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首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Population pharmacokinetic study of delayed methotrexate excretion in children with acute lymphoblastic leukemia
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Population pharmacokinetic study of delayed methotrexate excretion in children with acute lymphoblastic leukemia

机译:急性淋巴细胞白血病儿童延迟甲氨蝶呤排泄的人口药代动力学研究

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Objective: To investigate the population pharmacokinetics of delayed methotrexate (MTX) excretion in children with acute lymphoblastic leukemia (ALL). Materials and methods: A total of 1,659 plasma concentration samples of MTX from 190 patients with 1 - 4 courses (plasma concentrations > 0.1 mu mol/L) were collected in this study. The data analysis was performed using Phoenix NLME 1.3 software. The covariates included age, body surface area (BSA), body weight, alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine transaminase (ALT), total bilirubin (TBIL), and serum creatinine (SCr). The final model was validated by bootstrap resampling procedures (1,000 runs) and visual predictive check (VPC) method. Results: The data were best described by a two-compartment linear pharmacokinetic model. The mean values of clearance (CL) and distribution volume (V-d) of MTX were 6.53 L/h and 67.88 L, respectively. Analysis of covariates showed that BSA influenced the CL of MTX. Conclusion: The final model was demonstrated as appropriate and effective for assessing the pharmacokinetic parameters of delayed MTX excretion in children with ALL.
机译:目的:探讨急性淋巴细胞白血病儿童延迟甲氨蝶呤(MTX)排泄的人口药代动力学。材料和方法:在本研究中收集了190例1-4级疗程(血浆浓度>0.1μmol/ L)的190例MTX血浆浓度样品。使用Phoenix NLME 1.3软件进行数据分析。调节剂包括年龄,体表面积(BSA),体重,碱性磷酸酶(ALP),天冬氨酸氨基转移酶(AST),丙氨酸转氨酶(ALT),总胆红素(TBIL)和血清肌酐(SCR)。最终模型由Bootstrap重采样程序(1,000运行)和视觉预测检查(VPC)方法验证。结果:通过双隔室线性药代动力学模型最佳地描述了数据。 MTX的间隙(Cl)和分布体积(V-D)的平均值分别为6.53L / h和67.88L。协调因子分析表明,BSA影响了MTX的CL.结论:最终模型是适当的,可有效评估所有人中儿童延迟MTX排泄的药代动力学参数。

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