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评估唾液对基于紫外线的消毒技术的干扰。

Assessment of saliva interference with UV-based disinfection technologies.

机构信息

Polytechnique Montreal, CGM Department, CP 6079, succ. Centre-Ville, H3C 3A7, Canada.

Oranim College and University of Haifa l, Israel.

出版信息

J Photochem Photobiol B. 2021 Apr;217:112168. doi: 10.1016/j.jphotobiol.2021.112168. Epub 2021 Mar 4.

Abstract

Worldwide shortages of personal protective equipment during COVID-19 pandemic has forced the implementation of methods for decontaminating face piece respirators such as N95 respirators. The use of UV irradiation to reduce bioburden of used respirators attracts attention, making proper testing protocols of uttermost importance. Currently artificial saliva is used but its comparison to human saliva from the UV disinfection perspective is lacking. Here we characterize UV spectra of human and artificial saliva, both fresh and after settling, to test for possible interference for UV-based disinfection. ASTM 2720 artificial saliva recipe (with either porcine or bovine mucin) showed many discrepancies from average (N = 18) human saliva, with different mucins demonstrating very different UV absorbance spectra, resulting in very different UV transmittance at different wavelength. Reducing porcine mucin concentration from 3 to 1.7 g/L brought UVA in the artificial saliva to that of average human saliva (although not for other wavelengths), allowing 254 nm disinfection experiments. Phosphate saline and modified artificial saliva were spiked with 8.6 log CFU/ml B. subtilis spores (ATCC 6633) and irradiated at dose of up to 100 mJ/cm, resulting in 5.9 log inactivation for a saline suspension, and 2.8 and 1.1 log inactivation for ASTM-no mucin and ASTM-1.7 g/L porcine mucin 2 μL dried droplets, respectively. UVC irradiation of spores dried in human saliva resulted in 2.3 and 1.5 log inactivation, depending on the size of the droplets (2 vs 10 μL, respectively) dried on a glass surface. Our results suggest that in the presence of the current standard dried artificial saliva it is unlikely that UVC can achieve 6 log inactivation of B. subtilis spores using a realistic UV dose (e.g. less than 2 J/cm) and the ATSM saliva recipe should be revised for UV decontamination studies.

摘要

在 COVID-19 大流行期间,全球个人防护设备短缺,迫使人们不得不采用方法对 N95 等面罩式呼吸防护器进行消毒。使用紫外线照射来降低使用过的呼吸防护器的生物负荷引起了人们的关注,因此制定适当的测试方案至关重要。目前使用的是人工唾液,但从紫外线消毒的角度来看,它与人唾液的比较还很缺乏。在这里,我们对新鲜和沉降后的人工唾液和人唾液的紫外线光谱进行了特征描述,以测试紫外线消毒是否可能存在干扰。ASTM 2720 人工唾液配方(含有猪或牛粘蛋白)与平均(N=18)人唾液有许多差异,不同的粘蛋白表现出非常不同的紫外线吸收光谱,导致在不同波长下紫外线透过率非常不同。将猪粘蛋白的浓度从 3 降低到 1.7 g/L 使人工唾液中的 UVA 达到了平均人唾液的水平(尽管其他波长不是),从而允许进行 254nm 的消毒实验。磷酸盐生理盐水和改良人工唾液中加入 8.6 log CFU/ml 的枯草芽孢杆菌孢子(ATCC 6633),并在高达 100 mJ/cm 的剂量下进行照射,结果表明生理盐水悬浮液的灭活率为 5.9 log,ASTM 无粘蛋白和 ASTM-1.7 g/L 猪粘蛋白 2μL 干燥液滴的灭活率分别为 2.8 和 1.1 log。在人唾液中干燥的孢子经 UVC 照射后,灭活率分别为 2.3 和 1.5 log,这取决于在玻璃表面上干燥的液滴大小(分别为 2 和 10μL)。我们的研究结果表明,在当前标准的干燥人工唾液存在的情况下,使用实际的紫外线剂量(例如小于 2 J/cm)不太可能使枯草芽孢杆菌孢子达到 6 log 的 UVC 灭活,并且 ATSM 唾液配方应进行修订,以用于 UV 消毒研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cad/8614578/5e5b053d8f23/gr1_lrg.jpg

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