Branfman A R, Bruni R J, Merrill Y N, Chadwick M, Strong J M, Ervin T J
J Chromatogr. 1980 May 9;182(2):163-9. doi: 10.1016/s0378-4347(00)81620-5.
N-(Phosphonacetyl)-L-aspartic acid (PALA) is an antitumor agent which is currently under clinical study. A gas chromatography--mass spectrometry--selected ion monitoring assay procedure using [13C]PALA as the internal standard has been developed for the quantitation of PALA in biological samples. Standard curves which related ion intensity peak height ratios (m/e 220/221) to PALA concentrations in plasma and urine were described by a non-linear least square analysis with correlation coefficients of R2 greater than 0.995 and greater than 0.996, respectively. Over concentration ranges for PALA of 1--60 micrograms/ml of plasma and 1--160 micrograms/ml of urine the coefficient of variation from the fitted curve was 4--18%. This methodology has been used to quantitate PALA in human plasma samples in a study on the clinical pharmacology of the drug.
N-(膦酰乙酰基)-L-天冬氨酸(PALA)是一种目前正在进行临床研究的抗肿瘤药物。已开发出一种以[13C]PALA为内标的气相色谱-质谱-选择离子监测分析方法,用于定量生物样品中的PALA。通过非线性最小二乘法分析描述了离子强度峰高比(m/e 220/221)与血浆和尿液中PALA浓度的标准曲线,相关系数R2分别大于0.995和大于0.996。在PALA浓度范围为1-60微克/毫升血浆和1-160微克/毫升尿液时,拟合曲线的变异系数为4-18%。在一项该药物临床药理学研究中,此方法已用于定量人血浆样品中的PALA。