Piscitelli S C, Amatea M A, Vogel S, Bechtel C, Metcalf J A, Kovacs J A
Department of Pharmacy, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, USA.
Antimicrob Agents Chemother. 1996 Jan;40(1):161-5. doi: 10.1128/AAC.40.1.161.
The effects of cytokines on the pharmacokinetics of nucleoside analogs were evaluated in two separate studies using zidovudine in combination with interleukin-2 and didanosine in combination with alpha interferon. In each study, drug interactions were evaluated by using both a standard method (Student's t test) and bioequivalence testing. Serial blood samples were collected from human immunodeficiency virus-infected patients prior to and during cytokine therapy for determination of nucleoside analog concentrations. Concentrations were fit separately to a two-compartment model by using the iterative two-stage approach to population analysis. No alterations in area under the curve or oral clearance were observed for either drug during combination therapy. In general, there was good agreement between statistical methods for determining if antiviral pharmacokinetic parameters were altered by concomitant cytokine therapy. However, large individual changes in the maximum concentration of zidovudine in serum were detected by bioequivalence testing but no difference was found by Student's t test. For didanosine, significant but clinically irrelevant decreases determined by standard hypothesis testing were seen for both the volume of the central compartment (1.91 to 1.86 liters) and the absorption rate constant (0.79 to 0.73 h-1) in the presence of alpha interferon. No interaction was noted for these parameters by using bioequivalence guidelines. Bioequivalence testing may provide an alternative approach to assessment of drug interactions. Interleukin-2 and alpha interferon do not alter the pharmacokinetics of zidovudine and didanosine, respectively.
在两项独立研究中,分别使用齐多夫定与白细胞介素-2联合以及去羟肌苷与α干扰素联合,评估了细胞因子对核苷类似物药代动力学的影响。在每项研究中,通过使用标准方法(学生t检验)和生物等效性测试来评估药物相互作用。在细胞因子治疗之前和期间,从感染人类免疫缺陷病毒的患者中采集系列血样,以测定核苷类似物浓度。通过使用群体分析的迭代两阶段方法,将浓度分别拟合到二室模型。联合治疗期间,两种药物的曲线下面积或口服清除率均未观察到改变。总体而言,在确定抗病毒药代动力学参数是否因同时进行的细胞因子治疗而改变的统计方法之间,存在良好的一致性。然而,通过生物等效性测试检测到血清中齐多夫定的最大浓度存在较大个体差异,但学生t检验未发现差异。对于去羟肌苷,在存在α干扰素的情况下,通过标准假设检验确定中央室容积(从1.91升降至1.86升)和吸收速率常数(从0.79 h⁻¹降至0.73 h⁻¹)均有显著但临床无关紧要的降低。使用生物等效性指南未发现这些参数存在相互作用。生物等效性测试可能为评估药物相互作用提供一种替代方法。白细胞介素-2和α干扰素分别不会改变齐多夫定和去羟肌苷的药代动力学。