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Fewer Bacteria Adhere to Softer Hydrogels

机译:较少的细菌粘附于较软的水凝胶

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Clinically, biofilm-associated infections commonly form on intravascular catheters and other hydrogel surfaces. The overuse of antibiotics to treat these infections has led to the spread of antibiotic resistance and underscores the importance of developing alternative strategies that delay the onset of biofilm formation. Previously, it has been reported that during surface contact, bacteria can detect surfaces through subtle changes in the function of their motors. However, how the stiffness of a polymer hydrogel influences the initial attachment of bacteria is unknown. Systematically, we investigated poly(ethylene glycol) dimethacrylate (PEGDMA) and agar hydrogels that were 20 times thicker than the cumulative size of bacterial cell appendages, as a function of Young's moduli. Soft (44.05-308.5 kPa), intermediate (1495-2877 kPa), and stiff (5152-6489 kPa) hydrogels were synthesized. Escherichia coli and Staphylococcus aureus attachment onto the hydrogels was analyzed using confocal microscopy after 2 and 24 h incubation periods. Independent of hydrogel chemistry and incubation time, E. coli and S. aureus attachment correlated positively to increasing hydrogel stiffness. For example, after a 24 h incubation period, there were 52 and 82% fewer E. coil adhered to soft PEGDMA hydrogels than to the intermediate and stiff PEGDMA hydrogels, respectively. A 62 and 79% reduction in the area coverage by the Gram-positive microbe S. aureus occurred after 24 h incubation on the soft versus intermediate and stiff PEGDMA hydrogels. We suggest that hydrogel stiffness is an easily tunable variable that could potentially be used synergistically with traditional antimicrobial strategies to reduce early bacterial adhesion and therefore the occurrence of biofilm-associated infections.
机译:临床上,与生物膜相关的感染通常在血管内导管和其他水凝胶表面上形成。过度使用抗生素治疗这些感染导致了抗生素耐药性的传播,并强调了开发替代策略以延缓生物膜形成的开始的重要性。以前,据报道,在表面接触过程中,细菌可以通过其马达功能的细微变化来检测表面。然而,聚合物水凝胶的刚度如何影响细菌的初始附着尚不清楚。我们系统地研究了聚(乙二醇)二甲基丙烯酸酯(PEGDMA)和琼脂水凝胶,它们的厚度是细菌细胞附件累积大小的20倍,这是杨氏模量的函数。合成了软凝胶(44.05-308.5 kPa),中间凝胶(1495-2877 kPa)和硬凝胶(5152-6489 kPa)。孵育2和24小时后,使用共聚焦显微镜分析大肠杆菌和金黄色葡萄球菌在水凝胶上的附着。不受水凝胶化学和孵育时间的影响,大肠杆菌和金黄色葡萄球菌的附着与水凝胶硬度的增加呈正相关。例如,在经过24小时的温育期后,与软质PEGDMA水凝胶相比,粘附到软PEGDMA水凝胶上的大肠杆菌线圈分别减少了52和82%。在软,中,硬PEGDMA水凝胶上孵育24小时后,革兰氏阳性微生物金黄色葡萄球菌的面积覆盖范围分别减少了62%和79%。我们建议水凝胶硬度是一个易于调节的变量,可以与传统的抗菌策略协同使用,以减少早期细菌粘附,从而减少与生物膜相关的感染的发生。

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