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The influence of Co–Cr and UHMWPE particles on infection persistence: An in vivo study in mice

✍ Scribed by Anton H. Hosman; Sjoerd K. Bulstra; Jelmer Sjollema; Henny C. van der Mei; Henk J. Busscher; Daniëlle Neut


Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
484 KB
Volume
30
Category
Article
ISSN
0736-0266

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✦ Synopsis


Abstract

Wear of metal‐on‐metal (cobalt–chromium, Co–Cr particles) and metal‐on‐polyethylene (ultra‐high‐molecular‐weight polyethylene, UHMWPE particles) bearing surfaces in hip prostheses is a major problem in orthopedics. This study aimed to compare the influence of Co–Cr and UHMWPE particles on the persistence of infection. Bioluminescent Staphylococcus aureus Xen36 were injected in air pouches prepared in subcutaneous tissue of immuno‐competent BALB/c mice (control), as a model for the joint space, in the absence or presence of Co–Cr or UHMWPE particles. Bioluminescence was monitored longitudinally up to 21 days, corrected for absorption and reflection by the particles and expressed relative to the bioluminescence found in the presence of staphylococci only. After termination, air pouch fluid and air pouch membrane were cultured and histologically analyzed. Bioluminescence was initially lower in mice exposed to UHMWPE particles with staphylococci than in mice injected with staphylococci only, possibly because UHMWPE particles initially stimulated a higher macrophage presence in murine air pouch membranes. For mice exposed to Co–Cr particles with staphylococci, bioluminescence was observed to be higher in two out of six animals compared to the presence of staphylococci alone. In the majority of mice, infection risk in the absence or presence of Co–Cr and UHMWPE particles appeared similar, assuming that the longevity of an elevated bioluminescence is indicative of a higher infection risk. However, the presence of Co–Cr particles yielded a higher bioluminescence in two out of six mice, possibly because the macrophage degradative function was hampered by the presence of Co–Cr particles. © 2011 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 30:341–347, 2012


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