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羟丙基-β-环糊精通过超临界流体包合作用包载黄芩苷的传递。

Hydroxypropyl-β-cyclodextrin for Delivery of Baicalin via Inclusion Complexation by Supercritical Fluid Encapsulation.

机构信息

School of Pharmaceutical Sciences, Health Science Center, Shenzhen University, Shenzhen 518060, China.

出版信息

Molecules. 2018 May 14;23(5):1169. doi: 10.3390/molecules23051169.

Abstract

Over the years, various methods have been developed to enhance the solubility of insoluble drugs; however, most of these methods are time-consuming and labor intensive or involve the use of toxic materials. A method that can safely and effectively enhance the solubility of insoluble drugs is lacking. This study adopted baicalin as an insoluble drug model, and used hydroxypropyl-β-cyclodextrin for the delivery of baicalin via the inclusion complexation by supercritical fluid encapsulation. Different parameters for the complex preparation as well as the physicochemical properties of the complex have been investigated. Our results showed that when compared to the conventional solution mixing approach, supercritical fluid encapsulation enables a more precise control of the properties of the complex, and gives higher loading and encapsulation efficiency. It is anticipated that our reported method can be useful in enhancing the preparation efficiency of inclusion complexes, and can expand the application potential of insoluble herbal ingredients in treatment development and pharmaceutical formulation.

摘要

多年来,已经开发出各种方法来提高难溶性药物的溶解度;然而,这些方法大多耗时耗力,或者涉及使用有毒材料。缺乏一种安全有效提高难溶性药物溶解度的方法。本研究以黄芩苷为难溶性药物模型,采用羟丙基-β-环糊精通过超临界流体包合作用包载黄芩苷。考察了不同的包合物制备参数和包合物的理化性质。结果表明,与常规溶液混合法相比,超临界流体包封能更精确地控制包合物的性质,具有更高的载药量和包封效率。预计本报告的方法可以提高包合物的制备效率,并扩大难溶性草药成分在治疗开发和药物制剂中的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d28f/6099545/5bce7403d200/molecules-23-01169-g001.jpg

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