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应用定量载体试验评估抗分枝杆菌的杀菌剂。

Application of a quantitative carrier test to evaluate microbicides against mycobacteria.

作者信息

Springthorpe V Susan, Sattar Syed A

机构信息

University of Ottawa, Faculty of Medicine, Centre for Research on Environmental Microbiology (CREM), 451 Smyth Rd, Ottawa, ON, KlH 8M5, Canada.

出版信息

J AOAC Int. 2007 May-Jun;90(3):817-24.

Abstract

Microbicides for reprocessing heat-sensitive medical devices, such as flexible endoscopes, must be mycobactericidal to reduce the risk of nosocomial infections. Suspension test methods currently used for efficacy evaluation lack the stringency required for assessing inactivation of mycobacteria on surfaces. The quantitative carrier test method reported here is based on mycobacteria-contaminated reference carrier disks of brushed stainless steel. Each disk was contaminated with 10 microL of a suspension of Mycobacterium terrae containing a soil load. Each disk with a dried inoculum was placed in a glass or Teflon vial, and then overlaid with 50 microL of the test formulation or 50 microL saline for the control carriers. Five test and 3 control disks were used in each run. At the end of the contact time, each vial received 9.95 mL neutralizer solution with 0.1% Tween-80 to stop the reaction and perform the initial microbicide dilution. The inoculum was eluted by mixing on a Vortex mixer for 60 s, and the eluates and saline used to subsequently wash the vials and the funnels were membrane-filtered. Filters were placed on plates of Middlebrook 7H11 agar and incubated at 37 degrees C for at least 30 days before colonies were counted and log10 reductions were calculated in colony-forming units. Tests with a range of commercially available products, having claims against mycobacteria, or believed to be broad-spectrum microbicides, showed that the method gave reproducible results. Products used included oxidizing agents (sodium hypochlorite and an iodophore), a phenolic, a quaternary ammonium compound, and ortho-phthalaldehyde. This method represents a much more realistic evaluation than the currently used quantitative suspension test method for the evaluation of mycobactericidal formulations for registration and, when performed at different product concentrations, allows an assessment of any safety margin or risks in using the test formulation in the field.

摘要

用于对热敏医疗设备(如软性内窥镜)进行再处理的杀菌剂必须具有杀分枝杆菌的作用,以降低医院感染风险。目前用于疗效评估的悬液测试方法缺乏评估分枝杆菌在表面灭活所需的严格性。本文报道的定量载体测试方法基于被分枝杆菌污染的拉丝不锈钢参考载体盘。每个盘用10微升含有土壤负荷的地分枝杆菌悬液污染。每个带有干燥接种物的盘被放入玻璃或聚四氟乙烯小瓶中,然后用50微升测试制剂覆盖,对照载体则用50微升盐水覆盖。每次运行使用5个测试盘和3个对照盘。在接触时间结束时,每个小瓶加入9.95毫升含0.1%吐温80的中和剂溶液以终止反应并进行杀菌剂的初始稀释。通过在涡旋混合器上混合60秒洗脱接种物,将洗脱液和随后用于冲洗小瓶和漏斗的盐水进行膜过滤。将滤膜放置在Middlebrook 7H11琼脂平板上,在37℃下孵育至少30天,然后计数菌落并计算菌落形成单位的对数减少率。对一系列声称对分枝杆菌有作用或被认为是广谱杀菌剂的市售产品进行的测试表明,该方法可给出可重复的结果。使用的产品包括氧化剂(次氯酸钠和碘伏)、酚类、季铵化合物和邻苯二甲醛。与目前用于评估用于注册的杀分枝杆菌制剂的定量悬液测试方法相比,该方法代表了一种更实际的评估,并且当在不同产品浓度下进行时,允许评估在现场使用测试制剂时的任何安全余量或风险。

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