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猪去氧胆酸和胆酸在猪去氧胆酸钠-吐温40及胆酸钠-吐温40二元混合胶束中的pKa值:胶束的热力学稳定性以及与甾体骨架形成的协同氢键

pKa values of hyodeoxycholic and cholic acids in the binary mixed micelles sodium-hyodeoxycholate-Tween 40 and sodium-cholate-Tween 40: Thermodynamic stability of the micelle and the cooperative hydrogen bond formation with the steroid skeleton.

作者信息

Poša Mihalj, Pilipović Ana, Bećarević Mirjana, Farkaš Zita

机构信息

Department of Pharmacy, Faculty of Medicine, University of Novi Sad, Hajduk Veljkova 3, 21000 Novi Sad, Serbia.

Department of Pharmacy, Faculty of Medicine, University of Novi Sad, Hajduk Veljkova 3, 21000 Novi Sad, Serbia.

出版信息

Steroids. 2017 Jan;117:62-70. doi: 10.1016/j.steroids.2016.09.012. Epub 2016 Sep 17.

Abstract

Due to a relatively small size of bile acid salts, their mixed micelles with nonionic surfactants are analysed. Of the special interests are real binary mixed micelles that are thermodynamically more stable than ideal mixed micelles. Thermodynamic stability is expressed with an excess Gibbs energy (G) or over an interaction parameter (β). In this paper sodium salts of cholic (C) and hyodeoxycholic acid (HD) in their mixed micelles with Tween 40 (T40) are analysed by potentiometric titration and their pKa values are determined. Examined bile acids in mixed micelles with T40 have higher pKa values than free bile acids. The increase of ΔpKa acid constant of micellary bound C and HD is in a correlation with absolute values of an interaction parameter. According to an interaction parameter and an excess Gibbs energy, mixed micelle HD-T40 are thermodynamically more stable than mixed micelles C-T40. ΔpKa values are higher for mixed micelles with Tween 40 whose second building unit is HD, related to the building unit C. In both micellar systems, ΔpKa increases with the rise of a molar fraction of Tween 40 in binary mixtures of surfactants with sodium salts of bile acids. This suggests that, ΔpKa can be a measure of a thermodynamic stabilization of analysed binary mixed micelles as well as an interaction parameter. ΔpKa values are confirmed by determination of a distribution coefficient of HD and C in systems: water phase with Tween 40 in a micellar concentration and 1-octanol, with a change of a pH value of a water phase. Conformational analyses suggests that synergistic interactions between building units of analysed binary micelles originates from formation of hydrogen bonds between steroid OH groups and polyoxyethylene groups of the T40. Relative similarity and spatial orientation of C and C OH group allows cooperative formation of hydrogen bonds between T40 and HD - excess entropy in formation of mixed micelle. If a water solution of analysed binary mixtures of surfactants contains urea in concentration of 4M significant decreases of an interaction parameter value happens which confirms the importance of hydrogen bonds in synergistic interactions (urea compete in hydrogen bonds).

摘要

由于胆汁酸盐的尺寸相对较小,因此对其与非离子表面活性剂形成的混合胶束进行了分析。特别令人感兴趣的是真实的二元混合胶束,其热力学稳定性高于理想混合胶束。热力学稳定性用过量吉布斯自由能(G)或相互作用参数(β)表示。本文通过电位滴定法分析了胆酸(C)和猪去氧胆酸(HD)的钠盐与吐温40(T40)形成的混合胶束,并测定了它们的pKa值。与游离胆汁酸相比,在与T40形成的混合胶束中,所研究的胆汁酸具有更高的pKa值。胶束结合的C和HD的ΔpKa酸常数的增加与相互作用参数的绝对值相关。根据相互作用参数和过量吉布斯自由能,混合胶束HD-T40在热力学上比混合胶束C-T40更稳定。与以C为结构单元的情况相比,对于以HD为第二个结构单元的与吐温40形成的混合胶束,其ΔpKa值更高。在表面活性剂与胆汁酸钠盐的二元混合物中,随着吐温40摩尔分数的增加,两种胶束体系中的ΔpKa均升高。这表明,ΔpKa可以作为所分析的二元混合胶束热力学稳定性以及相互作用参数的一种度量。通过测定HD和C在以下体系中的分配系数来确认ΔpKa值:水相(含有胶束浓度的吐温40)和1-辛醇,同时改变水相的pH值。构象分析表明,所分析的二元胶束结构单元之间的协同相互作用源于甾体OH基团与T40的聚氧乙烯基团之间形成的氢键。C及其OH基团的相对相似性和空间取向使得T40与HD之间能够协同形成氢键——混合胶束形成过程中的过量熵。如果所分析表面活性剂二元混合物的水溶液中含有浓度为4M的尿素,则相互作用参数值会显著降低,这证实了氢键在协同相互作用中的重要性(尿素会竞争氢键)

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