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等离子体引发的聚丙烯膜上的聚乙二醇丙烯酸酯接枝聚合:化学表征及蛋白质吸附评价。

Plasma-induced graft-polymerization of polyethylene glycol acrylate on polypropylene films: chemical characterization and evaluation of the protein adsorption.

机构信息

Dipartimento di Fisica G. Occhialini, Università degli Studi di Milano-Bicocca, p.za della Scienza, 3 I-20126 Milano, Italy.

出版信息

J Colloid Interface Sci. 2010 Jan 1;341(1):53-8. doi: 10.1016/j.jcis.2009.09.012. Epub 2009 Sep 16.

Abstract

This work deals with the optimization of argon plasma-induced graft-polymerization of polyethylene glycol acrylate (PEGA) on polypropylene (PP) films in order to obtain surfaces with a reduced protein adsorption for possible biomedical applications. To this end, we examined the protein adsorption on the treated and untreated surfaces. The graft-polymerization process consisted of four steps: (a) plasma pre-activation of the PP substrates; (b) immersion in a PEGA solution; (c) argon plasma-induced graft-polymerization; (d) washing and drying of the samples. The efficiency of these processes was evaluated in terms of the amount of grafted polymer, coverage uniformity and substrates wettability. The process was monitored by contact angle measurements, attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), X-ray Photoelectron Spectroscopy (XPS) and atomic force microscopy (AFM) analyses. The stability of the obtained thin films was evaluated in water and in Phosphate Buffer Saline (PBS) at 37 degrees C. The adsorption of fibrinogen and green fluorescent protein (GFP)--taken as model proteins--on the differently prepared surfaces was evaluated through a fluorescence approach using laser scanning confocal microscopy with photon counting detection. After plasma treatments of short duration, the protein adsorption decreases by about 60-70% with respect to that of the untreated film, while long plasma exposure resulted in a higher protein adsorption, due to damaging of the grafted polymer.

摘要

这项工作涉及优化氩等离子体引发的聚乙二醇丙烯酸酯(PEGA)在聚丙烯(PP)薄膜上的接枝聚合,以获得具有降低蛋白质吸附能力的表面,用于可能的生物医学应用。为此,我们研究了处理和未处理表面上的蛋白质吸附。接枝聚合过程包括四个步骤:(a)PP 基底的等离子体预活化;(b)浸入 PEGA 溶液中;(c)氩等离子体引发接枝聚合;(d)样品的清洗和干燥。这些过程的效率通过接枝聚合物的量、覆盖均匀性和基底润湿性来评估。通过接触角测量、衰减全反射傅里叶变换红外光谱(ATR-FTIR)、X 射线光电子能谱(XPS)和原子力显微镜(AFM)分析来监测该过程。在 37°C 的水中和磷酸盐缓冲盐水(PBS)中评估了所得薄膜的稳定性。通过使用具有光子计数检测的激光扫描共聚焦显微镜的荧光方法评估了纤维蛋白原和绿色荧光蛋白(GFP)(作为模型蛋白)在不同制备表面上的吸附。经过短时间的等离子体处理后,与未处理的薄膜相比,蛋白质吸附减少了约 60-70%,而长时间的等离子体暴露会导致更高的蛋白质吸附,这是由于接枝聚合物的损坏。

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