通过主成分分析和偏最小二乘法回归分析材料特性对可压片性的影响。

IF 4.3 3区 医学 Q1 PHARMACOLOGY & PHARMACY European Journal of Pharmaceutical Sciences Pub Date : 2024-06-18 DOI:10.1016/j.ejps.2024.106836
Lena Mareczek , Carolin Riehl , Meike Harms , Stephan Reichl
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引用次数: 0

摘要

本研究结合了主成分分析(PCA)和偏最小二乘法回归(PLS),以确定决定直接压片和辊压压片性能的关键材料描述因子。为了系统地阐明不同的材料描述因子、原料药和填料特性以及工艺路线对压片性的影响,我们建立了一个庞大的材料库,其中包括 119 种材料描述因子以及 44 种粉末和辊压材料在不同药物负荷下的片剂拉伸强度。建立的 PCA 模型强调了不同粉末描述因子与相应表征方法之间的相关性,因此可以减少分析次数,在一定程度上节省资源。随后,建立了 PLS 模型,以确定可压片性的关键材料属性,如密度和粒度,以及表面能、内聚功和壁面摩擦力。此外,基于大量材料表征的 PLS 能够预测模型未知材料的可压片性。因此,本研究强调了 PCA 和 PLS 如何成为阐明粉末与可压片性之间相关性的有用工具,这将有助于在制剂开发过程中对可制造性进行更可靠的预测。
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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Analysis of the impact of material properties on tabletability by principal component analysis and partial least squares regression

Principal component analysis (PCA) and partial least squares regression (PLS) were combined in this study to identify key material descriptors determining tabletability in direct compression and roller compaction. An extensive material library including 119 material descriptors and tablet tensile strengths of 44 powders and roller compacted materials with varying drug loads was generated to systematically elucidate the impact of different material descriptors, raw API and filler properties as well as process route on tabletability. A PCA model was created which highlighted correlations between different powder descriptors and respective characterization methods and, thus, can enable reduction of analyses to save resources to a certain extent. Subsequently, PLS models were established to identify key material attributes for tabletability such as density and particle size but also surface energy, work of cohesion and wall friction, which were for the first time demonstrated by PLS as highly relevant for tabletability in roller compaction and direct compression. Further, PLS based on extensive material characterization enabled the prediction of tabletability of materials unknown to the model. Thus, this study highlighted how PCA and PLS are useful tools to elucidate the correlations between powder and tabletability, which will enable more robust prediction of manufacturability in formulation development.

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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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