Werner E R, Fuchs D, Hausen A, Reibnegger G, Wachter H
Institute for Medical Chemistry and Biochemistry, Innsbruck, Austria.
Clin Chem. 1987 Nov;33(11):2028-33.
This is a method for the simultaneous determination of neopterin, a product of interferon-gamma-activated macrophages, and creatinine in serum. Acidified, but not deproteinized serum is applied to a 4-propylbenzene sulfonic acid-modified silica sorbent cartridge, which quantitatively retains the analytes but not the serum proteins. The retained analytes are then eluted from the cartridge directly onto the liquid-chromatography column. Elution from the cartridge is facilitated by a pulse of 0.4 mol/L, pH 6.8 potassium phosphate buffer. On isocratic elution from an octadecylsilica column with potassium phosphate buffer (15 mmol/L, pH 6.0), neopterin is detected by its native fluorescence, creatinine by ultraviolet absorption. Detection limits are 0.5 nmol/L for neopterin, 1 mumol/L for creatinine at a sample volume of 100 microL. The standard curve is linear over the range of concentrations encountered in sera. For both neopterin and creatinine in serum, concentrations so measured agree well with results by established methods.
这是一种同时测定血清中γ-干扰素激活巨噬细胞产物新蝶呤和肌酐的方法。将酸化但未脱蛋白的血清应用于4-丙基苯磺酸改性硅胶吸附柱,该柱能定量保留分析物而不保留血清蛋白。然后将保留的分析物从柱中直接洗脱到液相色谱柱上。通过0.4 mol/L、pH 6.8的磷酸钾缓冲液脉冲促进从柱中的洗脱。在十八烷基硅胶柱上用磷酸钾缓冲液(15 mmol/L,pH 6.0)进行等度洗脱时,新蝶呤通过其天然荧光检测,肌酐通过紫外吸收检测。在进样量为100 μL时,新蝶呤的检测限为0.5 nmol/L,肌酐的检测限为1 μmol/L。标准曲线在血清中遇到的浓度范围内呈线性。对于血清中的新蝶呤和肌酐,如此测量的浓度与既定方法的结果非常吻合。