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首页> 外文期刊>Current drug delivery >In vitro Methods for In vitro-In vivo Correlation (IVIVC) for Poorly Water Soluble Drugs: Lipid Based Formulation Perspective
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In vitro Methods for In vitro-In vivo Correlation (IVIVC) for Poorly Water Soluble Drugs: Lipid Based Formulation Perspective

机译:用于差的水溶性药物(IVIVC)的体外方法的体外方法:脂质的制剂观点

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摘要

A great number of new drug candidates identified from the discovery pipeline are poorly water soluble, which is a drawback to bring such candidates into the pharmaceutical market. Formulating these compounds as self-emulsifying/microemulsifying/nanoemulsifying drug delivery systems (SEDDS/SMEDDS/SNEDDS) within lipid based formulations is of growing interest. Some of the recent studies have resulted in commercial products that provided improved bioavailability and dissolution due to the better dispersion properties of SEDDS/SMEDDS/SNEDDS. An ongoing challenge that the pharmaceutical industry is facing is identifying in vitro tests that are needed in order to predict the behavior of dosage forms in the GI tract. The goal of the current review is to present the various levels of in vitro-in vivo correlations (IVIVCs) and to provide tools on the utilization of the IVIVCs in product development and optimization of SEDDS/SMEDDS/SNEDDS.
机译:从发现管道确定的大量新药物候选者是可靠的差,这是将这种候选人带入制药市场的缺点。 将这些化合物作为自乳化/微乳化/纳米乳化药物递送系统(SEDDS / SMEDDS / SNEDDS)在脂质的制剂中具有越来越感兴趣。 最近的一些研究导致商业产品提供了改善的生物利用度和溶解,因为潜水/ SMEDDS / SNEDDS的更好分散性能。 持续的挑战,制药行业面临的是鉴定需要进行的体外试验,以预测GI在GI道中的剂型形式的行为。 目前审查的目的是呈现各种水平的体外相关(IVIVC),并提供有关在产品开发和优化潜水/ SMEDDS / SNEDDS中的IVIVC的工具。

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