Abstract |
It was the aim of this study to investigate whether leukemia P388 being an important murine transplantation tumor may alter the plasma concentration-time profiles of the alkylating antineoplastic agent bendamustine (1) in mice. In an advanced tumor stage the rapid decline of 1 plasma levels was found to be retarded in tumor-bearing in comparison to tumor-free animals both after i.v. and p.o. drug administration. These changes cannot be explained by the neoplasia-related depression of drug metabolism whereas the 1-containing ascitic fluid may be a possible reason for the prolonged drug levels in plasma. After p.o. administration of 1, the bioavailability of the drug was found to be increased in the leukemia-bearing animals.
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Authors | R Amlacher, H Weber, R Preiss, H Hoffmann |
Journal | Die Pharmazie
(Pharmazie)
Vol. 47
Issue 5
Pg. 378-81
(May 1992)
ISSN: 0031-7144 [Print] Germany |
PMID | 1409829
(Publication Type: Journal Article)
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Chemical References |
- Nitrogen Mustard Compounds
- Bendamustine Hydrochloride
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Topics |
- Administration, Oral
- Animals
- Bendamustine Hydrochloride
- Female
- Injections, Intravenous
- Leukemia P388
(metabolism)
- Mice
- Mice, Inbred Strains
- Nitrogen Mustard Compounds
(pharmacokinetics)
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