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软胶囊溶出方法开发的挑战

Challenges of Dissolution Methods Development for Soft Gelatin Capsules.

作者信息

Damian Festo, Harati Mohammad, Schwartzenhauer Jeff, Van Cauwenberghe Owen, Wettig Shawn D

机构信息

School of Pharmacy, University of Waterloo, 200 University Ave W, Waterloo, ON N2L 3G1, Canada.

Department of Natural Sciences, University of Michigan, 2209 Natural Sciences Building, 4901 Evergreen Rd, Dearborn, MI 48128, USA.

出版信息

Pharmaceutics. 2021 Feb 4;13(2):214. doi: 10.3390/pharmaceutics13020214.

Abstract

Recently, the development of soft gelatin capsules (SGCs) dosage forms has attracted a great deal of interest in the oral delivery of poorly water-soluble drugs. This is attributed to the increased number of poorly soluble drugs in the pipeline, and hence the challenges of finding innovative ways of developing bioavailable and stable dosage forms. Encapsulation of these drugs into SGCs is one of the approaches that is utilized to deliver the active ingredients to the systemic circulation to overcome certain formulation hurdles. Once formulated, encapsulated drugs in the form of SGCs require suitable in vitro dissolution test methods to ensure drug product quality and performance. This review focuses on challenges facing dissolution test method development for SGCs. A brief discussion of the physicochemical and formulation factors that affect the dissolution properties of SGCs will be highlighted. Likewise, the influence of cross-linking of gelatin on the dissolution properties of SGCs will also be discussed.

摘要

最近,软胶囊(SGCs)剂型的开发在口服递送难溶性药物方面引起了极大的关注。这归因于研发中的难溶性药物数量增加,因此在寻找开发具有生物利用度和稳定性剂型的创新方法方面面临挑战。将这些药物封装到软胶囊中是用于将活性成分递送至体循环以克服某些制剂障碍的方法之一。一旦制成,软胶囊形式的封装药物需要合适的体外溶出度测试方法来确保药品质量和性能。本综述重点关注软胶囊溶出度测试方法开发面临的挑战。将简要讨论影响软胶囊溶出特性的物理化学和制剂因素。同样,也将讨论明胶交联对软胶囊溶出特性的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac8e/7913951/4cc34aa3009d/pharmaceutics-13-00214-g001.jpg

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