Abstract | OBJECTIVES: We have reported that oral erythromycin (EM) inhibits periprosthetic tissue inflammation in a group of patients with aseptic loosening. The purpose of this study was to assess the efficacy of local, periprosthetic EM delivery in a rat model. METHODS: Uncoated Ti pins were press-fit into the right tibia of fourteen Sprague-Dawley rats following an intramedullar injection of UHMWPE ( ultra high molecular weight polyethylene) particles. Revision surgeries were performed 2 months after the primary surgery. EM was applied to the Peri-Apatite™ (PA) layer of the titanium (Ti) pins. The previously implanted Ti pins were withdrawn and replaced with Ti pins coated either with (n = 7) or without (n = 7) EM. The rats were killed 1 month after " revision surgery". The EM efficacy was evaluated by (MicroCT) μCT and histology. RESULTS: μCT analysis showed that bone volume percentage (BV/TV) was significantly higher in the EM-treated group compared to the untreated group (p < 0.05). Histological analysis showed that EM treatment inhibits UHMWPE particle-induced periprosthetic tissue inflammation compared to the untreated group. CONCLUSION: This study demonstrated that periprosthetic EM delivery reduced periprosthetic inflammation and improved the quality of surrounding bone.
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Authors | Weiping Ren, Renwen Zhang, Monica Hawkins, Tong Shi, David C Markel |
Journal | Inflammation research : official journal of the European Histamine Research Society ... [et al.]
(Inflamm Res)
Vol. 59
Issue 12
Pg. 1091-7
(Dec 2010)
ISSN: 1420-908X [Electronic] Switzerland |
PMID | 20607583
(Publication Type: Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Bacterial Agents
- Coated Materials, Biocompatible
- Polyethylenes
- ultra-high molecular weight polyethylene
- Erythromycin
- Titanium
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Topics |
- Animals
- Anti-Bacterial Agents
(administration & dosage, therapeutic use)
- Coated Materials, Biocompatible
(metabolism)
- Erythromycin
(administration & dosage, therapeutic use)
- Humans
- Implants, Experimental
- Inflammation
(drug therapy, etiology, pathology)
- Osteolysis
(drug therapy, etiology, pathology)
- Polyethylenes
(metabolism)
- Prosthesis Failure
- Rats
- Rats, Sprague-Dawley
- Tibia
(pathology)
- Titanium
(metabolism)
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