Zinc and melatonin mediated antimicrobial, anti-inflammatory, and antioxidant coatings accelerate bone defect repair.

IF 5.4 2区 医学 Q1 BIOPHYSICS
Fengzhen Jia, Jiaxin Guan, Jiali Wang, Meiyu Li, Yasi Zhang, Lei Xie, Pengde Han, He Lin, Xiao Huang, Jinping Lan, Yong Huang
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Abstract

Inflammation and bacterial infection are important causes of implant failure, and the development of multifunctional titanium surfaces to address these issues is an effective means of treating infected bone defects. In this study, polyphenols (EGCG) and Zn2+ were first loaded onto the titanium surface to construct an EGCG/Zn2+ polyphenol metal network coating. Then melatonin (MT) was loaded into the EGCG/Zn2+ network structure to prepare the EGCG/Zn2+/MT composite coating. The results proved that the EGCG/Zn2+/MT coating had good mechanical properties, hydrophilicity, corrosion resistance and bioactivity. In vitro, the inhibition rates of EGCG/Zn2+/MT against E. coli and S. aureus were about 97 % and 81 %, respectively. In vitro experiments revealed that EGCG/Zn2+/MT could regulate the polarization of macrophages (RAW264.7) to M2 type, could induce vascularization of human umbilical vein endothelial cells (HUVEC), and could promote the differentiation of pro-osteoblasts (MC3T3-E1) to osteogenesis. Meanwhile, EGCG/Zn2+/MT achieved effective ROS scavenging within HUVEC and MC3T3-E1. In vivo experiments demonstrated that the EGCG/Zn2+/MT coatings possessed favorable biosafety, anti-inflammatory, antimicrobial, and bone repair capabilities. This study provides a simple and versatile strategy for designing multifunctional surfaces with both antimicrobial, anti-inflammatory, antioxidant, angiogenic and osteogenic properties.

锌和褪黑激素介导的抗菌、消炎和抗氧化涂层可加速骨缺损修复。
炎症和细菌感染是导致植入失败的重要原因,开发多功能钛表面来解决这些问题是治疗感染性骨缺损的有效手段。在这项研究中,首先将多酚(EGCG)和 Zn2+ 添加到钛表面,以构建 EGCG/Zn2+ 多酚金属网络涂层。然后将褪黑素(MT)加入到 EGCG/Zn2+ 网络结构中,制备出 EGCG/Zn2+/MT 复合涂层。结果表明,EGCG/Zn2+/MT 涂层具有良好的机械性能、亲水性、耐腐蚀性和生物活性。在体外实验中,EGCG/Zn2+/MT 对大肠杆菌和金黄色葡萄球菌的抑制率分别为 97% 和 81%。体外实验表明,EGCG/Zn2+/MT 可调节巨噬细胞(RAW264.7)向 M2 型极化,可诱导人脐静脉内皮细胞(HUVEC)血管化,并可促进成骨细胞(MC3T3-E1)向成骨分化。同时,EGCG/Zn2+/MT 还能有效清除 HUVEC 和 MC3T3-E1 中的 ROS。体内实验表明,EGCG/Zn2+/MT涂层具有良好的生物安全性、抗炎、抗菌和骨修复能力。这项研究为设计具有抗菌、抗炎、抗氧化、血管生成和成骨特性的多功能表面提供了一种简单而多用途的策略。
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来源期刊
Colloids and Surfaces B: Biointerfaces
Colloids and Surfaces B: Biointerfaces 生物-材料科学:生物材料
CiteScore
11.10
自引率
3.40%
发文量
730
审稿时长
42 days
期刊介绍: Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields. Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication. The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.
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