文献类型：期刊文献

中文题名：等离子体辅助纳米涂层的构建及其成骨性能

英文题名：Construction and Osteogenic Properties of Plasma-Assisted Nano-Coating

作者：郭西萌[1];金莉莉[1];李春旺[1];何宏燕[1];刘昌胜[1]

机构：[1]华东理工大学材料科学与工程学院,材料生物学与动态化学前沿科学中心,教育部医用生物材料工程研究中心,上海200237

年份：2022

卷号：35

期号：1

起止页码：54

中文期刊名：功能高分子学报

外文期刊名：Journal of Functional Polymers

收录：CSTPCD;;北大核心:【北大核心2020】；CSCD:【CSCD2021_2022】；

基金：国家自然科学基金创新群体项目(51621002);国家重点研发计划战略性国际科技创新合作重点专项(SQ2018YF020328)。

语种：中文

中文关键词：聚对苯二甲酸乙二酯;骨形态发生蛋白;成骨分化;生物相容性;骨间充质干细胞

外文关键词：polyethylene terephthalate(PET);rhBMP-2;bone repair;biocompatibility;bone mesenchymal stem cell

摘要：通过氧等离子体处理,在聚对苯二甲酸乙二酯(PET)表面引入羟基,提高了其表面的亲水性。利用静电吸附等方式在PET材料表面先后载入表没食子儿茶素没食子酸酯(EGCG)、纤维黏连蛋白(Fn)和骨形态发生蛋白-2 (rhBMP-2),构建了rhBMP-2/EGCG/Fn有机组装的纳米涂层,改性后的PET表面表现出优异的细胞相容性,rhBMP-2的高效载入、活性维持、以及缓慢释放,赋予了改性表面高诱骨活性和成骨分化能力。
In recent years, polyethylene terephthalate(PET) based Ligament Advanced Reinforcement System(LARS)artificial ligaments have become popular in anterior cruciate ligament(ACL) reconstruction. However, due to its poor biological activity and high hydrophobicity, its application is limited to clinical uses. In order to improve the biological activity of materials and enhance the tendon-bone healing effect, oxygen plasma was used to introduce hydroxyl groups on the surface of PET. It has been found that the surface physiochemical treatment and immobilization of bioactive molecules have great effects on the bioactivity improvement of the inert surfaces. Therefore, bone morphogenetic proteins(rhBMP-2)with typical indicator and fibronectin(Fn) for enhancing the binding capacity of rhBMP-2 molecules were chosen as modifying molecules. The functional molecules such as epigallocatechin-3-gallate(EGCG) were coated on the PET surface first. There are six ortho phenolic hydroxyl groups in the molecular structure of EGCG. Fn molecules were then easily immobilized on the EGCG-PET surfaces. Since each subunit of Fn had a high-affinity binding site for rhBMP-2, rhBMP-2 molecules are biological anchored on the surface through long-chained Fn, which simulates the biomimetic design in the extracellular matrix. Thus, such molecules EGCG, Fn, and rhBMP-2 are sequentially immobilized on the PET surfaces. The nanocoating of rhBMP-2/EGCG/Fn is assembled to further enhance the loading efficiency of rhBMP-2 and control the release of rhBMP-2. Therefore, the surface-modified B/E-Fn-PET exhibits excellent cell compatibility. Moreover, effective loading,activity maintaining, and controlled release of rhBMP-2 give the implant surface high osteoinduction and better osteogenesis.Predictably, the integrated influences of these factors will provide technical support for designing the insert implantable surface with high bioactivities.