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Advanced Lipid Technologies? (ALT?): A Proven Formulation Platform to Enhance the Bioavailability of Lipophilic Compounds

机译:高级脂质技术? (alt?):一种探明的配方平台,可增强亲脂化合物的生物利用度

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Despite recent advances, the drug development process continues to face significant challenges to efficiently improve the poor solubility of active pharmaceutical ingredients (API) in aqueous media or to improve the bioavailability of lipid-based formulations. The inherent high intra- and interindividual variability of absorption of oral lipophilic drug leads to inconsistent and unpredictable bioavailability and magnitude of the therapeutic effect. For this reason, the development of lipid-based drugs remains a challenging endeavour with a high risk of failure. Therefore, effective strategies to assure a predictable, consistent, and reproducible bioavailability and therapeutic effect for lipid-based medications are needed. Different solutions to address this problem have been broadly studied, including the approaches of particle size reduction, prodrugs, salt forms, cocrystals, solid amorphous forms, cyclodextrin clathrates, and lipid-based drug delivery systems such as self-emulsifying systems and liposomes. Here, we provide a brief description of the current strategies commonly employed to increase the bioavailability of lipophilic drugs and present Advanced Lipid Technologies? (ALT?), a combination of different surfactants that has been demonstrated to improve the absorption of omega-3 fatty acids under various physiological and pathological states.
机译:尽管最近进展,药物开发过程继续面临有效改善活性药物成分(API)在水性介质中的差的溶解度或改善基于脂质的制剂的生物利用度的显着挑战。口服脂性药物吸收的固有的高内和切性可变异导致治疗效果的不一致和不可预测的生物利用度和幅度。因此,脂质的药物的发展仍然是具有高风险的挑战性努力。因此,需要有效的策略来确保可预测,一致,可重复和可重复的生物利用度和对基于脂质的药物的治疗效果。已经大致研究了解决这个问题的不同解决方案,包括粒度减少,前药,盐形式,碳酸酯,固体无定形形式,环糊精克拉族和脂质的药物递送系统,例如自乳化体系和脂质体。在这里,我们提供了通常用于增加亲脂性药物的生物利用度的现有策略以及现有先进的脂质技术的简要说明? (ALT?),已经证明了不同表面活性剂的组合,以改善各种生理和病理状态下ω-3脂肪酸的吸收。

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