Itoh Tatsuya, Takemoto Isao, Itagaki Shirou, Sasaki Kentaro, Hirano Takeshi, Iseki Ken
Department of Pharmacy, Sapporo Social Insurance General Hospital, Chuo-2-jo, 6-chome, Atsubetsu-ku, Sapporo, Japan.
J Pharm Pharm Sci. 2004 Jan 23;7(1):13-8.
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.
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.
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.
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.
本研究旨在探讨静脉注射喜树碱-11(CPT-11)的内酯型和羧酸盐型后,CPT-11及其代谢产物经胆汁途径排入胃肠道管腔的情况。
采用大鼠体内给药研究,考察CPT-11及其代谢产物SN-38和SN-38-葡萄糖醛酸苷的胆汁排泄情况。测定了CPT-11及其代谢产物的内酯型和羧酸盐型的胆汁排泄谱。
静脉注射CPT-11内酯型后,SN-38-葡萄糖醛酸苷的累积胆汁排泄量远大于CPT-11和SN-38,且SN-38的胆汁排泄量小于CPT-11。此外,CPT-11和SN-38主要以羧酸盐形式排泄到胆汁中。给予CPT-11羧酸盐型后,SN-38-葡萄糖醛酸苷的胆汁排泄量明显小于给予CPT-11内酯型后的排泄量。另一方面,给予CPT-11羧酸盐型后,CPT-11和SN-38的胆汁排泄量大于给予CPT-11内酯型后的排泄量。
结果表明,CPT-11及其代谢产物从内酯型转化为羧酸盐型的速率在这些化合物的胆汁排泄中起主要作用。