Abstract

Bacterial infection and corrosion are two of the most common causes of the failure for the use of biomedical metallic implants. In this paper, we developed a facile two-step approach for synthesizing a TiO2-PTFE nanocomposite coating on stainless steel substrate with both antibacterial and anticorrosion properties by using a sol-gel dip coating technique. A sub-layer of bioinspired polydopamine (PDA) was first coated on the stainless steel substrate to improve the adhesion and reactivity, then TiO2-PTFE was uniformly co-deposited onto the PDA sub-layer. Both PTFE and TiO2 contents had a significant influence on the surface energy of the TiO2-PTFE coating. The coating with the total surface energy of 26 mJ/m2 exhibited minimal bacterial adhesion against both Gram-negative Escherichia coli WT F1693 and Gram-positive Staphylococcus aureus F1557, which was explained using the extended DLVO theory. Benefiting from the synergistic effect between TiO2 and PTFE, the TiO2-PTFE coating showed improved corrosion resistance in artificial body fluids compared with the sole TiO2 coating or PTFE coating. The TiO2-PTFE coating also demonstrated extraordinary biocompatibility with fibroblast cells in culture, making it a prospective strategy to overcome current challenges in the use of metallic implants.

Highlights

  • Metallic implants are engineered systems designed to provide internal support to biological tissues and have been used extensively in dental, endovascular and orthopaedic surgery [1,2]

  • In a typical sol-gel TiO2 coating process, the formation of crystalline anatase TiO2 usually requires calcination at over 400 °C [39], but this temperature is much higher than the glass-transition temperature (Tg) and melting point of PTFE [40]

  • To synthesise coatings with photocatalytic activity, a range of anatase TiO2 nanoparticles was incorporated into the sol and the TiO2-PTFE coatings were heat treated at 100 °C (Fig. 1a)

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Summary

Introduction

Metallic implants are engineered systems designed to provide internal support to biological tissues and have been used extensively in dental, endovascular and orthopaedic surgery [1,2]. Despite extensive local tissue debridement and prolonged systemic and targeted local antimicrobial therapy, the infected device often must be removed to fully resolve the problem [5]. Current strategies for preventing infections include coating or impregnating antibacterial agents such as antibiotics [6], nano‐silver [7] and other antiseptics [8,9] onto the implant surface. Most of these attempts fail to deliver sustained antibacterial effects as the coatings are prone to loss of activity after covalent bonding [10]. Microbes being exposed to sub-lethal levels of the antimicrobials may trigger the emergence of resistance in situ

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