Yin Jianming, Aviles Pablo, Lee William, Ly Carl, Guillen Maria Jose, Munt Simon, Cuevas Carmen, Faircloth Glynn
PharmaMar USA, Inc., 320 Putnam Avenue, Cambridge, MA 02139-4616, USA.
Rapid Commun Mass Spectrom. 2005;19(5):689-95. doi: 10.1002/rcm.1848.
A rapid and sensitive liquid chromatography/tandem mass spectrometry (LC/MS/MS) assay was developed and validated to quantify a novel antineoplastic agent, PM00104, in mouse, rat, dog, and human plasma. The method was validated to demonstrate the specificity, limit of quantification (LOQ), accuracy, and precision of measurements. The calibration range for PM00104 was established using PM00104 standards from 0.01-5.0 ng/mL in blank plasma. The selected reaction monitoring (SRM), based on the m/z 692.2 --> 218.2 transition, was specific for PM00104, and that based on the m/z 697.2 --> 218.2 transition was specific for PM00104 ((13)C(2),(2)H(3)) (the internal standard, IS); no endogenous materials interfered with the analysis of PM00104 and IS from blank plasma. The assay was linear over the concentration range 0.01-5.0 ng/mL. The correlation coefficients for the calibration curves ranged from 0.9981-0.9999. The mean intra-day and inter-day accuracies for all calibration standards (n = 8) ranged from 97-105% (< or =5% bias) in human plasma, and the mean inter-day precision for all calibration standards was less than 8.5%. The mean intra- and inter-day assay accuracy for all quality control (QC) replicates in human plasma (n = 9), determined at each QC level throughout the validated runs, ranged from 96-112% (< or =12% bias) and from 102-105% (< or =5% bias), respectively. The mean intra- and inter-day assay precision was less than 15.0 and 11.8% for all QC levels, respectively. For the QC samples prepared in animal species plasma, the %CV values of the assays ranged from 1.8-8.8% in mouse plasma, from 3.7-13.8% in rat plasma, and from 3.0-7.2% in dog plasma. The assay accuracies ranged from 92-102% (< or =8% bias) for all QC levels prepared in mouse plasma; ranged from 93-106% (< or =7% bias) in rat plasma; and ranged from 95-114% (< or =14% bias) in dog plasma. The assay has been used to support preclinical pharmacokinetic and toxicokinetic studies and is currently used to measure PM00104 plasma concentrations to support clinical trials.
开发并验证了一种快速灵敏的液相色谱/串联质谱(LC/MS/MS)分析法,用于定量测定小鼠、大鼠、犬和人血浆中的新型抗肿瘤药物PM00104。该方法经过验证,以证明测量的特异性、定量限(LOQ)、准确性和精密度。使用空白血浆中浓度为0.01 - 5.0 ng/mL的PM00104标准品建立了PM00104的校准范围。基于m/z 692.2 --> 218.2跃迁的选择反应监测(SRM)对PM00104具有特异性,基于m/z 697.2 --> 218.2跃迁的SRM对PM00104((13)C(2),(2)H(3))(内标,IS)具有特异性;空白血浆中的内源性物质不干扰PM00104和IS的分析。该分析方法在0.01 - 5.0 ng/mL的浓度范围内呈线性。校准曲线的相关系数范围为0.9981 - 0.9999。所有人血浆校准标准品(n = 8)的日内和日间平均准确度范围为97 - 105%(偏差≤5%),所有校准标准品的日间平均精密度小于8.5%。在整个验证运行过程中,在每个质量控制(QC)水平测定的所有人血浆QC重复样品(n = 9)的日内和日间分析准确度分别为96 - 112%(偏差≤12%)和102 - 105%(偏差≤5%)。所有QC水平的日内和日间分析精密度分别小于15.0%和11.8%。对于在动物血浆中制备的QC样品,该分析方法在小鼠血浆中的变异系数(%CV)值范围为1.8 - 8.8%,在大鼠血浆中为3.7 - 13.8%,在犬血浆中为3.0 - 7.2%。所有在小鼠血浆中制备的QC水平的分析准确度范围为92 - 102%(偏差≤8%);在大鼠血浆中为93 - 106%(偏差≤7%);在犬血浆中为95 - 114%(偏差≤14%)。该分析方法已用于支持临床前药代动力学和毒代动力学研究,目前用于测量PM00104血浆浓度以支持临床试验。