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药物制剂研发与生产中的非环境条件

Non-ambient Conditions in the Investigation and Manufacturing of Drug Forms.

作者信息

Boldyreva Elena

机构信息

Institute of Solid State Chemistry and Mechanochemistry, Siberian Branch of the Russian Academy of Sciences, ul. Kutateladze, 18, Novosibirsk, 630128, Russian Federation.

出版信息

Curr Pharm Des. 2016;22(32):4981-5000. doi: 10.2174/1381612822666160804093120.

Abstract

For the formation of a drug, a pharmacologically active compound must be prepared in a specific form. The drug must be manufactured, packaged, stored, transported, administred and delivered to a target in the body. To successfully prepare a drug form that will be robust through manufacturing, stable before administration and active with high bioavailability after administration, one needs to produce solid forms with controlled crystal structure and particle size and shape - often as multi-component composites. Considering drugs as materials, one can apply the knowledge of solid-state chemistry and materials science and non-ambient conditions to obtain solid forms with optimized properties. These conditions include, among others, different types of mechanical and ultrasonic treatment, hydrostatic compression, high-temperature or cryogenic spray-drying and crystallization from supercritical solvents. Solid-state reactions (e.g. dehydration or clathrate decomposition) can be effective in accessing metastable polymorphs or in micronizing a sample uniformly. To achieve control over the drug forms and the processes used for their robust manufacturing, one needs to take into account both the thermodynamic and kinetic aspects of their transformations.

摘要

为了形成药物,必须将药理活性化合物制备成特定形式。药物必须经过制造、包装、储存、运输、给药并送达体内的靶点。为了成功制备出一种在制造过程中稳定、给药前稳定且给药后具有高生物利用度的活性药物剂型,需要制备具有可控晶体结构、粒径和形状的固体形式——通常为多组分复合材料。将药物视为材料,可以应用固态化学和材料科学知识以及非环境条件来获得具有优化性能的固体形式。这些条件包括不同类型的机械和超声处理、静水压缩、高温或低温喷雾干燥以及超临界溶剂结晶。固态反应(如脱水或包合物分解)在获得亚稳多晶型物或均匀微粉化样品方面可能有效。为了控制药物剂型及其稳健制造所使用的过程,需要考虑其转变的热力学和动力学方面。

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