Zirconia-Toughened Alumina Ceramic Wear Particles Do Not Elicit Inflammatory Responses in Human Macrophages

Author:

Porporati Alessandro Alan12ORCID,Mödinger Yvonne1,Fischer Sarah3ORCID,Polajžer Sara4,Mettang Melanie1,Deisinger Ulrike1,Podlogar Matejka5,Trebše Rihard67ORCID,Lovšin Nika4

Affiliation:

1. Medical Products Division, CeramTec GmbH, 73207 Plochingen, Germany

2. Department of Engineering and Architecture, University of Trieste, 34127 Trieste, Italy

3. Medizintechnik, University of Stuttgart, 70174 Stuttgart, Germany

4. Faculty of Pharmacy, University of Ljubljana, Aškerčeva 7, 1000 Ljubljana, Slovenia

5. Jozef Stefan Institute, 1000 Ljubljana, Slovenia

6. Valdoltra Orthopaedic Hospital, 6280 Ankaran, Slovenia

7. Faculty of Medicine, University of Ljubljana, Vrazov trg 2, 1000 Ljubljana, Slovenia

Abstract

Ten percent of patients undergoing total hip arthroplasty (THA) require revision surgery. One of the reasons for THA are wear particles released from the implants that can activate the immune defense and cause osteolysis and failure of the joint implant. The discrepancies between reports on toxicity and immunogenicity of the implant materials led us to this study in which we compared toxicity and immunogenicity of well-defined nanoparticles from Al2O3, zirconia-toughened alumina (ZTA), and cobalt chrome (CoCr), a human THP-1 macrophage cell line, human PBMCs, and therefrom-derived primary macrophages. None of the tested materials decreased the viability of THP-1 macrophages nor human primary macrophages at the 24 h time point, indicating that at concentrations from 0.05 to 50 µm3/cell the tested materials are non-toxic. Forty-eight hours of treatment of THP-1 macrophages with 5 µm3/cell of CoCr and Al2O3 caused 8.3-fold and 4.6-fold increases in TNF-α excretion, respectively, which was not observed for ZTA. The comparison between THP-1 macrophages and human primary macrophages revealed that THP-1 macrophages show higher activation of cytokine expression in the presence of CoCr and Al2O3 particles than primary macrophages. Our results indicate that ZTA is a non-toxic implant material with no immunogenic effects in vitro.

Funder

Slovenian Research Agency

University of Ljubljana”

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference37 articles.

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2. MacInnes, S.J., Gordon, A., and Wilkinson, J.M. (2012). Risk Factors for Aseptic Loosening Following Total Hip Arthroplasty, IntechOpen.

3. National Joint Registry (2023, March 09). 2017 14th Annual Report National Joint Registry. Available online: https://www.hqip.org.uk/resource/national-joint-registry-14th-annual-report-2017/.

4. Aseptic loosening, not only a question of wear: A review of different theories;Sundfeldt;Acta Orthop.,2006

5. Particle disease: Biologic mechanisms of periprosthetic osteolysis in total hip arthroplasty;Gallo;Innate. Immun.,2013

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