Dai Haiqing, Chen Ying, Elmquist William F
Department of Pharmaceutics, University of Minnesota, Minneapolis MN 55455, USA.
J Pharmacol Exp Ther. 2005 Oct;315(1):222-9. doi: 10.1124/jpet.105.090043. Epub 2005 Jun 29.
Pemetrexed disodium is a novel antifolate that exhibits potent inhibitory effects on multiple enzymes in folate metabolism. Phase II/III clinical trials have shown that pemetrexed is effective against various solid tumors. Like methotrexate, pemetrexed may be useful in treatment of primary and secondary brain tumors. In this study, we examined the central nervous system (CNS) distribution of pemetrexed and the interaction with an organic anion transport inhibitor indomethacin. Male Wistar rats were administered pemetrexed by either single intravenous bolus or constant intravenous infusion. Unbound pemetrexed in blood and brain was measured by simultaneous arterial blood and frontal cortex microdialysis sampling. In the i.v. bolus experiments, indomethacin was administered by i.v. bolus (10 mg/kg) followed by i.v. infusion (0.1 mg/kg/h) in a crossover manner. In the infusion experiments, the same dose of indomethacin was administered after a steady state was reached for pemetrexed. CNS distributional kinetics was analyzed by compartmental and noncompartmental methods. Both bolus and infusion studies showed that pemetrexed has a limited CNS distribution. The mean area under concentration-time curve (AUC)(brain)/AUC(plasma) ratio of unbound pemetrexed was 0.078 +/- 0.038 in the i.v. bolus study. The pemetrexed steady-state brain-to-plasma unbound concentration ratio after i.v. infusion was 0.106 +/- 0.054. The distributional clearance into the brain was approximately 10% of the clearance out of the brain in both the compartmental and noncompartmental analyses. Indomethacin had no effect on either the brain-to-plasma AUC ratio or the steady-state brain-to-plasma concentration ratio. The distribution of pemetrexed into the brain is limited, and an efflux clearance process, such as an efflux transporter, may be involved.
培美曲塞二钠是一种新型抗叶酸药物,对叶酸代谢中的多种酶具有强大的抑制作用。II/III期临床试验表明,培美曲塞对多种实体瘤有效。与甲氨蝶呤一样,培美曲塞可能对原发性和继发性脑肿瘤的治疗有用。在本研究中,我们检测了培美曲塞在中枢神经系统(CNS)的分布以及与有机阴离子转运抑制剂吲哚美辛的相互作用。雄性Wistar大鼠通过单次静脉推注或持续静脉输注给予培美曲塞。通过同时采集动脉血和额叶皮质微透析样本测定血液和脑中未结合的培美曲塞。在静脉推注实验中,吲哚美辛以交叉方式先静脉推注(10mg/kg),然后静脉输注(0.1mg/kg/h)。在输注实验中,在培美曲塞达到稳态后给予相同剂量的吲哚美辛。通过房室和非房室方法分析CNS分布动力学。推注和输注研究均表明培美曲塞在CNS中的分布有限。在静脉推注研究中,未结合培美曲塞的浓度-时间曲线下平均面积(AUC)(脑)/AUC(血浆)比值为0.078±0.038。静脉输注后培美曲塞的稳态脑-血浆未结合浓度比值为0.106±0.054。在房室和非房室分析中,进入脑内的分布清除率约为从脑内清除率的10%。吲哚美辛对脑-血浆AUC比值或稳态脑-血浆浓度比值均无影响。培美曲塞进入脑内的分布有限,可能涉及一种外排清除过程,如外排转运体。