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Original

Analysis of isoflavonoids from leguminous plant extracts by RPHPLC/DAD and electrospray ionization mass spectrometry

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Pages 116-124 | Published online: 06 Jul 2009

References

  • Aguiar, CL. 2004. Physical and biochemical transformations of soybean isoflavone (Glycine, max L.) and the effect on biological activities. PhD thesis, State University of Campinas.
  • Atkinson C, Warren RML, Sala E, Dowsett M, Dunning AM, Healey CS, Runswick S, Day NE, Bingham SA. Red clover-derived isoflavones and mammographic breast density: a double-blind, randomized, placebo controlled trial. Breast Cancer Res 2004; 6: 170–179
  • Bau HM, Villaume C, Méjean L. Effects of soybean (Glycine max) germination on biologically active components, nutritional values of seeds, and biological characteristics in rats. Nahrung 2000; 44: 2–6
  • Dewick PM. Isoflavones. Chapman & Hall, London 1993; 117–238
  • Fukutake M, Takahashi M, Ishida K, Kawamura H, Sugimura T, Wakabayashi K. Quantification of genistein and genistin in soybeans and soybean products. Food Chem Toxicol 1996; 34: 457–461
  • Griffith AP, Collison MW. Improved methods for the extraction and analysis of isoflavones from soy-containing foods and nutritional supplements by reversed-phase high-performance liquid chromatography and liquid chromatography–mass spectrometry. J Chromatogr 2001; 913: 397–413
  • Hagmann M, Grisebach H. Enzymatic rearrangement of flavanone to isoflavone. FEBS Lett 1984; 175: 199–202
  • Harborne JB, Williams CA. Advances in flavonoid research since 1992. Phytochemistry 2000; 55: 481–504
  • Hartwig UA, Maxwell CA, Joseph CM, Phillips DA. Chrysoeriol and luteolin released from alfalfa seeds induce nod genes in Rhizobium meliloti. Plant Physiol 1990; 92: 116–122
  • Heller W, Forkmann G. Biosynthesis of flavonoids. Chapman & Hall, London 1993; 499–535
  • Hirakura K, Morita M, Nakajima K, Sugama K, Takagi K, Niitsu K, Ikeya Y, Maruno M, Okada M. Phenolic glucosides from the root of Pueraria lobata. Phytochemistry 1997; 46: 921–928
  • Ho HM, Chen RY, Leung LK, Chan FL, Huang Y, Chen ZY. Difference in flavonoid and isoflavone profile between soybean and soy leaf. Biomed Pharmacother 2002; 56: 289–295
  • Katagiri Y, Ibrahim RK, Tahara S. HPLC analysis of white lupin isoflavonoids. Biosci Biotechnol Biochem 2000; 64: 1118–1125
  • Lima VLAG, Melo EA, Maciel MIS, Silva GSB, Lima DES. Fenólicos totais e atividade antioxidante do extrato aquoso de broto de feijão-mungo (Vigna radiata L.). Rev Nutr 2004; 17: 53–57
  • Malhotra B, Onyilagha JC, Bohm BA, Towers GHN, James D, Harborne JB, French CJ. Inhibition of tomato ringspot virus by flavonoids. Phytochemistry 1996; 43: 1271–1276
  • Merken HM, Beecher GR. Measurement of food flavonoids by high-performance liquid chromatography: a review. J Agric Food Chem 2000; 48: 577–599
  • Nitschke M, Haddad R, Costa GN, Gilioli R, Meurer EC, Gatti MSV, Eberlin MN, Höehr NF, Pastore GM. Structural characterization and biological properties of a lipopeptide surfactant produced by Bacillus subtilis on cassava wastewater medium. Food Sci Biotechnol 2004; 13: 591–596
  • Park YK, Alencar SM, Nery IA, Aguiar CL, Pacheco TARC. Enrichment of isoflavone aglycones in extracted soybean isoflavones by heat and fungal β-glucosidase. Food Sci Industry 2001a; 34: 14–34
  • Park YK, Aguiar CL, Alencar SM, Mascarenhas HAA, Scamparini ARP. Survey of isoflavone contents in Brazilian soybean. Cien Tecnol Aliment 2001b; 3: 156–160
  • Park YK, Aguiar CL, Alencar SM, Mascarenhas HAA, Scamparini ARP. Conversão de malonil-β-glicosil isoflavonas em isoflavonas glicosiladas presentes em alguns cultivares de soja brasileira. Cienc Tecnol Aliment 2002; 22: 130–135
  • Simmonds MSJ, Stevenson PC. Effects of isoflavonoids from Cicer on Larvae of Heliocoverpa armigera. J Chem Ecol 2001; 27: 965–977
  • Stroheker T, Chagnon MC, Pinnert MF, Berges R, Lavier MCC. Estrogenic effects of food wrap packaging xeno estrogens and flavonoids in female Wistar rats: a comparative study. Reprod Toxicol 2003; 17: 421–432
  • Sun Y, Wu Q, Van-Etten HD, Hrazdina G. Stereoisomerism in plant disease resistance: induction and isolation of the 7,2′-dihydroxy-4′,5′-methylenedioxyisoflavone oxidoreductase, an enzyme introducing chirality during synthesis of isoflavonoid phytoalexins in pea (Pisum sativum L.). Arch Biochem Biophys 1991; 284: 167–173
  • Tsukamoto C, Shimada S, Igita K, Kudou S, Kokubun M, Okubo K, Kitamura K. Factors affecting isoflavone content in soybean seeds. Changes in isoflavones, saponins, and composition of fatty acids at different temperatures during seed development. J Agric Food Chem 1995; 43: 1184–1192
  • Tsukamoto C, Kudou S, Kikuchi A, Carrão-Panizzi MC, Ono T, Kitamura K, Okubo K. Isoflavones in soybean products: composition, concentration, and physiological effects. Documentos Embrapa 2001; 169: 9–14
  • Vicent A, Fitzpatrick LA. Soy isoflavones: are they useful in menopause?. Mayo Clin Proc 2000; 75: 1174–1184

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