Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/6684
Type: Journal article
Title: Variation in cytokines induced by particles from different prosthetic materials
Author: Haynes, D.
Boyle, S.
Rogers, S.
Howie, D.
Vernon-Roberts, B.
Citation: Clinical Orthopaedics and Related Research, 1998; 352(352):223-230
Publisher: LIPPINCOTT WILLIAMS & WILKINS
Issue Date: 1998
ISSN: 0009-921X
1528-1132
Abstract: Particles of prosthetic material stimulate macrophages to release cytokines, which may cause bone loss and loosening of the prosthesis. This study investigates the possibility that particles of different prosthetic materials may induce different cytokines and thus have different effects on bone remodeling. The in vitro response of human monocytes to particles of cast and forged cobalt chrome alloy, stainless steel, and titanium aluminum vanadium alloy were compared. There was no difference in the biologic response to cobalt-chrome particles derived from cast or forged material. Cobalt-chrome particles were toxic to the cells, but titanium aluminum vanadium particles did not affect cell viability. Stainless steel particles were approximately 10 times more toxic than were cobalt-chrome particles. All particles induced the release of tumor necrosis factor and interleukin 1 beta; stainless steel particles were the most potent stimulators of interleukin 1 beta; titanium aluminum vanadium particles were the strongest stimulators of interleukin 6 and prostaglandin 2. The study showed that particles derived from prosthetic materials of different metal compositions can elicit significantly different biologic responses. Understanding these different responses may help identify materials better suited for prostheses.
Keywords: Monocytes; Cells, Cultured; Humans; Chromium Alloys; Titanium; Stainless Steel; Alloys; Dinoprostone; Tumor Necrosis Factor-alpha; Interleukin-1; Interleukin-6; Cytokines; Biocompatible Materials; Particle Size; Female; Male
RMID: 0030005856
Appears in Collections:Orthopaedics and Trauma publications

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