An Attempt to Degradation of Anticancer Drug and Odor in the Medical Environment by Photocatalyst

Currently, there is a need to reduce the occupational exposure of health care workers to anticancer drugs. Environmental contamination by anticancer drugs and subsequent exposure of health care workers are associated with vaporization of anticancer drugs. Furthermore, carcinomatous unpleasant odor i...

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Veröffentlicht in:YAKUGAKU ZASSHI 2012/10/01, Vol.132(10), pp.1189-1195
Hauptverfasser: Sato, Junya, Kudo, Kenzo, Hirano, Takahiro, Kuwashima, Takayuki, Yamada, Sonpei, Kijihana, Ichiro, Sato, Kazuhiko, Takahashi, Katsuo
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container_end_page 1195
container_issue 10
container_start_page 1189
container_title YAKUGAKU ZASSHI
container_volume 132
creator Sato, Junya
Kudo, Kenzo
Hirano, Takahiro
Kuwashima, Takayuki
Yamada, Sonpei
Kijihana, Ichiro
Sato, Kazuhiko
Takahashi, Katsuo
description Currently, there is a need to reduce the occupational exposure of health care workers to anticancer drugs. Environmental contamination by anticancer drugs and subsequent exposure of health care workers are associated with vaporization of anticancer drugs. Furthermore, carcinomatous unpleasant odor is an additional problem to vaporized anticancer drugs in the field of clinical cancer therapy. We attempted to degrade vaporized anticancer drug and unpleasant odor using a photocatalyst. Cyclophosphamide or unpleasant odors (ammonia, formaldehyde, isovaleric acid, and butyric acid) were vaporized by heating in a closed chamber. Plates of photocatalyst coated with titanium dioxide were placed into the chamber and irradiated by light source. Vaporized cyclophosphamide in the chamber was recovered by bubbling the internal air through acetone and derivatized by trifluoroacetic anhydride for analysis by gas chromatographic-mass spectrometric assay. Vaporized odors were determined using a gas-detector tube, which changed color depending on the concentration. Following activation of the photocatalyst by a light source, the residual amounts of anticancer drug and unpleasant odor components were significantly decreased compared with when the photocatalyst was not activated without a light source. These results indicate that the photocatalysts can accelerate the degradation of vaporized anticancer drugs and odor components. Air-cleaning equipment using a photocatalyst is expected to be useful in improving the QOL of cancer patients experiencing carcinomatous unpleasant odor, and in reducing occupational exposure of health care workers to anticancer drugs.
doi_str_mv 10.1248/yakushi.12-00173
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Environmental contamination by anticancer drugs and subsequent exposure of health care workers are associated with vaporization of anticancer drugs. Furthermore, carcinomatous unpleasant odor is an additional problem to vaporized anticancer drugs in the field of clinical cancer therapy. We attempted to degrade vaporized anticancer drug and unpleasant odor using a photocatalyst. Cyclophosphamide or unpleasant odors (ammonia, formaldehyde, isovaleric acid, and butyric acid) were vaporized by heating in a closed chamber. Plates of photocatalyst coated with titanium dioxide were placed into the chamber and irradiated by light source. Vaporized cyclophosphamide in the chamber was recovered by bubbling the internal air through acetone and derivatized by trifluoroacetic anhydride for analysis by gas chromatographic-mass spectrometric assay. Vaporized odors were determined using a gas-detector tube, which changed color depending on the concentration. 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source MEDLINE; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; Alma/SFX Local Collection
subjects Antineoplastic Agents
cyclophosphamide
Cyclophosphamide - analysis
Environmental Pollution - prevention & control
Light
occupational exposure
Occupational Exposure - prevention & control
Odorants
photocatalyst
Photochemistry
Titanium
titanium dioxide
unpleasant odor
Volatilization
title An Attempt to Degradation of Anticancer Drug and Odor in the Medical Environment by Photocatalyst
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