Antibacterial and biocompatible polyaniline‐doped titanium oxide layers

材料科学 金红石 聚苯胺 苯胺 锐钛矿 阳极氧化 光催化 氧化钛 氧化物 电解质 二氧化钛 化学工程 核化学 无机化学 聚合物 化学 有机化学 复合材料 冶金 电极 催化作用 聚合 物理化学 工程类
作者
Aya Ali,Sheetal Chowdhury,Mary A. Carr,Amol V. Janorkar,Mary E. Marquart,Jason A. Griggs,Joel D. Bumgardner,Michael D. Roach
出处
期刊:Journal of Biomedical Materials Research Part B [Wiley]
卷期号:111 (5): 1100-1111 被引量:4
标识
DOI:10.1002/jbm.b.35217
摘要

Abstract Titanium anodization has been shown to produce crystalline oxides exhibiting photocatalytic reactions that form reactive oxygen species (ROS) when exposed to UV light. The ROS subsequently attack bacteria cells, and thus reduce bacteria attachment on titanium implant surfaces. Polyaniline (PANI) is a conductive polymer that has shown antibacterial properties when electropolymerized onto titanium. Our research group hypothesized the addition of PANI to crystalline titanium oxide surfaces would increase the available free electrons and thus increase photocatalytic activity (PCA). This research led to the development of a novel single‐step anodization approach for PANI doping crystalline titanium oxide layers. The objective of the present study was to determine the proper aniline electrolyte concentration needed to maximize the PCA and reduce bacterial attachment on the formed oxides. Aniline concentrations up to 1 M were added into a 1 M sulfuric acid electrolyte. The formed oxides exhibited increased PANI surface coverage but decreased anatase and rutile crystalline titanium oxide phase formation with increasing aniline electrolyte concentrations. Despite exhibiting the lowest levels of anatase and rutile formation, the 0.75 M and 1 M aniline oxides with the greatest PANI surface coverage also exhibited the highest PCA levels. 1 M aniline oxides showed significantly higher PCA under UVA irradiation compared to oxides formed from aniline concentrations up to 0.5 M ( p < 0.001). 0.75 M aniline oxides exhibited significant reductions in Staphylococcus aureus attachment with or without UVA irradiation compared to control oxides without PANI. MTT and live/dead assays confirmed cytocompatibility and nearly 100% cell viability for the PANI doped oxides.
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