Madison N Brown, Danielle M Bryant, Bailey Bond, Harrison Smith, Richard A Smith, William M Mihalko
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引用次数: 0
Abstract
Background: This study examined the impact of simulated wear particles on inflammatory cell-induced corrosion (ICIC).
Methods: A 30-day macrophage-lymphocyte co-culture experiment was conducted using American Society of Testing and Materials F1537 cobalt-chromium-molybdenum (CoCrMo) disks, with activators and CoCrMo particles added at none, low (1:10), medium (1:100), and high (1:500) cell-particle ratios. Supernatants collected on days 10 and 30 were analyzed for tissue necrosis factor alpha (TNFα) and interleukin 6 (IL-6) levels via enzyme-linked immunosorbent assay. Disks were examined for ICIC damage using scanning electron microscopy (SEM), and the oxygen percentage on their surfaces was analyzed with energy-dispersive X-ray spectrometry (EDS) and X-ray photoelectron spectrometry (XPS).
Results: Most disks showed damage consistent with ICIC. Day 10 TNFα was higher in medium and high particle groups compared to groups without particles, while IL-6 was unexpectedly lower in those groups. On day 30, the activated medium particle group showed higher IL-6 than the non-activated group. The EDS showed no significant differences in %O (P = 0.77), but XPS results indicated significant differences (P < 0.0001) at high particle concentrations.
Conclusion: Overall, the data suggested that increased TNFα reflected a heightened inflammatory response, particles might temporarily inhibit IL-6 release, and there is likely a synergistic effect between activators and particles on cellular responses.
期刊介绍:
The Journal of Arthroplasty brings together the clinical and scientific foundations for joint replacement. This peer-reviewed journal publishes original research and manuscripts of the highest quality from all areas relating to joint replacement or the treatment of its complications, including those dealing with clinical series and experience, prosthetic design, biomechanics, biomaterials, metallurgy, biologic response to arthroplasty materials in vivo and in vitro.