HPTLC and reverse phase HPLC methods for the simultaneous quantification and in vitro screening of antioxidant potential of isolated sesquiterpenoids from the rhizomes of Cyperus rotundus

Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences

Volumn 904, Issue , 2012, Pages 22-28

  Priya Rani, M ^a   Padmakumari, K P ^a  

^a REGIONAL RESEARCH LABORATORY CSIR   (India)

Author keywords

Aristoloen; HPLC; HPTLC; NMR; Nootkatone; Solavetivone

Indexed keywords

ARISTOLOEN; HPLC; HPTLC; NOOTKATONE; SOLAVETIVONE;

ACETONE; NUCLEAR MAGNETIC RESONANCE; SILICA GEL; SPECTROSCOPIC ANALYSIS;

PLANTS (BOTANY);

1,1 DIPHENYL 2 PICRYLHYDRAZYL; ANTIOXIDANT; ARISTOLONE; CYPERUS ROTUNDUS EXTRACT; GALLIC ACID; MOLYBDENUM; NOOTKATONE; SCAVENGER; SESQUITERPENOID; SILICA GEL; SOLAVETIVONE; UNCLASSIFIED DRUG;

ACCURACY; ANTIOXIDANT ACTIVITY; ARTICLE; COLUMN CHROMATOGRAPHY; CYPERUS ROTUNDUS; DRUG ISOLATION; DRUG SCREENING; DRUG STRUCTURE; HIGH PERFORMANCE THIN LAYER CHROMATOGRAPHY; IC 50; IN VITRO STUDY; LIMIT OF DETECTION; LIMIT OF QUANTITATION; NONHUMAN; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; RHIZOME; SENSITIVITY ANALYSIS; STANDARDIZATION; ULTRAVIOLET IRRADIATION;

ANALYSIS OF VARIANCE; ANTIOXIDANTS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CHROMATOGRAPHY, REVERSE-PHASE; CYCLOPROPANES; CYPERUS; FURANS; LIMIT OF DETECTION; LINEAR MODELS; MOLYBDENUM; OXIDATION-REDUCTION; REPRODUCIBILITY OF RESULTS; RHIZOME; SESQUITERPENES; TETRAHYDRONAPHTHALENES;

CYPERUS ROTUNDUS;

EID: 84865395138     PISSN: 15700232     EISSN: 1873376X     Source Type: Journal    
DOI: 10.1016/j.jchromb.2012.05.042     Document Type: Article

References (20)

1. Halliwell B., Gutteridge J.M.C. Free Radicals in Biology and Medicine 1989, Oxford University Press, Oxford, UK, 96-98.
2. Heo H.J., Lee C.Y. J. Agric. Food Chem. 2005, 53:1984.
3. Seo W.G., Pae H.O., Oh G.S., Chai K.Y., Kwon T.O., Yun Y.G., Kim N.Y., Chung H.T. J. Ethnopharmacol. 2001, 76:59.
4. Gupta M.B., Palit T.K., Singh N., Bhargawa K.P. Indian J. Med. Res. 1971, 59:76.
5. Uddin S.J., Mondal K., Shilpi J.A., Rahman M.T. Fitoterapia 2006, 77:134.
6. Weenen H., Nkunya M.H.H., Bray D.H., Mwasumbi L.B., Kinabo L.S., Kilimali V.A.E.B., Wijnberg J.B.P.A. Planta Med. 1990, 56:371.
7. Thebtaranonth C., Thebtaranonth Y., Wanauppathamkul S., Yuthavong Y. Phytochemistry 1995, 40:125.
8. Trivedi V.P., Mann A.S. Q. J. Crude Drug Res. 1972, 12:1988.
9. Raut N.A., Gaikwad N.J. Fitoterapia 2006, 77:585.
10. Jeong S.J., Miyamoto T., Inagaki M., Kim Y.C., Higuchi R. J. Nat. Prod. 2000, 63:673.
11. Holm L.G., Plucknett D.L., Pancho J.V., Herberger J.V. The world's Worst Weeds: Distribution and Biology 1991, Krieger Publications, Malabar, Florida.
12. Morales-Payan J.P., Santos B.M., Stall W.M., Bewick T.A. Weed Technol. 1997, 11:672.
13. Prieto P., Pineda M., Aguilar M. Anal. Biochem. 1999, 269:337.
14. Brand-Williams W., Cuvelier M.E., Berset C. Lebens. Wissen. Tech. 1995, 28:25.
15. Coxon D.T., Price K.R., Howard B., Osman S.F., Kalan E.B., Zacharius R.M. Tetrahedron Lett. 1974, 34:2921.
16. Fujimori T., Kasuga R., Kaneko H., Noguchi M. Phytochemistry 1977, 16:392.
17. Shi Y.C., Zhi H.W., Shang K.W., Michael Y.C., Ali A.H.E.G., Chang F.D., Chang Y.D. Chem. Biodivers. 2009, 6:86.
18. Miyazawa M., Tougo H., Ishihara M. Nat. Prod. Lett. 2001, 15:201.
19. Anna G., Agnieszka Ł., Tomasz J., Marta Ś., Joanna W., Czesław W. Bioorg. Med. Chem. 2011, 19:2464.
20. Duh P.D. J. Am. Oil Chem. Soc. 1998, 75:455.