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The CMF-regimen. Modulation of cyclophosphamide uptake and clearance by methotrexate and fluorouracil

โœ Scribed by Ernst A. De Bruijn; Yi Geng; Jo Hermans; Oscar Driessen


Book ID
102276828
Publisher
John Wiley and Sons
Year
1990
Tongue
French
Weight
481 KB
Volume
45
Category
Article
ISSN
0020-7136

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โœฆ Synopsis


Influence of the 2 antimetabolites used in the CMFregimen, methotrexate (MTX, M) and fluorouracil (FUra, F) on in vivo pharmacokinetics of orally administered cyclophosphamide (CY, c), were studied in WAG/Rij rats. Blood plasma concentrations of CY following oral administration were monitored in single-agent CY, in C Y + MTX (CM), in CY + FUra (CF) and in CY + MTX + FUra (CMF) treatments. Each treatment group consisted of at least 10 rats. CY was determined in 50 pl of plasma by capillary gas chromatography on the first day of chemotherapy. Statistical analysis of blood plasma concentration data revealed a significant influence of both MTX and FUra on CY inputloutput function (p : 0.01). MTX and FUra significantly increased the area under the plasma concentration time-curve, whereas t , , was significantly prolonged in CF and CMF treatment groups (p : 0.01). It is suggested that MTX and FUra interact at the site of CY pre-systemic metabolism, including first-pass metabolism, subsequently resulting in prolonged absorption.


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The CMF-regimen. Toxicity patterns follo
โœ Ernst A. De Brulin; Oscar M.J. Driessen; Jo Hermans ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 614 KB

The contribution of the agents used in the CMF regimen, i.e.. cyclophosphamide (CY), methotrexate (MTX) and fluorouracil (FUra), to the development of toxicity was determined in tumor-bearing WAClRij rats. Data from untreated (U) rats were compared with data from rats treated with single-agent thera