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体外扩散床,抗菌伤口敷料的3天重复挑战“能力”测试。

In vitro diffusion bed, 3-day repeat challenge 'capacity' test for antimicrobial wound dressings.

作者信息

Greenman John, Thorn Robin M S, Saad Saliah, Austin Andrew J

机构信息

Centre for Research in Biomedicine, University of West of England, Frenchay Campus, Coldharbour Lane, Bristol, UK.

出版信息

Int Wound J. 2006 Dec;3(4):322-9. doi: 10.1111/j.1742-481X.2006.00268.x.

Abstract

The aim of this study was to develop an in vitro wound infection model that allows the comparison of the bacterial kill rate of antimicrobial wound dressings over the course of 3 days, with renewed microbial challenges each day, under realistic wound-like conditions. A test bed model of a moderately exuding wound was constructed from a hydrogel containing releasable foetal calf serum (FCS), and cellulose discs dosed with test microbes (Methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa) suspended in 50% FCS applied at the interface between the test dressing and the hydrogel test bed. Freshly prepared discs were used to challenge the same dressing over a 23-hour period for a course of 3 days. Different test dressings produced differing kill rates, allowing quantitative comparison of both their immediate activity and their capacity to continue working over 3 days, within a fluid-donating system similar to the situation in vivo. The reported method has significant advantages over established test procedures since it enables the researcher to assess the antimicrobial capacity of wound dressings to continue working under conditions that match those encountered in wounds. These key conditions are those that would be expected to impede the action of the dressing and protect the infecting organisms.

摘要

本研究的目的是建立一种体外伤口感染模型,该模型能够在类似真实伤口的条件下,比较抗菌伤口敷料在3天内的细菌杀灭率,且每天都有新的微生物挑战。一个中度渗出伤口的试验台模型由含有可释放胎牛血清(FCS)的水凝胶构建而成,在测试敷料和水凝胶试验台之间的界面处,放置浸有悬浮于50% FCS中的测试微生物(耐甲氧西林金黄色葡萄球菌和铜绿假单胞菌)的纤维素圆盘。在23小时内使用新制备的圆盘对同一敷料进行为期3天的挑战。不同的测试敷料产生不同的杀灭率,从而能够在类似于体内情况的液体供应系统中,对它们的即时活性以及在3天内持续发挥作用的能力进行定量比较。与既定的测试程序相比,所报道的方法具有显著优势,因为它使研究人员能够评估伤口敷料在与伤口中遇到的条件相匹配的情况下继续发挥作用的抗菌能力。这些关键条件是那些预计会阻碍敷料作用并保护感染生物体的条件。

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