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体外生物预测方法:研讨会总结报告。

In Vitro Biopredictive Methods: A Workshop Summary Report.

机构信息

New Modalities and Parenteral Development, Pharmaceutical Technology & Development, Operations, AstraZeneca, Macclesfield, UK.

Fraunhofer Institute for Molecular Biology and Applied Ecology and Goethe University, Frankfurt, Germany.

出版信息

J Pharm Sci. 2021 Feb;110(2):567-583. doi: 10.1016/j.xphs.2020.09.021. Epub 2020 Sep 19.

Abstract

This workshop report summarizes the proceedings of Day 1 of a three-day workshop on "Current State and Future Expectations of Translational Modeling Strategies to Support Drug Product Development, Manufacturing Changes and Controls". Physiologically based biopharmaceutics models (PBBM) are tools which enable the drug product quality attributes to be linked to the in vivo performance. These tools rely on key quality inputs in order to provide reliable predictions. After introducing the objectives of the workshop and the expectations from the breakout sessions, Day 1 of the workshop focused on the best practices and challenges in measuring in vitro inputs needed for modeling, such as the drug solubility, the dissolution rate of the drug product, potential precipitation of the drug and drug permeability. This paper reports the podium presentations and summarizes breakout session discussions related to A) the best strategies for determining solubility, supersaturation and critical supersaturation; B) the best strategies for the development of biopredictive (clinically relevant) dissolution methods; C) the challenges associated with describing gastro-intestinal systems parameters such as mucus, liquid volume and motility; and D) the challenges with translating biopharmaceutical measures of drug permeability along the gastrointestinal tract to a meaningful model parameter.

摘要

本研讨会报告总结了为期三天的“支持药物产品开发、制造变更和控制的转化建模策略的现状和未来期望”研讨会第一天的会议内容。生理相关的生物药剂学模型 (PBBM) 是将药物产品质量属性与体内性能联系起来的工具。这些工具依赖于关键质量输入以提供可靠的预测。在介绍了研讨会的目标和分组讨论的期望之后,研讨会的第一天重点讨论了测量建模所需的关键体外输入(如药物溶解度、药物产品的溶出率、药物潜在沉淀和药物渗透性)的最佳实践和挑战。本文报告了专题演讲,并总结了与以下方面相关的分组讨论内容:A)确定溶解度、过饱和度和关键过饱和度的最佳策略;B)开发生物预测性(临床相关)溶解方法的最佳策略;C)描述诸如粘液、液体体积和蠕动等胃肠道系统参数的相关挑战;以及 D)将药物渗透性的生物药剂学测量值沿胃肠道转化为有意义的模型参数的相关挑战。

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