Ti surfaces must exhibit antibacterial activity without cytotoxicity to promote bone reconstruction and prevent infection simultaneously. In this study, we employed a two-step electrochemical treatment process, namely, microarc oxidation (MAO) and cathodic electrochemical deposition (CED), to modify Ti surfaces. During the MAO step, a porous TiO (pTiO) layer with a surface roughness of approximately 2.0 μm was generated on the Ti surface, and in the CED step, Cu was deposited onto the pTiO layer on the Ti surface, forming Cu@pTiO. Cu@pTiO exhibited a similar structure, adhesion strength, and crystal phase to pTiO. Moreover, X-ray photoelectron spectroscopy (XPS) confirmed the presence of Cu in Cu@pTiO at an approximate concentration of 1.0 atom %. Cu@pTiO demonstrated a sustained release of Cu ions for a minimum of 28 days in a simulated in vivo environment. In vitro experiments revealed that Cu@pTiO effectively eradicated approximately 99% of and and inhibited biofilm formation, in contrast to the Ti and pTiO surfaces. Moreover, Cu@pTiO supported the proliferation of osteoblast-like cells at a rate comparable to that observed on the Ti and pTiO surfaces. Similar to pTiO, Cu@pTiO promoted the calcification of osteoblast-like cells compared with Ti. In summary, we successfully conferred antibacterial and pro-osteogenic activities to Ti surfaces without inducing cytotoxic effects or structural and mechanical alterations in pTiO through the application of MAO and CED processes. Moreover, we found that the pTiO layer promoted bacterial growth and biofilm formation more effectively than the Ti surface, highlighting the potential drawbacks of rough and porous surfaces. Our findings provide fundamental insights into the surface design of Ti-based medical devices for bone reconstruction and infection prevention.

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http://dx.doi.org/10.1021/acsabm.3c00860DOI Listing

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