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Simultaneous determination of anthraquinone derivatives in Radix et Rhizoma Rhei-based medicines by ultra-performance LC-ESCI-MS/MS multiple reaction monitoring

Autorzy
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A new method using ultra-performance liquid chromatography (UPLC) in combination with tandem mass spectrometry and a multiple reaction monitoring mode (UPLC-MS/MS-MRM) was developed for simultaneous quantitative determination of anthraquinone derivatives in Radix et Rhizoma Rhei-based medicines. A multi-mode electrospray/chemical ionization (ESCI) and negative ion mode with [M-H]− and its fragments under collision-activated conditions were employed in MS/MS-MRM. The quantitative method was validated and applied to simultaneous determination of anthraquinone derivatives in 21 Radix et Rhizoma Rhei-based medicines. The limits of quantification were in the range of 3.90–9.09 ng mL -1. Average recoveries were between 95.5% and 99.8% with relative standard deviations from 1.8% to 5.3%.
Rocznik
Strony
229--242
Opis fizyczny
Bibliogr. 18 poz., rys., tab.
Twórcy
autor
  • Chinese Academy of Sciences Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics Lanzhou 730000 P. R. China
autor
  • Lanzhou University of Technology School of Petroleum and Chemical Engineering Lanzhou 730050 P. R. China
Bibliografia
  • [1] The State Pharmacopoeia Commission of PR China, Pharmacopoeia of PR China, Chemical Industry Press, Beijing, 2005, pp. 17–18
  • [2] Pharmaceutical and Food Safety Bureau, Japanese Pharmacopoeia, Ministry of Health, Labour and Welfare, Tokyo, 2006, pp. 1344–1345
  • [3] European Directorate for the Quality of Medicines, European Pharmacopoeia, Council of Europe, Strasbourg, 2001, pp. 1858–1859
  • [4] W. Jin, Y.F. Wang, R.L. Ge, H.M. Shi, C.Q. Jia, and P.F. Tu, Rapid Commun. Mass Spectrom., 21, 2351 (2007)
  • [5] World Health Organization, WHO Monographs on Selected Medicinal Plants, Geneva, 1999, pp. 231–240
  • [6] K.C. Huang, The Pharmacology of Chinese Herbs, CRC Press, Boca Raton, 1993, pp. 185–186
  • [7] J.B. Wang, H.F. Li, C. Jin, Y. Qu, and X.H. Xiao, J. Pharm. Biomed. Anal., 47, 765 (2008)
  • [8] The State Pharmacopoeia Commission of PR China, Pharmacopoeia of PR China, Chemical Industry Press, Beijing 2010, pp. 22–23
  • [9] G.Y. Wang, L.W. Xu, and Y.P. Shi, Acta Chromatogr., 23, 653 (2011)
  • [10] G.Y. Wang, H.Y. Qi, and Y.P. Shi, J. Sep. Sci., 33, 1730 (2010)
  • [11] N.P. Singh, A.P. Gupta, A.K. Sinha, and P.S. Ahuja, J. Chromatogr. A, 1077, 202 (2005)
  • [12] R. Liu, A. Li, and A. Sun, J. Chromatogr. A, 1052, 217 (2004)
  • [13] F.Q. Yang, T.Y. Zhang, G.L. Tian, H.F. Cao, Q.H. Liu, and Y. Ito, J. Chromatogr. A, 858, 103 (1999)
  • [14] F. Li, Q.E. Cao, and Z. Ding, Chromatograpia, 59, 753 (2004)
  • [15] C.C. Lin, C.I. Wu, T.C. Lin, and J.S. Sheu, J. Sep. Sci., 29, 2584 (2006)
  • [16] C.L. Liu, P.L. Zhu, and M.C. Liu, J. Chromatogr. A, 857, 167 (1999)
  • [17] J. Koyama, I. Morita, and N. Kobayashi, J. Chromatogr. A, 1145, 183 (2007)
  • [18] J. Stahl-Zeng, V. Lange, R. Ossola, K. Eckhardt, W. Krek, R. Aebersold, and B. Domon, Mol. Cell. Proteomics., 6, 1809 (2007)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-09da8385-6e00-494b-82e9-5691ef1f30ee
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