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Effects of soluble metals on human peri‐implant cells
Author(s) -
Hallab Nadim James,
Anderson Shelley,
Caicedo Marco,
Brasher Amee,
Mikecz Katalin,
Jacobs Joshua J.
Publication year - 2005
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.30345
Subject(s) - viability assay , materials science , toxicity , implant , cell growth , metal , necrosis , filopodia , biophysics , cell , chemistry , metallurgy , medicine , biochemistry , biology , pathology , surgery
Despite reports associating tissue necrosis with implant failure, the degree to which processes, such as metal toxicity, negatively impact implant performance is unknown. We evaluated representative human peri‐implant cells (i.e., osteoblasts, fibroblasts, and lymphocytes) when challenged by Al +3 , Co +2 , Cr +3 , Fe +3 , Mo +5 , Ni +2 , and V +3 chloride solutions (and Na +2 as a control) over a wide range of concentrations (0.01–10.0 m M ). Cell responses were measured using proliferation assays, viability assays, and microscopic cell morphology assessments. Differential effects were found to be less a function of the cell type than of the composition and concentration of metal challenge. No preferential immunosuppression was demonstrated. Below 0.01 m M , no metal was toxic. The most toxic metals (i.e., Co, Ni, and V) reduced proliferation (IC 50 ), and viability (LC50) and cell morphology of osteoblasts, fibroblasts, and lymphocytes by <50% at challenge concentrations <1 m M . All other metals tested required >5 m M to exact the same responses. Below 1 m M , these toxic metals also induced alterations in all cell morphology consisting of loss of filopodia or lamellipodia or changes in cell shape. Metals that were toxic at clinically relevant concentrations (less than previously reported values in peri‐implant tissues/fluids) include Co (0.6 m M ), Ni (0.8 m M ), V (0.5 m M ) for lymphocytes and Co (0.8 m M ), V (0.3 m M ), Al (1–5 m M ), Fe (1–5 m M ) for fibroblasts, and Co (0.8 m M ), Ni (0.7 m M ), V (0.1 m M ) for osteoblasts. Only Co and V were toxic in vitro at concentrations below that detected in vivo in synovial fluid (V at 0.1 m M and Co at 0.8 m M for fibroblasts, and V at 0.4 m M and Co at 0.8 m M on osteoblasts). Thus, soluble Co and V released from Co‐ and Ti‐based alloys, respectively, could be implicated as the most likely to mediate cell toxicity in the periprosthetic milieu. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2005