Department of Surgery, Davis Heart and Lung Research Institute, Center for Regenerative Medicine & Cell-Based Therapies, Wexner Medical Center, The Ohio State University, Columbus, 43210, United States of America.
Center for Regenerative Medicine and Cell-Based Therapies, The Ohio State University, Columbus, 43210, United States of America.
Sci Rep. 2018 Jan 17;8(1):873. doi: 10.1038/s41598-018-19175-7.
A 100% water-soluble surfactant polymer dressing (SPD) that is bio-compatible and non-ionic has been reported to improve wound closure in preliminary clinical studies. The mechanism of action of SPD in wound healing remains unclear. Biofilm infection is a significant problem that hinders proper wound closure. The objective of this study was to characterize the mechanism of action of SPD inhibition of bacterial biofilm development. Static biofilms (48 h) of the primary wound pathogens Pseudomonas aeruginosa (PA01), Staphylococcus aureus (USA300) were grown on polycarbonate membranes and treated with SPD with and without antibiotics for an additional 24 h. The standard antibiotics - tobramycin (10 μg/ml) for PA01 and rifampicin (10 μg/ml) for USA300, were used in these studies. Following 24 h treatment with and without antibiotics, the biofilms were characterized using scanning electron microscopy (SEM) structural imaging, in vitro imaging system (IVIS) proliferation imaging, colony forming units (CFU), viability assay, quantitative PCR (qPCR) for virulence gene expression. Because SPD is a surfactant based dressing, it potentially has a direct effect on Gram negative bacteria such as Pseudomonas primarily due to the lipid-based outer membrane of the bacteria. SPD is a surfactant based dressing that has potent anti-biofilm properties directly or in synergy with antibiotics.
一种 100%水溶性的表面活性剂聚合物敷料(SPD),具有生物相容性和非离子特性,据初步临床研究报道,它可以改善伤口闭合。SPD 在伤口愈合中的作用机制尚不清楚。生物膜感染是阻碍伤口正常闭合的一个重大问题。本研究的目的是描述 SPD 抑制细菌生物膜形成的作用机制。将原发性伤口病原体铜绿假单胞菌(PA01)和金黄色葡萄球菌(USA300)的静态生物膜(48 h)在聚碳酸酯膜上培养,并用 SPD 及有无抗生素处理 24 h。在这些研究中,使用了标准抗生素-妥布霉素(PA01 为 10μg/ml)和利福平(USA300 为 10μg/ml)。在有无抗生素处理 24 h 后,使用扫描电子显微镜(SEM)结构成像、体外成像系统(IVIS)增殖成像、菌落形成单位(CFU)、活力测定、定量聚合酶链反应(qPCR)检测毒力基因表达来对生物膜进行表征。由于 SPD 是一种基于表面活性剂的敷料,它可能主要由于细菌的脂质外层膜而对革兰氏阴性菌(如铜绿假单胞菌)具有直接作用。SPD 是一种具有直接或与抗生素协同抗生物膜特性的基于表面活性剂的敷料。