Degradation and inactivation efficacy of ozone water for antineoplastic drugs in hospital settings

Author:

Kato Ginjiro1,Mitome Hidemichi1,Shigematsu Saki1,Utsunomiya Aya1,Shimasaki Miho1,Sasaki Yuta2,Maki Tsuneo2,Yamamoto Hiroshi2,Tanabe Tomotaka3,Funahashi Tatsuya3,Hatae Noriyuki4,Hidaka Noriaki5,Tanaka Mamoru5,Akira Kazuki1ORCID

Affiliation:

1. Laboratory of Pharmaceutical Analytical Chemistry, College of Pharmaceutical Sciences, Matsuyama University, Japan

2. Division of Pharmacy, National Hospital Organization Shikoku Cancer Center Japan

3. Laboratory of Hygienic Chemistry, College of Pharmaceutical Sciences, Matsuyama University, Japan

4. Faculty of Pharmaceutical Sciences, Yokohama University of Pharmacy, Japan

5. Division of Pharmacy, Ehime University Hospital, Japan

Abstract

Purpose Occupational exposure to antineoplastic drugs in hospital settings is recognized to be hazardous, and as such environmental decontamination including degradation and inactivation of such drugs is recommended. To data, although various agents such as oxidants have been reported to be useful for decontamination, simpler, safer, and more convenient methods are required. In this study, the degradation and inactivation efficacy of ozone water, which has newly been introduced for decontamination of antineoplastic drugs in spills, was investigated for formulations of gemcitabine, irinotecan, and paclitaxel. Methods Antineoplastic formulations (medicinal ingredient: ∼1.5 μmol) were mixed with 50 mL of ozone water (>4 mg/L). The reactions were monitored by high-performance liquid chromatography, and the degradation mixtures were analyzed by 1H nuclear magnetic resonance spectroscopy in order to obtain the structural information of the degradation products. The formulations of gemcitabine and irinotecan and those degradation mixtures were evaluated for their mutagenicity using the Ames test and cytotoxicity against human cancer cells. Results gemcitabine and irinotecan were found to be readily degraded by the ozone treatment, and their active sites were suggested to be degraded. In contrast, paclitaxel was hard to be decomposed, possibly owing to the consumption of ozone by the polyoxyethylene castor oil added as a pharmaceutical additive of the formulation. No significant mutagenic changes of Salmonella typhimurium strains used for the Ames test were observed for the samples within the concentration ranges examined. The ozone treatment showed obvious increases in cell viability for gemcitabine formulation, and mild increases for irinotecan formulation. Conclusions Ozone water was shown to be effective as a decomposition agent for the antineoplastic drug formulations examined, although the efficacy depends on the chemical structures of the drugs and the pharmaceutical additives. It was also suggested that ozone treatment has a tendency to decrease the toxicity of the antineoplastic drug formulations. As such, further studies are required in order to clarify the effects and application limitations of ozone water.

Publisher

SAGE Publications

Subject

Pharmacology (medical),Oncology

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