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An approach to quantify ortho-phthalaldehyde contamination on work surfaces

Ortho-phthalaldehyde (OPA) is used as a high-level disinfectant for reusable medical devices in healthcare settings. The ACGIH recently adopted a Threshold Limit Value–Surface Limit (TLV–SL; 25 µg/100 cm(2)) for OPA surface contamination to prevent induction of dermal and respiratory sensitization f...

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Detalles Bibliográficos
Autores principales: Rogers, Caitlyn A, Gaskin, Sharyn E, Thredgold, Leigh D, Pukala, Tara L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410490/
https://www.ncbi.nlm.nih.gov/pubmed/37436000
http://dx.doi.org/10.1093/annweh/wxad039
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author Rogers, Caitlyn A
Gaskin, Sharyn E
Thredgold, Leigh D
Pukala, Tara L
author_facet Rogers, Caitlyn A
Gaskin, Sharyn E
Thredgold, Leigh D
Pukala, Tara L
author_sort Rogers, Caitlyn A
collection PubMed
description Ortho-phthalaldehyde (OPA) is used as a high-level disinfectant for reusable medical devices in healthcare settings. The ACGIH recently adopted a Threshold Limit Value–Surface Limit (TLV–SL; 25 µg/100 cm(2)) for OPA surface contamination to prevent induction of dermal and respiratory sensitization following dermal exposure. However, there is no current validated method to measure OPA surface contamination. This study aimed to develop a standardized approach for sample collection and quantitative determination of OPA from work surfaces for use in risk assessment practices. The reported method utilises readily available commercial wipes to collect surface samples coupled with direct detection of OPA via liquid chromatography time of flight mass spectrometry (LC–ToF–MS). This approach avoided complex derivatization steps commonly required for the analysis of aldehydes. Method evaluation was conducted in accordance with the Occupational Safety and Health Administration (OSHA) surface sampling guidelines. Overall recoveries of 25 µg/100 cm(2) of OPA from stainless steel and glass surfaces were 70% and 72%, respectively. The reported LOD for this method was 1.1 µg/sample and the LOQ was 3.7 µg/sample. OPA remained stable on the sampling medium for up to 10 days, when stored at 4 °C. The method was demonstrated in a workplace surface assessment at a local hospital sterilising unit, successfully detecting OPA on work surfaces. This method is intended to supplement airborne exposure assessment and provide a quantitative assessment tool for potential dermal exposure. When used in conjunction with a thorough occupational hygiene program that includes hazard communication, engineering controls, and personal protective equipment, skin exposure and consequent sensitization risks in the workplace can be minimized.
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spelling pubmed-104104902023-08-10 An approach to quantify ortho-phthalaldehyde contamination on work surfaces Rogers, Caitlyn A Gaskin, Sharyn E Thredgold, Leigh D Pukala, Tara L Ann Work Expo Health Original Articles Ortho-phthalaldehyde (OPA) is used as a high-level disinfectant for reusable medical devices in healthcare settings. The ACGIH recently adopted a Threshold Limit Value–Surface Limit (TLV–SL; 25 µg/100 cm(2)) for OPA surface contamination to prevent induction of dermal and respiratory sensitization following dermal exposure. However, there is no current validated method to measure OPA surface contamination. This study aimed to develop a standardized approach for sample collection and quantitative determination of OPA from work surfaces for use in risk assessment practices. The reported method utilises readily available commercial wipes to collect surface samples coupled with direct detection of OPA via liquid chromatography time of flight mass spectrometry (LC–ToF–MS). This approach avoided complex derivatization steps commonly required for the analysis of aldehydes. Method evaluation was conducted in accordance with the Occupational Safety and Health Administration (OSHA) surface sampling guidelines. Overall recoveries of 25 µg/100 cm(2) of OPA from stainless steel and glass surfaces were 70% and 72%, respectively. The reported LOD for this method was 1.1 µg/sample and the LOQ was 3.7 µg/sample. OPA remained stable on the sampling medium for up to 10 days, when stored at 4 °C. The method was demonstrated in a workplace surface assessment at a local hospital sterilising unit, successfully detecting OPA on work surfaces. This method is intended to supplement airborne exposure assessment and provide a quantitative assessment tool for potential dermal exposure. When used in conjunction with a thorough occupational hygiene program that includes hazard communication, engineering controls, and personal protective equipment, skin exposure and consequent sensitization risks in the workplace can be minimized. Oxford University Press 2023-07-12 /pmc/articles/PMC10410490/ /pubmed/37436000 http://dx.doi.org/10.1093/annweh/wxad039 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the British Occupational Hygiene Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Rogers, Caitlyn A
Gaskin, Sharyn E
Thredgold, Leigh D
Pukala, Tara L
An approach to quantify ortho-phthalaldehyde contamination on work surfaces
title An approach to quantify ortho-phthalaldehyde contamination on work surfaces
title_full An approach to quantify ortho-phthalaldehyde contamination on work surfaces
title_fullStr An approach to quantify ortho-phthalaldehyde contamination on work surfaces
title_full_unstemmed An approach to quantify ortho-phthalaldehyde contamination on work surfaces
title_short An approach to quantify ortho-phthalaldehyde contamination on work surfaces
title_sort approach to quantify ortho-phthalaldehyde contamination on work surfaces
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10410490/
https://www.ncbi.nlm.nih.gov/pubmed/37436000
http://dx.doi.org/10.1093/annweh/wxad039
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