药物开发中粉末和多颗粒单元可加工性表征的数学方法

Q4 Pharmacology, Toxicology and Pharmaceutics
Ivana Vasiljević, Erna Turković, I. Aleksić, J. Parojčić
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引用次数: 0

摘要

在药物开发的质量设计方法中,需要了解材料特性和加工对固体剂型性能的影响。几个研究小组已经开发了数学方法,旨在促进配方组成和制造技术的选择。这些方法基于材料颗粒、体积和压缩相关特性。本文提供了理论假设和不同的数学方法粉末和多颗粒单位的可加工性表征的关键审查。数学方法主要用于直接可压缩材料,但有时也考虑其他制造技术,如辊压实和湿造粒。获得的压实抗拉强度作为描述压实力学性能的重要特征,已在大多数方法中实现。流动性也应进行评估,因为它影响样品的可加工性。此外,颗粒大小和形状,材料密度和可压缩性,压实性和可溶性也被区分为固体剂型发展的相关特性。数学方法的应用可能有助于对关键材料属性的机理理解,并促进剂型的开发和优化。然而,根据预期剂型特性选择合适的剂型是至关重要的,以确保所有相关的粉末/多颗粒单位特性得到实施和严格评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mathematical approaches for powders and multiparticulate units processability characterization in pharmaceutical development
An understanding of material properties and processing effects on solid dosage forms performance is required within the Quality-by-design approach to pharmaceutical development. Several research groups have developed mathematical approaches aiming to facilitate the selection of formulation composition and the manufacturing technology. These approaches are based on material particulate, bulk and compression-related properties. This paper provides theoretical assumptions and a critical review of different mathematical approaches for processability characterization of powders and multiparticulate units. Mathematical approaches have mainly been developed for directly compressible materials, but sometimes other manufacturing technologies, such as roller compaction and wet granulation, are also considered. The obtained compact tensile strength has been implemented in the majority of approaches, as an important characteristic describing compact mechanical properties. Flowability should be also evaluated, since it affects sample processability. Additionally, particle size and shape, material density and compressibility, compactibility and tabletability profiles have been also distinguished as relevant properties for solid dosage form development. The application of mathematical approaches may contribute to the mechanistic understanding of critical material attributes and facilitate dosage form development and optimization. However, it is essential to select the appropriate one, based on the intended dosage form characteristics, in order to ensure that all relevant powder/multiparticulate units characteristics are implemented and critically evaluated.
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来源期刊
Arhiv za Farmaciju
Arhiv za Farmaciju Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
自引率
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发文量
19
审稿时长
12 weeks
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