<i>In Vivo</i> Prevention of Implant-Associated Infections Caused by Antibiotic-Resistant Bacteria through Biofunctionalization of Additively Manufactured Porous Titanium

Additively manufactured (AM) porous titanium implants may have an increased risk of implant-associated infection (IAI) due to their huge internal surfaces. However, the same surface, when biofunctionalized, can be used to prevent IAI. Here, we used a rat implant infection model to evaluate the bioco...

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Main Authors: Ingmar Aeneas Jan van Hengel, Bruce van Dijk, Khashayar Modaresifar, Johan Frederik Felix Hooning van Duyvenbode, Faisal Ruben Hamzah Aziz Nurmohamed, Marius Alexander Leeflang, Adriaan Camille Fluit, Lidy Elena Fratila-Apachitei, Iulian Apachitei, Harrie Weinans, Amir Abbas Zadpoor
Format: Article
Language:English
Published: MDPI AG 2023-10-01
Series:Journal of Functional Biomaterials
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Online Access:https://www.mdpi.com/2079-4983/14/10/520
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Summary:Additively manufactured (AM) porous titanium implants may have an increased risk of implant-associated infection (IAI) due to their huge internal surfaces. However, the same surface, when biofunctionalized, can be used to prevent IAI. Here, we used a rat implant infection model to evaluate the biocompatibility and infection prevention performance of AM porous titanium against bioluminescent methicillin-resistant <i>Staphylococcus aureus</i> (MRSA). The specimens were biofunctionalized with Ag nanoparticles (NPs) using plasma electrolytic oxidation (PEO). Infection was initiated using either intramedullary injection <i>in vivo</i> or with <i>in vitro</i> inoculation of the implant prior to implantation. Nontreated (NT) implants were compared with PEO-treated implants with Ag NPs (PT-Ag), without Ag NPs (PT) and infection without an implant. After 7 days, the bacterial load and bone morphological changes were evaluated. When infection was initiated through <i>in vivo</i> injection, the presence of the implant did not enhance the infection, indicating that this technique may not assess the prevention but rather the treatment of IAIs. Following <i>in vitro</i> inoculation, the bacterial load on the implant and in the peri-implant bony tissue was reduced by over 90% for the PT-Ag implants compared to the PT and NT implants. All infected groups had enhanced osteomyelitis scores compared to the noninfected controls.
ISSN:2079-4983