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有机溶剂对药物载入聚合物载体的影响及载药聚合物胶束的形态分析。

Effects of organic solvents on drug incorporation into polymeric carriers and morphological analyses of drug-incorporated polymeric micelles.

机构信息

Japan Science and Technology Agency, ERATO, Takahara Soft Interfaces Project, CE80, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.

出版信息

Int J Pharm. 2011 Feb 14;404(1-2):271-80. doi: 10.1016/j.ijpharm.2010.11.016. Epub 2010 Nov 18.

Abstract

We incorporated an anticancer agent, camptothecin (CPT), into polymeric micelle carriers by using two different solvents (TFE and chloroform) in the solvent-evaporation drug incorporation process. We observed significant differences in the drug-incorporation behaviors, in the morphologies of the incorporated drug and the polymeric micelles, and in the pharmacokinetic behaviors between the two solvents' cases. In particular, the CPT-incorporated polymeric micelles prepared with TFE as the incorporation solvent exhibited more stable circulation in blood than those prepared with chloroform. This contrast indicates a novel technological perspective regarding the drug incorporation into polymeric micelle carriers. Morphological analyses of the inner core have revealed the presence of the directed alignment of the CPT molecules and CPT crystals in the micelle inner core. This is the first report of the morphologies of the drug incorporated into the polymeric micelle inner cores. We believe these analyses are very important for further pharmaceutical developments of polymeric micelle drug-carrier systems.

摘要

我们通过使用两种不同的溶剂(TFE 和氯仿)在溶剂蒸发药物掺入过程中,将抗癌剂喜树碱(CPT)掺入聚合物胶束载体中。我们观察到两种溶剂情况下药物掺入行为、掺入药物和聚合物胶束的形态以及药代动力学行为之间存在显著差异。特别是,用 TFE 作为掺入溶剂制备的 CPT 掺入聚合物胶束在血液中的循环稳定性优于用氯仿制备的胶束。这种对比为将药物掺入聚合物胶束载体提供了一种新的技术视角。对内核形态的分析表明,CPT 分子和 CPT 晶体在胶束内核中存在定向排列。这是首次报道药物在聚合物胶束内核中的形态。我们相信这些分析对于进一步开发聚合物胶束药物载体系统具有非常重要的意义。

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