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通过分子模拟研究抗蛋白质黏附两性离子聚合物刷的水化斥力。

Study of Hydration Repulsion of Zwitterionic Polymer Brushes Resistant to Protein Adhesion through Molecular Simulations.

机构信息

Key Laboratory of High Efficiency and Clean Mechanical Manufacture of Ministry of Education, School of Mechanical Engineering, Shandong University, Jinan 250061, P. R. China.

Key National Demonstration Center for Experimental Mechanical Engineering Education, Shandong University, Jinan 250061, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2024 Apr 10;16(14):17145-17162. doi: 10.1021/acsami.3c18546. Epub 2024 Mar 27.

Abstract

The fabrication of antifouling zwitterionic polymer brushes represents a leading approach to mitigate nonspecific adhesion on the surfaces of medical devices. This investigation seeks to elucidate the correlation between the material composition and structural attributes of these polymer brushes in preventing protein adhesion. To achieve this goal, we modeled three different zwitterionic brushes, namely, carboxybetaine methacrylate (CBMA), sulfobetaine methacrylate (SBMA), and (2-(methacryloyloxy)ethyl)-phosphorylcholine (MPC). The simulations revealed that elevating the grafting density enhances the structural stability, hydration strength, and resistance to protein adhesion exhibited by the polymer brushes. PCBMA manifests a more robust hydration layer, while PMPC demonstrates the slightest interaction with proteins. In a comprehensive evaluation, PSBMA polymer brushes emerged as the best choice with superior stability, enhanced protein repulsion, and minimally induced protein deformation, resulting in effective resistance to nonspecific adhesion. The high-density SBMA polymer brushes significantly reduce the level of protein adhesion in AFM testing. In addition, we have pioneered the quantitative characterization of hydration repulsion in polymer brushes by analyzing the hydration repulsion characteristics at different materials and graft densities. In summary, our study provides a nuanced understanding of the material and structural determinants influencing the capacity of zwitterionic polymer brushes to thwart protein adhesion. Additionally, it presents a quantitative elucidation of hydration repulsion, contributing to the advancement and application of antifouling polymer brushes.

摘要

制备抗污的两性离子聚合物刷是减轻医疗器械表面非特异性黏附的主要方法。本研究旨在阐明这些聚合物刷的材料组成和结构特性与阻止蛋白质黏附之间的相关性。为实现这一目标,我们模拟了三种不同的两性离子聚合物刷,即羧基甜菜碱甲基丙烯酸酯(CBMA)、磺酸甜菜碱甲基丙烯酸酯(SBMA)和(2-(甲基丙烯酰氧)乙基)-磷酸胆碱(MPC)。模拟结果表明,增加接枝密度可以提高聚合物刷的结构稳定性、水合强度和抗蛋白质黏附能力。PCBMA 表现出更稳定的水合层,而 PMPC 与蛋白质的相互作用最小。综合评估表明,PSBMA 聚合物刷是最佳选择,具有更好的稳定性、增强的蛋白质排斥性和最小的蛋白质变形诱导,从而有效抵抗非特异性黏附。高密 SBMA 聚合物刷在 AFM 测试中显著降低了蛋白质黏附水平。此外,我们通过分析不同材料和接枝密度下的水合排斥特性,首次对聚合物刷中水合排斥的定量特征进行了量化表征。总之,本研究深入了解了影响两性离子聚合物刷阻止蛋白质黏附能力的材料和结构决定因素,并对水合排斥进行了定量阐述,为抗污聚合物刷的发展和应用提供了参考。

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