Gibb D, Barry M, Ormesher S, Nokes L, Seefried M, Giaquinto C, Back D
Institute of Child Health, University of London, UK.
Br J Clin Pharmacol. 1995 May;39(5):527-30. doi: 10.1111/j.1365-2125.1995.tb04490.x.
The pharmacokinetics of zidovudine (ZDV) and dideoxyinosine (ddI) were investigated following administration alone and in combination to children with symptomatic HIV disease. The children were studied on three separate occasions and received ZDV 200 mg m-2, ddI 100 mg m2 or a combination of ZDV 200 mg m-2 plus ddI 100 mg m-2. The administration of ddI did not significantly alter ZDV pharmacokinetics. The area under the curve (AUC) was 14.2 +/- 4.9 and 15.8 +/- 7.2 mumol l-1 h and elimination half-life (t1/2, z) was 1.4 +/- 0.4 and 1.2 +/- 0.2 h in the absence and presence of ddI respectively. The peak concentration (Cmax), time to peak (tmax) and apparent oral clearance (CL/F) were also unchanged. The administration of ZDV had no significant effect on ddI Cmax, tmax, t1/2,z, or CL/F, however the AUC was reduced by 19% (5.9 +/- 2.9 to 4.8 +/- 2.7 mumol l-1 h; P < 0.05). This study suggests that ZDV and ddI may be co-administered to children with symptomatic HIV disease without concern of a clinically relevant pharmacokinetic drug interaction.
对有症状的艾滋病患儿单独给药和联合给药后,研究了齐多夫定(ZDV)和去羟肌苷(ddI)的药代动力学。这些患儿分三次接受研究,分别给予ZDV 200 mg/m²、ddI 100 mg/m²或ZDV 200 mg/m²加ddI 100 mg/m²的联合用药。给予ddI并未显著改变ZDV的药代动力学。在不存在和存在ddI的情况下,曲线下面积(AUC)分别为14.2±4.9和15.8±7.2 μmol·l⁻¹·h,消除半衰期(t1/2,z)分别为1.4±0.4和1.2±0.2 h。峰浓度(Cmax)、达峰时间(tmax)和表观口服清除率(CL/F)也未改变。给予ZDV对ddI的Cmax、tmax、t1/2,z或CL/F没有显著影响,然而AUC降低了19%(从5.9±2.9降至4.8±2.7 μmol·l⁻¹·h;P<0.05)。该研究表明,对于有症状的艾滋病患儿,可以联合使用ZDV和ddI,而无需担心临床上有意义的药代动力学药物相互作用。