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首页> 外文期刊>BioMed research international >Use of Synthetic Single-Stranded Gligonucleotides as Artificial Test Soiling for Validation of Surgical Instrument Cleaning Processes
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Use of Synthetic Single-Stranded Gligonucleotides as Artificial Test Soiling for Validation of Surgical Instrument Cleaning Processes

机译:使用合成的单链寡核苷酸作为人工测试污物,以验证手术器械的清洁过程

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Surgical instruments are often strongly contaminated with patients' blood and tissues, possibly containing pathogens. The reuse of contaminated instruments without adequate cleaning and sterilization can cause postoperative inflammation and the transmission of infectious diseases from one patient to another. Thus, based on the stringent sterility requirements, the development of highly efficient, validated cleaning processes is necessary. Here, we use for the first time synthetic single-stranded DNA (ssDNA.ODN), which does not appear in nature, as a test soiling to evaluate the cleaning efficiency of routine washing processes. Stainless steel test objects were coated with a certain amount of ssDNA.ODN. After cleaning, the amount of residual ssDNA_ODN on the test objects was determined using quantitative real-time PCR. The established method is highly specific and sensitive, with a detection limit of 20 fg, and enables the determination of the cleaning efficiency of medical cleaning processes under different conditions to obtain optimal settings for the effective cleaning and sterilization of instruments. The use of this highly sensitive method for the validation of cleaning processes can prevent, to a significant extent, the insufficient cleaning of surgical instruments and thus the transmission of pathogens to patients.
机译:手术器械经常被患者的血液和组织严重污染,其中可能含有病原体。在没有充分清洁和消毒的情况下重复使用受污染的器械会导致术后发炎,并将传染病从一个患者传播到另一个患者。因此,基于严格的无菌要求,必须开发高效,经过验证的清洁工艺。在这里,我们首次使用天然不存在的合成单链DNA(ssDNA.ODN)作为测试污物,以评估常规洗涤过程的清洁效率。不锈钢测试对象涂有一定量的ssDNA.ODN。清洁后,使用定量实时PCR测定测试对象上的残留ssDNA_ODN量。所建立的方法具有很高的特异性和灵敏度,检测极限为20 fg,可确定不同条件下医疗清洁过程的清洁效率,从而获得有效清洁和消毒器械的最佳设置。使用这种高度敏感的方法来验证清洁过程可以在很大程度上防止手术器械清洁不足,从而避免病原体传播给患者。

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