Lokiec F, Poirier O, Gisselbrecht C, Marty M, Boiron M, Najean Y
Cancer Chemother Pharmacol. 1982;9(3):165-8. doi: 10.1007/BF00257746.
The kinetics of methotrexate were studied in a group of 59 patients after infusion of high doses. From the triexponential analysis of the serum concentration curve, rate constants and relative concentrations in non-circulating pools were calculated, using a linear 'mammillary' three-compartment model. No significant variation as a function of dose (300-6,000 mg/m2) was observed. In circumstances the rapidly exchanging pool was a reflection of the circulating pool, suggesting that it is an extravascular, protein-bound pool of methotrexate. Considerable variations of the relative concentration and rate constants of the slowly exchanging pool were observed to be a function of the duration of methotrexate infusion, the presence of other drugs, and the patient's age. If this compartment is assumed to include the target cells for methotrexate, then the large variations observed could be responsible for individual differences in toxicity and/or effectiveness.
在一组59例接受高剂量甲氨蝶呤输注的患者中研究了其动力学。通过对血清浓度曲线进行三指数分析,采用线性“乳突状”三室模型计算速率常数和非循环池中的相对浓度。未观察到随剂量(300 - 6000 mg/m²)变化的显著差异。在某些情况下,快速交换池反映了循环池,表明它是甲氨蝶呤的血管外、蛋白结合池。观察到缓慢交换池的相对浓度和速率常数存在相当大的变化,这是甲氨蝶呤输注持续时间、其他药物的存在以及患者年龄的函数。如果假定该隔室包含甲氨蝶呤的靶细胞,那么观察到的较大变化可能是毒性和/或有效性个体差异的原因。