Harmoinen A, Sillanaukee P, Jokela H
Department of Clinical Chemistry, Tampere University Hospital, Finland.
Clin Chem. 1991 Apr;37(4):563-5.
We describe an HPLC method for quantifying creatinine, separating the analyte from other compounds in serum and urine by cation-exchange chromatography and measuring its absorbance at 234 nm. The precision of the method (CV) varied from 2.9% (mean creatinine concentration, 31 mumol/L) to 1.7% (361 mumol/L) within a series of assays and from 3.9% (34 mumol/L) to 2.4% (391 mumol/L) between series. A comparison with the Jaffé method, as performed with a Technicon SMA analyzer, gave the regression line yHPLC = 1.00xJaffé - 12.0 (n = 141, r = 0.998, and Syx = 19). Results also are comparable with those of an enzymatic method, if the enzymatic method is standardized with a serum-based standard when serum samples are measured. An aqueous standard has to be used for enzymatic determination of creatinine in urine.
我们描述了一种用于定量肌酐的高效液相色谱法,该方法通过阳离子交换色谱将分析物与血清和尿液中的其他化合物分离,并在234nm处测量其吸光度。在一系列测定中,该方法的精密度(CV)在2.9%(平均肌酐浓度为31μmol/L)至1.7%(361μmol/L)之间变化,系列间在3.9%(34μmol/L)至2.4%(391μmol/L)之间变化。与用Technicon SMA分析仪进行的Jaffé法比较,得到回归线yHPLC = 1.00xJaffé - 12.0(n = 141,r = 0.998,Syx = 19)。如果在测量血清样本时用基于血清的标准对酶法进行标准化,结果也与酶法的结果相当。在对尿液中的肌酐进行酶法测定时必须使用水性标准品。