Non-Sterile Gloves as a Source of Radiation-Tolerant Microorganisms

Author:

Cabeau Celine1ORCID,Bolle-Reddat Romain1ORCID,Hauschild James2,McDonnell Gerald2ORCID

Affiliation:

1. Microbiological Quality & Sterility Assurance, DePuy Synthes, Chemin Blanc 38, 2400 Le Locle, Switzerland

2. Microbiological Quality & Sterility Assurance, Johnson & Johnson, Building 930 East, 1000 Route 202 South, Raritan, NJ 08869, USA

Abstract

Radiation methods are widely used for disinfection and sterilization applications. Microorganisms demonstrate known, variable tolerance levels to inactivation with lower doses of ionizing and non-ionizing radiation based on multiple mechanisms of resistance in their structures and nucleic acid repair mechanisms. The radiation dose required to ensure microbial inactivation during sterilization is typically based on the understanding and routine monitoring of the natural population and resistance of microorganisms on products exposed to radiation sterilization processes. This report describes the isolation of Roseomonas mucosa in a device manufacturing environment that was detected during routine device bioburden and dose verification monitoring. Sources of Gram-negative bacteria in the environment were investigated. Non-sterile examination gloves used during manufacturing were found to be a persistent source of R. mucosa and other microbial contaminants. The source of contamination was determined to be from the glove manufacturing process. Maintenance and routine microbiological controls during glove manufacturing, including water systems, are required to reduce the risks of gloves being a source of unexpected microbiological contamination.

Publisher

MDPI AG

Subject

Virology,Microbiology (medical),Microbiology

Reference27 articles.

1. McDonnell, G., and Hansen, J. (2020). Block’s Disinfection, Sterilization, and Preservation, Wolters Kluwer. [6th ed.]. Chapter 29.

2. McDonnell, G.E. (2017). Antisepsis, Disinfection, and Sterilization: Types, Action, and Resistance, ASM Press. [2nd ed.].

3. (2006). Sterilization of Health Care Products—Radiation—Part 1: Requirements for Development, Validation and Routine Control of a Sterilization Process for Medical Devices (Standard No. ISO 11137-1).

4. (2013). Sterilization of Health Care Products—Radiation—Part 2: Establishing the Sterilization Dose (Standard No. ISO 11137-2).

5. Radiation resistance of microorganisms comprising the bioburden of operating room packs;Whitby;Rad. Phys. Chem.,1977

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