THE PHARMACOKINETICS OF 5-FLUOROURACIL ADMINISTERED BY ARTERIAL INFUSION IN ADVANCED COLORECTAL HEPATIC METASTASES

被引:18
作者
GOLDBERG, JA
KERR, DJ
WATSON, DG
WILLMOTT, N
BATES, CD
MCKILLOP, JH
MCARDLE, CS
机构
[1] UNIV GLASGOW,GLASGOW ROYAL INFIRM,DEPT MED,GLASGOW,SCOTLAND
[2] UNIV STRATHCLYDE,DEPT PHARM,GLASGOW G1 1XW,SCOTLAND
[3] UNIV GLASGOW,DEPT MED ONCOL,GLASGOW G12 8QQ,SCOTLAND
[4] UNIV STRATHCLYDE,DEPT PHARMACEUT CHEM,BIOMED MASS SPECTROMETRY UNIT,GLASGOW G1 1XW,SCOTLAND
关键词
D O I
10.1038/bjc.1990.204
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The pharmacokinetics of 5-fluorouracil (5FU) following its administration via the hepatic artery in conjuction 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 angiotesin 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. © The MacMillan Press Ltd., 1990.
引用
收藏
页码:913 / 915
页数:3
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