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微米化药物粉末的研磨法工艺优化与颗粒工程。

Process optimization and particle engineering of micronized drug powders via milling.

机构信息

Division of Molecular Pharmaceutics and Drug Delivery, University of Texas at Austin College of Pharmacy, 2409 West University Avenue, PHR 4.214, Austin, TX, 78712, USA.

出版信息

Drug Deliv Transl Res. 2018 Dec;8(6):1740-1750. doi: 10.1007/s13346-017-0444-x.

Abstract

Process control and optimization is a critical aspect of process analytical technology (PAT), quality by design (QbD), and the implementation of continuous manufacturing procedures. While process control and optimization techniques have been utilized in other manufacturing industries for decades, the pharmaceutical industry has only recently begun to adopt these procedures. Micronization, particularly milling, is a generally low-yield, high-energy consumption process that is well suited for a process optimization mindset. This review discusses optimization of the pharmaceutical milling process through design space development, theoretical and empirical modeling, and monitoring of critical quality attributes.

摘要

过程控制和优化是过程分析技术(PAT)、质量源于设计(QbD)和连续制造程序实施的关键方面。虽然过程控制和优化技术在其他制造业已经使用了几十年,但制药行业直到最近才开始采用这些程序。微粉化,特别是研磨,是一种普遍低产、高能耗的工艺,非常适合采用过程优化的思维。本文通过设计空间开发、理论和经验建模以及关键质量属性监测,讨论了制药研磨过程的优化。

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