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通过pH调节实现界面处双嵌段共聚物单层的可逆活化,2:固/液界面处的膜相互作用

Reversible activation of diblock copolymer monolayers at the interface by pH modulation, 2: Membrane interactions at the solid/liquid interface.

作者信息

Rehfeldt Florian, Steitz Roland, Armes Steven P, von Klitzing Regine, Gast Alice P, Tanaka Motomu

机构信息

Physik Department E22, Technische Universität München, James-Franck-Str., D-85748 Garching, Germany.

出版信息

J Phys Chem B. 2006 May 11;110(18):9177-82. doi: 10.1021/jp054533b.

Abstract

A monolayer of the pH-responsive poly[2-(dimethylamino)ethyl methacrylate-block-methyl methacrylate] diblock copolymer [PDMAEMA-PMMA] was transferred from the air/water interface to a silicon substrate for evaluation as a tunable interlayer between biological material and solid substrates. Specular neutron reflectivity experiments revealed that the weak polyelectrolyte PDMAEMA chains at the solid/liquid interface can be reversibly activated by pH modulation. The thickness, scattering length density, and surface roughness of the polymer film can be systematically controlled by pH titration. As a simple model of plasma membranes, a lipid bilayer was deposited onto the polymer film. The membrane-substrate interaction was characterized by neutron reflectivity experiments, demonstrating that the membrane-substrate distance could be reversibly regulated by pH titration. These results confirm the potential of stimuli-responsive polymers for precise control of cell-surface interactions.

摘要

将pH响应性聚[2-(二甲基氨基)乙基甲基丙烯酸酯-嵌段-甲基丙烯酸甲酯]二嵌段共聚物[PDMAEMA-PMMA]的单分子层从空气/水界面转移到硅基底上,以评估其作为生物材料与固体基底之间的可调夹层。镜面中子反射率实验表明,固体/液体界面处的弱聚电解质PDMAEMA链可通过pH调节而可逆地活化。通过pH滴定可以系统地控制聚合物膜的厚度、散射长度密度和表面粗糙度。作为质膜的简单模型,将脂质双层沉积在聚合物膜上。通过中子反射率实验对膜-基底相互作用进行了表征,表明膜-基底距离可通过pH滴定进行可逆调节。这些结果证实了刺激响应性聚合物在精确控制细胞-表面相互作用方面的潜力。

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