A new method for in vivo evaluation of antimicrobial agents by translocation of complex dense populations of cutaneous bacteria.

J J Leyden, K J McGinley, A N Foglia, J E Wahrman, C N Gropper, B R Vowels
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引用次数: 8

Abstract

Previously, we described methods for measuring in vivo antimicrobial activity in which the resident bacterial flora of the forearm is expanded by occlusion with an impermeable plastic film, test agents are applied and quantitative cultures are obtained at varying time points. This methodology allows for an in vivo quantitative assessment of antimicrobial effects directed against a dense flora comprised primarily of staphylococci. This method may not be applicable to situations in which there is a high density of multiple species of bacteria. We describe herein new methods which permit in vivo determination of antimicrobial activity against a dense, mixed flora. Swabs moistened with a dilute nonionic detergent are used to remove bacteria from the subject's axilla or groin which are then translocated to the subject's forearm. Occlusion of the forearm with a large, sterile plastic chamber provides the necessary humid environment to yield a dense flora (10(5)-10(6) CFU) consisting of gram-positive cocci, gram-positive coryneforms and gram-negative rods. In this manner, multiple test sites are created on each forearm allowing for the simultaneous evaluation of multiple antimicrobial agents in a single subject. This method allows for the evaluation of the immediate, as well as sustained, in vivo bactericidal effect of an antimicrobial agent against a dense mixed flora with quantitative cultures obtained at varying time points after application of the test agent. Furthermore, ecological pressures which select for resistant organisms or allow for an overgrowth of nonsensitive bacteria can be evaluated by determining the composition of the flora after single or repeated applications of a test agent. The testing methodologies described herein can provide relevant information regarding the antimicrobial effectiveness of an agent in a variety of situations such as use against the axillary flora (including its utility as a deodorant), use as a perineal cleanser for critically ill, hospitalized patients and use in situations where a dense mixed flora exists, e.g. stasis ulcers and infected intertriginous dermatoses.

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一种通过复杂稠密的皮肤细菌群易位来评估体内抗菌药物的新方法。
以前,我们描述了测量体内抗菌活性的方法,其中前臂的常驻细菌菌群通过用不透水的塑料薄膜遮挡而扩大,应用测试剂,并在不同的时间点获得定量培养。这种方法允许在体内定量评估针对主要由葡萄球菌组成的密集菌群的抗菌作用。这种方法可能不适用于有多种细菌高密度的情况。我们在此描述的新方法,允许在体内测定抗微生物活性对密集,混合菌群。用用稀释的非离子清洁剂湿润的拭子去除受试者腋窝或腹股沟的细菌,然后将细菌转移到受试者的前臂。用一个大的无菌塑料腔封闭前臂,提供必要的潮湿环境,产生密集的菌群(10(5)-10(6)CFU),由革兰氏阳性球菌、革兰氏阳性棒状菌和革兰氏阴性杆状菌组成。以这种方式,在每个前臂上创建多个测试点,允许在单个受试者中同时评估多种抗菌剂。本方法允许评估抗菌剂对密集混合菌群的立即和持续的体内杀菌效果,并在施用试验剂后的不同时间点获得定量培养。此外,选择耐药生物或允许非敏感细菌过度生长的生态压力可以通过测定单次或多次使用试验剂后菌群的组成来评估。本文所描述的测试方法可以提供有关药剂在各种情况下的抗菌有效性的相关信息,例如用于腋窝菌群(包括其作为除臭剂的用途),用于危重病人、住院病人的会阴清洁剂,以及用于存在密集混合菌群的情况,例如,瘀疮和感染的三叶间性皮肤病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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