Oral delivery of glutathione: antioxidant function, barriers and strategies

Tielan Wei, Sachin S. Thakur, Mengyang Liu, Jingyuan Wen
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引用次数: 3

Abstract

Glutathione (GSH) is a tripeptide with potent antioxidant activity, which is involved in numerous basic biological processes and has been used for interventions in various degenerative diseases. However, oral delivery of GSH remains challenging, similarly to that of other protein and peptide drugs, because the physicochemical barriers in the gastrointestinal (GI) tract lead to low oral bioavailability. Although several approaches have been explored to improve delivery, such as co-administration with penetration enhancers and enzymatic inhibitors, or encapsulation into nanoparticles, microemulsions and liposomes, appropriate formulations with clinical therapeutic effects remain to be developed. This review discusses approaches explored to developing an oral GSH delivery system that could provide protection against proteolytic degradation in the GI tract and enhance molecular absorption across the epithelial membrane. This system may be beneficial for the design and development of an oral formulation of GSH in the future.
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口服谷胱甘肽:抗氧化功能、障碍和策略
谷胱甘肽(GSH)是一种具有强抗氧化活性的三肽,它参与了许多基本的生物过程,并被用于各种退行性疾病的干预。然而,与其他蛋白质和肽类药物一样,谷胱甘肽的口服递送仍然具有挑战性,因为胃肠道(GI)中的物理化学屏障导致口服生物利用度低。虽然已经探索了几种改善递送的方法,如与渗透增强剂和酶抑制剂共同给药,或包封在纳米颗粒、微乳液和脂质体中,但仍需开发具有临床治疗效果的适当配方。这篇综述讨论了开发口服谷胱甘肽递送系统的方法,该系统可以提供防止胃肠道蛋白水解降解的保护,并增强上皮膜上的分子吸收。该系统可为将来谷胱甘肽口服制剂的设计和开发提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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