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首页> 外文期刊>ACS nano >Designer Dual Therapy Nanolayered Implant Coatings Eradicate Biofilms and Accelerate Bone Tissue Repair
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Designer Dual Therapy Nanolayered Implant Coatings Eradicate Biofilms and Accelerate Bone Tissue Repair

机译:设计师双重疗法纳米层植入物涂层消除了生物膜并加速了骨组织修复

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Infections associated with orthopedic implants cause increased morbidity and significant healthcare cost. A prolonged and expensive two-stage procedure requiring two surgical steps and a 6-8 week period of joint immobilization exists as today's gold standard for the revision arthroplasty of an infected prosthesis. Because infection is much more common in implant replacement surgeries, these issues greatly impact long-term patient care for a continually growing part of the population. Here, we demonstrate that a single-stage revision using prostheses coated with self-assembled, hydrolytically degradable multi layers that sequentially deliver the antibiotic (gentamicin) and the osteoinductive growth factor (BMP-2) in a time staggered manner enables both eradication of established biofilms and complete and rapid bone tissue repair around the implant in rats with induced osteomyelitis. The nanolayered construct allows precise independent control of release kinetics and loading for each therapeutic agent in an infected implant environment. Antibiotics contained in top layers can be tuned to provide a rapid release at early times sufficient to eliminate infection, followed by sustained release for several weeks, and the underlying BMP-2 component enables a long-term sustained release of BMP-2, which induced more significant and mechanically competent bone formation than a short-term burst release. The successful growth factor mediated osteointegration of the multilayered implants with the host tissue improved bone-implant interfacial strength 15-fold when compared with the uncoated one. These findings demonstrate the potential of this layered release strategy to introduce a durable next-generation implant solution, ultimately an important step forward to future large animal models toward the clinic.
机译:与整形外科植入物有关的感染会增加发病率,并增加医疗费用。作为当今感染假体翻修的金标准,一种耗时且昂贵的两阶段手术需要两个手术步骤,并需要6-8周的关节固定时间。由于感染在植入物置换手术中更为常见,因此这些问题极大地影响了人口不断增长的长期患者护理。在这里,我们证明了使用自组装,可水解降解的多层包被的假体进行的单阶段修复,可以以交错的方式依次递送抗生素(庆大霉素)和骨诱导生长因子(BMP-2),从而消除了已建立的生物膜并在诱导性骨髓炎大鼠中对植入物周围的骨组织进行全面,快速的修复。纳米层构建体可在感染的植入物环境中精确独立地控制每种治疗剂的释放动力学和负载。可以调整顶层中包含的抗生素,以在早期提供足够的快速释放,以消除感染,然后持续释放数周,并且潜在的BMP-2成分可以使BMP-2长期持续释放,从而诱导比短期爆发释放更重要且在机械方面胜任的骨形成。与未包被的相比,成功的生长因子介导的多层植入物与宿主组织的骨整合将骨植入物的界面强度提高了15倍。这些发现证明了这种分层释放策略的潜力,可以引入耐用的下一代植入物解决方案,最终是朝着未来的大型动物模型迈向临床的重要一步。

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