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口服药物产品开发中渗透性评估的挑战。

Challenges in Permeability Assessment for Oral Drug Product Development.

作者信息

Koziolek Mirko, Augustijns Patrick, Berger Constantin, Cristofoletti Rodrigo, Dahlgren David, Keemink Janneke, Matsson Pär, McCartney Fiona, Metzger Marco, Mezler Mario, Niessen Janis, Polli James E, Vertzoni Maria, Weitschies Werner, Dressman Jennifer

机构信息

NCE Drug Product Development, Development Sciences, AbbVie Deutschland GmbH & Co. KG, 67061 Ludwigshafen, Germany.

Drug Delivery and Disposition, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, 3000 Leuven, Belgium.

出版信息

Pharmaceutics. 2023 Sep 28;15(10):2397. doi: 10.3390/pharmaceutics15102397.

Abstract

Drug permeation across the intestinal epithelium is a prerequisite for successful oral drug delivery. The increased interest in oral administration of peptides, as well as poorly soluble and poorly permeable compounds such as drugs for targeted protein degradation, have made permeability a key parameter in oral drug product development. This review describes the various in vitro, in silico and in vivo methodologies that are applied to determine drug permeability in the human gastrointestinal tract and identifies how they are applied in the different stages of drug development. The various methods used to predict, estimate or measure permeability values, ranging from in silico and in vitro methods all the way to studies in animals and humans, are discussed with regard to their advantages, limitations and applications. A special focus is put on novel techniques such as computational approaches, gut-on-chip models and human tissue-based models, where significant progress has been made in the last few years. In addition, the impact of permeability estimations on PK predictions in PBPK modeling, the degree to which excipients can affect drug permeability in clinical studies and the requirements for colonic drug absorption are addressed.

摘要

药物透过肠道上皮细胞是口服给药成功的前提条件。对肽类药物以及难溶性和低渗透性化合物(如用于靶向蛋白降解的药物)口服给药的兴趣日益增加,使得渗透性成为口服药物产品开发的关键参数。本综述描述了用于测定人体胃肠道药物渗透性的各种体外、计算机模拟和体内方法,并确定了它们在药物开发不同阶段的应用方式。讨论了用于预测、估计或测量渗透性值的各种方法,从计算机模拟和体外方法到动物和人体研究,探讨了它们的优点、局限性和应用。特别关注了诸如计算方法、芯片肠道模型和基于人体组织的模型等新技术,这些技术在过去几年中取得了显著进展。此外,还讨论了渗透性估计对生理药代动力学(PBPK)建模中药物动力学(PK)预测的影响、辅料在临床研究中对药物渗透性的影响程度以及结肠药物吸收的要求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b09/10609725/1579db8675b1/pharmaceutics-15-02397-g001.jpg

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