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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
|
pubmed:dateCreated |
1984-11-16
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pubmed:abstractText |
Ro 03-8799, a lipophilic nitroimidazole with a basic side chain, has now been administered intravenously to 69 patients. The elimination half-life in plasma was 5.1 hr and the plasma concentration at 30 min was 14.8 micrograms/ml standardized to a dose of 1 g per square meter of surface area. Immediate symptoms of malaise, heat, sweating and disorientation limit the amount of the drug which may be given on any one occasion. However, a dose of 750 mg per square meter of surface area may be given combined with daily radiotherapy. Our data suggest that when given with a 20 fraction course of radiotherapy, sensitization of hypoxic cells may be achieved equal to a 10-fold increase in the dose of misonidazole above that presently permitted.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0360-3016
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
10
|
pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1759-63
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6480459-Drug Evaluation,
pubmed-meshheading:6480459-Female,
pubmed-meshheading:6480459-Humans,
pubmed-meshheading:6480459-Male,
pubmed-meshheading:6480459-Neoplasms,
pubmed-meshheading:6480459-Nitroimidazoles,
pubmed-meshheading:6480459-Radiation-Sensitizing Agents,
pubmed-meshheading:6480459-Time Factors,
pubmed-meshheading:6480459-Tissue Distribution
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pubmed:year |
1984
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pubmed:articleTitle |
The clinical testing of Ro 03-8799--pharmacokinetics, toxicology, tissue and tumor concentrations.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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