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Evolution of Micelle Structure in Poly(ethylene oxide)-b-poly(γ-methyl-ε-caprolactone) Block Copolymers

机译:聚(环氧乙烷)-B-聚(γ-甲基-ε-己内酮)嵌段共聚物中胶束结构的演化

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The increased utilization of self-assembled nanoscale aggregates as drug delivery vehicles has motivated the progressive design of amphiphiles suited for biomedical applications. Micelles exhibiting biocompatibility and biodegradability can be generated through the integration of specific hydrophilic and hydrophobic polymers, while the tailoring of aggregate morphology has been shown tractable through control of amphiphile composition. Here we outline the spherical, cylindrical, and bilayered vesicle structures generated from the self-assembly of poly(ethylene oxide)-b-poly(γ-methyl-ε-caprolactone) (OMCL) diblock copolymers in water. The micelles, comprised of a biocompatible corona and an amorphous, low T_g, aliphatic polyester core, were formed at moderate temperatures without the use of a cosolvent.
机译:作为药物递送车辆的自组装纳米级骨料的利用率增加促使适用于生物医学应用的两亲的逐步设计。通过聚特亲水和疏水聚合物的整合,可以产生具有生物相容性和生物降解性的胶束,而聚集形态的剪裁已经显示通过控制两亲组合物的陶瓷。在这里,我们概述了从聚(环氧乙烷)-B-聚(γ-甲基-ε-己内酯)(OMCL)二嵌段共聚物的自组装产生的球形,圆柱形和双层囊泡结构。在中等温度下,在不使用助理剂的中等温度下形成由生物相容性电晕和无定形的电晕和无定形的低T_G,脂族聚酯芯的胶束。

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