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首页> 外文期刊>Drug delivery and translational research >Killing bacteria within biofilms by sustained release of tetracycline from triple-layered electrospun microanofibre matrices of polycaprolactone and poly(ethylene-co-vinyl acetate)
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Killing bacteria within biofilms by sustained release of tetracycline from triple-layered electrospun microanofibre matrices of polycaprolactone and poly(ethylene-co-vinyl acetate)

机译:通过从聚己内酯和聚(乙烯-乙酸乙烯酯)的三层电纺微/纳米纤维基质中持续释放四环素来杀死生物膜内的细菌

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摘要

We report the controlled release of the antibiotic tetracycline (tet) HCl from a triple-layered electrospun matrix consisting of a central layer of poly(ethylene-co-vinyl acetate (PEVA) sandwiched between outer layers of poly-ε-caprolactone (PCL). These microanofibre layers with tet successfully encapsulated (essentially quantitatively at 3 and 5 % w/w) in each layer, efficiently inhibited the growth of a panel of bacteria, including clinical isolates, as shown by a modified Kirby-Bauer disc assay. Furthermore, they demonstrated high biological activity in increasingly complex models of biofilm formation (models that are moving closer to the situation in a wound) by stopping biofilm formation, by killing preformed biofilms and killing mature, dense biofilm colonies of Staphylococcus aureus MRSA252. Tet is clinically useful with potential applications in wound healing and especially in complicated skin and skin-structure infections; electrospinning provides good encapsulation efficiency of tet within PCL/PEVA/PCL polymers in microanofibre layers which display sustained antibiotic release in formulations that are anti-biofilm.
机译:我们从三层静电纺丝基质中报告了抗生素四环素(tet)HCl的受控释放,该静电纺丝基质由夹在聚ε-己内酯(PCL)外层之间的聚(乙烯-醋酸乙烯酯(PEVA)的中央层)组成如改良的Kirby-Bauer圆盘分析所示,这些具有tet的微/纳米纤维层已成功封装(基本上以3%和5%w / w定量定量),有效抑制了包括临床分离株在内的细菌群的生长。此外,他们通过停止生物膜形成,杀死预先形成的生物膜并杀死金黄色葡萄球菌MRSA252成熟,致密的生物膜菌落,在日益复杂的生物膜形成模型(接近伤口情况的模型)中证明了高生物活性。在临床上具有潜在的伤口愈合应用潜力,尤其是在复杂的皮肤和皮肤结构感染中;静电纺丝可提供良好的包封效果微/纳米纤维层中PCL / PEVA / PCL聚合物中的tet cy在抗生物膜制剂中显示出持续的抗生素释放。

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