首页> 外文会议>International symposium on controlled release of bioactive materials >Novel micelle releasing systems; complex formation of poly(2-ethyl-2-oxazoline)/poly(epsilon-caprolactone) block copolymer micelles with poly(acrylic acid)
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Novel micelle releasing systems; complex formation of poly(2-ethyl-2-oxazoline)/poly(epsilon-caprolactone) block copolymer micelles with poly(acrylic acid)

机译:新型胶束释放系统;聚(2-乙基-2-恶唑啉)/聚(ε-己内酯)嵌段共聚物胶束的复合物形成(丙烯酸)

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Polymeric micelles derived from amphiphilic block copolymers have been widely pursued especially for the delivery of hydrophobic drugs because they have shown the enhanced therapeutic efficacy of drugs with reducing unwanted toxic side effects.~1,2 The high potnetial of polymeric micelles as a drug carrier lies in their unique characteristics such as nano-size and thermodynamic stability. In addition, their core-shell structure can mimic the naturally occurring transport systems such as plasma lipoproteins. Therefore, they may satisfy the structural aspect to act as a transport system. In recent researches, the hydrophilic outer shells of micelles were newly designed and modified to provide the system with another function other than their intrinsic functions of the micelle stabilization in an aqueous phase and the interaction with biocomponents. In a recnet report, we described the formation and characteristics of micelles based on diblock copolymers of poly(2-ethyl-2-oxazoline) (PEtOz) and poly(epsilon-caprolactone) (PCL)~3.
机译:衍生自两亲嵌段共聚物的聚合物胶束已被广泛追求,特别是为了递送疏水性药物,因为它们已经显示出药物的增强治疗效果,从而减少了不需要的有毒副作用。〜1,2聚合物胶束作为药物载体的高动加始在它们独特的特性,如纳米尺寸和热力学稳定性。另外,它们的核心壳结构可以模拟天然存在的传送系统,例如血浆脂蛋白。因此,它们可以满足结构方面充当运输系统。在最近的研究中,新设计和修饰的胶束亲水外壳,以提供除了胶束稳定化在水相中的内在功能之外的另一个功能,以及与生物组分的相互作用。在核记录报告中,我们描述了基于聚(2-乙基-2-恶唑啉)(PETOZ)和聚(ε-己内酯)(PCL)〜3的二嵌段共聚物的胶束的形成和特征。

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