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两亲性杯芳烃衍生物水溶液中的囊泡-胶束转变

Vesicle-to-micelle transition in aqueous solutions of amphiphilic calixarene derivatives.

作者信息

Micali Norberto, Villari Valentina, Consoli Grazia M L, Cunsolo Francesca, Geraci Corrada

机构信息

CNR-Istituto per i Processi Chimico-Fisici, Via La Farina 237, I-98123, Messina, Italy.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2006 May;73(5 Pt 1):051904. doi: 10.1103/PhysRevE.73.051904. Epub 2006 May 8.

Abstract

Structure and conformation of spontaneous self-assembled calix[8]arenes derivatives are studied by means of static and dynamic light scattering and electrophoretic mobility. These amphiphilic molecules are in the aggregated form in aqueous solution, in a wide range of pH; they take a vesicle structure in neutral and basic pH environment, but, in relatively strong acidic conditions (below pH=4.5), a transition from vesicle to micelle occurs. The structural change is driven by the surface charge density. At neutral pH calix[8]arenes take a negative surface charge, which prevents coagulation and ensures stability; at acidic pH the surface charge tend to become positive because of the protonation of the hydrophilic head. These pH-responsive aggregates, able to release an encapsulated hydrophilic guest, are promising systems for application as nanocarriers.

摘要

通过静态和动态光散射以及电泳迁移率研究了自发自组装杯[8]芳烃衍生物的结构和构象。这些两亲分子在广泛的pH范围内在水溶液中呈聚集形式;它们在中性和碱性pH环境中呈囊泡结构,但在相对强酸性条件下(pH低于4.5),会发生从囊泡到胶束的转变。结构变化由表面电荷密度驱动。在中性pH下,杯[8]芳烃带有负表面电荷,这可防止凝聚并确保稳定性;在酸性pH下,由于亲水头部的质子化,表面电荷趋于变为正电荷。这些能够释放包封的亲水性客体的pH响应性聚集体是作为纳米载体应用的有前景的体系。

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