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癌症患者口服和静脉注射5-氟尿嘧啶后的血浆水平。

Plasma levels of 5-fluorouracil after oral and intravenous administration in cancer patients.

作者信息

Finch R E, Bending M R, Lant A F

出版信息

Br J Clin Pharmacol. 1979 Jun;7(6):613-7. doi: 10.1111/j.1365-2125.1979.tb04651.x.

Abstract
  1. Plasma levels of 5-fluorouracil (5FU) have been determined in eleven cancer patients after 0.5 g and 1.0 g intravenous doses, and in one patient after paired 1.0 g oral and intravenous doses. 2. The plasma half-life after the 0.5 g intravenous dose was relatively constant, irrespective of the stage and spread of the disease. 3. Plasma kinetics of the drug were dose dependent. Doubling of the intravenous dose produced a 1.5-fold increase in plasma half life, a two-fold increase in initial plasma drug concentration, and a three-fold increase in area under the concentration/time curve. 4. In one patient receiving paired 1.0 g intravenous and oral doses nine weeks apart, an increase in the bioavailability of the drug coincided with a marked clinical regression in palpable intra-abdominal metastases. 5. The significance of measuring plasma drug kinetics and their relationship to drug efficacy and toxicity are discussed.
摘要
  1. 已测定11例癌症患者静脉注射0.5g和1.0g剂量的5-氟尿嘧啶(5FU)后的血浆浓度,并测定1例患者口服和静脉注射1.0g配对剂量后的血浆浓度。2. 0.5g静脉注射剂量后的血浆半衰期相对恒定,与疾病的阶段和扩散无关。3. 该药物的血浆动力学呈剂量依赖性。静脉注射剂量加倍使血浆半衰期增加1.5倍,初始血浆药物浓度增加两倍,浓度/时间曲线下面积增加三倍。4. 1例患者在相隔9周接受1.0g静脉注射和口服配对剂量后,药物生物利用度增加,同时可触及的腹腔内转移灶出现明显临床消退。5. 讨论了测量血浆药物动力学的意义及其与药物疗效和毒性的关系。

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