Ab'/> Ephemeral biogels to control anti-biofilm agent delivery: From conception to the construction of an active dressing
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Ephemeral biogels to control anti-biofilm agent delivery: From conception to the construction of an active dressing

机译:短暂的生物凝块,用于控制抗生物膜剂的递送:从概念到建造一个活跃的敷料

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AbstractChronic wound colonization by bacterial biofilms is common and can cause various complications. An anti-biofilm strategy was developed around the co-entrapment of a commercially available antiseptic, PHMB (polyhexamethylene biguanide 4mgmL?1), with EDTA (Ethylen diamine tetra acetic acid, 20mM) in a gelatin gel. The two active compounds act synergistically against bacterial biofilms, but their efficiency is strongly reduced (16-fold) when entrapped inside the 5% gelatin gel, and they weaken the mechanical properties (50-fold) of the gel. Increasing the gelatin concentration to 7% allows for good mechanical properties but large diffusional constraints. An active ephemeral gel, a chemical gel with controlled hydrolysis, was conceived and developed. When the ephemeral gel was solubilized after 48h, PHMB delivery increased, leading to good anti-biofilm activity. The various gels were examined over 24 and 48h of contact withP. aeruginosaandS. aureusbiofilms, two types of bacterial biofilms frequently encountered in chronic wounds. The ephemeral gel eradicated the dense biofilms (>6.107CFU·cm?2) produced by either single or mixed strains; a similar efficiency was measured for biofilms from strains of both laboratory and clinical origin. The formulation was then adapted to develop a dressing prototype that is active against biofilms and fulfils the requirements of an efficient wound care system.
机译:<![cdata [ 抽象 细菌生物膜的慢性伤口定植是常见的并且会导致各种并发症。围绕市售防腐剂,pHMB(聚环亚甲基双胍4mgml )围绕商业上可获得的防腐剂,pHMB(聚环萃取甲酯)围绕着抗生物膜策略。(乙烯二胺四醋酸酸,20mm)在明胶凝胶中。两种活性化合物对细菌生物膜协同作用,但是当夹住5%明胶凝胶内时它们的效率强烈降低(16倍),并且它们削弱了凝胶的机械性能(50倍)。将明胶浓度的增加至7%允许良好的机械性能,但是大的扩散限制。构思和开发了一种有源短暂的凝胶,具有受控水解的化学凝胶。当48小时后溶解短纤维凝胶时,PHMB递送增加,导致良好的抗生物膜活性。在与 p接触的24和48h中检查各种凝胶。铜绿假单胞菌 s。金黄色葡萄球菌生物膜,两种类型的慢性伤口经常遇到的细菌生物膜。短暂的凝胶消除了致密的生物膜(> 6.10 7 cfu·cm ?2 )单身或混合菌株;从实验室和临床来源的菌株测量生物膜的类似效率。然后调整制剂以开发一种敷料原型,该原型是对抗生物膜的活性,并满足有效的伤口护理系统的要求。

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