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

机译:羟丙基-β-环糊精通过超临界流体包封通过包合络合物递送黄ical苷

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摘要

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.
机译:多年来,已经开发出各种方法来增强不溶性药物的溶解性。但是,这些方法大多数都是耗时且劳动密集的,或者涉及使用有毒物质。缺乏能够安全有效地提高不溶性药物的溶解度的方法。本研究采用黄ical苷为不溶性药物模型,并使用羟丙基-β-环糊精通过超临界流体包封的包合复合物递送黄ical苷。已经研究了用于配合物制备的不同参数以及配合物的理化性质。我们的结果表明,与常规溶液混合方法相比,超临界流体包封可以更精确地控制复合物的性质,并提供更高的负载量和包封效率。可以预期,我们报道的方法可用于提高包合物的制备效率,并可以扩大不溶性草药成分在治疗开发和药物制剂中的应用潜力。

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