Alleviation of side effects induced by irinotecan hydrochloride (CPT-11) in rats by intravenous infusion

A Kurita, S Kado, N Kaneda, M Onoue… - Cancer chemotherapy …, 2003 - Springer
Abstract Purpose Irinotecan hydrochloride (CPT-11) is a potent topoisomerase I inhibitor
and is established and used widely as an antitumor agent. However, it sometimes causes …

Modified irinotecan hydrochloride (CPT-11) administration schedule improves induction of delayed-onset diarrhea in rats

A Kurita, S Kado, N Kaneda, M Onoue… - Cancer chemotherapy …, 2000 - Springer
Purpose: Clinically, diarrhea is the major dose-limiting toxicity of irinotecan hydrochloride
(CPT-11). Using a rat model, we attempted to decrease the incidence of delayed-onset …

The modulation of irinotecan-induced diarrhoea and pharmacokinetics by three different classes of pharmacologic agents

B Chowbay, A Sharma, QY Zhou… - Oncology …, 2003 - spandidos-publications.com
Diarrhoea is the major dose-limiting toxicity of irinotecan hydrochloride (CPT-11) in the
clinical setting. This study was designed to evaluate the effects of different pharmacological …

Phase I and pharmacokInetic (PK) study of Irinotecan (CPT11) with a prolonged (14D) infusion schedule

V Herben, J Schellens, M Swart, G Gruia… - European Journal of …, 1997 - elibrary.ru
CPT11 isa a topoisomerase I inhibitor with substantial anti tumor activity. Preclinical data
suggest that prolonged exposure has better efficacy and possibly less toxicity. A dose …

Comparison of the pharmacokinetics and efficacy of irinotecan after administration by the intravenous versus intraperitoneal route in mice

S Guichard, E Chatelut, I Lochon, R Bugat… - Cancer chemotherapy …, 1998 - Springer
Abstract Irinotecan (CPT-11) is a new drug active in colorectal cancer. A comparison was
made of the efficacy and pharmacokinetics of CPT-11 after ip versus iv administration to …

Simultaneous determination of the lactone and carboxylate forms of irinotecan (CPT-11) and its active metabolite SN-38 by high-performance liquid chromatography …

X Yang, Z Hu, SY Chan, BC Goh, W Duan… - … of Chromatography B, 2005 - Elsevier
Irinotecan (CPT-11) and its main metabolite SN-38 are potent anticancer derivatives of
camptothecin (CPT), with active lactone and inactive carboxylate forms coexisting. A simple …

Excretion into gastrointestinal tract of irinotecan lactone and carboxylate forms and their pharmacodynamics in rodents

K Arimori, N Kuroki, A Kumamoto, N Tanoue… - Pharmaceutical …, 2001 - Springer
Purpose. To investigate the excretion of irinotecan hydrochloride (CPT-11) and its active
metabolite, SN-38, into the gastrointestinal lumen via the biliary and/or intestinal membrane …

Phase I and pharmacokinetic study of the camptothecin derivative irinotecan, administered on a weekly schedule in cancer patients

M De Forni, R Bugat, GG Chabot, S Culine, JM Extra… - Cancer research, 1994 - AACR
Abstract Irinotecan (CPT-11) is a novel water-soluble, semisynthetic derivative of
camptothecin, with inhibitory effects on mammalian DNA topoisomerase I, high cytotoxic …

Influence of multiple dose activated charcoal on the disposition kinetics of irinotecan in rats

C Balram, QY Zhou, YB Cheung… - Drug metabolism and drug …, 2002 - degruyter.com
Introduction: The main clinical adverse effect of irinotecan (CPT-11) therapy is diarrhoea.
Using a rat model, we attempted to study the effects of activated charcoal on the prevention …

A review of the clinical experience with irinotecan (CPT-11)

RW Horowitz, S Wadler, PH Wiernik - American Journal of …, 1997 - journals.lww.com
Abstract Irinotecan (CPT-11) is a derivative of the chemotherapeutic agent camptothecin.
CPT-11 inhibits the nuclear enzyme topoisomerase I. It has demonstrated a broad spectrum …