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

IF 3.7 4区 医学 Q1 BIOCHEMICAL RESEARCH METHODS
Samuel T Shawn, Sean W Harshman, Christina N Davidson, Jae Hwan Lee, Anne E Jung, Ariel Parker, M Aaron Hawkins, Blake W Stamps, Rhonda L Pitsch, Jennifer A Martin
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引用次数: 0

Abstract

Exhaled breath research has been hindered by a lack of standardization in collection and analysis methodologies. Recently, the Respiration Collector forIn VitroAnalysis (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 (p= 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 1μm particles after five repetitive autoclaving cycles compared to new filters (p= 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 (p> 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.

用高压灭菌法消毒和重复使用用于标准化呼气收集装置的口罩。
由于缺乏标准化的收集和分析方法,呼出气体的研究一直受到阻碍。最近,用于体外分析的呼吸收集器(ReCIVA)采样装置显示了其潜力,可为在吸附介质上收集呼出气体提供一致而方便的方法。然而,与呼气袋相比,标准化收集器的成本较高,这被认为是呼气领域研究人员广泛使用有限的原因。例如,除了采样硬件外,每次呼出气体收集还需要一个一次性使用的硅胶面罩,上面贴有过滤器。为了减轻经济负担、简化设备维护、减少废料并减轻与一次性面罩相关的后勤负担,我们假设可对消耗性面罩和过滤器进行高压灭菌,以便重复使用。对口罩进行污染、高压灭菌,然后用孢子条标准和测量培养物的光密度来检测是否有病原体存活。通过热脱附气相色谱质谱法(TD-GC-MS),将使用 ReCIVA 和新口罩收集到的化合物背景与使用重复高压灭菌口罩收集到的化合物背景进行了比较。通过引入气溶胶并比较过滤前和过滤后的颗粒计数,测试了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了呼吸采样,以测试 TD-GC-MS 测量外源和内源化合物的变化。数据表明,高压灭菌循环可将添加了唾液的口罩灭菌到本底水平(p= 0.2527)。结果表明,随着口罩重复高压灭菌,硅氧烷化合物的本底水平会升高。数据显示,与新过滤器相比,重复高压灭菌五次后,口罩过滤器的 1 微米微粒明显减少(p= 0.0219)。最后,采用薄荷摄入方案的呼出气体结果表明,与薄荷有关的两种化合物--薄荷酮和 1-甲基-4-(1-甲基乙基)-环己醇,以及一种内源性呼出气体化合物--异戊二烯,在使用新口罩或经过五次高压灭菌的口罩采样时没有明显差异(p> 0.1063)。总之,这些数据表明 ReCIVA 口罩和过滤器可以通过高压灭菌器消毒并重复使用。结果表明,ReCIVA 喉罩和过滤器的重复使用次数应限制在三次以内,以限制可能产生问题的本底污染物和过滤器功能障碍。
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来源期刊
Journal of breath research
Journal of breath research BIOCHEMICAL RESEARCH METHODS-RESPIRATORY SYSTEM
CiteScore
7.60
自引率
21.10%
发文量
49
审稿时长
>12 weeks
期刊介绍: Journal of Breath Research is dedicated to all aspects of scientific breath research. The traditional focus is on analysis of volatile compounds and aerosols in exhaled breath for the investigation of exogenous exposures, metabolism, toxicology, health status and the diagnosis of disease and breath odours. The journal also welcomes other breath-related topics. Typical areas of interest include: Big laboratory instrumentation: describing new state-of-the-art analytical instrumentation capable of performing high-resolution discovery and targeted breath research; exploiting complex technologies drawn from other areas of biochemistry and genetics for breath research. Engineering solutions: developing new breath sampling technologies for condensate and aerosols, for chemical and optical sensors, for extraction and sample preparation methods, for automation and standardization, and for multiplex analyses to preserve the breath matrix and facilitating analytical throughput. Measure exhaled constituents (e.g. CO2, acetone, isoprene) as markers of human presence or mitigate such contaminants in enclosed environments. Human and animal in vivo studies: decoding the ''breath exposome'', implementing exposure and intervention studies, performing cross-sectional and case-control research, assaying immune and inflammatory response, and testing mammalian host response to infections and exogenous exposures to develop information directly applicable to systems biology. Studying inhalation toxicology; inhaled breath as a source of internal dose; resultant blood, breath and urinary biomarkers linked to inhalation pathway. Cellular and molecular level in vitro studies. Clinical, pharmacological and forensic applications. Mathematical, statistical and graphical data interpretation.
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