KINETICS OF MERCAPTOPURINE AND THIOGUANINE NUCLEOTIDES IN RENAL-TRANSPLANT RECIPIENTS DURING AZATHIOPRINE TREATMENT

被引:29
作者
BERGAN, S
RUGSTAD, HE
BENTDAL, O
ENDRESEN, L
STOKKE, O
机构
[1] UNIV OSLO,RIKSHOSP,NATL HOSP,DEPT CLIN PHARMACOL,OSLO,NORWAY
[2] UNIV OSLO,RIKSHOSP,NATL HOSP,DEPT SURG,OSLO,NORWAY
关键词
AZATHIOPRINE; 6-MERCAPTOPURINE; 6-THIOGUANINE NUCLEOTIDES; PHARMACOKINETICS; RENAL TRANSPLANTATION;
D O I
10.1097/00007691-199402000-00002
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The purpose of this study was to examine the pharmacokinetics of mercaptopurine (6-MP) and thioguanine nucleotides (6-TGN) during azathioprine treatment. Plasma profiles and urinary excretion of 6-MP and 6-TGN concentrations in red blood cells (RBCs) were measured repeatedly during the first 3 weeks following transplantation in 10 adults, who had received kidney grafts from living related donors. Mean maximal 6-MP plasma concentration (C-max) was 340 nmol/L (SD = 290), mean time to C-max (T-max) was 2 h (SD = 1.8), and mean area under the plasma concentration-time curve (AUC) was 930 nmol/L/h (SD = 770). The mean fraction of azathioprine dose excreted as 6-MP in urine was 1.32% (SD = 1.11). Up to eightfold variability of C-max and AUC was observed from day to day within each patient. The correlation between 6-MP AUC and amount excreted in the urine was weak (r = 0.37, 95% CI from 0.02 to 0.64). In this group of patients the observed 6-TGN levels in RBCs were low; maxima during the observation period ranged from undetectable to 250 pmol/8 x 10(8) RBCs. In individual patients, 6-TGN levels were relatively stable throughout the dosing interval (''within-dose-interval-CV'' <19%), even when sharp and high 6-MP peaks in plasma were observed.
引用
收藏
页码:13 / 20
页数:8
相关论文
共 23 条
[1]  
ALTMAN DG, 1989, STATISTICS CONFIDENC, P34
[3]   AZATHIOPRINE METABOLISM - PHARMACOKINETICS OF 6-MERCAPTOPURINE, 6-THIOURIC ACID AND 6-THIOGUANINE NUCLEOTIDES IN RENAL-TRANSPLANT PATIENTS [J].
CHAN, GLC ;
ERDMANN, GR ;
GRUBER, SA ;
MATAS, AJ ;
CANAFAX, DM .
JOURNAL OF CLINICAL PHARMACOLOGY, 1990, 30 (04) :358-363
[4]  
CHAN GLC, 1987, PHARMACOTHERAPY, V7, P165
[5]  
ELION GB, 1961, CANCER CHEMOTH REP, P93
[6]   SIGNIFICANCE OF AZATHIOPRINE METABOLITES [J].
ELION, GB .
PROCEEDINGS OF THE ROYAL SOCIETY OF MEDICINE-LONDON, 1972, 65 (03) :257-+
[7]   PHARMACOKINETICS OF ORAL 6-MERCAPTOPURINE - RELATIONSHIP BETWEEN PLASMA-LEVELS AND URINE EXCRETION OF PARENT DRUG [J].
ENDRESEN, L ;
LIE, SO ;
STORMMATHISEN, I ;
RUGSTAD, HE ;
STOKKE, O .
THERAPEUTIC DRUG MONITORING, 1990, 12 (03) :227-234
[8]   6-MERCAPTOPURINE PLASMA-LEVELS IN CHILDREN WITH ACUTE LYMPHOBLASTIC-LEUKEMIA - RELATION TO RELAPSE RISK AND MYELOTOXICITY [J].
HAYDER, S ;
LAFOLIE, P ;
BJORK, O ;
PETERSON, C .
THERAPEUTIC DRUG MONITORING, 1989, 11 (06) :617-622
[9]   6-MERCAPTOPURINE - APPARENT LACK OF RELATION BETWEEN PRESCRIBED DOSE AND BIOLOGICAL EFFECT IN CHILDREN WITH LEUKEMIA [J].
HERBER, S ;
LENNARD, L ;
LILLEYMAN, JS ;
MADDOCKS, J .
BRITISH JOURNAL OF CANCER, 1982, 46 (01) :138-141
[10]   DETERMINATION OF 6-MERCAPTOPURINE IN ACUTE LYMPHOBLASTIC-LEUKEMIA PATIENTS PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
KATO, Y ;
MATSUSHITA, T ;
YOKOYAMA, T ;
MOHRI, K .
THERAPEUTIC DRUG MONITORING, 1991, 13 (03) :220-225