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采用高压蒸汽灭菌法对标准化呼气收集装置的口罩进行消毒和重复使用。

Sterilization and reuse of masks for a standardized exhaled breath collection device by autoclaving.

机构信息

Air Force Research Laboratory, 711th Human Performance Wing/RHBBA, 2510 Fifth Street, Area B, Building 840, Wright- Patterson AFB, OH 45433, United States of America.

UES Inc., 711th Human Performance Wing/RHBBA, 2510 Fifth Street, Area B, Building 840, Wright- Patterson AFB, OH 45433, United States of America.

出版信息

J Breath Res. 2023 Jun 30;17(3). doi: 10.1088/1752-7163/ace127.

Abstract

Exhaled breath research has been hindered by a lack of standardization in collection and analysis methodologies. Recently, the Respiration Collector forAnalysis (ReCIVA) sampling device has illustrated the potential to provide a consistent and convenient method for exhaled breath collection onto adsorbent media. However, the significant costs, compared to exhaled breath bags, associated with the standardized collector is believed to be the reason for limited widespread use by researchers in the exhaled breath field. For example, in addition to the sampling hardware, a single-use disposable silicon mask affixed with a filter is required for each exhaled breath collection. To reduce the financial burden, streamline device upkeep, reduce waste material, and ease the logistical burden associated with the single use masks, it is hypothesized that the consumable masks and filters could be sterilized by autoclaving for reuse. The masks were contaminated, autoclaved, and then tested for any surviving pathogens with spore strip standards and by measuring the optical density of cultures. The compound background collected when using the ReCIVA with new masks was compared to that collected with repeatedly autoclaved masks via thermal desorption gas chromatography mass spectrometry (TD-GC-MS). The capacity to block particulate matter of new filters was tested against that of autoclaved filters by introducing an aerosol and comparing pre-filter and post-filter particle counts. Finally, breath samplings were conducted with new masks and autoclaved masks to test for changes in measurements by TD-GC-MS of exogenous and endogenous compounds. The data illustrate the autoclave cycle sterilizes masks spiked with saliva to background levels (= 0.2527). The results indicate that background levels of siloxane compounds are increased as masks are repetitively autoclaved. The data show that mask filters have significant breakthrough of 1m particles after five repetitive autoclaving cycles compared to new filters (= 0.0219). Finally, exhaled breath results utilizing a peppermint ingestion protocol indicate two compounds associated with peppermint, menthone and 1-Methyl-4-(1-methylethyl)-cyclohexanol, and an endogenous exhaled breath compound, isoprene, show no significant difference if sampled with a new mask or a mask autoclaved five times (> 0.1063). Collectively, the data indicate that ReCIVA masks and filters can be sterilized via autoclave and reused. The results suggest ReCIVA mask and filter reuse should be limited to three times to limit potentially problematic background contaminants and filter dysfunction.

摘要

呼气研究一直受到收集和分析方法缺乏标准化的阻碍。最近,呼吸采集分析器(ReCIVA)采样设备展示了提供一种用于将呼气收集到吸附剂介质上的一致且方便的方法的潜力。然而,与呼气袋相比,标准化采集器的显著成本被认为是研究人员在呼气领域中有限使用的原因。例如,除了采样硬件外,每次呼气采集还需要一个一次性使用的带有过滤器的硅口罩。为了降低经济负担、简化设备维护、减少浪费材料以及减轻与一次性使用口罩相关的后勤负担,假设可以通过高压灭菌对消耗性口罩和过滤器进行消毒以重复使用。口罩被污染,进行高压灭菌,然后用孢子带标准和培养物的光密度测量来测试任何存活的病原体。通过热解吸气相色谱质谱(TD-GC-MS)比较使用新口罩和反复高压灭菌的口罩时收集的复合背景。通过引入气溶胶并比较预滤器和后滤器的颗粒计数,测试新过滤器和高压灭菌过滤器阻挡颗粒物的能力。最后,使用新口罩和高压灭菌口罩进行呼吸采样,以通过 TD-GC-MS 测试外源性和内源性化合物的测量值变化。数据表明,高压灭菌周期可将唾液污染的口罩消毒至背景水平(= 0.2527)。结果表明,随着口罩的反复高压灭菌,硅氧烷化合物的背景水平会升高。数据表明,与新过滤器相比,口罩过滤器在经过五次重复高压灭菌循环后,1m 颗粒的突破率显著增加(= 0.0219)。最后,使用薄荷醇摄入协议的呼气结果表明,与薄荷醇相关的两种化合物,薄荷酮和 1-甲基-4-(1-甲基乙基)-环己醇,以及一种内源性呼气化合物,异戊二烯,如果使用新口罩或五次高压灭菌的口罩采样,则没有显著差异(> 0.1063)。总的来说,数据表明 ReCIVA 口罩和过滤器可以通过高压灭菌进行消毒并重复使用。结果表明,ReCIVA 口罩和过滤器的重复使用次数应限制在三次以内,以限制潜在的有问题的背景污染物和过滤器功能障碍。

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