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在水中,2-氧代辛酸纳自发形成囊泡并向胶束转化。

Spontaneous vesicle formation and vesicle-to-micelle transition of sodium 2-ketooctanate in water.

机构信息

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

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

出版信息

J Colloid Interface Sci. 2018 Jan 1;509:265-274. doi: 10.1016/j.jcis.2017.09.023. Epub 2017 Sep 7.

DOI:10.1016/j.jcis.2017.09.023
PMID:28915484
Abstract

Single-tailed short-chain alkyl keto-acids/salts, a class of fatty acid/salt derivatives, such as sodium 2-ketooctanate (KOCOONa), are a kind of weakly acid/salt type amphiphiles and plausible prebiotic molecules, and the current understanding of their aggregation behavior in aqueous solutions is still limited. Herein, the aggregation behavior of KOCOONa in aqueous solution was studied by changing its concentration (C), using equilibrium surface tension, conductivity, and fluorescence measurements. The aggregates formed were characterized using freeze-fracture and cryogenic transmission electron microscopy, dynamic light scattering, atomic force microscopy, and confocal laser scanning microscopy. A concentration-driven stepwise aggregation was identified in the KOCOONa solution. Vesicles can spontaneously form from the single-component aqueous solution, with a critical vesicle concentration (CVC) of ∼15mM, which is obviously lower than that of octanoic acid/salt (120-200mM). With increasing C, a vesicle-to-micelle transition can occur, showing a critical micelle concentration (CMC) of ∼80mM. In addition, the membrane permeability of the KOCOONa vesicles was examined using small-size Calcein and large-size FITC-BSA as fluorescence probes, showing a size-selective permeability, similar to short-chain (C8-C11) fatty acid vesicles. For the first time, the aggregation behavior of single-tailed keto-acid salt surfactant is reported.

摘要

单尾短链烷基酮酸/盐,一类脂肪酸/盐衍生物,如 2-酮辛酸钠(KOCOONa),是一种弱酸/盐型两亲分子,也是合理的前生物分子,目前对其在水溶液中的聚集行为的了解仍然有限。在此,通过改变浓度(C),使用平衡表面张力、电导率和荧光测量来研究 KOCOONa 在水溶液中的聚集行为。使用冷冻断裂和低温传输电子显微镜、动态光散射、原子力显微镜和共聚焦激光扫描显微镜对形成的聚集体进行了表征。在 KOCOONa 溶液中确定了浓度驱动的逐步聚集。囊泡可以从单一组分的水溶液中自发形成,临界囊泡浓度(CVC)约为 15mM,明显低于辛酸/盐(120-200mM)。随着 C 的增加,可能会发生囊泡到胶束的转变,表现出临界胶束浓度(CMC)约为 80mM。此外,使用小尺寸 Calcein 和大尺寸 FITC-BSA 作为荧光探针研究了 KOCOONa 囊泡的膜通透性,表现出类似短链(C8-C11)脂肪酸囊泡的尺寸选择性通透性。首次报道了单尾酮酸盐表面活性剂的聚集行为。

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