de Bruijn E A, Driessen O, Leeflang P, van Strijen E, van den Bosch N, Hermans J
Department of Pharmacology, University of Leiden, The Netherlands.
Cancer Treat Rep. 1987 Dec;71(12):1267-9.
The interaction of methotrexate and/or cyclophosphamide with the pharmacokinetics of 5-fluorouracil (5-FU) was studied in tumor-bearing WAG/Rij rats. Four groups were formed including treatment with single-agent 5-FU (eight rats); 5-FU plus methotrexate (11 rats); 5-FU plus cyclophosphamide (12 rats); and 5-FU, cyclophosphamide, and methotrexate (13 rats). The area-under-the-plasma-concentration/time curve, total-body clearance, elimination half-life, mean residence time, and steady-state volume of distribution were computed and compared. The mean residence time and elimination half-life of 5-FU increased when methotrexate was included in the combination. The increase was significant (P less than 0.05) for 5-FU, cyclophosphamide, and methotrexate versus 5-FU and cyclophosphamide.
在荷瘤WAG/Rij大鼠中研究了甲氨蝶呤和/或环磷酰胺与5-氟尿嘧啶(5-FU)药代动力学的相互作用。将大鼠分为四组,包括单药5-FU治疗组(8只大鼠);5-FU加甲氨蝶呤组(11只大鼠);5-FU加环磷酰胺组(12只大鼠);以及5-FU、环磷酰胺和甲氨蝶呤组(13只大鼠)。计算并比较了血浆浓度/时间曲线下面积、全身清除率、消除半衰期、平均驻留时间和稳态分布容积。当联合使用甲氨蝶呤时,5-FU的平均驻留时间和消除半衰期增加。与5-FU和环磷酰胺相比,5-FU、环磷酰胺和甲氨蝶呤联合使用时的增加具有显著性(P小于0.05)。