamed College (Autonomous), Tiruchirappalli- 620 020, Tamil Nadu, India
ABSTRACT
The aim of the study was to investigate the phytochemical compounds of Wattakaka volubilis ethanolic leaf extracts. The phytochemical compounds were screened by GC-MS method. The ethanolic leaf extracts presented 32 bioactive compounds. The identification of phytochemical compounds is based on the peak area, molecular weight and molecular formula. Diethyl phthalate C12H14O4 has peak area 37.31, 2-pentanone, 3, 3, 4, 4-tetramethyl C9H18O has peak area 17.58 and propane 1, 1, 3-trimethoxy C9H20O3 has peak area 10.20 and the results were presented.
Keywords:
Wattakaka volubilis, Phytochemical analysis, |
Leaf extract
INTRODUCTION:Plants have been an important source of medicines for thousands of years. Everyday, the World Health Organization estimates that upto 80 percent of people still rely mainly on traditional remedies such as herbs for their medicines. Its civilization is very ancient and the country of a whole has long been known for its rich resources medicinal plants. Today, ayurvedic, homeo and unani physicians utilize numerous species of medicinal plants are possibly utilized as antiseptic and antimicrobial substances.
Wattakaka volubilis (Linn F.) Stapf (Family- Asclipidiaceae) is a large climber with green flowers in drooping umbels with smooth bank and ash coloured leaves rounded at the base. It is found in India and South East Asia. The root is applied to snake bites and given to women to cure head ache after child birth and the leaves are applied to boils and abscesses to promote suppuration. It is an emetic, diphoretic and diuretic 2. Traditional healers of Kerala used its leaves to treat inflammatory and painful conditions 3. However, till date no scientific validation of these properties has been reported.
Here, the present study has been made to identify the Phytochemical compounds of W. volubilis by GC-MS analysis.
MATERIALS AND METHODS:
Collection of Plant Material: The plant W. volubilis was collected from the garden of Jamal Mohamed College, Tiruchirappalli. The plant was identified and voucher specimen was deposited in the Rapinet Herbarium, St. Joseph’s College, Tiruchirappalli.
Preparation of Extracts: The plant leaves wereair dried and crushed to small piece using mortar and pestle and powdered in an electric grinder. Dried and powdered plant material was extracted using soxhlet apparatus with ethanol as solvent (50-60oC) for 72 hrs.
The obtained extracts were evaporated in vacuum to give residues. A semi solid residual extract was obtained. It was stored at 4oC until used. When needed, the residual extract was dissolved in distilled water and used in the study. The extracts preparations were done as previously described by Allade and Irobi 4.
GC-MS Analysis: The GC-MS analysis of unknown compounds of W. volubilis deals with using a Clarus 500 Perkin Elmer Gas Chromatography ionizes compounds and measures their mass number equipped with Elite-5-Capillary Column (5% phenyl 95% dimethyl poly siloxane) (30 mm x 0.25 mm ID x 0.25 µmdf) and mass detector turbomass gold of the company which was operated at in EI mode. Helium was carried the gas at the flow rate of 1 ml / min, the injector was operated at 280oC and the oven temperature was programmed as follows : 70oC @ 8 oC/min to 150oC (1 min) @ 8oC / min to 280oC (10 min). The identification of components was based on comparison of their mass spectra with those of Wiley and NBS Libraries and those described by Adams 5 as well as on comparison of their retention indices with literature 6.
RESULTS AND DISCUSSION: The present study carried out on the W. volubilis revealed the presence of medicinal active constituents. In GC-MS analysis 32 bioactive phytochemical components were identified in the ethanolic extract of W. volubilis. The identification of phytochemical compounds is based on the peak area, molecular weight and molecular formula. Diethyl phthalate (C12H14O4) with RT 16.55 has peak area 37.31, 2-pentanone, 3, 3, 4, 4-tetramethyl (C9H18O) with RT 14.93 has peak area 17.58 and propane 1, 1, 3-trimethoxy (C9H20O3) with RT 6.84 has peak area 10.20, the results were presented in table 1, figure 1.
TABLE: CONSTITIENTS AND PERCENTAGE COMPOSITION OF THE ETHANOLIC LEAF EXTRACT OF W.VOLUBILIS
S. No | Peak name | Retention time | Peak area | % Peak area |
1 | Propane, 1,1,3-triethoxy-
Formula: C9H20O3 MW: 176 |
6.84 | 6359325 | 10.2012 |
2 | Ethane, 1,1-diethoxy-
Formula: C6H14O2 MW: 118 |
7.29 | 99703 | 0.1599 |
3 | Tridecane
Formula: C13H28 MW: 184 |
9.17 | 442012 | 0.7090 |
4 | Benzoic acid, 2-hydroxy-, methyl ester
Formula: C8H8O3 MW: 152 |
9.34 | 3260023 | 5.2295 |
5 | 1,2-Benzenedicarboxylic acid
Formula: C8H6O4 MW: 166 |
11.74 | 104790 | 0.1681 |
6 | Decane, 6-ethyl-2-methyl-
Formula: C13H28 MW: 184 |
13.02 | 573829 | 0.9205 |
7 | 1,2,3,4-Cyclohexanetetrol
Formula: C6H12O4 MW: 148 |
13.41, 14.27, 13.71 | 1753306 | 2.8125 |
8 | Dodecane, 1-chloro-
Formula: C12H25Cl MW: 204 |
14.42 | 103779 | 0.1665 |
9 | 1-Dodecanol
Formula: C12H26O MW: 186 |
14.48 | 139343 | 0.2235 |
10 | 2-Pentanone, 3,3,4,4-tetramethyl-
Formula: C9H18O MW: 142 |
14.93 | 10961298 | 17.5833 |
11 | n-Decanoic acid
Formula: C10H20O2 MW: 172 |
15.96 | 145530 | 0.2334 |
12 | Diethyl Phthalate
Formula: C12H14O4 MW: 222 |
16.55 | 23263070 | 37.3169 |
13 | 1-Undecanol
Formula: C11H24O MW: 172 |
18.01 | 282572 | 0.4533 |
14 | Isooctanol
Formula: C8H18O MW: 130 |
18.50 | 52380 | 0.0840 |
15 | 2-Piperidinone, N-[4-bromo-n-butyl]-
Formula: C9H16BrNO MW: 233 Alkaloid (piperidine type) |
19.13 | 146969 | 0.2358 |
16 | Sulfurous acid, 2-ethylhexyl isohexyl ester
Formula: C14H30O3S MW: 278 |
19.53 | 247774 | 0.3975 |
17 | 3-Butylindolizidine
Formula: C12H23N MW: 181 Alkaloid (indole group) |
19.71 | 53083 | 0.0852 |
18 | 3,7,11,15-Tetramethyl-2-hexadecen-1-ol
Formula: C20H40O MW: 296 |
20.05,20.64 | 1880117 | 3.0159 |
19 | á-k-Strophanthin
Formula: C36H54O14 MW: 710 |
20.16,21.60, 31.73 | 2295909 | 3.6829 |
20 | Uridine, 2'-deoxy-3-methyl-3',5'-di-O-methyl-
Formula: C12H18N2O5 MW: 270 |
20.28 | 92554 | 0.1485 |
21 | 1-Hexadecyne
Formula: C16H30 MW: 222 |
20.38 | 244581 | 0.3923 |
22 | Undecanoic acid
Formula: C11H22O2 MW: 186 |
21.76 | 749327 | 1.2020 |
23 | Decanoic acid, ethyl ester
Formula: C12H24O2 MW: 200 |
22.10 | 382719 | 0.6139 |
24 | Cyclohexanone, 2-ethyl-4-methoxy-
Formula: C9H16O2 MW: 156 |
22.26 | 90720 | 0.1455 |
25 | 4-Oxazolecarboxylic acid, 4,5-dihydro-2-phenyl-, 1-methylethyl ester
Formula: C13H15NO3 MW: 233 |
23.12 | 26531 | 0.0426 |
26 | Phytol
Formula: C20H40O MW: 296 |
23.57 | 1919497 | 3.0791 |
28 | Oxirane, (7-octenyl)-
Formula: C10H18O MW: 154 |
24.21 | 177971 | 0.2855 |
29 | Hexadecane, 1,2-epoxy
Formula: C16H32O MW: 240 |
26.01 | 450888 | 0.7233 |
30 | Hexanedioic acid, mono(2-ethylhexyl)ester
Formula: C14H26O4 MW: 258 |
26.64 | 970462 | 1.5567 |
31 | Pentadecanal-
Formula: C15H30O MW: 226 |
28.17 | 2326460 | 3.7319 |
32 | trans-Squalene
Formula: C30H50 MW: 410 |
32.24 | 2742765 | 4.3997 |
100.0000 |
FIGURE 1: GC-MS CHROMATOGRAM OF ETHANOLIC EXTRACTS OF W.VOLUBILIS
Arunkumar and Muthuselvam reported in the GC-MS analysis, 26 bioactive phytochemical compounds were identified in the ethanolic extrct of Aloe vera. The identification of phytochemical compounds is based on the peak area, molecular weight and molecular formula. J. sitostera (C29H50O) with RT 38.78 has peak area 13.19%, Oleic Acid (C18H34O2) with RT (21.85) and 9,12,15-Octadecatrienoic acid methyl ester (Z, Z, Z) (C19H33C2) with RT 22.6 ranks next having peak area 11.74% and 11.36% respectively 7.
Investigated fourteen aromatic and 24 aliphatic acids were determined by GC-MS analysis of acidic fractions obtained from Paronia peregrine and Paeonia tenifolia roots. Benzoic acid and its monohydroxy-dihydroxy and tri-hydroxy derivatives are the main acid components of both Paronia species. Some fractions could serve as a source of benzoic 4-hydroxy benzoic, vanillic and gallic acids as well as of ethyl gallate 8.
GC-MS results revealed phenols, aromatic carboxylic acids and esters in the chloroform extract 9. The GC-MS analysis of a botanically certified Oleogama Resin of Boswellia sacra essential oil revealed the presence of 34 monoterpenes and 16-sesquiterpens 10.
CONCLUSION: This study revealed the presence of 32 phytochemical compounds. The identification of the compounds W. volubilis could be exploited for new potent antidiabetic agents.
ACKNOWLEDGEMENT: The authors are thankful to the Centre for Advanced Research in Indian System of Medicine (CARISM), Sastra University, Thanjavur, for offering facilities to carryout this study.
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Article Information
55
1867-1871
529KB
1532
English
IJPSR
Karuppusamy Sridhara Vishnusithan and Malaiyandi Kamaraj*
P.G. and Research Department of Botany, Jamal Mohamed College (Autonomous), Tiruchirappalli- 620 020, Tamil Nadu, India
20 February, 2012
25 May, 2012
29 May, 2012
http://dx.doi.org/10.13040/IJPSR.0975-8232.3(6).1867-71
01 June, 2012