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: Comparing ASTM F1671 with a Modified Dot-Blot Method to Evaluate Personal Protective Materials.

作者信息

Nandy Poulomi, Zhu Chengru, Young Megan, Wood Steven C, Lucas Anne D

出版信息

Biomed Instrum Technol. 2020 Mar/Apr;54(2):102-109. doi: 10.2345/0899-8205-54.2.102.

DOI:10.2345/0899-8205-54.2.102
PMID:32186903
Abstract

Effective personal protective equipment (PPE) is critical in preventing the spread of infectious diseases. Appropriate test systems and test soils are needed to adequately evaluate PPE. ASTM test method F903, which specifies the test method setup also used in ASTM F1670 and F1671, has been used for decades to test liquid (ASTM F1670) or viral (ASTM F1671) penetration resistance of PPE fabrics. However, an alteration of the bacteriophage propagation method detailed in the standard was necessary to obtain consistent titers of virus. In this study, modification of the nutrient broth provided consistently higher titers of virus and the use of the top agar in smaller increments prevented premature solidification. This study then compared the standard ASTM F1671 (using bacteriophage ϕχ174) with a modified dot-blot method to assess viral penetration of PPE materials. The results indicated that ASTM F1671 and the dot-blot apparatus methods were equivalent. The dot-blot method described here is less labor intensive and faster than the ASTM F1671 method. However, using the dot-blot system, which uses antibodies to detect the bacteriophage and signal amplification, does not indicate if virus viability or infectivity is retained, whereas the ASTM F1671 method indicates both. Nonetheless, the method presented in this investigation is a substantial improvement of a standard method for viral challenge testing of PPE materials.

摘要

相似文献

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引用本文的文献

1
Can qPCR replace the standard plaque assay in the ASTM F1671 to assess personal protective equipment barrier performance?定量聚合酶链反应(qPCR)能否取代美国材料与试验协会(ASTM)F1671标准中的噬斑测定法来评估个人防护装备的屏障性能?
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