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Metabolism of Irlnotecan to SN-38 in a Tissue-Isolated Tumor Model

机译:在组织分离的肿瘤模型中,伊尔替康对SN-38的代谢

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摘要

The objective of this study is to investigate the metabolism of the antitumor drug, irinotecan (CPT-11), to its active metabolite, SN-38, in tumor tissue. Using Walker 256 carcinoma, we prepared a tissue-isolated tumor model: tumor preparation was continuously perfused with Krebs-Henseleit bicarbonate buffer containing 4% bovine serum albumin (BSA) and CPT-11 (10 /Jg/ml), and the concentration of SN-38 in the perfusate was monitored using HPLC. The concentration of SN-38 in the perfusate was gradually increased to a level of 9.69ng/ml 60min after the start of perfusion. As a control, an aliquot of the perfusate was separately incubated; however, no significant increase in SN-38 levels was observed. At the end of the perfusion, a part of the tumor tissue was homogenized and the level of SN-38 was determined; the levels in tumor tissue were 2.2-4.5 times higher than in the perfusate. From above results, CPT-11 was found to be metabolized to its active metabolite, SN-38, in tumor tissue- a desirable feature of an antitumor prodrug.
机译:这项研究的目的是研究抗肿瘤药伊立替康(CPT-11)在肿瘤组织中向其活性代谢产物SN-38的代谢。使用Walker 256癌,我们制备了一个组织分离的肿瘤模型:用含4%牛血清白蛋白(BSA)和CPT-11(10 / Jg / ml)的Krebs-Henseleit碳酸氢盐缓冲液连续灌注肿瘤制备物,使用HPLC监测灌流液中的SN-38。灌注开始后60min,灌注液中SN-38的浓度逐渐增加至9.69ng / ml。作为对照,将等分的灌注液分别孵育;然而,没有观察到SN-38水平的显着增加。灌注结束时,将一部分肿瘤组织匀浆并确定SN-38的水平。肿瘤组织中的水平是灌注液中的2.2-4.5倍。从以上结果中,发现CPT-11在肿瘤组织中被代谢成其活性代谢产物SN-38,这是抗肿瘤前药的理想特征。

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