Best Practices and Recommendations for Non-Liquid Matrices Bioanalysis.

IF 5 3区 医学 Q1 PHARMACOLOGY & PHARMACY AAPS Journal Pub Date : 2025-03-11 DOI:10.1208/s12248-025-01033-w
Faye Vazvaei-Smith, Wenkui Li, Omar S Barnaby, Sanjeev Bhardwaj, Juyao Dong, Carolyne Dumont, Carmen Fernández-Metzler, Brian Geist, Mohamed Hassanein, Amanda Hays, Anna Ilinskaya, Eugene P Kadar, Kris King, Nadia Kulagina, Murali K Matta, Krishna Midde, Rina Pan, Divya Pathania, Thomas Tarnowski, Eric Tewalt, Eric Thomas, Enaksha Wickremsinhe, Deqing Xiao
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Abstract

The analysis of Non-Liquid Matrices (NLMs) can provide key information on many aspects in drug discovery and development. These include but are not limited to drug uptake and distribution, engagement and modulation, and target exposure. A thorough understanding of these aspects is fundamental to the progression of drug development. In many cases, such an understanding can only be achieved through quantitative analysis of NLMs. Such dependence can lead to bottlenecks in the drug development process-as the practices and regulations that govern bioanalysis of conventional liquid matrices typically cannot be directly applied to NLMs. This paper strives to fill this crucial gap. To this end, subject matter experts from across the industry, through the auspices of the AAPS Bioanalytical Community, have combined their collective best practices for NLM bioanalysis in this paper. Certainly, this endeavor came with challenges, the most prominent of which also serves as the impetus for this project, the lack of literature on NLM bioanalysis dealing with different types of NLM, analysis rigor, and best practices to draw from. This paper aims to serve as a comprehensive set of best practices drawn from the experiences of leading scientists across the industry-for NLM bioanalysis in drug development.

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对非液体基质(NLM)的分析可以提供药物发现和开发过程中许多方面的关键信息。这些方面包括但不限于药物吸收和分布、参与和调节以及靶点暴露。全面了解这些方面对于药物开发的进展至关重要。在许多情况下,只有通过对无损检测指标进行定量分析才能实现这种理解。这种依赖性可能会导致药物开发过程中出现瓶颈--因为管理传统液体基质生物分析的实践和法规通常无法直接应用于非淋菌物质。本文致力于填补这一重要空白。为此,来自业界的主题专家们在 AAPS 生物分析社区的支持下,在本文中汇集了他们对 NLM 生物分析的集体最佳实践。当然,这项工作也面临着挑战,其中最突出的挑战也是本项目的动力,那就是缺乏有关无损检测生物分析的文献资料,这些文献资料涉及不同类型的无损检测、分析的严谨性以及可借鉴的最佳实践。本文旨在从业界顶尖科学家的经验中总结出一套全面的最佳实践,用于药物开发过程中的无损检测生物分析。
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来源期刊
AAPS Journal
AAPS Journal 医学-药学
CiteScore
7.80
自引率
4.40%
发文量
109
审稿时长
1 months
期刊介绍: The AAPS Journal, an official journal of the American Association of Pharmaceutical Scientists (AAPS), publishes novel and significant findings in the various areas of pharmaceutical sciences impacting human and veterinary therapeutics, including: · Drug Design and Discovery · Pharmaceutical Biotechnology · Biopharmaceutics, Formulation, and Drug Delivery · Metabolism and Transport · Pharmacokinetics, Pharmacodynamics, and Pharmacometrics · Translational Research · Clinical Evaluations and Therapeutic Outcomes · Regulatory Science We invite submissions under the following article types: · Original Research Articles · Reviews and Mini-reviews · White Papers, Commentaries, and Editorials · Meeting Reports · Brief/Technical Reports and Rapid Communications · Regulatory Notes · Tutorials · Protocols in the Pharmaceutical Sciences In addition, The AAPS Journal publishes themes, organized by guest editors, which are focused on particular areas of current interest to our field.
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