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The Role of Functional Excipients in Solid Oral Dosage Forms to Overcome Poor Drug Dissolution and Bioavailability

机译:功能性赋形剂在固体口服剂型中克服药物溶解不良和生物利用度的作用

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摘要

Many active pharmaceutical ingredients (APIs) exhibit poor solubility and low dissolution rates in aqueous environments such as the luminal fluids of the gastrointestinal tract. The oral bioavailability of these compounds is usually very low as a result of their poor solubility properties. In order to improve the bioavailability of these poorly soluble drugs, formulation strategies have been applied as a means to improve their aqueous solubility and dissolution rates. With respect to formulation approaches, excipients can be incorporated in the formulation to assist in the dissolution process of the drug, or specialized dosage forms can be formulated that improve dissolution rate through various mechanisms. This paper provides an overview of selected excipients (e.g., alkalinizing agents, surfactants and sugars) that can be used in formulations to increase the dissolution rate as well as specialized dosage forms such as self-emulsifying delivery systems and formulation techniques such as inclusion complexes and solid dispersions. These formulation approaches are discussed with available examples with specific reference to positive outcomes in terms of drug solubility and bioavailability enhancement.
机译:许多活性药物成分(API)在水性环境(例如胃肠道腔液)中显示出较差的溶解度和低溶解度。这些化合物的口服生物利用度通常由于其不良的溶解性而非常低。为了提高这些难溶性药物的生物利用度,已采用制剂策略作为改善其水溶性和溶解速率的手段。关于制剂方法,可以将赋形剂掺入制剂中以辅助药物的溶解过程,或者可以配制专门的剂型以通过各种机制提高溶解速率。本文概述了可用于制剂中以提高溶出度的选定赋形剂(例如,碱化剂,表面活性剂和糖)以及专用剂型(例如自乳化递送系统)和制剂技术(例如包合配合物和固体分散体。通过可用的实例讨论了这些配制方法,并具体参考了药物溶解度和生物利用度提高方面的积极成果。

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