Subramaniam B, Rajewski R A, Snavely K
Department of Chemical and Petroleum Engineering, and Center for Drug Delivery Research, University of Kansas, Lawrence 66045, USA.
J Pharm Sci. 1997 Aug;86(8):885-90. doi: 10.1021/js9700661.
Replacement of traditional solvents with "environmentally benign" carbon dioxide is receiving increased attention in pharmaceutical processing. Among the reported applications, particle formation with dense carbon dioxide and the "clean" synthesis of drug compounds using carbon dioxide as a reaction medium hold immense potential for large-scale application in the pharmaceutical industry. This paper provides an overview of these rapidly emerging technologies along with examples of the wide variety of relatively contaminant-free pharmaceutical compounds that have been processed via these technologies on a laboratory scale. Challenges facing successful implementation in practice include demonstration of continuous production and harvesting of particles with desired and reproducible product characteristics. Mathematical models aimed at a better fundamental understanding of the underlying thermophysical phenomena are essential for rational design and scale-up of these technologies.
在药物加工过程中,用“环境友好型”二氧化碳替代传统溶剂正受到越来越多的关注。在已报道的应用中,利用超临界二氧化碳制备颗粒以及以二氧化碳作为反应介质“清洁”合成药物化合物,在制药行业大规模应用方面具有巨大潜力。本文概述了这些迅速兴起的技术,并列举了多种已在实验室规模通过这些技术加工的相对无污染药物化合物的实例。在实际中成功实施所面临的挑战包括证明能够连续生产以及收获具有所需且可重现产品特性的颗粒。旨在更好地从根本上理解潜在热物理现象的数学模型,对于这些技术的合理设计和放大至关重要。