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钙表面活性剂的亲水基团和 C(n)DMAO 的疏水链对配位囊泡形成的影响。

Effect of hydrophilic groups of Ca surfactants and hydrophobic chains of C(n)DMAO on coordinated vesicle formation.

机构信息

Key Laboratory of Colloid and Interface Chemistry, Shandong University, Ministry of Education, Jinan 250100, China.

出版信息

Langmuir. 2010 Dec 21;26(24):18652-8. doi: 10.1021/la102847f. Epub 2010 Nov 18.

Abstract

The effects of hydrophilic headgroups of Ca surfactants, calcium dodecylsulfate (Ca(DS)(2)), calcium dodecylsulfonate (Ca(DSA)(2)), and calcium laurate (CaL(2)) and hydrophobic chains of alkyldimethylamine oxide (C(n)DMAO, n = 12, 14, 16) on the formation of Ca(2+)-ligand coordinated vesicles was investigated in detail. On the basis of phase behavior studies, rheological properties and freeze-fracture transmission electron microscope (FF-TEM) images were measured. Quite different phase behaviors were observed in different surfactant systems. For a Ca surfactant with a highly polar group, Ca(DS)(2), vesicles were observed in all Ca(DS)(2)/C(n)DMAO (n = 12, 14, and 16) systems, whereas for Ca surfactant with lower polar group, Ca(DSA)(2), vesicles can form in Ca(DSA)(2)/C(n)DMAO systems of n = 14 and 16 but not for n = 12. For CaL(2), the surfactant with the least polar group, vesicles form only in the CaL(2)/C(16)DMAO system. The results demonstrate that in the systems formed by Ca surfactants and C(n)DMAO, the formation of vesicles is driven not only by interaction between Ca(2+) and the N → O groups of C(n)DMAO but also by electrostatic and hydrophobic interactions. Vesicles prefer to form in Ca surfactants with highly polar headgroups and C(n)DMAO with long chain length.

摘要

详细研究了钙表面活性剂(十二烷基硫酸钠(Ca(DS)(2))、十二烷基磺酸钠(Ca(DSA)(2))和月桂酸钙(CaL(2))的亲水基团和烷基二甲基氧化胺(C(n)DMAO,n = 12、14、16)的疏水链对 Ca(2+)-配体配位囊泡形成的影响。在基于相行为研究的基础上,测量了流变性能和冷冻断裂透射电子显微镜(FF-TEM)图像。在不同的表面活性剂体系中观察到了非常不同的相行为。对于具有高极性基团的钙表面活性剂 Ca(DS)(2),在所有 Ca(DS)(2)/C(n)DMAO(n = 12、14 和 16)体系中都观察到了囊泡,而对于具有较低极性基团的钙表面活性剂 Ca(DSA)(2),在 Ca(DSA)(2)/C(n)DMAO 体系中 n = 14 和 16 可以形成囊泡,但 n = 12 不行。对于具有最小极性基团的钙表面活性剂 CaL(2),只有在 CaL(2)/C(16)DMAO 体系中才能形成囊泡。结果表明,在由钙表面活性剂和 C(n)DMAO 形成的体系中,囊泡的形成不仅由 Ca(2+)与 C(n)DMAO 的 N → O 基团之间的相互作用驱动,还由静电和疏水相互作用驱动。囊泡更倾向于在具有高极性头基的钙表面活性剂和具有长链长度的 C(n)DMAO 中形成。

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