Synthesis and study of a disinfectant based on diethanolamine

V. Farzaliev, M. Abbasova, Oruc Garib Nabiev, N. A. Alieva, L. Safarova, G. M. Kulieva
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引用次数: 0

Abstract

The interaction of diethanolamine with formaldehyde at a ratio of initial reagents of 2?:?3, respectively, obtained a preparation that is an equimolar mixture of 3-(?-hydroxyethyl)-1,3-oxazolidine and its methylol derivative – 3-(?-hydroxyoxymethyl-ethyl)-1,3-oxazolidine. The paper presents the results of a study of the antimicrobial activity of the preparation against microorganisms – S. aureus, E. coli, as the most resistant species of bacteria that cause nosocomial infection. The tests were carried out by three methods: the test object method, as well as suspension and adsorption methods. The minimum effective concentration and exposure time of the preparation, which ensure the complete destruction of these microorganisms, have been established. The effect of organic substances and neutralizers on the antimicrobial activity of the preparation was studied. «Sulfonol» (a mixture of stereoisomers of the sodium salt of alkylbenzenesulfonic acid) at a concentration of 0,2?% and ten percent milk were used as neutralizers, and 10?% horse serum was used as protein. The concentration of the preparation and the exposure time required for the complete disinfection of dishes, glass and metlakh tiles infected with S. aureus and E. coli were determined. Disinfection of surfaces is achieved by treatment with a 3?% solution of the preparation during an exposure of 60 minutes, and dishes – with 3–5?% solutions for 45 minutes. It has been established by the thermoanalytical method of analysis that the preparation is stable at normal temperature and does not change its physicochemical properties during storage for 18 months or more. The preparation is recommended as a disinfectant for medical purposes. Keywords: 1,3-oxazolidine derivatives, 3-(?-hydroxyethyl)-1,3-oxazolidine, 3-(?-hydroxyoxymethylethyl)-1,3-oxazolidine, antimicrobial activity, bactericidal activity, nosocomial infection, bacteria, S. aureus, E. coli, disinfection, disinfectant.
二乙醇胺类消毒剂的合成与研究
二乙醇胺与甲醛在初始试剂比例为2∶3时的相互作用3分别获得了3-(?-羟乙基)-1,3-恶唑烷及其甲基衍生物- 3-(?-羟氧甲基乙基)-1,3-恶唑烷的等摩尔混合物的制剂。本文介绍了该制剂对微生物的抗菌活性的研究结果-金黄色葡萄球菌,大肠杆菌,作为引起医院感染的最耐药的细菌物种。试验采用试验对象法、悬浮法和吸附法三种方法进行。已经确定了制剂的最低有效浓度和暴露时间,以确保这些微生物的完全破坏。研究了有机物质和中和剂对该制剂抑菌活性的影响。磺胺醇(烷基苯磺酸钠盐的立体异构体混合物)浓度为0.2 ?%和10%的牛奶被用作中和剂,10%的牛奶被用作中和剂。蛋白质采用%马血清。测定了对感染金黄色葡萄球菌和大肠杆菌的餐具、玻璃和面砖进行彻底消毒所需的制剂浓度和暴露时间。表面消毒是用3?%溶液的制备过程中暴露60分钟,盘子- 3-5 ?%溶液浸泡45分钟。经热分析分析方法确定,该制剂在常温下稳定,在18个月以上的贮存期间,其理化性质不发生变化。该制剂推荐作为医疗用途的消毒剂。关键词:1,3-恶唑烷衍生物,3-(?-羟乙基)-1,3-恶唑烷,3-(?-羟基氧甲基乙基)-1,3-恶唑烷,抗菌活性,杀菌活性,医院感染,细菌,金黄色葡萄球菌,大肠杆菌,消毒,消毒剂
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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