首页> 外文会议>International symposium on controlled release of bioactive materials;Consumer and diversified products conference >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)嵌段共聚物胶束与聚丙烯酸的复合形成

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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高分子胶束已被广泛追求,特别是对于疏水性药物的输送,因为它们显示出增强的药物治疗效果并减少了有害的毒副作用。〜1,2高分子胶束作为药物载体的高电势在于具有独特的特性,例如纳米尺寸和热力学稳定性。另外,它们的核-壳结构可以模仿天然存在的转运系统,例如血浆脂蛋白。因此,它们可以满足用作运输系统的结构方面的要求。在最近的研究中,对胶束的亲水性外壳进行了新的设计和改进,为系统提供了除其在水相中稳定胶束的固有功能以及与生物组分的相互作用之外的其他功能。在一篇回顾报告中,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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