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利用肠道 OATP 转运体的口服药物递送。

Oral drug delivery utilizing intestinal OATP transporters.

机构信息

Department of Membrane Transport and Biopharmaceutics, Faculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Japan.

出版信息

Adv Drug Deliv Rev. 2012 May 1;64(6):508-14. doi: 10.1016/j.addr.2011.07.007. Epub 2011 Jul 30.

Abstract

Transporters play important roles in tissue distribution and urinary- and biliary-excretion of drugs and transporter molecules involved in those processes have been elucidated well. Furthermore, an involvement of efflux transporters such as P-glycoproteins, multidrug resistance associated protein 2, and breast cancer resistance protein as the intestinal absorption barrier and/or intestinal luminal secretion mechanisms has been demonstrated. However, although there are many suggestions for the contribution of uptake/influx transporters in intestinal absorption of drugs, information on the transporter molecules responsible for the intestinal absorptive process is limited. Among them, most studied absorptive drug transporter is peptide transporter PEPT1. However, utilization of PEPT1 for oral delivery of drugs may not be high due to the chemical structural requirement of PEPT1 limited to peptide-mimetics. Recently, organic anion transporting polypeptide (OATP) family such as OATP1A2 and OATP2B1 has been suggested to mediate intestinal absorption of several drugs. Since OATPs exhibit species difference in expressed tissues and functional properties between human and animals, human studies are essential to clarify the intestinal absorption mechanisms of drugs via OATPs. Recent pharmacogenomic studies demonstrated that OATP2B1 is involved in the drug absorption in human. In addition, information of drug-juice interaction in the intestine also uncovered the contribution of OATP1A2 and OATP2B1 in drug absorption. Since OATP1A2 and OATP2B1 exhibit broader substrate selectivity compared with PEPT1, their potential to be applied for oral delivery should be high. In this review, current understanding of characteristics and contribution as the absorptive transporters of OATPs in small intestine in human is described. Now, it is getting clearer that OATPs have significant roles in intestinal absorption of drugs, therefore, there are higher possibility to utilize OATPs as the tools for oral delivery.

摘要

转运蛋白在药物的组织分布和尿液及胆汁排泄中起着重要作用,涉及这些过程的转运蛋白分子已经得到了很好的阐明。此外,已经证明外排转运蛋白如 P-糖蛋白、多药耐药相关蛋白 2 和乳腺癌耐药蛋白作为肠道吸收屏障和/或肠道腔分泌机制的参与。然而,尽管有许多关于摄取/内流转运蛋白在药物肠道吸收中作用的建议,但负责肠道吸收过程的转运蛋白分子的信息有限。在这些转运蛋白中,研究最多的吸收性药物转运蛋白是肽转运蛋白 PEPT1。然而,由于 PEPT1 的化学结构要求仅限于肽类似物,因此 PEPT1 用于药物的口服给药可能效果不高。最近,有机阴离子转运多肽 (OATP) 家族,如 OATP1A2 和 OATP2B1,被认为介导了几种药物的肠道吸收。由于 OATPs 在表达组织和人类与动物之间的功能特性上存在种属差异,因此人类研究对于阐明 OATPs 介导的药物肠道吸收机制至关重要。最近的药物基因组学研究表明,OATP2B1 参与了人类的药物吸收。此外,药物与肠道内液相互作用的信息也揭示了 OATP1A2 和 OATP2B1 在药物吸收中的作用。由于 OATP1A2 和 OATP2B1 与 PEPT1 相比具有更广泛的底物选择性,因此它们作为口服给药的应用潜力应该很高。在这篇综述中,描述了人类小肠中 OATP 作为吸收转运蛋白的特性和作用。现在,越来越清楚的是,OATPs 在药物的肠道吸收中起着重要作用,因此,将 OATPs 用作口服给药工具的可能性更高。

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