Kamel R S, al-Hakiem M H, Rademaker M, Meyrick Thomas R H, Munro D D
Department of Chemical Pathology, St Bartholomew's Hospital, London, England.
Acta Derm Venereol. 1988;68(3):267-70.
The pharmacokinetics of methotrexate was studied in 23 patients with chronic plaque psoriasis. Ten patients received a single oral does and 13 patients a single intramuscular injection of 25 mg methotrexate. Serum methotrexate was measured for 24 hours following administration of the drug using a magnetizable solid-phase radio-immunoassay. The disappearance of methotrexate from the serum fitted a two-compartment model with a distribution phase half-life of 1.18 +/- 0.12 h and an elimination phase half-life of 5.35 +/- 0.62 h following the oral dose and 1.45 +/- 0.22 h and 4.71 +/- 0.32 h, respectively following the intramuscular dose. Peak serum methotrexate concentrations varied greatly between patients but the mean area below the curve for the two routes of administration did not differ significantly. In a further 18 psoriatic patients receiving long-term maintenance methotrexate therapy there was no consistent relationship between salivary and serum methotrexate levels.
对23例慢性斑块状银屑病患者的甲氨蝶呤药代动力学进行了研究。10例患者口服单次剂量,13例患者单次肌内注射25mg甲氨蝶呤。给药后24小时内,采用可磁化固相放射免疫分析法测定血清甲氨蝶呤。口服给药后,甲氨蝶呤从血清中的消失符合二室模型,分布相半衰期为1.18±0.12小时,消除相半衰期为5.35±0.62小时;肌内注射给药后,分布相半衰期为1.45±0.22小时,消除相半衰期为4.71±0.32小时。患者之间血清甲氨蝶呤峰值浓度差异很大,但两种给药途径的曲线下平均面积无显著差异。在另外18例接受长期维持性甲氨蝶呤治疗的银屑病患者中,唾液和血清甲氨蝶呤水平之间没有一致的关系。