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Human & Experimental Toxicology
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Kinetic Aspects of Misonidazole and its Major Metabolite in Radiotherapy

P.G. Meering

Centre for Human Toxicology, State University of Utrecht, Vondellaan 14, 3521 GE Utrecht

D. Gonzalez Gonzalez

Department of Radiotherapy, University of Amsterdam, Wilhelmina Gasthuis, Eerste Helmersstraat 104, 1054 EG Amsterdam

R.A.A. Maes

Centre for Human Toxicology, State University of Utrecht, Vondellaan 14, 3521 GE Utrecht

H.A. van Peperzeel

Department of Radiotherapy, State University of Utrecht, Academic Hospital, Catharijnesingel 101, 3511 GV Utrecht, The Netherlands

1 Oral doses of misonidazole between 0.75 and 1.3 g/m2 were administered during 3-5 days per week to 21 patients with various malignancies.

2 Mean plasma levels of misonidazole and desmethylmisonidazole at the times of radiotherapy were in the range 20-50 and 2-12 mg/l respectively.

3 Slight accumulation of misonidazole and desmethylmisonidazole in plasma was observed with a dosage interval of 24 h.

4 In patients with anticonvulsant comedication plasma elimination half-lives of misonidazole of 4.1-8.9 h were found.

5 Observed side-effects were nausea and vomiting (9%), exanthema or rashes (14%) and mild peripheral neuropathy (9%).

Human & Experimental Toxicology, Vol. 4, No. 4, 425-434 (1985)
DOI: 10.1177/096032718500400409


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