PMID- 23289150 OWN - NLM STAT- MEDLINE DCOM- 20131021 LR - 20131121 IS - 0513-4870 (Print) IS - 0513-4870 (Linking) VI - 47 IP - 10 DP - 2012 Oct TI - [Pharmacokinetics of S-1 capsule in patients with advanced gastric cancer]. PG - 1363-9 AB - The study is to investigate the pharmacokinetics of S-1 capsule (tegafur, gimeracil and potassium oxonate capsule) in patients with advanced gastric cancer after single and multiple oral administration. Twelve patients with advanced gastric cancer were recruited to the study. The dose of S-1 for each patient was determined according to his/her body surface area (BSA). The dose for single administration was 60 mg every subject. The dose for multiple administration for one subject was as follows: 100 mg x d(-1) or 120 mg x d(-1), 28-days consecutive oral administration. The pharmacokinetic parameters of tegafur, 5-fluorouracil, gimeracil, potassium oxonate and uracil after single oral administration were as follows: (2,207 +/- 545), (220.0 +/- 68.2), (374.9 +/- 103.0), (110.5 +/- 100.8) and (831.1 +/- 199.9) ng x mL(-1) for Cmax; (11.8 +/- 3.8), (4.4 +/- 3.3), (7.8 +/- 5.1), (3.1 +/- 0.9) and (8.8 +/- 4.1) h for t1/2, respectively. After six days oral administration, the average steady state plasma concentrations (Cav) of tegafur, 5-fluorouracil, gimeracil, potassium oxonate and uracil were (2,425 +/- 1,172), (73.88 +/- 18.88), (162.6 +/- 70.8), (36.89 +/- 29.35) and (435.3 +/- 141.0) ng x mL(-1), respectively, and the degree of fluctuation (DF) were (1.0 +/- 0.2), (2.5 +/- 0.4), (3.1 +/- 0.8), (2.4 +/- 0.8) and (1.5 +/- 0.3), respectively. The cumulative urine excretion percentage of tegafur, 5-fluorouracil, gimeracil and potassium oxonate in urine within 48 h were (4.2 +/- 2.8) %, (4.7 +/- 1.6) %, (18.5 +/- 6.0) % and (1.7 +/- 1.2) %, repectively, after single oral administration of S-1. The results exhibited that tegafur had some drug accumulation observed, and gimeracil, potassium oxonate, 5-fluorouracil and uracil had no drug accumulation observed. FAU - Liu, He-ying AU - Liu HY AD - Department of PharmaceuticalAnalysis, China Pharmaceutical University, Nanjing, China FAU - Ding, Li AU - Ding L FAU - Yu, Yong AU - Yu Y FAU - Chu, Yan AU - Chu Y FAU - Zhu, He AU - Zhu H LA - chi PT - English Abstract PT - Journal Article PL - China TA - Yao Xue Xue Bao JT - Yao xue xue bao = Acta pharmaceutica Sinica JID - 21710340R RN - 0 (Antimetabolites, Antineoplastic) RN - 0 (Capsules) RN - 0 (Drug Combinations) RN - 0 (Pyridines) RN - 150863-82-4 (S 1 (combination)) RN - 1548R74NSZ (Tegafur) RN - 4R7FFA00RX (potassium oxonate) RN - 56HH86ZVCT (Uracil) RN - 5VT6420TIG (Oxonic Acid) RN - U3P01618RT (Fluorouracil) RN - UA8SE1325T (gimeracil) SB - IM MH - Administration, Oral MH - Adult MH - Aged MH - Antimetabolites, Antineoplastic/*pharmacokinetics MH - Capsules MH - Drug Combinations MH - Female MH - Fluorouracil/blood/urine MH - Humans MH - Male MH - Middle Aged MH - Neoplasm Staging MH - Oxonic Acid/blood/*pharmacokinetics/urine MH - Pyridines/blood/urine MH - Stomach Neoplasms/blood/*metabolism/pathology/urine MH - Tegafur/blood/*pharmacokinetics/urine MH - Uracil/blood/urine EDAT- 2013/01/05 06:00 MHDA- 2013/10/22 06:00 CRDT- 2013/01/05 06:00 PHST- 2013/01/05 06:00 [entrez] PHST- 2013/01/05 06:00 [pubmed] PHST- 2013/10/22 06:00 [medline] PST - ppublish SO - Yao Xue Xue Bao. 2012 Oct;47(10):1363-9.