学术纳米医学研究中的药物质量设计:通过约束扼杀创新还是创造力?

Lea Ann Dailey
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引用次数: 5

摘要

药物设计质量(QbD)是一种系统的药物开发方法,从预定义的目标开始,强调基于健全的科学和质量风险管理的产品和工艺理解和控制。首先,QbD是一种实验设计哲学,强调在实验室研究开始前进行彻底的智力规划的价值。志在转化科学的学术研究人员可能会受益于制药行业在将QbD纳入其发展理念后所吸取的教训。然而,由于学术纳米医学研究的跨学科性质,可能很少有研究人员了解QbD,以及如何在学术研究环境中明智地实施QbD。这篇综述介绍了QbD的主要元素,并举例说明QbD应用于纳米医学研究的案例研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pharmaceutical quality by design in academic nanomedicine research: stifling innovation or creativity through constraint?

Pharmaceutical quality by design in academic nanomedicine research: stifling innovation or creativity through constraint?

Pharmaceutical quality by design (QbD) is a systematic approach to drug development that begins with predefined objectives and emphasises product and process understanding and control based on sound science and quality risk management. First and foremost, QbD is an experimental design philosophy, which emphasises the value of thorough intellectual planning prior to the commencement of laboratory studies. Academic researchers whose ambitions lie in translational science may benefit from the lessons learned by the pharmaceutical industry following implementation of QbD into their development philosophy. However, because of the very interdisciplinary nature of academic nanomedicine research, it is likely that very few investigators are aware of QbD and how aspects of it may be judiciously implemented in an academic research setting. This review provides an introduction to the main elements of QbD and gives examples of case studies where QbD has been applied to nanomedicine research.

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