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Studies of the pharmacokinetic properties of nimorazole.
The pharmacokinetics of the hypoxic radio-sensitizer nimorazole were studied in 19 individuals after single oral doses of between 0.5-3.5 g. HPLC measurements showed, after a rapid absorption, a linear relationship between peak plasma concentration and given dose. Mean elimination half life was 3.1...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1983
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2011427/ https://www.ncbi.nlm.nih.gov/pubmed/6871077 |
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author | Overgaard, J. Overgaard, M. Timothy, A. R. |
author_facet | Overgaard, J. Overgaard, M. Timothy, A. R. |
author_sort | Overgaard, J. |
collection | PubMed |
description | The pharmacokinetics of the hypoxic radio-sensitizer nimorazole were studied in 19 individuals after single oral doses of between 0.5-3.5 g. HPLC measurements showed, after a rapid absorption, a linear relationship between peak plasma concentration and given dose. Mean elimination half life was 3.1 h. A tendency to a dose-dependent variation in the apparent volume of distribution, total body clearance and elimination half life suggest non-linear pharmacokinetics of nimorazole. Tumour concentrations measured in 5 patients gave tumour/plasma ratios between 0.8-1.3. No toxicity was observed. The results indicate that nimorazole may have potential as a clinically useful hypoxic radiosensitizer. |
format | Text |
id | pubmed-2011427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1983 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20114272009-09-10 Studies of the pharmacokinetic properties of nimorazole. Overgaard, J. Overgaard, M. Timothy, A. R. Br J Cancer Research Article The pharmacokinetics of the hypoxic radio-sensitizer nimorazole were studied in 19 individuals after single oral doses of between 0.5-3.5 g. HPLC measurements showed, after a rapid absorption, a linear relationship between peak plasma concentration and given dose. Mean elimination half life was 3.1 h. A tendency to a dose-dependent variation in the apparent volume of distribution, total body clearance and elimination half life suggest non-linear pharmacokinetics of nimorazole. Tumour concentrations measured in 5 patients gave tumour/plasma ratios between 0.8-1.3. No toxicity was observed. The results indicate that nimorazole may have potential as a clinically useful hypoxic radiosensitizer. Nature Publishing Group 1983-07 /pmc/articles/PMC2011427/ /pubmed/6871077 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Overgaard, J. Overgaard, M. Timothy, A. R. Studies of the pharmacokinetic properties of nimorazole. |
title | Studies of the pharmacokinetic properties of nimorazole. |
title_full | Studies of the pharmacokinetic properties of nimorazole. |
title_fullStr | Studies of the pharmacokinetic properties of nimorazole. |
title_full_unstemmed | Studies of the pharmacokinetic properties of nimorazole. |
title_short | Studies of the pharmacokinetic properties of nimorazole. |
title_sort | studies of the pharmacokinetic properties of nimorazole. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2011427/ https://www.ncbi.nlm.nih.gov/pubmed/6871077 |
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