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近年来改善非水溶性药物在无定形药物固体中溶解和过饱和的进展:综述。

Recent Advances in Enhancement of Dissolution and Supersaturation of Poorly Water-Soluble Drug in Amorphous Pharmaceutical Solids: A Review.

机构信息

School of Pharmacy, Jiangsu Vocational College of Medicine, Yancheng, 224005, China.

Department of Cancer Biology and Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, 27157, USA.

出版信息

AAPS PharmSciTech. 2021 Dec 10;23(1):16. doi: 10.1208/s12249-021-02137-0.

Abstract

Amorphization is one of the most effective pharmaceutical approaches to enhance the dissolution and oral bioavailability of poorly water-soluble drugs. In recent years, amorphous formulations have been experiencing rapid development both in theoretical and practical application. Based on using different types of stabilizing agents, amorphous formulations can be mainly classified as polymer-based amorphous solid dispersion, coamorphous formulation, mesoporous silica-based amorphous formulation, etc. This paper summarizes recent advances in the dissolution and supersaturation of these amorphous formulations. Moreover, we also highlight the roles of stabilizing agents such as polymers, low molecular weight co-formers, and mesoporous silica. Maintaining supersaturation in solution is a key factor for the enhancement of dissolution profile and oral bioavailability, and thus, the strategies and challenges for maintaining supersaturation are also discussed. With an in-depth understanding of the inherent mechanisms of dissolution behaviors, the design of amorphous pharmaceutical formulations will become more scientific and reasonable, leading to vigorous development of commercial amorphous drug products.

摘要

无定形化是提高难溶性药物溶解和口服生物利用度的最有效药物制剂方法之一。近年来,无定形制剂在理论和实际应用方面都得到了快速发展。基于使用不同类型的稳定剂,无定形制剂主要可以分为聚合物基无定形固体分散体、共无定形制剂、介孔硅基无定形制剂等。本文总结了这些无定形制剂在溶解和过饱和方面的最新进展。此外,我们还强调了聚合物、低分子量共晶形成剂和介孔硅等稳定剂的作用。在溶液中维持过饱和度是提高溶解曲线和口服生物利用度的关键因素,因此,也讨论了维持过饱和度的策略和挑战。通过深入了解溶解行为的内在机制,无定形药物制剂的设计将变得更加科学合理,从而推动商业无定形药物产品的蓬勃发展。

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