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克服溶解性挑战:用于增强难溶性抗病毒药物递送的自乳化系统

Overcoming Solubility Challenges: Self-emulsifying Systems for Enhancing the Delivery of Poorly Water-Soluble Antiviral Drugs.

作者信息

Kapoor Devesh U, Sharma Deepak, Gaur Mansi, Prajapati Bhupendra G, Limmatvapirat Sontaya, Sriamornsak Pornsak

机构信息

Dr. Dayaram Patel Pharmacy College, Bardoli, 394601, Gujarat, India.

Institute of Pharmacy, Assam Don Bosco University, Tapesia, Sonapur Gaon, 78240, Assam, India.

出版信息

Pharm Nanotechnol. 2025;13(1):117-132. doi: 10.2174/0122117385280541231130055458.

Abstract

The primary goal of drug formulation is to improve a drug's bioavailability in the body. However, poorly water-soluble drugs present challenging issues related to their solubility and bioavailability factors. Emerging technologies, such as lipid-based drug delivery systems, including micro- or nanoemulsifying drug delivery systems, have become increasingly relevant to address the above challenges. This review presents a thorough overview of self-emulsifying drug delivery systems (SEDDS). It covers the properties, principles, self-emulsification mechanism, formulation strategies, and characterization methods of SEDDS. This review also addresses the delivery of antiviral agents through SEDDS. Moreover, it summarizes the marketed formulations of SEDDS consisting of antiviral agents. This review offers a comprehensive and valuable resource for future perspectives on SEDDS and their potential applications in antiviral drug delivery.

摘要

药物制剂的主要目标是提高药物在体内的生物利用度。然而,水溶性差的药物在其溶解度和生物利用度因素方面存在具有挑战性的问题。新兴技术,如基于脂质的药物递送系统,包括微乳或纳米乳药物递送系统,对于应对上述挑战变得越来越重要。本综述全面概述了自乳化药物递送系统(SEDDS)。它涵盖了SEDDS的性质、原理、自乳化机制、制剂策略和表征方法。本综述还讨论了通过SEDDS递送抗病毒药物的情况。此外,它总结了由抗病毒药物组成的SEDDS的上市制剂。本综述为SEDDS的未来前景及其在抗病毒药物递送中的潜在应用提供了全面且有价值的资源。

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