白藜芦醇
伊布替尼
药理学
体内
最大值
化学
药代动力学
体外
微粒体
医学
生物化学
内科学
生物
白血病
生物技术
慢性淋巴细胞白血病
作者
Jian Wen,Su‐su Bao,Bo-Wen Zhang,Tenghui Liu,Qiu-Geng Ouyang,Jianping Cai,Hong-Yu Zhou
标识
DOI:10.1080/03639045.2018.1514044
摘要
Objective: To investigate the impact of resveratrol on the metabolism of ibrutinib in vitro and in vivo.Methods: In vitro, rat liver microsomes (RLM) and human liver microsomes (HLM) were used to study. In vivo, 18 male SD rats were randomly divided into three groups (n = 6): ibrutinib and the multiple dose of 100 mg/kg resveratrol for consecutive 7 days (Group A), ibrutinib and the single dose of 100 mg/kg resveratrol (Group B), ibrutinib (Group C). Processed samples were analyzed by UPLC–MS/MS.Results: Resveratrol showed inhibition on RLM and HLM in vitro. The IC50 of resveratrol was 8.745 µM in RLM and 7.789 µM in HLM. Furthermore, Groups A and B both increased the AUC and reduced the CLz/F. The Cmax of Group A and the MRT(0–t) of Group B were significantly improved.Conclusions: Resveratrol inhibits the pharmacokinetic of ibrutinib in vitro and in vivo. It is necessary to pay more attention to adjust the dose of the drug when resveratrol is used in combination with ibrutinib.
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