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DOI 10.1007/s00011-010-0229-x

Медицинская библиотека · Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2010

Efficacy of periprosthetic erythromycin delivery for wear debris-induced inflammation and osteolysis.

Ren Weiping, Zhang Renwen, Hawkins Monica, Shi Tong, Markel David C

Оценочное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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 The previously implanted Ti pins were withdrawn and replaced with Ti pins coated either with (n = 7) or without (n = 7) EM.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.

Для цитирования: Ren Weiping, Zhang Renwen, Hawkins Monica, Shi Tong, Markel David C. Efficacy of periprosthetic erythromycin delivery for wear debris-induced inflammation and osteolysis.. Inflammation research : official journal of the European Histamine Research Society ... [et al.]. 2010. DOI: 10.1007/s00011-010-0229-x.

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