MEASUREMENT AND MITIGATION OF MICROBIAL CONTAMINATION ON VARIOUS PERSONAL PROTECTIVE EQUIPMENT

Embargo until
2025-08-01
Date
2023-07-20
Journal Title
Journal ISSN
Volume Title
Publisher
Johns Hopkins University
Abstract
Recent global health crisis has called for methods to measure and mitigate microbial contamination on various personal protective equipment. Particularly, this document focu sed on: the implementation of modified AATCCAATCC-100 with qRT qRT-PCR assisted absolute and relative quantification for quantifiable tracing of both antimicrobial and microbial behavioral properties; the comparison of pipette tip repurposing efficiencies among lab detergent, ozone, and CAP; and the prospective application of vapor hydrogen peroxide, ozone, and CAP for mask repurposing. Log reductions from modified AATCC - 100 were compared to identify time dependent antimicrobial were compared to identify time dependent antimicrobial properties from silver ion containi containing wound dressing samples. A ntimicrobial properties of wound dressing samples diminished as incubation days are increased for both PCR and cell viability assay, while d ata from qRT qRT- PCR generally produced lower standard deviation than that of culture method s, hence shown to be more precise. Complementary parallel analysis of samples using both methods better characterized antimicrobial properties of the tested samples. A p arallel analysis using classical methods alongside the application of relative quantifi cation displayed changes in expression of virulence related genes. Although molecular assays targeting specific virulence activities are needed to verify the change in activities, relative quantification efficiently provided insight into changechanges specific t o virulence in model organisms. A c ontamination evaluation protocol were outlined t o evaluate the efficacies of the following repurposing methods: washing wit h a common laboratory detergent, exposure of ozone vapor, and CAP. Efficacy was determined by turn over ratio and log reduction in detectable genomic material of the contaminated products via re real -time quantitative PCR (qPCR). Ozone at 14400 PPM * minute is fully optimized while CAP shows promising potential post optimization. The application of ozone, hydrogen peroxide, and CAP is further explored for mask repurposing. Although further experimentation with BFE is needed, minimal change in physical properties of post post-repurposed masks showed promising potential as non non-destructive repurposing methods.
Description
Keywords
Antimicrobial, Decontamination, PCR, Ozone, Cold Atmospheric Plasma, Regulatory Science
Citation