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作者:

Wang, X.-N. (Wang, X.-N..) | Guan, H. (Guan, H..) | Zhou, P.-K. (Zhou, P.-K..) | Cai, Y. (Cai, Y..) | Qian, X.-H. (Qian, X.-H..)

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摘要:

OBJECTIVE: To develop a quick, sensitive and accurate high performance liquid chromatography tandem mass spectrometric(HPLC-MS/MS) method for quantification of VND3207 and its metabolites in rat plasma and to investigate pharmacokinetics of VND3207 in SD rats. METHODS: Rats were ig given VND3207 70 mg·kg-1. Blood samples were collected and separated by liquid chromatography on a C18 reversion phase chromatographic column with gradient elution. Concentration of VND3207 and its metabolites syringic acid and syringic alcohol were detected by HPLC-MS/MS in positive multiple reaction monitoring mode. Pharmacokinetic parameters of VND3207 and its metabolites were calculated. RESULTS: Calibration curves of VND3207 and its metabolites syringic acid and syringic alcohol were linear within the range of 2-2000 μg·L -1, ranged from quantification limit 2 μg·L-1. Intra- and inter-day precision was both less than 15%, and accuracy with 91.2%-110.7%. The concentrations of VND3207 and its metabolites were detected in plasma of rats up to 12 h after VND3207 was ig given to rats. AUC 0-∞ of VND3207, syringic acid and syringic alcohol were 19.37 ± 10.56, 1825.32 ± 719.97 and (9.89 ± 1.75) mg·L-1·min, and T1/2 was 78.0 ± 44.6, 114.4 ± 17.9 and (66.0 ± 23.8) min, respectively. CONCLUSION: A quick, sensitive and accurate HPLC-MS/MS method is developed for quantification of VND3207 and its metabolites in rat plasma. VND3207 is absorbed and metabolized rapidly. A large amount of VND3207 is oxidized to syringic acid while a small amount is reduced to syringic alcohol.

关键词:

Liquid chromatography tandem mass spectrometry; Pharmacokinetics; Radiation; Syringic acid; Syringic alcohol; Vanillin derivative; VND3207

作者机构:

  • [ 1 ] [Wang, X.-N.]Molecular Design and Protein Function Group, College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China
  • [ 2 ] [Wang, X.-N.]Beijing Institute of Radiation Medicine, Beijing 100850, China
  • [ 3 ] [Wang, X.-N.]Beijing Proteome Research Center, Beijing 102206, China
  • [ 4 ] [Guan, H.]Beijing Institute of Radiation Medicine, Beijing 100850, China
  • [ 5 ] [Zhou, P.-K.]Beijing Institute of Radiation Medicine, Beijing 100850, China
  • [ 6 ] [Cai, Y.]Beijing Institute of Radiation Medicine, Beijing 100850, China
  • [ 7 ] [Cai, Y.]Beijing Proteome Research Center, Beijing 102206, China
  • [ 8 ] [Qian, X.-H.]Molecular Design and Protein Function Group, College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China
  • [ 9 ] [Qian, X.-H.]Beijing Institute of Radiation Medicine, Beijing 100850, China
  • [ 10 ] [Qian, X.-H.]Beijing Proteome Research Center, Beijing 102206, China

通讯作者信息:

  • [Qian, X.-H.]Molecular Design and Protein Function Group, College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China

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来源 :

Chinese Journal of Pharmacology and Toxicology

ISSN: 1000-3002

年份: 2013

期: 2

卷: 27

页码: 216-221

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