Abstract

Plasma electrolytic oxidation (PEO) can provide an ideal surface for osteogenic cell attachment and proliferation with further successful osteointegration. However, the same surface is attractive for bacteria due to similar mechanisms of adhesion in prokaryotic and eukaryotic cells. This issue requires the application of additional surface treatments for effective prevention of postoperative infectious complications. In the present work, ZrNb alloy was treated in a Ca-P solution with Ag nanoparticles (AgNPs) for the development of a new oxide layer that hosted osteogenic cells and prevented bacterial adhesion. For the PEO, 0.5 M Ca(H2PO2)2 solution with 264 mg L−1 of round-shaped AgNPs was used. Scanning electron microscopy with energy-dispersive x-ray and x-ray photoelectron spectroscopy were used for morphology and chemical analysis of the obtained samples; the SBF immersion test, bacteria adhesion test, and osteoblast cell culture were used for biological investigation. PEO in a Ca-P bath with AgNPs provides the formation of a mesoporous oxide layer that supports osteoblast cell adhesion and proliferation. Additionally, the obtained surface with incorporated Ag prevents bacterial adhesion in the first 6 h after immersion in a pathogen suspension, which can be an effective approach to prevent infectious complications after implantation.

Highlights

  • Incomplete osteointegration and microbial infection represent major contributors to implant failure

  • A ZrNb alloy (Zr-2.5 wt % Nb) was obtained from Osteoplant R&D (Debica, Poland); 6 mm diameter cylindrical samples with a height of 6 mm were prepared for all investigations

  • The Ag nanoparticles (AgNPs) used in the experiment have a round shape with an average size of 27 ± 4.3 nm

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Summary

Introduction

Incomplete osteointegration and microbial infection represent major contributors to implant failure. Microbial populations use cell attachment to solid substrates to survive, forming biofilms [1]. Strategies for bone and dental implant development have focused on surface modification to improve implant osteointegration and reduce bacterial infection. The development of multifunctional strategies that promote osteointegration while mitigating bacterial colonization is clearly important because both effects are necessary to ensure optimal, long-term functionality of medical implants. The adhesion mechanisms of eukaryotic and prokaryotic cells are similar, and this is a critical consideration in multifunctional surface development.

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