光接枝
光化学
光致聚合物
银纳米粒子
光引发剂
材料科学
表面改性
化学
纳米颗粒
高分子化学
聚合
聚合物
有机化学
纳米技术
单体
物理化学
作者
Davy‐Louis Versace,Julien Ramier,Daniel Grande,Samir Abbad Andaloussi,Pierre Dubot,Nelly Hobeika,Jean‐Pierre Malval,Jacques Lalevée,Estelle Renard,Valérie Langlois
标识
DOI:10.1002/adhm.201200269
摘要
Abstract A straightforward and versatile method for immobilizing macromolecules and silver nanoparticles on the surface of poly(3‐hydroxybutyrate‐ co ‐3‐hydroxyvalerate) (PHBHV) electrospun fibers is developed with the objective of designing a new functional material having significant antibacterial activity. The approach relies on a two‐step procedure: UV photografting of poly(methacrylic acid) (PMAA) on the surface of PHBHV fibers according to a “grafting from” method, and complexation of in situ photogenerated silver nanoparticles (Ag NPs) by carboxyl groups from tethered PMAA chains. The photografting process is conducted through a photoinduced free‐radical process employing a ketone‐based photoinitiator in aqueous medium. Under appropriate conditions, the photogenerated radicals abstract hydrogen atoms from the PHBHV backbone, thus initiating the UV‐mediated photopolymerization of MAA from the PHBHV microfibrous surface. The photochemical mechanism of the ketone photolysis is entirely described by the electron spin resonance/spin‐trapping technique, and the modified PHBHV microfibrous scaffold is extensively characterized by ATR‐FTIR spectroscopy, water contact‐angle measurements, and mercury intrusion porosimetry. In a second step, the in situ synthesis of Ag NPs within the microfibrous scaffold is implemented by photoreduction reaction in the presence of both a silver precursor and a photosensitizer. The photoinduced formation of Ag NPs is confirmed by UV spectrophotometry and XPS analysis. SEM and TEM experiments confirm the formation and dispersion of Ag NPs on the surface of the modified fibers. Finally, a primary investigation is conducted to support the antibacterial activity of the new functionalized biomaterial against Staphylococcus aureus and Escherichia coli .
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