Construction and antibacterial performance study of strontium-doped TiO <sub>2</sub> coatings with photothermal-chemical synergistic antimicrobial properties
The inert surface of titanium (Ti) leads to inadequate osseointegration and bacterial infection, which are critical factors contributing to the failure of Ti implants. Micro-arc oxidation (MAO) technology enables the formation of a biocompatible porous TiO<sub>2</sub>coating on Ti surfaces, offering advantages such as a simple fabrication process, strong adhesion to the substrate, and the ability to incorporate functional ions (e.g. Ag<sup>+</sup>, Cu<sup>2+</sup>, Sr<sup>2+</sup>). This modification significantly enhances cellular adhesion and osteogenic activity. However, the TiO<sub>2</sub>produced via MAO exhibits a wide bandgap (3.2 eV), responding primarily to ultraviolet light, which results in low photothermal conversion efficiency in the near-infrared (NIR) region with greater tissue penetration, thereby limiting its application in photothermal therapy (PTT). This study was based on Sr<sup>2+</sup>-doped TiO<sub>2</sub>coating, and its NIR photothermal efficiency was improved through surface modification with a metal-polyphenol network (MPN). Additionally,<i>ϵ</i>-poly-L-lysine (EPL) antimicrobial peptides were grafted onto the surface to establish a synergistic photothermal-chemical antibacterial system. Experimental results demonstrated that the TiO<sub>2</sub>-MPN-EPL composite coating exhibited high-efficiency photothermal conversion under 808 nm laser irradiation, with the synergistic action of EPL providing targeted membrane disruption of bacteria. This system achieved a high bactericidal rate against<i>Staphylococcus aureus</i>and<i>Escherichia coli</i>while mitigating the thermal damage risks associated with standalone PTT. Furthermore, it promoted the proliferation of MC3T3-E1 osteoblasts.
Authors
- Han Xiang
- Wanming Lin
Institutions
- Shanxi Normal University (CN)
Publication Details
- Journal
- Biomedical Materials
- Published
- 2025-10-24
- DOI
- https://doi.org/10.1088/1748-605x/ae1777
- Primary Topic
- Nanoplatforms for cancer theranostics
- Type
- article
- Field-Weighted Citation Impact
- 0.00