从可提取数据到暴露数据:关注USP < 665 >的外推算法的敏感性分析。

IF 4.7 3区 医学 Q1 PHARMACOLOGY & PHARMACY European Journal of Pharmaceutical Sciences Pub Date : 2025-04-01 Epub Date: 2025-01-27 DOI:10.1016/j.ejps.2025.107026
Armin Hauk , Alexander Wildschütz , Ina Pahl , Daniel Canton , Roberto Menzel
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引用次数: 0

摘要

我们评估了用于推断可提取数据的算法,用于预测与工艺设备相关的可浸出物(PERL)和评估一次性使用系统(SUSs)及其组件中的PERL暴露。这些算法的鲁棒性和灵敏度针对输入数据的变化进行了测试,包括从USP < 665 >提供的标准化可提取协议中获得的短期和长期接触时间可提取数据的外推算法。我们的研究结果表明,SUS和组件的外推数据适用于安全评估。外推和汇总的数据不会系统地低估潜在的PERL暴露值,前提是可提取的数据来自与使用场景相比具有更高的接触表面积液体体积比和/或低液体与材料体积比的实验。该算法对输入数据中的偏差不敏感,因为这些偏差逐渐传播到外推数据和参数中。通过结合使用半极性有机溶液(如乙醇)的实验中可提取的研究数据,可以提高PERL暴露计算的质量和重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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From extractables to exposure data: Sensitivity analysis of extrapolation algorithms with focus on USP 〈665〉
We evaluated algorithms designed to extrapolate extractables data for predicting process equipment-related leachables (PERLs) and assessing PERL exposure in single-use systems (SUSs) and assemblies. The robustness and sensitivity of these algorithms were tested against variations in input data, including extrapolation algorithms for both short and long contact time extractables data obtained from the standardized extractables protocol provided in USP 〈665〉. Our findings demonstrate that extrapolated data for SUS and assemblies are suitable for safety assessments. Extrapolated and aggregated data do not systematically underestimate potential PERL exposure values, provided that the extractables data originate from experiments with a higher surface area to contact liquid volume ratio and/or a low liquid to material volume ratio compared to the use scenario. The algorithms are non-sensitive to deviations in input data, as these deviations are propagated decreasingly into extrapolated data and parameters. The quality and significance of PERL exposure calculations can be enhanced by incorporating extractables study data from experiments using a semipolar organic solution, such as ethanol.
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来源期刊
CiteScore
9.60
自引率
2.20%
发文量
248
审稿时长
50 days
期刊介绍: The journal publishes research articles, review articles and scientific commentaries on all aspects of the pharmaceutical sciences with emphasis on conceptual novelty and scientific quality. The Editors welcome articles in this multidisciplinary field, with a focus on topics relevant for drug discovery and development. More specifically, the Journal publishes reports on medicinal chemistry, pharmacology, drug absorption and metabolism, pharmacokinetics and pharmacodynamics, pharmaceutical and biomedical analysis, drug delivery (including gene delivery), drug targeting, pharmaceutical technology, pharmaceutical biotechnology and clinical drug evaluation. The journal will typically not give priority to manuscripts focusing primarily on organic synthesis, natural products, adaptation of analytical approaches, or discussions pertaining to drug policy making. Scientific commentaries and review articles are generally by invitation only or by consent of the Editors. Proceedings of scientific meetings may be published as special issues or supplements to the Journal.
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