首页> 外文期刊>Inflammation research: Official journal of the European Histamine Research Society >Vancomycin-loaded nano-hydroxyapatite pellets to treat MRSA-induced chronic osteomyelitis with bone defect in rabbits
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Vancomycin-loaded nano-hydroxyapatite pellets to treat MRSA-induced chronic osteomyelitis with bone defect in rabbits

机译:载有万古霉素的纳米羟基磷灰石小球用于治疗MRSA诱发的兔骨缺损慢性骨髓炎

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摘要

Objective: To investigate nano-hydroxyapatite (nHA) pellets as carriers for vancomycin in the treatment of chronic osteomyelitis and bone defects due to methicillin-resistant Staphylococcus aureus (MRSA) strains. Methods: Chronic osteomyelitis was induced in 45 New Zealand white rabbits. After 3 weeks (chronic infection), all animals were treated with debridement. The rabbits were divided into an experimental group (the bone was filled with vancomycin-loaded nHA pellets), a control group (the bone was filled with nHA pellets alone), and a blank group. The drug release profiles were determined in vitro and in vivo. X-rays, bone specimens, and microorganism cultures were used to evaluate the efficacy of the treatments. Results: Following a rapid initial release into the circulation, the drug concentration remained effective in the osseous and soft tissues for 12 weeks after debridement. Within 3 months, all rabbits in the experimental group recovered from osteomyelitis without a recurrence of the infection and the bone defects were partially repaired, whereas the infection and bone defects persisted in the control and blank groups. Conclusions: The results demonstrate that vancomycin-loaded nHA pellets successfully repair bone defects and control infection in MRSA-induced chronic osteomyelitis. In addition, nHA is an effective and safe controlled-release vancomycin carrier for chronic osteomyelitis with bone defects that is induced by MRSA.
机译:目的:研究纳米羟基磷灰石(nHA)颗粒作为万古霉素的载体,用于治疗耐甲氧西林金黄色葡萄球菌(MRSA)菌株引起的慢性骨髓炎和骨缺损。方法:在45只新西兰白兔中诱发慢性骨髓炎。 3周(慢性感染)后,对所有动物进行清创术治疗。将兔分为实验组(用万古霉素加载的nHA颗粒填充骨骼),对照组(仅用nHA的颗粒填充骨骼)和空白组。在体外和体内测定药物释放曲线。 X射线,骨标本和微生物培养物用于评估治疗效果。结果:在迅速释放到循环中之后,清创后12周内,骨和软组织中的药物浓度仍然有效。在3个月内,实验组的所有兔均从骨髓炎中恢复过来,没有感染复发,并且骨缺损得到了部分修复,而对照组和空白组的感染和骨缺损仍然存在。结论:结果表明,载有万古霉素的nHA颗粒可成功修复MRSA诱发的慢性骨髓炎的骨缺损并控制感染。此外,nHA是由MRSA诱导的具有骨骼缺陷的慢性骨髓炎的一种有效且安全的控释万古霉素载体。

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