Polymer-associated infections are a major problem in implanted or intravascular devices. Among others, microorganisms of the staphylococcal family have been identified as the most important culprit. Prevention of bacterial adhesion and colonization of polymeric surfaces by release of antimicrobial agents incorporated into the polymers itself are currently under study. We have developed a novel method for the functionalization of a polymeric surface which is based on the deposition of covalently coupled lipid structures from antibiotic loaded vesicles. We have found that such process significantly reduces the bacterial growth on polystyrene material. In this work, lipid coverage obtained from multilamellar (MLVs) and extruded unilamellar (LUVs) vesicles were analyzed with respect to their adhesion efficiency on three types of polystyrene (PS) well-plates. Two methods of lipid deposition were characterized and compared in terms of surface lipid density and time stability: deposition of cationic vesicles on negatively charged surfaces and formation of covalent linkages between functionalized lipids and amines enriched surfaces. In order to study the antibiotic encapsulation efficiency we measured how the rifampicin (RIF) loading was affected by changes of liposome charge upon introduction of various amounts of stearylamine (SA), distearoyl-trimethylammonium propane (DSTAP) or dioleoyloxypropyl-trimethylammonium chloride (DOTAP) into the liposomal formulation. RIF-coated polymeric surfaces were also tested against a Staphylococcus epidermidis strain to evaluate their efficacy in vitro, showing that only approximately 2% of such bacteria inoculated on MLV-treated PS substrate were able to proliferate. Covalently immobilized lipid films showed about a tenfold increase in time stability compared to electrostatically bonded lipid films. Furthermore, substrates covalently modified with RIF-loaded MLVs retained an antibacterial activity for up to 12 days when aged in buffer at 37 degrees C. Such antimicrobial polymer coatings show promise for their use as antibacterial barrier for the prevention of catheter-related infections.

译文

:与聚合物相关的感染是植入式或血管内装置的主要问题。其中,葡萄球菌家族的微生物已被确定为最重要的罪魁祸首。目前正在研究通过释放掺入到聚合物本身中的抗微生物剂来防止细菌粘附和聚合物表面定居。我们已经开发了一种用于聚合物表面功能化的新方法,该方法基于从载有抗生素的囊泡中共价偶联的脂质结构的沉积。我们已经发现,这种方法显着减少了细菌在聚苯乙烯材料上的生长。在这项工作中,分析了从多层(MLV)和单层挤出(LUV)囊泡获得的脂质覆盖度,分析了它们在三种类型的聚苯乙烯(PS)孔板上的粘附效率。表征了两种脂质沉积的方法,并根据表面脂质密度和时间稳定性进行了比较:阳离子小泡在带负电荷的表面上的沉积以及功能化脂质和富含胺的表面之间形成共价键。为了研究抗生素的包封效率,我们测量了引入各种量的硬脂胺(SA),二硬脂酰三甲基铵丙烷(DSTAP)或二油酰氧基丙基三甲基氯化铵(DOTAP)时脂质体电荷的变化如何影响利福平(RIF)的负载量进入脂质体制剂。还用RIF涂层的聚合物表面针对表皮葡萄球菌菌株进行了测试,以在体外评估其功效,结果表明,仅约2%的此类细菌接种在MLV处理的PS底物上能够繁殖。与静电结合的脂质膜相比,共价固定的脂质膜显示出约10倍的时间稳定性。此外,当在37摄氏度的缓冲液中老化时,用RIF负载的MLV共价修饰的底物在长达12天的时间内仍保留了抗菌活性。此类抗菌聚合物涂层有望将其用作预防导管相关感染的抗菌屏障。

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