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二正十二烷基二甲基氯化铵/聚氧乙烯烷基醚的水相混合物:尾-尾和头-头相互作用对共胶束化和杀菌活性的显著影响。

Aqueous mixtures of di-n-decyldimethylammonium chloride/polyoxyethylene alkyl ether: dramatic influence of tail/tail and head/head interactions on co-micellization and biocidal activity.

机构信息

Laboratoires Anios, Pavé du Moulin, F-59260 Hellemmes Lille, France.

出版信息

J Colloid Interface Sci. 2012 May 15;374(1):176-86. doi: 10.1016/j.jcis.2012.02.006. Epub 2012 Feb 21.

Abstract

Mixed aggregate formation and synergistic interactions of binary surfactant mixtures of di-n-decyldimethylammonium chloride, [DiC(10)][Cl], with polyoxyethylene alkyl ethers, C(i)E(j) (i=10, 12, j=4, 6, 8), have been investigated for various [DiC(10)][Cl]/C(i)E(j) ratios. The critical aggregation concentration of the binary mixtures has been determined by tensiometry, and the aggregate characteristics (i.e., size and composition, free ammonium concentration) have been estimated using the pulsed field gradient NMR spectroscopy and a [DiC(10)]-selective electrode. Diffusion coefficient measurements of micelles confirmed the synergistic interaction between the surfactants. It is thus shown that the formation of surface monolayers and mixed aggregates from [DiC(10)][Cl]/C(10)E(j) mixtures is driven by both tail/tail and head/head interactions, whereas [DiC(10)][Cl]/C(12)E(j) co-aggregation is mainly driven by tail/tail interactions. As a consequence, the co-aggregation phenomenon notably influences the biocidal activity of [DiC(10)][Cl] on the Candida albicans fungi. In the presence of C(12)E(j), the biocidal activity of the ammonium salt is inhibited due to the trapping of the cationic surfactants in the mixed aggregates, whereas in the presence of C(10)E(j), the biocidal activity of the surfactant mixture is maintained. The mode of action is also confirmed by a faster increase in the zeta potential of a C. albicans suspension in the presence of [DiC(10)][Cl]/C(10)E(8) than in the presence of [DiC(10)][Cl]/C(12)E(8). Therefore, a judicious adjustment of the alkyl (i) and polyoxyethylene (j) chain lengths of C(i)E(j) avoids its antagonistic effect on the biocidal activity of [DiC(10)][Cl].

摘要

二癸基二甲基氯化铵([DiC(10)][Cl])与聚氧乙烯烷基醚 C(i)E(j)(i=10、12,j=4、6、8)的二元表面活性剂混合物的混合聚集形成和协同相互作用已针对各种[DiC(10)][Cl]/C(i)E(j)比例进行了研究。通过张力法测定了二元混合物的临界聚集浓度,并使用脉冲梯度 NMR 光谱和[DiC(10)]选择性电极估算了聚集特性(即尺寸和组成、游离铵浓度)。胶束的扩散系数测量证实了两种表面活性剂之间的协同相互作用。因此,表明[DiC(10)][Cl]/C(10)E(j)混合物形成表面单层和混合聚集物的驱动力既有尾部/尾部相互作用,也有头部/头部相互作用,而[DiC(10)][Cl]/C(12)E(j)共聚则主要由尾部/尾部相互作用驱动。因此,共聚现象显著影响[DiC(10)][Cl]对白色念珠菌真菌的杀菌活性。在存在 C(12)E(j)的情况下,由于阳离子表面活性剂被捕获在混合聚集物中,铵盐的杀菌活性受到抑制,而在存在 C(10)E(j)的情况下,表面活性剂混合物的杀菌活性得以维持。这种作用模式也通过在存在[DiC(10)][Cl]/C(10)E(8)的情况下,白色念珠菌悬浮液的 ζ 电位更快地增加得到证实,而在存在[DiC(10)][Cl]/C(12)E(8)的情况下则较慢。因此,通过明智地调整 C(i)E(j)的烷基(i)和聚氧乙烯(j)链长,可以避免其对[DiC(10)][Cl]杀菌活性的拮抗作用。

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