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
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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.
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页码:13 / 18
页数:6
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