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Dynamically Crosslinked Polymer Nanocomposites to Treat Multidrug-Resistant Bacterial Biofilms

机译:动态交联的聚合物纳米复合材料用于治疗耐多药细菌生物膜。

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摘要

Multidrug-resistant biofilms are highly resistant to current antimicrobial therapies. We have developed an antimicrobial platform that integrates the bacteria-killing phytochemical carvacrol into dynamically crosslinked polymer nanocomposites (DCPNs). Taking advantage of a reversibly crosslinked Schiff-base scaffold throughout the engineered emulsions, DCPNs exhibited long-term shelf-life and good stability in serum, while readily disassembling in acidic microenvironments. Furthermore, we demonstrated that DCPNs efficiently penetrate the biofilm matrix, eradicating both Gram-negative/positive bacteria enclosed within. Moreover, DCPNs showed no observable toxicity to fibroblast mammalian cells within the same antimicrobial concentrations necessary to eradicate MDR biofilms. Given their potent antimicrobial and stimuli-responsive dissociation characteristics in a biofilm setting, DCPNs are a suitable therapeutic platform for combating MDR bacterial infections.
机译:耐多药生物膜对当前的抗菌疗法具有高度抵抗力。我们已经开发了一种抗菌平台,该平台将杀死细菌的植物化学香芹酚整合到动态交联的聚合物纳米复合材料(DCPNs)中。利用整个工程乳液中可逆交联的席夫碱支架的优势,DCPNs表现出长期的保存期限和在血清中的良好稳定性,同时在酸性微环境中易于分解。此外,我们证明了DCPNs可以有效地穿透生物膜基质,从而消除了封闭在其中的革兰氏阴性/阳性细菌。此外,在根除MDR生物膜所需的相同抗菌浓度下,DCPNs对成纤维细胞哺乳动物细胞没有观察到毒性。鉴于它们在生物膜环境中具有强大的抗菌和刺激响应解离特性,DCPNs是对抗MDR细菌感染的合适治疗平台。

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