S. Ohlman et al., DAY-TO-DAY VARIABILITY IN AZATHIOPRINE PHARMACOKINETICS IN RENAL-TRANSPLANT RECIPIENTS, Clinical transplantation, 8(3), 1994, pp. 217-223
The intraindividual and the interindividual variability in the pharmac
okinetics of azathioprine (Aza) and its main metabolite 6-mercaptopuri
ne (6-MP) were investigated in 10 renal transplant patients on 2 conse
cutive days, after repeated oral doses of Aza. On the 1st study, the d
ose-adjusted Aza AUC (0-6 h) ranged from 8.4 to 129.1 nghml-1/mg* kg-
1, mean 41.4 (+/- 37.6) nghml-1/mg*kg-1. The corresponding values for
the dose-adjusted 6-MP AUC (0-6 h) ranged from 37.9 to 172.0 nghml-1
/mgkg-1, mean 91.7 (+/- 50.7) ngh*ml-1/mg*kg-1. The absolute percenta
ge intraindividual difference in Aza AUC (0-6 h) between the two days
ranged from 1.2% to 256.6% (mean 64.7%), and for 6-MP AUC (0-6 h) from
5.9% to 98.5% (mean 49.8%). However, no statistically significant dif
ference was found when comparing the pharmacokinetics on the 2 study d
ays. The mean half-life of Aza was 1.7 h and of 6-MP 1.2 h. Impaired r
enal function did not seem to affect the pharmacokinetics. No correlat
ion was found between the given dose of Aza and AUC (0-6 h) for Aza or
6-MP. A strong correlation was found between the concentrations of Az
a and 6-MP obtained at 2 h after the oral dose and the corresponding A
UCs (0-6 h) (Aza: r = 0.85, p < 0.001, n = 20; 6-MP: r = 0.9, p < 0.00
1, n = 20). We conclude that the intraindividual variability in Aza p
harmacokinetics is marked. but it is less pronounced than the even lar
ger interpatient variability found in this study and previously descri
bed.