期刊
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
卷 112, 期 -, 页码 152-158出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejps.2017.11.021
关键词
Capecitabine; 5'-Deoxy-5-fluorocytidine; 5'-Deoxy-5-fluorouridine; 5-Fluorouracil; Chronomodulated chemotherapy; Chronopharmacokinetics
资金
- Ministry of Education, Culture, Sports, Science, and Technology of Japan [15K18937]
- Grants-in-Aid for Scientific Research [15K18937] Funding Source: KAKEN
Capecitabine, an orally available prodrug of 5-fluorouracil, is widely used to treat patients with colorectal cancer. Although various studies have shown circadian variations in plasma 5-fluorouracil concentrations during long-term infusion, it is still unknown whether circadian variations also exist following administration of capecitabine. The present study aimed to investigate whether the pharmacokinetics of capecitabine and its metabolites, including 5-fluorouracil, vary according to administration time in rats. Rats were orally administered capecitabine (180 mg/kg) at 07: 00 (23 h after light onset, HALO), 13: 00 (5 HALO), or 19: 00 h (11 HALO). Plasma concentrations of capecitabine and its metabolites, such as 5'-deoxy-5-fluorocytidine (5'-DFCR), 5'-deoxy-5-fluorouridine (5'-DFUR), and 5-fluorouracil, were determined after capecitabine administration. The results showed that the t(1/2) and AUC(0-infinity) values of 5-fluorouracil differed as a function of the dosing time of capecitabine. The maximum and minimum mean t(1/2) values of 5-fluorouracil were obtained when the drug was administered at 07: 00 h (23 HALO: 3.1 +/- 1.2 h) and 13: 00 h (5 HALO: 1.5 +/- 0.6 h), respectively. The AUC(0-infinity) value of 5-fluorouracil at 07: 00 h (23 HALO: 533.9 +/- 195.7 mu mol.h/L) was 1.8-fold higher than the value at 13: 00 h (5 HALO: 302.5 +/- 157.1 mu mol.h/L). The clearance of 5-fluorouracil followed a cosine circadian curve, and the simulated population mean clearance was highest at rest times and lowest during active times in rats. The results for the plasma 5'-DFCR and 5'-DFUR levels indicated that circadian variations in the sequential metabolism of capecitabine to 5-fluorouracil would also affect plasma 5-fluorouracil levels following capecitabine administration. In conclusion, the pharmacokinetics of capecitabine and its metabolites, including 5-fluorouracil, varied according to time of dosing, suggesting that the capecitabine administration time is an important factor in achieving sufficient efficacy and reducing toxicity in patients.
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