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受生物启发的聚多巴胺和多酚单宁酸功能化钛抑制破骨细胞分化:一种在骨-植入界面调节破骨细胞活性的简便高效策略。

Bioinspired polydopamine and polyphenol tannic acid functionalized titanium suppress osteoclast differentiation: a facile and efficient strategy to regulate osteoclast activity at bone-implant interface.

机构信息

Department of Orthopaedic Surgery, National University of Singapore , NUHS Tower Block Level 11, 1E Kent Ridge Road, Singapore 119228 , Republic of Singapore.

出版信息

J R Soc Interface. 2019 Mar 29;16(152):20180799. doi: 10.1098/rsif.2018.0799.

Abstract

Osseointegration of metallic implants in porous osteoporotic bone remains a challenge. Surface modification of implants to reduce peri-implant osteoclastic bone resorption was explored in the study. Bioinspired polydopamine (pDOP) and polyphenol tannic acid (pTAN) are nature-derived universal coating systems that have emerged either as a sole coating or ad-layer for biomolecular conjugation on different biomaterials. The effects pDOP and pTAN on osteoclast development have not been reported before. In this study, osteoclast development was investigated on titanium (Ti) substrates coated with pDOP (Ti-pDOP) and pTAN (Ti-pTAN). The results showed that Ti-pDOP and Ti-pTAN coating reduced tartrate-resistant acid phosphatase activity and osteoclast cell number as compared with pristine Ti. Intriguingly, the reduction was higher on Ti-pTAN than on Ti-pDOP. Economical and biocompatible tannic acid serves as a superior coating in decreasing osteoclast activity when compared with that of pDOP coating and could be used to modulate osteoclast activity at bone-implant interfaces.

摘要

金属植入物在多孔骨质疏松骨中的骨整合仍然是一个挑战。本研究探索了通过表面改性植入物来减少种植体周围破骨细胞的骨吸收。生物启发的聚多巴胺(pDOP)和多酚单宁酸(pTAN)是天然衍生的通用涂层系统,它们要么作为单独的涂层,要么作为生物分子在不同生物材料上接枝的 ad-layer。pDOP 和 pTAN 对破骨细胞发育的影响以前尚未报道过。在这项研究中,研究了涂有 pDOP(Ti-pDOP)和 pTAN(Ti-pTAN)的钛(Ti)基底上的破骨细胞发育。结果表明,与原始 Ti 相比,Ti-pDOP 和 Ti-pTAN 涂层降低了抗酒石酸酸性磷酸酶活性和破骨细胞数量。有趣的是,Ti-pTAN 上的减少量高于 Ti-pDOP。与 pDOP 涂层相比,经济且生物相容的单宁酸作为一种优越的涂层,可降低破骨细胞的活性,可用于调节骨-植入物界面处的破骨细胞活性。

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