Distribution of the novel antifolate pemetrexed to the brain

被引:29
作者
Dai, HQ [1 ]
Chen, Y [1 ]
Elmquist, WF [1 ]
机构
[1] Univ Minnesota, Dept Pharmaceut, Minneapolis, MN 55455 USA
关键词
D O I
10.1124/jpet.105.090043
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 concentrationtime 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.
引用
收藏
页码:222 / 229
页数:8
相关论文
共 59 条
[1]   Pemetrexed: A multitargeted antifolate agent with promising activity in solid tumors [J].
Adjei, AA .
ANNALS OF ONCOLOGY, 2000, 11 (10) :1335-1341
[2]  
ALLEN JC, 1980, CANCER TREAT REP, V64, P1261
[3]  
Banerjee D, 1995, ACTA BIOCHIM POL, V42, P457
[4]   The blood-brain barrier and oncology: new insights into function and modulation [J].
Bart, J ;
Groen, HJM ;
Hendrikse, NH ;
van der Graaf, WTA ;
Vaalburg, W ;
de Vries, EGE .
CANCER TREATMENT REVIEWS, 2000, 26 (06) :449-462
[5]   Interaction of ochratoxin A with human intestinal Caco-2 cells: possible implication of a multidrug resistance-associated protein (MRP2) [J].
Berger, V ;
Gabriel, AF ;
Sergent, T ;
Trouet, A ;
Larondelle, Y ;
Schneider, YJ .
TOXICOLOGY LETTERS, 2003, 140 :465-476
[6]   ODE TO METHOTREXATE [J].
BERTINO, JR .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (01) :5-14
[7]   Accumulation of methotrexate in systemic tissues after intrathecal administration [J].
Bleyer, WA ;
Nelson, JA ;
Kamen, BA .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1997, 19 (06) :530-532
[8]  
BLEYER WA, 1978, CANCER, V41, P2431, DOI 10.1002/1097-0142(197806)41:6<2431::AID-CNCR2820410650>3.0.CO
[9]  
2-3
[10]   Blood-brain barrier transport and brain distribution of morphine-6-glucuronide in relation to the antinociceptive effect in rats-pharmacokinetic/pharmacodynamic modelling [J].
Bouw, MR ;
Xie, RJ ;
Tunblad, K ;
Hammarlund-Udenaes, M .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 134 (08) :1796-1804