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Vol. 30, Issue 11, 1221-1229, November 2002
Groupe de Résonance Magnétique Nucléaire
Biomédicale, Unité Mixte Recherche Centre National de la
Recherche Scientifique 5623, Université Paul Sabatier, Toulouse,
France
Capecitabine (Xeloda; CAP) is a recently developed oral
antineoplastic prodrug of 5-fluorouracil (5-FU) with enhanced tumor selectivity. Previous studies have shown that CAP activation follows a
pathway with three enzymatic steps and two intermediary metabolites, 5'-deoxy-5-fluorocytidine (5'-DFCR) and 5'-deoxy-5-fluorouridine (5'-DFUR), to form 5-FU preferentially in tumor tissues. In the present
work, we investigated all fluorinated compounds present in liver, bile,
and perfusate medium of isolated perfused rat liver (IPRL) and in
liver, plasma, kidneys, bile, and urine of healthy rats. Moreover, data
obtained from rat urine were compared with those from mice and human
urine. According to a low cytidine deaminase (3.5.4.5) activity in
rats, 5'-DFCR was by far the main product in perfusate medium from IPRL
and plasma and urine from rats. Liver and circulating 5'-DFCR in
perfusate and plasma equilibrated at the same concentration value in
the range 25 to 400 µM, which supports the involvement of
es-type nucleoside transporter in the liver. 5'-DFUR and
-fluoro-
-ureidopropionic acid (FUPA) +
-fluoro-
-alanine
(FBAL) were the main products in urine of mice, making up 23 to 30% of
the administered dose versus 3 to 4% in rat. In human urine, FUPA + FBAL represented 50% of the administered dose, 5'-DFCR 10%, and
5'-DFUR 7%. Since fluorine-19 nuclear magnetic resonance spectroscopy
gives an overview of all the fluorinated compounds present in a sample,
we observed the following unreported metabolites of CAP: 1)
5-fluorocytosine and its hydroxylated metabolite,
5-fluoro-6-hydroxycytosine, 2) fluoride ion, 3)
2-fluoro-3-hydroxypropionic acid and fluoroacetate, and 4) a
glucuroconjugate of 5'-DFCR.
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