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A Review on Novel Therapeutic Strategies for the Enhancement of Solubility for Hydrophobic Drugs through Lipid and Surfactant Based Self Micro Emulsifying Drug Delivery System: A Novel Approach

机译:通过基于脂质和表面活性剂的自微乳化药物递送系统提高疏水性药物溶解性的新治疗策略的综述:一种新方法

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Self micro-emulsifying drug delivery systems (SMEDDS) are vital tool for enhancement of oral bioavailability of hydrophobic drugs. These systems are currently of interest to the researchers because of their significant capability to act as drug delivery vehicles by incorporating a extensive range of drug molecules. The present communication embodies approaches in the design of lipid based formulation, evaluation processes, mechanism involved there in, updated with latest findings from literature reports and patents. Also, this comprehensive review offers an explicit discussion on vital possibilities of the SMEDDS in bioavailability improvement of various drugs. A pseudo ternary phase diagram is used for identifying the micro-emulsification region. Thus, this current article provides an updated compilation of extensive information and result on all the unexplored areas of the self micro emulsifying drug delivery systems, thus encouraging the researchers to accelerate their research work in this direction for the development and enhancement of dissolution profile of hydrophobic drugs and pay a novel approach to pharmaceutical research.
机译:自微乳化药物输送系统(SMEDDS)是增强疏水性药物口服生物利用度的重要工具。这些系统目前对研究人员很感兴趣,因为它们具有通过掺入多种药物分子而充当药物传递媒介的显着能力。本交流体现了基于脂质的制剂设计,评估过程,其中涉及的机制的方法,并根据文献报告和专利的最新发现进行了更新。此外,本综述还对SMEDDS在改善各种药物的生物利用度方面的重要可能性进行了明确的讨论。伪三元相图用于识别微乳化区域。因此,本文为自微乳化药物递送系统的所有未开发领域提供了广泛的信息和结果的最新汇编,从而鼓励研究人员在该方向上加快研究工作,以开发和增强疏水性的溶出度药物并为药物研究支付一种新颖的方法。

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