Sindelar W F
Ann Surg. 1985 Mar;201(3):337-43. doi: 10.1097/00000658-198503000-00014.
Isolation-perfusion of the liver was performed in ten pigs using 5-fluorouracil administered in the perfusion circuit at doses of 100, 250, 500, and 1000 mg/kg body weight. Perfusion was performed for 60 minutes at normothermic (37 C) or hyperthermic (41 C) temperatures. One animal died shortly after perfusion. Incomplete isolation of the hepatic vasculature in two animals resulted in significant drug leakage into the systemic circulation with resulting hematologic toxicity. Perfusion with 5-fluorouracil at 1000 mg/kg produced hepatic necrosis. Perfusion with 5-fluorouracil at doses of 100, 250, or 500 mg/kg produced no hepatic toxicity except for transient elevations of hepatic enzymes and resulted in no systemic drug toxicity. Levels of 5-fluorouracil tolerated by the liver in the isolation-perfusion system were more than 1000-fold greater than the maximum drug levels achievable by routine systemic, intra-arterial, or intraperitoneal administration.
对10头猪进行肝脏隔离灌注,在灌注回路中以100、250、500和1000mg/kg体重的剂量给予5-氟尿嘧啶。在常温(37℃)或高温(41℃)下进行60分钟的灌注。1只动物在灌注后不久死亡。2只动物的肝血管系统隔离不完全,导致药物大量漏入体循环,从而产生血液学毒性。1000mg/kg的5-氟尿嘧啶灌注导致肝坏死。100、250或500mg/kg剂量的5-氟尿嘧啶灌注除了导致肝酶短暂升高外,未产生肝毒性,也未导致全身药物毒性。在隔离灌注系统中,肝脏耐受的5-氟尿嘧啶水平比常规全身、动脉内或腹腔内给药所能达到的最大药物水平高1000倍以上。