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The pharmacokinetics of 5-fluorouracil administered by arterial infusion in advanced colorectal hepatic metastases.

机译:5-氟尿嘧啶通过动脉输注在晚期大肠肝转移中的药代动力学。

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摘要

The pharmacokinetics of 5-fluorouracil (5FU) following its administration via the hepatic artery in conjunction with biodegradable albumin microspheres and angiotensin II have been studied. Peripheral venous concentrations of 5FU are lower and plasma clearance values higher following intrahepatic arterial administration compared with a similar dose administered by intravenous infusion over both 2 h and 24 h. For the 2 h drug infusions, plasma 5FU concentrations following co-treatment with angiotensin II and microspheres via the hepatic artery were intermediate between those of arterial and venous infusions of 5FU alone. There was a trend towards the peak plasma drug concentrations and the area under the plasma concentration-time curve (AUC) being significantly lower following co-treatment with angiotensin II and microspheres compared with intra-arterial and intravenous infusions of 5FU over 24 h. Co-administration of 5FU, angiotensin II and microspheres via the hepatic artery may reduce drug exposure in the systemic compartment and therefore may increase the therapeutic ratio of 5FU administration via the hepatic artery.
机译:已经研究了5-氟尿嘧啶(5FU)通过肝动脉与可生物降解的白蛋白微球和血管紧张素II联合给药后的药代动力学。与2小时和24小时静脉内输注的相似剂量相比,肝内动脉给药后5FU的外周静脉浓度较低,血浆清除率值较高。对于2小时的药物输注,与血管紧张素II和微球经肝动脉共同治疗后的血浆5FU浓度介于单独的5FU的动脉和静脉输注之间。与24小时内动脉内和静脉内输注5FU相比,与血管紧张素II和微球共同治疗后,血浆药物浓度达到峰值,血浆浓度-时间曲线下面积(AUC)明显降低。经由肝动脉共同给药5FU,血管紧张素II和微球可减少全身腔室中的药物暴露,因此可增加经由肝动脉给药5FU的治疗率。

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