吗替麦考酚酸酯及其活性代谢物麦考酚酸的跨膜转运机制研究

余自成, 田薇薇, 马明华, 刘霞, 陈红君, 陈红专

中国药学杂志 ›› 2014, Vol. 49 ›› Issue (4) : 322-328.

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中国药学杂志 ›› 2014, Vol. 49 ›› Issue (4) : 322-328. DOI: 10.11669/cpj.2014.03.015
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吗替麦考酚酸酯及其活性代谢物麦考酚酸的跨膜转运机制研究

  • 余自成1, 田薇薇1, 马明华1, 刘霞1, 陈红君1, 陈红专2
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Investigation on the Mechanism of Transmembrane Transport of Mycophenolate Mofetil and Its Active Metabolite Mycophenolic Acid

  • YU Zi-cheng1, TIAN Wei-wei1, MA Ming-hua1, LIU Xia1, CHEN Hong-jun1, CHEN Hong-zhuan2
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摘要

目的 研究吗替麦考酚酸酯(mycophenolate mofetil, MMF)及其活性代谢物麦考酚酸(mycophenolic acid, MPA)的跨膜转运机制。方法 建立Caco-2细胞单层模型, 进行吗替麦考酚酸酯及麦考酚酸转运实验, 用LC-MS/MS方法测定转运实验样品中吗替麦考酚酸酯和麦考酚酸浓度, 计算表观通透系数Papp和外排率Pratio, 评价药物转运及外排作用, P-糖蛋白(P-glycoprotein, P-gp)抑制剂维拉帕米用于评价P-gp在吗替麦考酚酸酯和麦考酚酸肠道吸收转运中的作用。结果 麦考酚酸在10、50和100 μmol·L-1的双向转运的表观通透系数Papp, ab 分别为(9.70±0.40)×106 cm·s-1、(9.35±0.62)×106cm·s-1和(8.69±0.69)×106cm·s-1;外排率Pratio分别为1.39、1.22和1.22, 维拉帕米明显降低了外排率。吗替麦考酚酸酯在穿过Caco-2细胞单层转运过程中大部分被水解为麦考酚酸, 麦考酚酸转运的量随转运时间延长而不断增加, 而吗替麦考酚酸酯转运的量随时间无明显变化。维拉帕米对吗替麦考酚酸酯转运无明显影响。结论 麦考酚酸的跨膜转运受到由转运载体介导的主动转运外排作用影响, P-gp参与了麦考酚酸的跨膜转运。吗替麦考酚酸酯的跨膜转运不存在P-gp的作用, 为被动转运。

Abstract

OBJECTIVE To investigate the mechanism of transmembrane transport of mycophenolate mofetil (MMF) and its active metabolite mycophenolic acid (MPA). METHODS Caco-2 cell monolayer model was developed for MMF and MPA transport experiment, and the LC-MS/MS method was used for the determination of MMF and MPA concentration in transport medium. The apparent permeability coefficient (Papp) and efflux ratio (Pratio) were calculated and used for the evaluation of the ability of drug transport and drug efflux across Caco-2 cell monolayer. RESULTSThe Papp of MPA in two-way transport experiment (Papp, ab and Papp, ba) at 10, 50 and 100 μmol·L-1 were(9.70±0.40)×106 cm·s-1, (9.35±0.62)×106cm·s-1, (8.69±0.69)×106cm·s-1, respectively. Pratiowere 1.39, 1.22 and 1.22, respectively.Pratioof MPA was reduced by verapamil, a well-known P-glycoprotein inhibitor. MMF was mostly hydrolyzed to MPA during the transport process across the Caco-2 cell monolayer. The amount of MPA transported increased with time, but the amount of MMF transported changed not significantly over time and no significant effect of verapamil was observed. CONCLUSION The transmembrane transport of MPA is affected by active transportefflux mediated by transporter with P-gp involved. No effect of P-gp is found in MMF transmembrane transport, which is passive transport.

关键词

吗替麦考酚酸酯 / 麦考酚酸 / 跨膜转运 / 机制 / P-糖蛋白

Key words

mycophenolate mofetil / mycophenolic acid / transmembrane transport / mechanism / P-glycoprotein

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余自成, 田薇薇, 马明华, 刘霞, 陈红君, 陈红专. 吗替麦考酚酸酯及其活性代谢物麦考酚酸的跨膜转运机制研究[J]. 中国药学杂志, 2014, 49(4): 322-328 https://doi.org/10.11669/cpj.2014.03.015
YU Zi-cheng, TIAN Wei-wei, MA Ming-hua, LIU Xia, CHEN Hong-jun, CHEN Hong-zhuan. Investigation on the Mechanism of Transmembrane Transport of Mycophenolate Mofetil and Its Active Metabolite Mycophenolic Acid[J]. Chinese Pharmaceutical Journal, 2014, 49(4): 322-328 https://doi.org/10.11669/cpj.2014.03.015
中图分类号: R285.5   

参考文献

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