Ahern M, Booth J, Loxton A, McCarthy P, Meffin P, Kevat S
Department of Medicine, Flinders University of South Australia.
J Rheumatol. 1988 Sep;15(9):1356-60.
Pharmacokinetic drug interaction between methotrexate (MTX) and nonsteroidal anti-inflammatory drugs (NSAID) has been implicated in several case reports of MTX related toxicity. We therefore studied the kinetics of low dose (15 mg) oral MTX with and without concomitant NSAID therapy after preliminary determination of the systemic bioavailability of commercial tablets. Fourteen patients with rheumatoid arthritis, age range 44-77 years, participated in paired kinetic studies performed 1-4 weeks apart. The Abbott TDx fluorescence polarization immunoassay was used to measure serum levels and urinary excretion of MTX over 72 h after a single dose. The mean systemic bioavailability was 73% for the 15 mg oral dose. Area under the serum concentration versus time curve for a 50 mg oral dose was 1.1-2.7 times that of the 15 mg oral dose indicating dose dependent absorption. Mean kinetic variables after oral MTX did not differ significantly with and without NSAID therapy despite apparent interactions in individual patients. Renal clearance of MTX correlated with creatinine clearance (r = 0.8, p less than 0.01).
甲氨蝶呤(MTX)与非甾体抗炎药(NSAID)之间的药代动力学药物相互作用在几例MTX相关毒性的病例报告中有所涉及。因此,在初步测定市售片剂的全身生物利用度后,我们研究了低剂量(15毫克)口服MTX在有和没有NSAID伴随治疗情况下的动力学。14名年龄在44至77岁之间的类风湿性关节炎患者参与了相隔1至4周进行的配对动力学研究。使用雅培TDx荧光偏振免疫分析法测量单剂量后72小时内MTX的血清水平和尿排泄量。15毫克口服剂量的平均全身生物利用度为73%。50毫克口服剂量的血清浓度-时间曲线下面积是15毫克口服剂量的1.1至2.7倍,表明吸收呈剂量依赖性。尽管个别患者存在明显相互作用,但口服MTX后平均动力学变量在有和没有NSAID治疗情况下并无显著差异。MTX的肾清除率与肌酐清除率相关(r = 0.8,p小于0.01)。