Abstract
Crosslinked polyethylene (XPE) was developed to reduce wear in hip and knee arthroplasty. Periprosthetic osteolysis depends on many factors including biological activity of wear particles. This study examines the relative inflammatory effect of different crosslinked polyethylenes compared to ultra-high-molecular-weight-polyethylene (UHMWPE) particles in vivo.
Materials and Methods: Wear particles of 3 XPE- (1 sequential irradiated/annealed; 2 remelted inserts) and 1 UHMWPE-insert were isolated from a knee joint simulator (20nm-nucleopore-filter;acid digestion method;ISO). Particles were analysed by scanning electron microscopy (n=66000). For all groups the particles were smooth, granular, irregular and less fibrillar. More than 85% of the particles were submicron. After removal of endotoxin the particles were suspended in a phosphate buffered saline solution (0.1% vol/vol (particle volume/PBS volume)). Endotoxin levels were controlled using standardised endotoxin detection tests (Lonza) in all samples.
40 female Balb/c mice were randomly assigned to one of five treatment groups (according to the national guidelines of animal protection laws): control (n=8); XPE1 (95 kGy E-beam, remelted; n=8); XPE2 (65 kGy E-beam, remelted; n=8), XPE3 (3x30 kGy Gamma, annealed and sequential irradiated; n=8) and UHMWPE particles (n=8). 50 μl of the particle suspension were injected into the murine left knee under sterile conditions. The leukocyte–endothelial cell interactions and the synovial microcirculation were performed by intra-vital fluorescence microscopy one week after particle injection to assess the inflammatory reaction to the particles (by measuring the rolling fraction of leukocytes, the adherent cells and the functional capillary density (FCD)). Data analysis was performed using a computer-assisted microcirculation analysis system (Cap-Image).
For the statistical analysis the Kruskal-Wallis test was used to determine differences within the groups, followed by an all pairwise multiple comparison procedure with a Bonferoni correction. The level of significance was set at p< 0.05.
Results: The fraction of the rolling leukocytes, adherent cells and FCD increased significantly (p< 0.05) in all bio-materials compared to control group. However, there was no significant difference between the UHMWPE and the XPE particle groups (p> 0.05).
Conclusion: Our data suggest that crosslinked polyethylene wear particles do not lead to a higher inflammatory reaction in vivo compared to UHMWPE particles.
Correspondence should be addressed to: EFORT Central Office, Technoparkstrasse 1, CH – 8005 Zürich, Switzerland. Tel: +41 44 448 44 00; Email: office@efort.org
Author: Sandra Utzschneider, Germany