Kase S, Kubota T, Watanabe M, Furukawa T, Tanino H, Kuo T H, Saikawa Y, Teramoto T, Kitajima M
Department of Surgery, School of Medicine, Keio University, Tokyo, Japan.
Anticancer Res. 1995 Jan-Feb;15(1):153-5.
We investigated the modulating effect of recombinant human interferon alpha-2a (IFN-alpha) on the antitumor activity of 5-fluorouracil (5-FU) against a human colon carcinoma xenograft (Co-4) in nude mice with reference to changes in the pharmacokinetic pattern of 5-FU. Mice bearing Co-4 received 5-FU ip at a dose of 90 mg/kg once with or without IFN-alpha, which was administered sc at a dose of 60.000 IU/mouse daily for 7 days before 5-FU treatment. When the area under the curve (AUC) and peak plasma concentration (Cmax) of 5-FU with or without IFN-alpha were measured as pharmacokinetic parameters, the pharmacokinetics of 5-FU was not changed by IFN-alpha administration. This result suggests that the modulating effect of IFN-alpha on 5-FU does not involve augmentation of 5-FU pharmacokinetic parameters.
我们参照5-氟尿嘧啶(5-FU)药代动力学模式的变化,研究了重组人α-2a干扰素(IFN-α)对5-氟尿嘧啶(5-FU)抗人结肠癌裸鼠移植瘤(Co-4)抗肿瘤活性的调节作用。携带Co-4移植瘤的小鼠接受一次腹腔注射剂量为90 mg/kg的5-FU,注射时伴有或不伴有IFN-α,IFN-α在5-FU治疗前7天每天以60000 IU/小鼠的剂量皮下注射。当将伴有或不伴有IFN-α的5-FU的曲线下面积(AUC)和血浆峰浓度(Cmax)作为药代动力学参数进行测量时,给予IFN-α后5-FU的药代动力学未发生改变。该结果表明,IFN-α对5-FU的调节作用不涉及5-FU药代动力学参数的增加。