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Validation is the key to autoclave performance

机译:验证是高压灭菌器性能的关键

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摘要

Sterilisation is critical to many of the activities that are carried out in cleanrooms, from life science research to contact lens manufacturing, and steam sterilisation using an autoclave is the preferred technique. A failure of product sterilisation has far-reaching consequences, but a failure of a laboratory steriliser can produce spurious results causing unnecessary product wastage or loss of research data. How can you be certain that your autoclave is working properly? When using steam for sterilisation, it is critical to know that the correct pressure and temperature have been reached and that both parameters have been held for long enough to ensure the total destruction of any microorganisms, bacteria and spores. This means that the instrumentation (temperature and pressure sensors and timers) that controls your autoclave must be functioning correctly and producing accurate readings. In other words, they must be properly calibrated.
机译:从生命科学研究到隐形眼镜制造,灭菌对于在洁净室中进行的许多活动至关重要,而使用高压灭菌器进行蒸汽灭菌是首选技术。产品灭菌失败会产生深远的影响,但是实验室灭菌器的失败会产生虚假结果,从而导致不必要的产品浪费或研究数据丢失。您如何确定高压灭菌器正常工作?当使用蒸汽进行灭菌时,至关重要的是要知道达到了正确的压力和温度,并且两个参数的保持时间已经足够长,以确保完全破坏任何微生物,细菌和孢子。这意味着控制高压灭菌器的仪器(温度和压力传感器以及计时器)必须正常运行并产生准确的读数。换句话说,它们必须正确校准。

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    《Cleanroom technology》 |2019年第10期|18-18|共1页
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