STUDY ON GAS CHROMATOGRAPHY AND MASS SPECTROSCOPY ANALYSIS, ANTIOXIDANT, AND NUTRITIVE PROPERTIES OF AERVA LANATA (L.) JUSS. COLLECTED FROM SELECTED REGIONS OF SHIMOGA, KARNATAKA, INDIA
DOI:
https://doi.org/10.22159/ajpcr.2019.v12i2.27998Keywords:
Aerva lanata (L) Juss, Antioxidant activity, GC-MS, nutritive propertiesAbstract
Objective: Aerva lanata (L.) Juss., the plant ethanolic extract was subjected to gas chromatography and mass spectroscopy, antioxidant, and nutritive experiment using standard methods.
Methods: Antioxidant experiment is done using 2, 2‑diphenyl‑1‑picrylhydrazyl, 2, 2‑azobis‑3‑ethylbenthiozoline‑6‑sulfonic acid, superoxide radical scavenging, hydroxy radical scavenging, and metal‑chelating assays. Nutritive value is performed by double acid digestion followed by atomic absorption spectroscopy.
Results: Antioxidant experiment revealed that A. lanata (L.) Juss. the plant ethanolic extract has good medicinal compounds exhibits excellent antioxidant activity in all tested experiments, but comparably less with the standards used. From nutritive value experiment, it is revealed that A. lanata (L.) Juss the plant has high iron content with rich macro‑ and micro‑nutrients.
Conclusion: A. lanata (L.) Juss. could be exploited as a valuable source of antioxidant agent enriching with nutrients.
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References
Goyal M, Pareek A, Nagori BP, Sasmal D. Aerva lanata: A review on phytochemistry and pharmacological aspects. Pharm Rev 2011;5:195 8.
Payal C, Gurlaganjeet K, Davinder K, Gagan S, Amit C, Dhawan RK. A review on phytochemistry and biological activity of Aerva lanata L. Med Pharm Plants 2015;4:2 4.
Malode UG. Pharmacognostic studies on ethnomedicinal plant Aerva lanata (L.) juss. Int J Pharm Biosci 2017;8:229 34.
Athira P, Sreesha N. Pharmacognostic review of medicinal plant Aerva lanata (L.). J Pharm Sci Res 2017;9:1420 3.
Nevin KG, Vijayammal PL. Pharmacological and immunomodulatory effects of Aerva lanata. in daltons lymphomaascites–bearing mice. Pharm Biol 2008;43:640 6.
Rajesh R, Chitra K, Padmaa M, Paarakh A, Chidambaranathan N. Anticancer activity of aerial parts of Aerva lanata (L.) Juss. Ex Schultagainst dalton’s ascitic lymphoma. Eur J Integr Med 2011;3:245 50.
Rajesh R, Chitra K, Padmaa M, Paarakh. In vitro anthelmintic activity of aerial parts of Aerva lanata Linn Juss. Int J Pharm Sci Drug Res 2010;2:269 71.
Arthi I, Subburaju T, Laxminarayanan B, Rajkumar LA. In vitro evaluation of antioxidant activity of aqueous extract of Aerva lanata (L.). J Pharm Res 2012;5:66 8.
Kumar G, Karthik L, Rao VB. Phytochemical composition of in vitro antioxidant activity of aqueous extract of Aerva lanata (L.) juss. Ex schult. stem (Amaranthaceae). Asian Pac J Trop Med 2013;6:180 7.
Ganesan P, Ramachandran T, Karthik T, Anand VS, Gowthaman T. Process optimization of Aerva lanata extract treated textile material for microbial resistance in healthcare textiles. Fibers Polym 2013;14:1663 73.
Thangavel A, Balakrishnan S, Armugam A, Duraisamy S, Muthusamy S. Phytochemical screaning, GCMS analysis of phytochemical constituents and antibacterial activity of Aerva lanata (L.) leaves. Afr J Pharm Pharm 2014;8:126 35.
Bitasta M, Madan S. Aerva lanata (L.): A blessing of mother nature. J Pharm Phytochem 2016;5:92 101.
Kayalvizhi D, Shivakumar V, Jayanthi M. Phytochemical screening and antinephrolithiasis activity of ethanol extract of Aerva lanata on ethylene glycol induced renal stone in rats. J Pharm Technol 2015;8:1481 6.
Krishnamurthi R. Phytochemical analysis and antioxidant property of Aerva lanata (L.). Int J Pharm 2015;2:426 9.
Manohari R, Prasanna G. In vitro antioxidants and antimicrobial activities of Aerva lanata L. Int J Pharm Pharm Res 2016;6:191 201.
Vidhya R, Udaykumar R. Phytochemical screening and evaluation of in vitro haemolytic, thrombolytic and anti inflamatory activities of Aerva lanata (L.). Indo Am J Pharm Res 2016;6:5965 73.
Abdulmuthalib U, Manjur Shah M. Phytochemical screening on the antioxidant properties of Aerva lanata flower extracts and their in vitro anti proliferative effects on human liver cancer cell line running head phytochemical screening of flower extracts of Aerva lanata. J Biol Nat 2017;7:81 90.
Gujjeti RP, Mamidala E. Anti HIV Activity of phytosterol isolated from Aerva lanata Roots. Rev J Field Pharm 2017;9:112 6.
Harborne JB. Phytochemical Methods: A Guide to Modern Techniques of Plant Analysis. 3rd ed. New York: Chapman and Hall Co.; 1998. p. 1 302.
Thangavel A, Balakrishnan S, Duraisamy SV. Phytochemical screening, gas chromatography mass spectrometry (GC MS) analysis of phytochemical constituents and antibacterial activity of Coriandrum sativum (l) seeds. Int J Pharm Pharm Sci 2015;7:153 9.
Alzoreky N, Nakahara N. Antioxidant activity of edible Yemeni plants evaluated by ferryl myoglobin/ABTS assay. Food Sci Techno Res 2001;7:141 4.
Ang H, Lee K. Analysis of mercury in Malaysian herbal preparations; a peer review. Biomed Sci 2005;4:31 6.
Uddin AB, Khalid RS, Alaama M, Abdualkader AM, Kasmuri A, Abbas SA. Comparitive study of three digestion methods for elemental analysis in traditional medicine products using atomic absorption spectrometry. J Anal Sci Technol 2016;7:2 7.
PubChem Glycerin/C3H8O3. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/glycerol.
Hiramoto K, Nasuhara A, Michikoshi K, Kato T, Kikugawa K. DNA strand breaking activity and mutagenicity of 2,3 dihydro 3,5 dihydroxy 6 methyl 4H pyran 4 one (DDMP), a Maillard reaction product of glucose and glycine. Mutat Res/Genet Toxicol Environ Mutagen 1997;395:47 56.
Kumar PP, Kumaravel S, Lalitha C. Screening of antioxidant activity, total phenolics and GC MS study of Vitex negundo. Afr J Biochem Res 2010;4:191 5.
Yu X, Zhao M, Liu F, Zeng S, Hu J. Identification of 2,3 dihydro 3,5 dihydroxy 6 methyl 4H pyran 4 one as a strong antioxidant in glucose–histidine Maillard reaction products. Food Res Int 2013;51:397 403.
Gopalakrishnan S, Vadivel E. GC MS analysis of some bioactive constituents of Mussaenda frondosa LINN. Int J Pharm Bio Sci 2011;2:313 20.
PubChem 5 (Hydroxymethyl) 2 furaldehyde/C6H6O3. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/5 hydroxymethylfurfural.
PubChem 1,2,3 Propanetriol, Monoacetate/C5H10O4. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/Acetin.
PubChem 4 Methyltridecane/C14H30. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/4 Methyltridecane.
PubChem 2 Methoxy 4 vinylphenol/C9H10O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/2 Methoxy 4 vinylphenol.
PubChem Undecanoic acid/C11H22O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/undecanoic_acid.
PubChem Sucrose/C12H22O11. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/sucrose.
PubChem Levoglucosan/C6H10O5. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/Leucoglucosan.
PubChem Lauric acid/C12H24O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/lauric_acid.
PubChem 2 Nonenal/C9H16O. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/trans 2 Nonenal.
PubChem Limonene dioxide/C10H16O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/Limonene_dioxide.
PubChem Phytol/C20H40O. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/3_7_11_15 tetramethyl 2 hexadecen 1 ol.
PubChem 6,10,14 Trimethylpentadecan 2 one/C18H36O. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/6_10_14 Trimethylpentadecan 2 one.
PubChem Pentadecanoic acid/C15H30O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/pentadecanoic_acid.
PubChem Ethyl palmitate/C18H36O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/ethyl_palmitate.
PubChem Oleic acid/C18H34O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/oleic_acid.
PubChem Myristic acid/C14H28O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/Tetradecanoic_acid.
PubChem Phytol/C20H40O. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/Phytol.
PubChem Octadeca 9,12 dienoic acid/C18H32O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/3931.
PubChem Isoambrettolide/C16H28O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/Isoambrettolide.
PubChem delta Octadecalactone/C18H34O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/518573.
Wikipedia Propylhexedrine. Available from: https://www.en.wikipedia.org/wiki/Propylhexedrine.
PubChem Squalene/C30H50. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/squalene.
Wikipedia 1 Hexacosanol. Available from: https://www.en.wikipedia.org/wiki/1 Hexacosanol.
PubChem delta Tocopherol/C27H46O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/586537.
PubChem gamma Tocopherol/C28H48O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/gamma Tocopherol.
PubChem Vitamin E/C29H50O2. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/alpha Tocopherol.
PubChem Campesterol/C28H48O. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/campesterol.
PubChem Stigmasterol/C29H48O. Available from: https://www. pubchem.ncbi.nlm.nih.gov/compound/Stigmasterin.
PubChem Lanosterol/C30H50O. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/lanosterol.
PubChem gamma Sitosterol/C29H50O. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/Clionasterol.
PubChem Stigmastanol/C29H52O. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/Fucostanol.
PubChem Stigmast 7 en 3 ol, (3beta, 5alpha) /C29H50O https://www.pubchem.ncbi.nlm.nih.gov/compound/6432515.
PubChem Lupeol/C30H50O. Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/Lupeol.
Saleem M. Lupeol. A Novel anti inflammatory and anti cancer dietary triterpene. Cancer Lett 2009;5:109 15.
PubChem 3alpha, 7beta Dihydroxy 5beta, 6beta epoxycholestane/C27H46O3 . Available from: https://www.pubchem.ncbi.nlm.nih.gov/compound/2221626.
Cai L, Wu CD. Compounds from Syzygium aromaticum possessing growth inhibitory activity against oral pathogens. J Nat Prod 1996;59:987 90.
Mittal M, Gupta N, Parashar P, Mehra V, Khatri M. Phytochemical evaluation and pharmacological activity of Syzygium aromaticum: A comprehensive review. Int J Pharm Pharm Sci 2014;6:67 72.
Kamurthy H, Ch S, Rao SN, Sudhakar M. Antinocieptive activity of stigmasterol 3 glyceryl 2 linoleiate, campesterol and daucosterol isolated from Aerva lanata Linn. Aerial parts. Asian J Pharm Clin Res 2013;6:149 50.
Choi J, Lee E, Lee H, Kim K, Ahn K, Shim B, et al. Identification of campesterol from Chrysanthemum coronarium L. And its antiangiogenic activities. J Phytother Res 2007;21:954 9.
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