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Application of ozone gas for decontamination of nucleoside anticancer drugs
BACKGROUND: Exposure to anticancer drugs is hazardous and may lead to chromosomal abnormalities and spontaneous abortion in healthcare workers. Guidelines recommend surface decontamination and cleaning in order to minimize the occupational exposure to anticancer drugs, although no single process has...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5048470/ https://www.ncbi.nlm.nih.gov/pubmed/27729988 http://dx.doi.org/10.1186/s40780-016-0058-3 |
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author | Tsukamoto, Ayumi Ishiwata, Shunji Kajimoto, Asami Murata, Ryusuke Kitano, Rika Inoue, Tomomi Kotake, Takeshi |
author_facet | Tsukamoto, Ayumi Ishiwata, Shunji Kajimoto, Asami Murata, Ryusuke Kitano, Rika Inoue, Tomomi Kotake, Takeshi |
author_sort | Tsukamoto, Ayumi |
collection | PubMed |
description | BACKGROUND: Exposure to anticancer drugs is hazardous and may lead to chromosomal abnormalities and spontaneous abortion in healthcare workers. Guidelines recommend surface decontamination and cleaning in order to minimize the occupational exposure to anticancer drugs, although no single process has been found to deactivate all currently available hazardous drugs. Ozone gas is oxidative and a decontaminant for bacteria; its characteristic as a gas has advantages in that it does not need to be wiped off or neutralized after use. METHODS: The nucleoside anticancer drugs, cytarabine and fluorouracil, were exposed to ozone gas on plates under controlled humidity. The levels of exposed ozone were evaluated using the concentration-time (CT) value, which is the mathematical product of ozone concentration and exposure time. The effects of exposure to ozone on levels of the anticancer drugs were determined by high-performance liquid chromatography (HPLC). RESULTS: The levels of cytarabine decreased with increasing CT value and were not detected beyond 40,000 CT. The decomposition levels of the anticancer drug by ozone were CT-dependent irrespective of the maximum concentration of ozone. Higher humidity in the range from 70 to 90 % accelerated the decomposition of cytarabine and fluorouracil, and neither of the drugs were detected at 90 % humidity after exposure to ozone gas. CONCLUSIONS: Ozone gas decomposed these nucleoside anticancer drugs. This is the first report of the applicability of ozone gas as a decontaminator for anticancer drugs. |
format | Online Article Text |
id | pubmed-5048470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50484702016-10-11 Application of ozone gas for decontamination of nucleoside anticancer drugs Tsukamoto, Ayumi Ishiwata, Shunji Kajimoto, Asami Murata, Ryusuke Kitano, Rika Inoue, Tomomi Kotake, Takeshi J Pharm Health Care Sci Research Article BACKGROUND: Exposure to anticancer drugs is hazardous and may lead to chromosomal abnormalities and spontaneous abortion in healthcare workers. Guidelines recommend surface decontamination and cleaning in order to minimize the occupational exposure to anticancer drugs, although no single process has been found to deactivate all currently available hazardous drugs. Ozone gas is oxidative and a decontaminant for bacteria; its characteristic as a gas has advantages in that it does not need to be wiped off or neutralized after use. METHODS: The nucleoside anticancer drugs, cytarabine and fluorouracil, were exposed to ozone gas on plates under controlled humidity. The levels of exposed ozone were evaluated using the concentration-time (CT) value, which is the mathematical product of ozone concentration and exposure time. The effects of exposure to ozone on levels of the anticancer drugs were determined by high-performance liquid chromatography (HPLC). RESULTS: The levels of cytarabine decreased with increasing CT value and were not detected beyond 40,000 CT. The decomposition levels of the anticancer drug by ozone were CT-dependent irrespective of the maximum concentration of ozone. Higher humidity in the range from 70 to 90 % accelerated the decomposition of cytarabine and fluorouracil, and neither of the drugs were detected at 90 % humidity after exposure to ozone gas. CONCLUSIONS: Ozone gas decomposed these nucleoside anticancer drugs. This is the first report of the applicability of ozone gas as a decontaminator for anticancer drugs. BioMed Central 2016-10-04 /pmc/articles/PMC5048470/ /pubmed/27729988 http://dx.doi.org/10.1186/s40780-016-0058-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Tsukamoto, Ayumi Ishiwata, Shunji Kajimoto, Asami Murata, Ryusuke Kitano, Rika Inoue, Tomomi Kotake, Takeshi Application of ozone gas for decontamination of nucleoside anticancer drugs |
title | Application of ozone gas for decontamination of nucleoside anticancer drugs |
title_full | Application of ozone gas for decontamination of nucleoside anticancer drugs |
title_fullStr | Application of ozone gas for decontamination of nucleoside anticancer drugs |
title_full_unstemmed | Application of ozone gas for decontamination of nucleoside anticancer drugs |
title_short | Application of ozone gas for decontamination of nucleoside anticancer drugs |
title_sort | application of ozone gas for decontamination of nucleoside anticancer drugs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5048470/ https://www.ncbi.nlm.nih.gov/pubmed/27729988 http://dx.doi.org/10.1186/s40780-016-0058-3 |
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