Bratlid D, Moe P J
Eur J Clin Pharmacol. 1978 Nov 16;14(2):143-7. doi: 10.1007/BF00607446.
The pharmacokinetics of intravenous high-dose methotrexate were studied in two groups of children being treated for malignant diseases, mostly acute lymphatic leukemia. The peak serum level of methotrexate of 2.32--10(-5) mol/1 was found in children given 500 mg methotrexate/m2 by a 24 h infusion, and another group given 2790 mg/m2 during a 6 h infusion had serum levels as high as 2.16--10(-4) mol/1. The decay of serum concentration of methotrexate after completion of the infusion followed a diphasic curve, with an initial serum half-life of 4.8 h, followed by a second half-life of 34.4 h at distribution equilibrium. The apparent volume of distribution was 56.8 litres/m2. Significant levels of methotrexate were found in cerebrospinal fluid, but penetration into cerebrospinal fluid was slow. Urinary excretion of methotrexate was considerable. Four to five days after commencement of the infusion, urinary concentrations of methotrexate still exceeded the serum levels.
对两组患有恶性疾病(主要是急性淋巴细胞白血病)的儿童进行了静脉注射大剂量甲氨蝶呤的药代动力学研究。通过24小时输注给予500mg甲氨蝶呤/m²的儿童中,甲氨蝶呤的血清峰值水平为2.32×10⁻⁵mol/L,而另一组在6小时输注期间给予2790mg/m²的儿童血清水平高达2.16×10⁻⁴mol/L。输注结束后甲氨蝶呤血清浓度的衰减呈双相曲线,初始血清半衰期为4.8小时,随后在分布平衡时第二个半衰期为34.4小时。表观分布容积为56.8升/m²。脑脊液中发现了显著水平的甲氨蝶呤,但进入脑脊液的速度较慢。甲氨蝶呤的尿排泄量相当可观。输注开始后四至五天,尿中甲氨蝶呤浓度仍超过血清水平。