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Effects of Fuzheng Huayu recipe on entecavir pharmacokinetics in normal and dimethylnitrosamine-induced hepatic fibrosis rats

CONTEXT: Fuzheng Huayu recipe (FZHY) combined with entecavir (ETV) is used to treat the cirrhosis caused by chronic hepatitis B (CHB) infection. OBJECTIVE: To investigate the effect of FZHY on ETV pharmacokinetics under different conditions. MATERIALS AND METHODS: A model of liver fibrosis was creat...

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Autores principales: Yang, Tao, Zheng, Tian-Hui, Zhao, Qiang, Liu, Wei, Li, Shu-Ping, Tao, Yan-Yan, Wang, Chang-Hong, Liu, Cheng-Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968529/
https://www.ncbi.nlm.nih.gov/pubmed/31847670
http://dx.doi.org/10.1080/13880209.2019.1687527
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author Yang, Tao
Zheng, Tian-Hui
Zhao, Qiang
Liu, Wei
Li, Shu-Ping
Tao, Yan-Yan
Wang, Chang-Hong
Liu, Cheng-Hai
author_facet Yang, Tao
Zheng, Tian-Hui
Zhao, Qiang
Liu, Wei
Li, Shu-Ping
Tao, Yan-Yan
Wang, Chang-Hong
Liu, Cheng-Hai
author_sort Yang, Tao
collection PubMed
description CONTEXT: Fuzheng Huayu recipe (FZHY) combined with entecavir (ETV) is used to treat the cirrhosis caused by chronic hepatitis B (CHB) infection. OBJECTIVE: To investigate the effect of FZHY on ETV pharmacokinetics under different conditions. MATERIALS AND METHODS: A model of liver fibrosis was created by intraperitoneal injection of dimethylnitrosamine (DMN; 10 μg/kg) for 4 weeks in Wistar rats. Ultra-high-performance liquid chromatography–tandem mass spectrometry was used to determine the blood concentration of ETV. Pharmacokinetic characteristics of ETV (0.9 mg/kg) were investigated after co-administration with FZHY (0.55 g/kg) at certain time intervals in normal and model rats. RESULTS: The analytical method for ETV was validated at 0.5–50 μg/L with a correlation coefficient = 0.9996, lower limit of quantitation of 0.5 μg/L and mean accuracy of 104.18 ± 9.46%. Compared with the ETV-N group, the pharmacokinetic parameters of the EF-2 group did not change significantly, but that of the EF-0 group decreased in C(max) to 27.38 μg/L, in AUC(0–)(t) from 323.84 to 236.67 μg/h/L, and a delay in T(max) from 0.75 to 6.00 h; that of the EF-0 group presented a decrease in C(max) of 61.92%, delay in t(1/2) of 2.45 h and delay in T(max) of 2.92 h. The t(1/2e) and V(d)/F of ETV were increased significantly to 8.01 h and 24.38 L/kg in the ETV-M group. CONCLUSIONS: The effects of FZHY on ETV pharmacokinetics were diminished with an increase of interval time. The best time to administer both drugs is >2 h apart.
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spelling pubmed-69685292020-01-30 Effects of Fuzheng Huayu recipe on entecavir pharmacokinetics in normal and dimethylnitrosamine-induced hepatic fibrosis rats Yang, Tao Zheng, Tian-Hui Zhao, Qiang Liu, Wei Li, Shu-Ping Tao, Yan-Yan Wang, Chang-Hong Liu, Cheng-Hai Pharm Biol Article CONTEXT: Fuzheng Huayu recipe (FZHY) combined with entecavir (ETV) is used to treat the cirrhosis caused by chronic hepatitis B (CHB) infection. OBJECTIVE: To investigate the effect of FZHY on ETV pharmacokinetics under different conditions. MATERIALS AND METHODS: A model of liver fibrosis was created by intraperitoneal injection of dimethylnitrosamine (DMN; 10 μg/kg) for 4 weeks in Wistar rats. Ultra-high-performance liquid chromatography–tandem mass spectrometry was used to determine the blood concentration of ETV. Pharmacokinetic characteristics of ETV (0.9 mg/kg) were investigated after co-administration with FZHY (0.55 g/kg) at certain time intervals in normal and model rats. RESULTS: The analytical method for ETV was validated at 0.5–50 μg/L with a correlation coefficient = 0.9996, lower limit of quantitation of 0.5 μg/L and mean accuracy of 104.18 ± 9.46%. Compared with the ETV-N group, the pharmacokinetic parameters of the EF-2 group did not change significantly, but that of the EF-0 group decreased in C(max) to 27.38 μg/L, in AUC(0–)(t) from 323.84 to 236.67 μg/h/L, and a delay in T(max) from 0.75 to 6.00 h; that of the EF-0 group presented a decrease in C(max) of 61.92%, delay in t(1/2) of 2.45 h and delay in T(max) of 2.92 h. The t(1/2e) and V(d)/F of ETV were increased significantly to 8.01 h and 24.38 L/kg in the ETV-M group. CONCLUSIONS: The effects of FZHY on ETV pharmacokinetics were diminished with an increase of interval time. The best time to administer both drugs is >2 h apart. Taylor & Francis 2019-12-18 /pmc/articles/PMC6968529/ /pubmed/31847670 http://dx.doi.org/10.1080/13880209.2019.1687527 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Yang, Tao
Zheng, Tian-Hui
Zhao, Qiang
Liu, Wei
Li, Shu-Ping
Tao, Yan-Yan
Wang, Chang-Hong
Liu, Cheng-Hai
Effects of Fuzheng Huayu recipe on entecavir pharmacokinetics in normal and dimethylnitrosamine-induced hepatic fibrosis rats
title Effects of Fuzheng Huayu recipe on entecavir pharmacokinetics in normal and dimethylnitrosamine-induced hepatic fibrosis rats
title_full Effects of Fuzheng Huayu recipe on entecavir pharmacokinetics in normal and dimethylnitrosamine-induced hepatic fibrosis rats
title_fullStr Effects of Fuzheng Huayu recipe on entecavir pharmacokinetics in normal and dimethylnitrosamine-induced hepatic fibrosis rats
title_full_unstemmed Effects of Fuzheng Huayu recipe on entecavir pharmacokinetics in normal and dimethylnitrosamine-induced hepatic fibrosis rats
title_short Effects of Fuzheng Huayu recipe on entecavir pharmacokinetics in normal and dimethylnitrosamine-induced hepatic fibrosis rats
title_sort effects of fuzheng huayu recipe on entecavir pharmacokinetics in normal and dimethylnitrosamine-induced hepatic fibrosis rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968529/
https://www.ncbi.nlm.nih.gov/pubmed/31847670
http://dx.doi.org/10.1080/13880209.2019.1687527
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