PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Pharmacokinetics and bioavailability of liensinine in mouse blood by UPLC-MS/MS

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Liensinine is a bisbenzyltetrahydroisoquinoline alkaloid extracted from lotus (Nelumbo nucifera GAERTNER., Nelumbonaceae), especially in its embryo loti “Lien Tze Hsin” (green embryo of mature seed). A rapid and simple UPLC-MS/MS method was developed to determine liensinine in mouse blood and its application to a pharmacokinetic study. The blood samples were preprocessed by protein precipitation using acetonitrile. Midazolam (internal standard, IS) and liensinine were gradient eluted by mobile phase of methanol and water (0.1% formic acid) in a Waters UPLC BEH C18 column. The multiple reaction monitoring of m/z 611.3 → 206.1 for liensinine and m/z 326.2 → 291.1 for IS with an electrospray ionization (ESI) source was used for quantitative detection. The calibration curve ranged from 0.5 to 400 ng/mL (r > 0.995). The accuracy ranged from 92.2 to 108.2%, the precision of intra-day and inter-day was less than 14%, and the matrix effect was between 100.0% and 109.6%, the recovery was better than 71.0%. The developed UPLC-MS/MS method was successfully used for a pharmacokinetic study of liensinine in mice after oral (5 mg/kg) and intravenous administration (1 mg/kg), and the absolute availability of liensinine was 1.8%.
Słowa kluczowe
Rocznik
Strony
333--337
Opis fizyczny
Bibliogr. 15 poz., rys., tab.
Twórcy
autor
  • Department of Pharmacy, Maternal and Child Health Hospital of Hubei Province, Wuhan, China
autor
  • Laboratory Animal Centre, Wenzhou Medical University, Wenzhou, China
autor
  • Laboratory Animal Centre, Wenzhou Medical University, Wenzhou, China
autor
  • Laboratory Animal Centre, Wenzhou Medical University, Wenzhou, China
Bibliografia
  • 1. Zhang, X.; Xiang, Q.; Zhao, X.; Ma, L.; Cui, Y. J. Clin. Pharm. Ther. 2019, 44, 163–73.
  • 2. Millar, S. A.; Stone, N. L.; Yates, A. S.; O'Sullivan, S. E. Front Pharmacol. 2018, 9, 1365.
  • 3. Hu, G.; Xu, R. A.; Dong, Y. Y.; Wang, Y. Y.; Yao, W. W.; Chen, Z. C.; Chen, D.; Bu, T.; Ge, R. S. J. Ethnopharmacol. 2015, 163, 94–8.
  • 4. Huang, Y.; Zhao, L.; Bai, Y.; Liu, P.; Wang, J.; Xiang, J. Arzneimittelforschung 2011, 61, 347–52.
  • 5. Lv, S. F.; Wang, X. H.; Li, H. W.; Zhang, X. L.; Wang, B. J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 2015, 992, 43–6.
  • 6. Peng, L. S.; Jiang, X. Y.; Li, Z. X.; Yi, T. G.; Huang, B.; Li, H. L.; Zeng, Z.; Liu, Y.; Peng, S. L.; He, J. S.; He, L.; Peng, L. P. J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 2015, 991, 29–33.
  • 7. US Department of Health and Human Services, F.a.D.A. Guidance for Industry: Bioanalytical Method Validation, 2013.
  • 8. Qiu, E. J.; Wang, H. Z.; Yu, Y.; Song, D. Z.; Cai, J. Z.; Ye, F. F. Lat. Am. J. Pharm. 2020, 39, 1171–5.
  • 9. Nie, J. J.; Chen, F.; Wang, F. W.; Luo, W. C.; Shen, X. W. Lat. Am. J. Pharm. 2020, 39, 612–6.
  • 10. Lu, M. F.; Feng, T. T.; Hu, Y. J.; Wang, H. Z.; Yang, X. Z. Lat. Am. J. Pharm. 2020, 39, 459–63.
  • 11. Li, T. R.; Ye, W. J.; Huang, B. G.; Lu, X. J.; Chen, X. X.; Lin, Y. J.; Wen, C. C.; Wang, X. Q. J. Pharm. Biomed. Anal. 2019, 168, 133–7.
  • 12. Zhou, Q.; Ma, J. S.; Chen, L. M. J. Anal. Methods Chem. 2020, 2020, 7204315.
  • 13. Shen, X. W.; Ma, J. S.; Wang, X. Q.; Wen, C. C.; Zhang, M. L. Biomed. Res. Int. 2020, 2020, 8247270.
  • 14. Lin, G. T.; Chen, Y. Y.; Yu, Y.; Wang, H. Z.; Wang, X. Q.; Chen, L. M. Lat. Am. J. Pharm. 2020, 39, 1105–9.
  • 15. Weng, B. X.; Zhong, Z. Q.; Yu, Y.; Lin, J.; Wen, C. C. Lat. Am. J. Pharm. 2020, 39, 1100–4.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-0b1ef5a5-baaa-4eb7-bb58-7cb122c2da65
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.