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利用无细胞渗透工具进行药物渗透特性分析:概述及应用。

Drug permeability profiling using cell-free permeation tools: Overview and applications.

机构信息

Drug Delivery and Disposition, KU Leuven, Gasthuisberg O&N II, Herestraat 49, Box 921, 3000 Leuven, Belgium.

Drug Transport and Delivery Group, Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense DK-5230, Denmark.

出版信息

Eur J Pharm Sci. 2018 Jul 1;119:219-233. doi: 10.1016/j.ejps.2018.04.016. Epub 2018 Apr 13.

DOI:10.1016/j.ejps.2018.04.016
PMID:29660464
Abstract

Cell-free permeation systems are gaining interest in drug discovery and development as tools to obtain a reliable prediction of passive intestinal absorption without the disadvantages associated with cell- or tissue-based permeability profiling. Depending on the composition of the barrier, cell-free permeation systems are classified into two classes including (i) biomimetic barriers which are constructed from (phospho)lipids and (ii) non-biomimetic barriers containing dialysis membranes. This review provides an overview of the currently available cell-free permeation systems including Parallel Artificial Membrane Permeability Assay (PAMPA), Phospholipid Vesicle-based Permeation Assay (PVPA), Permeapad®, and artificial membrane based systems (e.g. the artificial membrane insert system (AMI-system)) in terms of their barrier composition as well as their predictive capacity in relation to well-characterized intestinal permeation systems. Given the potential loss of integrity of cell-based permeation barriers in the presence of food components or pharmaceutical excipients, the superior robustness of cell-free barriers makes them suitable for the combined dissolution/permeation evaluation of formulations. While cell-free permeation systems are mostly applied for exploring intestinal absorption, they can also be used to evaluate non-oral drug delivery by adjusting the composition of the membrane.

摘要

无细胞渗透系统作为一种工具,在药物发现和开发中越来越受到关注,可用于可靠预测被动肠吸收,而不会产生与基于细胞或组织的渗透性分析相关的缺点。根据屏障的组成,无细胞渗透系统分为两类,包括(i)仿生屏障,由(磷酸)脂质构建,以及(ii)包含透析膜的非仿生屏障。本文综述了目前可用的无细胞渗透系统,包括平行人工膜渗透测定法(PAMPA)、基于磷脂囊泡的渗透测定法(PVPA)、Permeapad®以及基于人工膜的系统(例如人工膜插入系统(AMI 系统)),就其屏障组成以及与经过充分表征的肠渗透系统的预测能力而言。鉴于存在食物成分或药物赋形剂时基于细胞的渗透屏障完整性可能丧失,无细胞屏障的卓越稳健性使其适合用于制剂的组合溶解/渗透评估。虽然无细胞渗透系统主要用于探索肠吸收,但通过调整膜的组成,它们也可用于评估非口服药物传递。

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