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Combinative Particle Size Reduction Technologies for the Production of Drug Nanocrystals

机译:组合粒度减小技术,用于生产药物纳米晶体

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Nanosizing is a suitable method to enhance the dissolution rate and therefore the bioavailability of poorly soluble drugs. The success of the particle size reduction processes depends on critical factors such as the employed technology, equipment, and drug physicochemical properties. High pressure homogenization and wet bead milling are standard comminution techniques that have been already employed to successfully formulate poorly soluble drugs and bring them to market. However, these techniques have limitations in their particle size reduction performance, such as long production times and the necessity of employing a micronized drug as the starting material. This review article discusses the development of combinative methods, such as the NANOEDGE, H 96, H 69, H 42, and CT technologies. These processes were developed to improve the particle size reduction effectiveness of the standard techniques. These novel technologies can combine bottom-up and/or top-down techniques in a two-step process. The combinative processes lead in general to improved particle size reduction effectiveness. Faster production of drug nanocrystals and smaller final mean particle sizes are among the main advantages. The combinative particle size reduction technologies are very useful formulation tools, and they will continue acquiring importance for the production of drug nanocrystals.
机译:纳米化是一种提高溶解速度,从而提高难溶性药物生物利用度的合适方法。减小粒度过程的成功取决于关键因素,例如所采用的技术,设备和药物的物理化学性质。高压均质化和湿珠磨是标准的粉碎技术,已成功用于配制难溶性药物并将其投放市场。但是,这些技术在减小粒度的性能方面存在局限性,例如生产时间长以及必须使用微粉化药物作为起始原料。本文将讨论诸如NANOEDGE,H 96,H 69,H 42和CT技术之类的组合方法的发展。开发这些方法是为了提高标准技术的粒度减小效果。这些新颖的技术可以在两步过程中结合自下而上和/或自上而下的技术。组合方法通常导致改进的粒度减小效力。药物纳米晶体的更快生产和较小的最终平均粒径是主要优势。组合粒径减小技术是非常有用的配制工具,它们将继续在药物纳米晶体的生产中获得重要性。

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