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界面吸附酰基辅酶 A 的结构特征。

Structural features of interfacially adsorbed acyl-l-carnitines.

机构信息

Biological Physics Laboratory, School of Physics and Astronomy, University of Manchester, Oxford Road, Manchester M13 9PL, UK.

ISIS Neutron Facility, Rutherford Appleton Laboratory, STFC, Chilton, Didcot, Oxon OX11 0QX, UK.

出版信息

J Colloid Interface Sci. 2022 Oct;623:368-377. doi: 10.1016/j.jcis.2022.05.024. Epub 2022 May 7.

Abstract

HYPOTHESIS

Acyl-l-carnitines (CLCs) are potentially important as biosurfactants in drug delivery and tissue engineering due to their good biocompatibility. However, little is currently known about the basic interfacial behavior underlying their technological applications. Following our previous characterization of their solution aggregation and adsorption at the air/water interface, this work examines how they adsorb at the hydrophilic solid/liquid interface.

EXPERIMENTS

As the SiO/water interface has served as the model substrate for many interfacial adsorption studies, so it has been used in this work as the solid substrate to facilitate dynamic adsorption by spectroscopic ellipsometry (SE) and structural determination of the adsorbed layers by neutron reflection (NR) under different conditions at the SiO/water interface from a group of CLC (n = 12, 14, and 16).

FINDINGS

CLC surfactants are zwitterionic at neutral pH. They reached saturated adsorption above their critical micellar concentrations (CMCs) and formed a sandwich bilayer with a head-tail-head structure at the hydrophilic SiO/water interface. The total thicknesses of the adsorbed layers at CMC were found to be 33 ± 2, 35 ± 2, and 37 ± 2 Å for CLC, CLC, and CLC, respectively, with their inner and outer head layers remaining similar but the thickness of the interdigitated middle layer increasing with acyl chain length. As the solution becomes acidic, the carboxyl groups become protonated and the l-carnitine heads are net positively charged, resulting in increased repulsion between the head groups. In this situation, the CLC surfactants are adsorbed as distinct aggregates to reduce repulsive interaction, resulting in reduced surfactant volume fraction and layer thickness. However, a high ionic strength can screen the repulsive interaction and enhance the adsorbed amount, effectively diminishing the impact of pH. This information provides a useful basis for exploring the technological applications of CLCs involving a solid substrate.

摘要

假设

酰基辅氨酸 (CLCs) 由于其良好的生物相容性,作为药物输送和组织工程中的生物表面活性剂具有潜在的重要性。然而,目前对于它们在技术应用中的基本界面行为知之甚少。在我们之前对其在空气/水界面的溶液聚集和吸附进行了表征之后,本工作研究了它们在亲水固/液界面的吸附方式。

实验

由于 SiO2/水界面已作为许多界面吸附研究的模型底物,因此在本工作中,SiO2/水界面被用作固体底物,以通过光谱椭圆术 (SE) 促进动态吸附,并通过中子反射 (NR) 确定不同条件下吸附层的结构。使用一组 CLC(n=12、14 和 16)在 SiO2/水界面。

发现

CLC 表面活性剂在中性 pH 下为两性离子。它们在达到临界胶束浓度 (CMC)以上时达到饱和吸附,并在亲水 SiO2/水界面上形成具有头尾头结构的三明治双层。在 CMC 下,吸附层的总厚度分别为 33±2、35±2 和 37±2 Å,对于 CLC、CLC 和 CLC,其内层和外层头层保持相似,但交错中间层的厚度随酰链长度增加而增加。随着溶液变酸,羧基质子化,l-肉碱头带净正电荷,导致头基之间的排斥增加。在这种情况下,CLC 表面活性剂被吸附为不同的聚集体以减少排斥相互作用,从而减少表面活性剂的体积分数和层厚度。然而,高离子强度可以屏蔽排斥相互作用并增加吸附量,从而有效降低 pH 的影响。这些信息为探索涉及固体底物的 CLC 技术应用提供了有用的基础。

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