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胶束和非胶束溶液中溶酶体靶向物质衍生物吸附的动力学。

Dynamics of adsorption in micellar and non micellar solutions of derivatives of lysosomotropic substances.

机构信息

Institute of Chemical Technology and Engineering, Poznan University of Technology, Pl. Marii Sklodowskiej-Curie 2, 60-965 Poznan, Poland.

出版信息

Adv Colloid Interface Sci. 2010 Apr 22;156(1-2):62-9. doi: 10.1016/j.cis.2010.02.008. Epub 2010 Feb 17.

Abstract

Dynamics of adsorption in micellar and non micellar solutions of derivatives of lysosomotropic substances was studied. The following compounds were considered in our research work: alkyl N,N-dimethyl-alaninates methobromides (DMALM-n), alkyl N,N-dimethylglycinates methobromides (DMGM-n), fatty acids N,N-dimethylaminoethylesters methobromides (DMM-n), fatty acids N,N-dimethylaminopropylesters methobromides (DMPM-n), fatty acids 1-dimethylamino-2-propyl methobromides (DMP(2)M-n), and derivatives of aminoesters with double alkyl chains (M(2)M-n). The examined compounds show interesting biological properties which can be useful, especially in medicine. The exact mechanism of interaction of such compounds with biological membrane is not fully known. However, it is supposed that the presence of micelles has an important role in biological systems. In this paper we show the results of dynamic surface tension measurements in solutions containing the investigated compounds at concentrations above and below cmc. Moreover, we analyzed the influence of the chemical structure of molecules on the diameters of the micelles formed in the solutions. It was found that adsorption dynamics for the studied compounds is strongly affected by the chemical structure of the considered derivatives, especially by the presence of the ester bond, linearity of the molecule, as well as its hydrophobicity. The obtained results show that the structure of the bromide M(2)M-n with two short hydrocarbon chains favors a faster and more efficient adsorption of the molecules at the air/water interface, compared with compounds having one long alkyl chain. Moreover, the double chained derivatives of the M(2)M-n type do not form typical spherical micelles but bilayer structures probably exist in these solutions. The micelles present in the solutions influence the dynamics of adsorption drastically. Moreover, the obtained results indicated that the compounds with especially high biological activity form rather small aggregates.

摘要

研究了溶酶体亲和物质衍生物在胶束和非胶束溶液中的吸附动力学。在我们的研究工作中考虑了以下化合物:烷基 N,N-二甲基丙氨酸甲酯溴化物(DMALM-n)、烷基 N,N-二甲基甘氨酸甲酯溴化物(DMGM-n)、脂肪酸 N,N-二甲氨基乙酯甲酯溴化物(DMM-n)、脂肪酸 N,N-二甲基氨基丙酯甲酯溴化物(DMPM-n)、脂肪酸 1-二甲基氨基-2-丙基甲酯溴化物(DMP(2)M-n)和双烷基链氨基酸酯衍生物(M(2)M-n)。这些被研究的化合物表现出有趣的生物特性,特别是在医学方面可能具有应用价值。这些化合物与生物膜相互作用的确切机制尚未完全了解。然而,据推测,胶束的存在在生物体系中起着重要作用。本文介绍了在浓度高于和低于 cmc 的含有所研究化合物的溶液中动态表面张力测量的结果。此外,还分析了分子的化学结构对溶液中形成的胶束直径的影响。结果表明,研究化合物的吸附动力学强烈受考虑的衍生物的化学结构的影响,特别是受酯键、分子的线性和疏水性的影响。研究结果表明,具有两个短烃链的溴化物 M(2)M-n 的结构有利于分子更快、更有效地在气/水界面上吸附,与具有一条长烷基链的化合物相比。此外,M(2)M-n 型的双链衍生物可能不会形成典型的球形胶束,而是在这些溶液中可能存在双层结构。溶液中的胶束对吸附动力学有很大的影响。此外,研究结果表明,具有特别高生物活性的化合物形成了较小的聚集物。

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