PRELIMINARY PHYTOCHEMICAL ANALYSIS AND GAS CHROMATOGRAPHY MASS SPECTROMETRY SPECTRA OF CHLOROFORM EXTRACT FROM SPERMACOSE HISPIDA L. SEED

Authors

  • Gokula Krishnan Anantharaman Department of Biochemistry, Vels University, Chennai, Tamil Nadu, India.
  • Gayathri Krishnamoorthy Department of Biochemistry, Vels University, Chennai, Tamil Nadu, India.

DOI:

https://doi.org/10.22159/ajpcr.2017.v10i6.18090

Keywords:

Physicochemical analysis, Primary metabolites, Secondary metabolites, Yield, Gas chromatography mass spectrometry spectra

Abstract

  Objectives: Globally, scientific evaluation of traditional uses of herbal medicine, isolation, and characterization of bioactive constituents from herbs are some of the leading research areas. Spermacoce hispida (SH) is well known for its hypolipidemic and anti-obesity activity. The aim of this study is to qualitatively analyze the presence of primary and secondary metabolites in various extracts of SH seeds and to examine the presence of bioactive principles of chloroform extract from SH seeds.

Methods: Physicochemical analysis such as ash content, acid-soluble ash, water-soluble ash, moisture content, fiber content, ethanol soluble extractive value, and water-soluble extractive value for seeds of SH was determined as per WHO guidelines. Cold percolative extracts of seeds of SH with different solvents were carried out. Preliminary phytochemical analysis for the presence of various primary and secondary metabolites in extracts was determined. Gas chromatography mass spectrometry (GC-MS) analysis of chloroform extract was carried out.

Results: Physicochemical analysis values were found to be present in permissible level (<5%). Yield of ethyl acetate (4.9/100 g), ethanolic (4.2/100 g), and hydroalcoholic extract (4.0/100 g) of seeds of SH was found to be higher than that of extract obtained by soaking with different low polar solvents. Secondary metabolites such as phenol, flavonoid, and tannin are present in ethyl acetate, ethanolic, hydroalcoholic extract. Fat and alkaloid are present in chloroform extract. GC-MS spectra show the presence of 30 different bioactive constituents. Among them, n-hexadecanoic acid was found to constitute (5.83%) highest peak area than the remaining compounds.

Conclusion: Seeds of SH is a rich source of primary and secondary metabolites and various bioactive phytoconstituents.

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References

Bernerjee BG. Folk Illness and Ethnomedicine. New Delhi: Northern Book Center; 1988. p. 19.

Mosihuzzaman M. Herbal medicine in healthcare - An overview. Nat Prod Commun 2012;7(6):807-12.

Rajkumar T. Antimicrobial studies of Spermacose hispida seed oil. Int J Innov Pharm Sci Res 2013;1(1):62-70.

Dhevi R, Elango V. GC-MS evaluation of bioactive compounds from the seeds of Spermacoce hispida Linn. World J Pharm Res 2015;4(2):1171-80.

Kaviarasan K, Kalaiarasi P, Pugalendi V. Antioxidant efficacy of flavonoid rich fraction from Spermacoce hispida in hyperlipidemic rats. J Appl Biomed 2008;6:165-76.

Parthasarathy G. Evaluation of anti-inflammatory activity of methanolic extract of Spermacoce hispida Linn. J Pharm Res 2010;3(7):1516-7.

Rathi MA, Meenakshi P, Kumar DG, Raj CA, Sunitha M, Gopalakrishnan VK. Leaves of Spermacoce hispida as a novel cancer therapeutic - An in vitro study. Res J Pharm Technol 2011;4(8):1288-91.

Vinayagam R, Xu B. Antidiabetic properties of dietary flavonoids: A cellular mechanism review. Nutr Metab (Lond) 2015;12:60.

Yue-Tao L, Bi-Nan L, Li-Na X, Lian-Hong Y, Xiao-Na W, Jin-Yong P, et al. The antioxidant activity and hypolipidemic activity of the total flavonoids from the fruit of Rosa laevigata Michx. Nat Sci2012;2(3): 175-83.

Serafini M, Peluso I, Raguzzini A. Flavonoids as anti-inflammatory agents. Proc Nutr Soc 2010;69(3):273-8.

Prassas I, Diamandis EP. Novel therapeutic applications of cardiac glycosides. Nat Rev Drug Discov 2008;7(11):926-35.

Okuda T, Yoshida T, Hatano T. Pharmacologically active tannins isolated from medicinal plants. Basic Life Sci 1992;59:539-69.

Raisa HL, Jyothilakshmi M, Latha MS. Isolation and quantification of tannins from the root bark of Clerodendrum infortunatum Linn. And assessment of their antioxidant potential and antiproliferative effect on HCT-15 cells. Int J Pharm Pharm Sci 2015;7(10):170-5.

Antony de PB. An overview on the biological and pharmacological activities of saponins. Int J Pharm Pharm Sci 2014;6(8):47-50.

Yu F, Lu S, Yu F, Shi J, McGuire PM, Wang R. Cytotoxic activity of an octadecenoic acid extract from Euphorbia kansui (Euphorbiaceae) on human tumour cell strains. J Pharm Pharmacol 2008;60(2):253-9.

Aparna V, Dileep KV, Mandal PK, Karthe P, Sadasivan C, Haridas M. Anti-inflammatory property of n-hexadecanoic acid: Structural evidence and kinetic assessment. Chem Biol Drug Des 2012;80(3):434-9.

Kim JY, Oh TH, Kim BJ, Kim SS, Lee NH, Hyun CG. Chemical composition and anti-inflammatory effects of essential oil from Farfugium japonicum flower. J Oleo Sci 2008;57(11):623-8.

Abdelwahab SI, Zaman FQ, Mariod AA, Yaacob M, Abdelmageed AH, Khamis S. Chemical composition, antioxidant and antibacterial properties of the essential oils of Etlingera elatior and Cinnamomum pubescens Kochummen. J Sci Food Agric 2010;90(15):2682-8.

Swayamsiddha P, Meenakshi SM, Ravichandran N, Brindha P. Anticancer activity of ethanolic extract of Solanum torvum SW. Int J Pharm Pharm Sci 2014;6(1):93-8.

Published

01-06-2017

How to Cite

Anantharaman, G. K., and G. Krishnamoorthy. “PRELIMINARY PHYTOCHEMICAL ANALYSIS AND GAS CHROMATOGRAPHY MASS SPECTROMETRY SPECTRA OF CHLOROFORM EXTRACT FROM SPERMACOSE HISPIDA L. SEED”. Asian Journal of Pharmaceutical and Clinical Research, vol. 10, no. 6, June 2017, pp. 331-5, doi:10.22159/ajpcr.2017.v10i6.18090.

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