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首页> 外文期刊>Acta biomaterialia >Structure-property effects of novel bioresorbable hybrid structures with controlled release of analgesic drugs for wound healing applications
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Structure-property effects of novel bioresorbable hybrid structures with controlled release of analgesic drugs for wound healing applications

机译:新型生物可吸收杂化结构的结构性质效应,具有用于伤口愈合应用的镇痛药的控制释放

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Over the last decades, wound dressings have developed from the traditional gauze dressing to tissue-engineered scaffolds. A wound dressing should ideally maintain a moist environment at the wound surface, allow gas exchange, act as a barrier to micro-organisms and remove excess exudates. In order to provide these characteristics, we developed and studied bioresorbable hybrid structures which combine a synthetic porous drug-loaded top layer with a spongy collagen sublayer. The top layer, prepared using the freeze-drying of inverted emulsions technique, was loaded with the analgesic drugs ibuprofen or bupivacaine, for controlled release to the wound site. Our investigation focused on the effects of the emulsion's parameters on the microstructure and on the resulting drug-release profile, as well as on the physical and mechanical properties. The structure of the semi-occlusive top layer enables control over vapor transmission, in addition to strongly affecting the drug release profile. Release of the analgesic drugs lasted from several days to more than 100 days. Higher organic:aqueous phase ratios and polymer contents reduced the burst release of both drugs and prolonged their release due to a lower porosity. The addition of reinforcing fibers to this layer improved the mechanical properties. Good binding of the two components, PDLGA and collagen, was achieved due to our special method of preparation, which enables a third interfacial layer in which both materials are mixed to create an "interphase". These new PDLGA/collagen structures demonstrated a promising potential for use in various wound healing applications.
机译:在过去的几十年中,伤口敷料已经从传统的纱布敷料发展到组织工程的支架。伤口敷料在理想情况下应在伤口表面保持湿润的环境,允许气体交换,充当微生物的屏障并清除多余的渗出物。为了提供这些特性,我们开发并研究了可生物吸收的杂化结构,该结构将合成的多孔药物顶层与海绵状胶原子层相结合。使用反相乳液冷冻干燥技术制备的顶层装有镇痛药布洛芬或布比卡因,以控制释放到伤口部位。我们的研究集中在乳剂参数对微观结构和所产生的药物释放曲线以及物理和机械性能的影响上。半封闭顶层的结构除了可以强烈影响药物释放曲线外,还可以控制蒸气的传输。镇痛药的释放持续了几天到超过100天。较高的有机相,水相比和聚合物含量可降低两种药物的爆炸释放,并由于较低的孔隙率而延长了释放时间。向该层添加增强纤维改善了机械性能。由于我们特殊的制备方法,PDLGA和胶原蛋白这两种成分之间实现了良好的结合,这使得第三界面层得以实现,在这两种材料中混合形成了“界面相”。这些新的PDLGA /胶原蛋白结构显示了在各种伤口愈合应用中使用的有前途的潜力。

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