Effect of wettability and surface roughness on the adhesion properties of collagen on PDMS films treated by capacitively coupled oxygen plasma

润湿 聚二甲基硅氧烷 粘附 傅里叶变换红外光谱 材料科学 表面粗糙度 接触角 复合材料 双层 表面改性 扫描电子显微镜 胶粘剂 聚合物 高分子化学 化学工程 分析化学(期刊) 化学 图层(电子) 有机化学 工程类 生物化学
作者
Juan Antonio Juárez‐Moreno,Alejandro Ávila‐Ortega,A.I. Oliva,F. Avilés,J.V. Cauich-Rodríguez
出处
期刊:Applied Surface Science [Elsevier BV]
卷期号:349: 763-773 被引量:118
标识
DOI:10.1016/j.apsusc.2015.05.063
摘要

Abstract Direct chemical bonding of biomolecules to the surface of chemically inert polymers such as polydimethylsiloxane (PDMS) is not easily achieved. Therefore, pre-activation of such materials, followed by attachment of the biomolecule is necessary. This paper describes a procedure to functionalize a PDMS surface by oxygen-based plasma followed by the adhesion of collagen type I for the preparation of adhesive-free bilayer composite intended as skin substitute. Plasma treatments between 40 and 120 W for 5 to 15 min were used and the extent of surface modification was followed by contact angle, Fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM), scanning electron microscopy (SEM) and adhesion test. It was found that as the plasma power and time were increased, PDMS contact angle decreased while surface roughness increased as revealed by SEM and AFM. The formation of oxygen-containing functional groups at the surface was detected by FTIR. T-peel tests, performed on PDMS treated at 80 W/13 min and covered with collagen showed maximum peel strength of 0.1 N/mm which was 3 times higher than that measured for the untreated bilayer composite. The observed enhancement in the adhesion strength was attributed to the increased mechanical interlocking driven by the increased roughness and the formation of hydrophilic functional groups.
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