Biliary excretion of irinotecan and its metabolites.

被引:0
作者
Itoh, T
Takemoto, I
Itagaki, S
Sasaki, K
Hirano, T
Iseki, K
机构
[1] Sapporo Social Insurance Gen Hosp, Dept Pharm, Sapporo, Hokkaido, Japan
[2] Hokkaido Univ, Dept Clin Pharmaceut & Therapeut, Grad Sch Pharmaceut Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
来源
JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES | 2004年 / 7卷 / 01期
关键词
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
PURPOSE: The aim of this study was to investigate the excretion of irinotecan hydrochloride (CPT-11) and its metabolites into the gastrointestinal lumen via the biliary route after intravenous administration of lactone and carboxylate forms of CPT-11. METHODS: Biliary excretions of CPT-11 and its metabolites, SN-38 and SN-38-glucuronide, were investigated by an in vivo administration study using rats. The biliary excretion profiles for both the lactone and carboxylate forms of CPT-11 and its metabolites were determined. RESULTS: After the i.v. injection of the lactone form of CPT-11, the cumulative biliary excretion of SN-38-glucuronide was much greater than that of CPT-11 and SN-38, and biliary excretion of SN-38 was less than that of CPT-11. Further, CPT-11 and SN-38 were mainly excreted into bile as carboxylate forms. After the administration of the CPT-11 carboxylate form, biliary excretion of SN-38-glucuronide was significantly smaller than that after the administration of CPT-11 lactone form. On the other hand, biliary excretion of CPT-11 and SN-38 was greater after dosing with the CPT-11 carboxylate form than that after the CPT-11 lactone form. CONCLUSIONS: The results suggest that the rate of conversion of lactone to carboxylate forms of CPT-11 and its metabolites plays a major role in the biliary excretion of these compounds.
引用
收藏
页码:13 / 18
页数:6
相关论文
共 50 条
  • [31] BILIARY-EXCRETION OF DOXORUBICIN (ADRIAMYCIN) AND ITS METABOLITES IN A PATIENT WITH SEVERE HEPATOBILIARY DISEASE
    RIGGS, CE
    CHANG, P
    BACHUR, NR
    CLINICAL RESEARCH, 1982, 30 (02): : A635 - A635
  • [32] BILIARY-EXCRETION OF [C-14]-LABELED TEMAZEPAM AND ITS METABOLITES IN THE RAT
    TSE, FLS
    BALLARD, F
    JAFFE, JM
    JOURNAL OF PHARMACEUTICAL SCIENCES, 1983, 72 (03) : 311 - 312
  • [33] Effect of several compounds on biliary excretion of paclitaxel and its metabolites in guinea-pigs
    Bun, SS
    Giacometti, S
    Fanciullino, R
    Ciccolini, J
    Bun, H
    Aubert, C
    ANTI-CANCER DRUGS, 2005, 16 (06) : 675 - 682
  • [34] SEX DIFFERENCE IN THE BILIARY-EXCRETION OF DIGOXIN AND ITS METABOLITES IN AGING WISTAR RATS
    KITANI, K
    OHTA, M
    KANAI, S
    SATO, Y
    ARCHIVES OF GERONTOLOGY AND GERIATRICS, 1985, 4 (01) : 1 - 12
  • [35] BILIARY-EXCRETION OF DIAZEPAM AND ITS METABOLITES IN MAN AFTER REPEATED ORAL DOSES
    SELLMAN, R
    HURME, M
    KANTO, J
    EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1977, 12 (03) : 209 - 212
  • [36] BILIARY-EXCRETION OF DIGITOXIN AND ITS METABOLITES IN YOUNG AND OLD MALE WISTAR RATS
    KITANI, K
    KANAI, S
    SATO, Y
    NOKUBO, M
    EXPERIMENTAL GERONTOLOGY, 1982, 17 (06) : 407 - 416
  • [37] IMPAIRED BILIARY-EXCRETION OF DIGITOXIN AND ITS METABOLITES AFTER TREATMENT WITH POLYCHLORINATED BIPHENYLS
    SCHMOLDT, A
    BENTHE, HF
    HABERLAND, G
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 1979, 47 (03) : 483 - 491
  • [38] EFFECT OF MODERATE HEPATIC IMPAIRMENT ON THE PHARMACOKINETICS OF AFICAMTEN AND ITS METABOLITES.
    Xu, D.
    Divanji, P.
    Kim, E.
    Li, J.
    Benattia, Y.
    Griffith, A.
    Kupfer, S.
    German, P.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2024, 115 : S8 - S9
  • [39] Development of a population pharmacokinetic model for Genasense™ and its active metabolites.
    Gupta, M
    Julian, TN
    Barrett, JS
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2006, 79 (02) : P54 - P54
  • [40] Ion chromatography for the analysis of glyphosate and its selected metabolites. A review
    Michalski, Rajmund
    Pecyna-Utylska, Paulina
    JOURNAL OF SEPARATION SCIENCE, 2023, 46 (12)