Vaks J E
Advanced Technology Center, Beckman Instruments, Inc., Brea, CA, USA.
Clin Chem. 1996 Jul;42(7):1074-8.
Linearity, interference evaluations of the performance of clinical chemistry systems, mathematical model selection for nonlinear calibration, and other assessments often involve several human sample pools with equally spaced analyte concentrations. Sequential mixing of equal volumes, first of the low and high pools to produce the middle pool, then of the low and middle pools to produce the mid-low pool, and of the high and middle pools to produce the mid-high pool, is recommended in the NCCLS EP7-P guideline for interference studies. Proportional mixing of the low and high pools to produce all of the required pool concentrations is recommended in the NCCLS EP6-P guideline for linearity studies. Mathematical analysis and computer simulation show that the sequential mixing is much more accurate and precise than the proportional mixing. Therefore, we recommend sequential mixing for clinical chemistry application.
临床化学系统性能的线性、干扰评估、非线性校准的数学模型选择以及其他评估通常涉及几个具有等距分析物浓度的人体样本池。NCCLS EP7-P干扰研究指南建议依次等量混合,先将低浓度和高浓度样本池混合产生中间浓度样本池,然后将低浓度和中间浓度样本池混合产生中低浓度样本池,将高浓度和中间浓度样本池混合产生中高浓度样本池。NCCLS EP6-P线性研究指南建议按比例混合低浓度和高浓度样本池以产生所有所需的样本池浓度。数学分析和计算机模拟表明,依次混合比按比例混合更准确、更精确。因此,我们建议在临床化学应用中采用依次混合。