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首页> 外文期刊>Biomedical Engineering: Applications, Basis and Communications >STERILIZATION PERFORMANCE OF AUTOCLAVE UNITS ON CANNULAR MATERIALS
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STERILIZATION PERFORMANCE OF AUTOCLAVE UNITS ON CANNULAR MATERIALS

机译:高压灭菌器在管状材料上的灭菌性能

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Autoclaves are devices that are used for sterilization of medical devices under high pressure and temperatures. As with all medical devices, the correct operation of autoclave units is vital for their performance and for successful sterilization. Thus, they should be tested to investigate their technical performance and biological effects within the studies of hospital quality control. Starting from setting the temperature and the pressure parameters up to taking out the materials from the autoclave after sterilization, all steps of the process need to be revised at these control stages. In this study, biological effects of sterilization were tested on microorganisms placed in cannular materials by using different temperatures and sterilization durations. As for the sterilization unit, a vertical type autoclave was used. The technical parameters of the autoclave during the sterilization process were measured by using a temperature-pressure data logger device. Bacillus subtilis var. niger strain was used to examine the biological performance of the sterilization unit. We performed different experiments by changing the temperature and the duration of the sterilization, and using several sizes of cannular materials. Experiments were made at 100°C, 95°C, 90°C, 85°C, 80°C, 75°C, 70°C and for 1 and 5 min. Additionally, two different cannula type sterile glass pipettes (1 and 10 ml) were used in experiments to compare the status of sterilization for different volumetric materials. Biological and technical results obtained for both test and control parameters were compared. The percent of bacteria reduction (Bacteria reduction% = (Test Number/Control Number) x 100) was calculated for biological tests. Technical tests resulted that the autoclave was not able to provide a stable output for temperatures from 70° C to 100° C, and for durations of 1 and 5 min. However, biological tests showed that the sterilization was achieved for the strain at all test conditions. It was observed that the autoclave provided technical requirements for sterilization even for short sterilization durations and low temperature, as such no microbial growth was observed. In short, the bacteria reduction percent was 100%. It was explained that the reason for biological sterilization at these low parameters is because the autoclave generated higher pressure and higher temperature than the set pressure and temperature values. Consequently, the results of the biological tests were supported by measuring the technical parameters of the autoclave.
机译:高压灭菌器是用于在高压和高温下对医疗设备进行灭菌的设备。与所有医疗设备一样,高压灭菌器的正确操作对其性能和成功灭菌至关重要。因此,应在医院质量控制研究中对它们​​进行测试,以研究其技术性能和生物学效果。从设置温度和压力参数直到灭菌后从高压釜中取出物料开始,在这些控制阶段都需要修改过程的所有步骤。在这项研究中,通过使用不同的温度和消毒持续时间,对放置在导管材料中的微生物测试了消毒的生物学效应。至于灭菌单元,使用立式高压釜。高压灭菌器在灭菌过程中的技术参数通过使用温度-压力数据记录器设备进行测量。枯草芽孢杆菌变种使用尼日尔菌株检测灭菌单元的生物学性能。我们通过改变温度和消毒持续时间,并使用多种尺寸的套管材料进行了不同的实验。在100°C,95°C,90°C,85°C,80°C,75°C,70°C下分别进行1分钟和5分钟的实验。另外,在实验中使用了两种不同的插管型无菌玻璃移液器(1和10 ml)来比较不同体积材料的灭菌状态。比较了测试参数和控制参数的生物学和技术结果。计算出细菌减少的百分比(细菌减少%=(测试编号/对照编号)x 100)以进行生物学测试。技术测试结果表明,高压釜无法在70°C至100°C的温度下以及1分钟和5分钟的时间内提供稳定的输出。但是,生物学测试表明,在所有测试条件下均实现了菌株的灭菌。观察到高压灭菌器即使在短的灭菌持续时间和低温下也提供了灭菌的技术要求,因为没有观察到微生物的生长。简而言之,细菌减少率是100%。解释了在这些低参数下进行生物灭菌的原因是因为高压灭菌器产生的压力和温度高于设定压力和温度值。因此,通过测试高压釜的技术参数来支持生物学测试的结果。

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