Chemical analysis of Eriocaulon buergerianum and adulterating species by high-performance liquid chromatography with diode array detection and electrospray ionization tandem mass spectrometry

Journal of Pharmaceutical and Biomedical Analysis

Volumn 57, Issue 1, 2012, Pages 133-142

  Qiao, Xue ^a   Ye, Guan ^b   Liu, Chun Fang ^a   Zhang, Zhi Xiang ^c   Tu, Qiang ^c   Dong, Jing ^d   Li, Yue Qi ^d   Guo, De An ^a   Ye, Min ^a  

^a PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

^b Central Research Institute of Shanghai Pharmaceutical Group   (China)

^c BEIJING FORESTRY UNIVERSITY   (China)

^d Shimadzu International Trading Shanghai Co Ltd   (China)

Author keywords

Chinese herbal medicine; Eriocaulon buergerianum; Flavonoids; HPLC DAD ESI MS n; Naphthopyranones

Indexed keywords

CHINESE DRUG; ERIOCAULON BUERGERIANUM EXTRACT; FLAVONE; FLAVONOID; FLAVONOL; GU JING CAO; ISOFLAVONE; METHANOL; NAPHTHOPYRANONE; PHENOL DERIVATIVE; PLANT EXTRACT; PYRAN DERIVATIVE; UNCLASSIFIED DRUG; XANTHONE DERIVATIVE;

ARTICLE; CHEMICAL ANALYSIS; CHINESE MEDICINE; DIODE; ERIOCAULON BUERGERIANUM; ERIOCAULON CINEREUM; ERIOCAULON FABERI; ERIOCAULON SEXANGULARE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ION TRAP MASS SPECTROMETRY; NEGATIVE ION ELECTROSPRAY; PRINCIPAL COMPONENT ANALYSIS; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS;

CHROMATOGRAPHY, HIGH PRESSURE LIQUID; ERIOCAULACEAE; PRINCIPAL COMPONENT ANALYSIS; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; TANDEM MASS SPECTROMETRY;

EID: 80054034084     PISSN: 07317085     EISSN: 1873264X     Source Type: Journal    
DOI: 10.1016/j.jpba.2011.08.033     Document Type: Article

References (28)

1. Chinese Pharmacopoeia Commission Pharmacopoeia of the People's Republic of China 2010, vol. 1. Chinese Medical Science and Technology Press, Beijing, pp. 168. 2010 ed.
2. Fang J.J., Ye G., Chen W.L., Zhao W.M. Antibacterial phenolic components from Eriocaulon buergerianum. Phytochemistry 2008, 69:1279-1286.
3. Ho J.C., Chen C.M. Flavonoids from the aquatic plant Eriocaulon buergerianum. Phytochemistry 2002, 61:405-408.
4. Bate-Smith E.C., Harborne J.B. Quercetagetin and patuletin in Eriocaulon. Phytochemistry 1969, 8:1035-1037.
5. Liao Z.L., Tian C.Y., Chen L., Zhou X.J., Sun K. Textual criticism on the original plant of Flos Eriocauli in great compendium of Chinese Materia Medica. Shanghai Zhongyiyao Zazhi 2004, 38:60-62.
6. Flora of China Editorial, Committee Flora of China 1979, vol. 133. Science Press, Beijing, pp. 20-63.
7. Zhang Z.X., Stützel T. SEM studies on morphology of seed surface structure of Eriocaulon from eastern and southeastern Asia. J. Beijing Forestry Univ. 2002, 24:81-83.
8. Yang W.C., Liu H., Ni S.F., Luo R.F., Li Z.X., Chen Q.L. Recent progress on Eriocaulon species: a review. Acta Chin. Med. Pharmcol. 2009, 37:92-93.
9. Tistaert C., Dejaegher B., Heyden Y.V. Chromatographic separation techniques and data handling methods for herbal fingerprints: a review. Anal. Chim. Acta 2011, 690:148-161.
10. Zhou J.L., Qi L.W., Li P. Herbal medicine analysis by liquid chromatography/time-of-flight mass spectrometry. J. Chromatogr. A 2009, 1216:7582-7594.
11. Scatena V.L., Giulietti A.M., Borba E.L., van den Berg C. Anatomy of Brazilian Eriocaulaceae: correlation with taxonomy and habitat using multivariate analyses. Plant Syst. Evol. 2005, 253:1-22.
12. Cuyckens F., Claeys M. Mass spectrometry in the structural analysis of flavonoids. J. Mass Spectrom. 2004, 39:1-15.
13. Vukics V., Guttman A. Structural characterization of flavonoid glycosides by multi-stage mass spectrometry. Mass Spectrom. Rev. 2010, 29:1-16.
14. Fabre N., Rustan I., Hoffmann E., Quetin-Leclercq J. Determination of flavone, flavonol, and flavanone aglycones by negative Ion liquid chromatography electrospray ion trap mass spectrometry. J. Am. Soc. Mass Spectrom. 2001, 12:707-715.
15. Justesen U. Collision-induced fragmentation of deprotonated methoxylated flavonoids, obtained by electrospray ionization mass spectrometry. J. Mass Spectrom. 2001, 36:169-178.
16. Qiao X., Zhang X., Ye M., Su Y.F., Dong J., Han J., Yin J., Guo D.A. Rapid characterization of triterpene saponins from Conyza blinii by liquid chromatography coupled with mass spectrometry. Rapid Commun. Mass Spectrom. 2010, 24:3340-3350.
17. Ye M., Yan Y.N., Guo D.A. Characterization of phenolic compounds in the Chinese herbal drug Tu-Si-Zi by liquid chromatography coupled to electrospray ionization mass spectrometry. Rapid Commun. Mass Spectrom. 2005, 19:1469-1484.
18. Ye M., Han J., Chen H.B., Zheng J.H., Guo D.A. Analysis of phenolic compounds in rhubarbs using liquid chromatography coupled with electrospray ionization mass spectrometry. J. Am. Soc. Mass Spectrom. 2007, 18:82-91.
19. da Silva M.A., Oliveira A.P.S., Sannomiya M., Sano P.T., Varanda E.A., Vilegas W., dos Santos L.C. Flavonoids and a naphthopyranone from Eriocaulon ligulatum and their mutagenic activity. Chem. Pharm. Bull. 2007, 55:1635-1639.
20. dos Santos L.C., Rodrigues C.M., da Silva M.A., Coelho R.G., Sannomiya M., Vilegas W. Chemical profile of Eriocaulon ligulatum (Vell.) L.B. Smith (Eriocaulaceae). Biochem. Syst. Ecol. 2005, 33:1159-1166.
21. Iinuma M., Tosa H., Toriyama N., Tanaka T., Ito T., Chelladurai V. Six xanthones from Calophyllum austroindicum. Phytochemistry 1996, 43:681-685.
22. Lee J.H., Baek I.Y., Kang N.S., Ko J.M., Han W.Y., Kim H.T., Oh K.W., Suh D.Y., Ha T.J., Park K.H. Isolation and characterization of phytochemical constituents from soybean (Glycine max L. Merr.). Food Sci. Biotechnol. 2006, 15:392-398.
23. Rehman A., Malik A., Riaz N., Nawaz H.R., Ahmad H., Nawaz S.A., Choudhary M.I. Lipoxygenase inhibitory constituents from Periploca aphylla. J. Nat. Prod. 2004, 67:1450-1454.
24. Kang S.W., Kim M.C., Kim C.Y., Jung S.H., Um B.H. The rapid identification of isoflavonoids from Belamcanda chinensis by LC-NMR and LC-MS. Chem. Pharm. Bull. 2008, 56:1452-1454.
25. Mina S.W., Kimb N.J., Baekc N.I., Kima D.H. Inhibitory effect of eupatilin and jaceosidin isolated from Artemisia princeps on carrageenan-induced inflammation in mice. J. Ethnopharmacol. 2009, 125:497-500.
26. Miyazawa M., Okuno Y., Nakamura S., Kosaka H. Antimutagenic activity of flavonoids from Pogostemon cablin. J. Agric. Food Chem. 2000, 48:642-647.
27. 1H-NMR studies. Helv. Chim. Acta 2010, 93:466-481.
28. Salatino A., Salatino M.L.F., dos Santos D.Y.A.C., Patricio M.C.B. Distribution and evolution of secondary metabolites in Eriocaulaceae, Lythraceae and Velloziaceae from " campos rupestres" Genet. Mol. Biol. 2000, 23:931-940.