首页> 美国卫生研究院文献>Cancer Science >Relationship between Development of Diarrhea and the Concentration of SN‐38 an Active Metabolite of CPT‐11 in the Intestine and the Blood Plasma of Athymic Mice Following Intraperitoneal Administration of CPT‐11
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Relationship between Development of Diarrhea and the Concentration of SN‐38 an Active Metabolite of CPT‐11 in the Intestine and the Blood Plasma of Athymic Mice Following Intraperitoneal Administration of CPT‐11

机译:腹膜内给予CPT-11后腹泻的发展与肠道和CPT-11活性代谢产物SN-38的浓度之间的关系与无胸腺小鼠的血浆

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摘要

Severe diarrhea occurred during daily intraperitoneal administration of 7‐ethyl‐10‐[4‐(l‐piperidino)‐l‐piperidino]carbonyloxycamptothecin (CPT‐11) at a dose of 50 mg/kg in athymic mouse. Serial determination of CPT‐11 and 7‐ethyl‐10‐hydroxycamptothecin (SN‐38), with the use of an on‐line solid extraction HPLC system, demonstrated that much higher levels of the compounds are retained in the intestine and the blood plasma after five consecutive daily injections than after a single injection. Histologic examination of the gastrointestinal tract showed hemorrhagic colitis on day 7 and later after five consecutive daily injections of CPT‐11. The direct cause of diarrhea associated with CPT‐11 administration is considered to be enterocolitis caused by high levels of SN‐38 and/or CPT‐11 retained for a long period in the intestine.
机译:在无胸腺小鼠中,每天腹腔注射7-乙基-10- [4-(1-哌啶子基)-1-哌啶子基]羰氧基喜树碱(CPT-11)时会出现严重腹泻。使用在线固相萃取HPLC系统对CPT-11和7-乙基-10-羟基喜树碱(SN-38)进行的连续测定表明,肠道和血浆中保留了更高水平的化合物连续五次每日注射后比一次注射后。胃肠道的组织学检查在第7天以及连续5天每天注射CPT-11后发现出血性结肠炎。与CPT-11给药相关的腹泻的直接原因被认为是肠道小肠结肠炎,原因是肠道中长时间保留高水平的SN-38和/或CPT-11。

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