Miller M E, Cosgriff J M, Schwartz R H
Clin Chem. 1985 Oct;31(10):1715-6.
For the diagnosis of cystic fibrosis, we use the "Macroduct Sweat Collection System" (Wescor) to sample sweat, and anion-exchange chromatography to determine its chloride content. The chromatographic system consists of a Whatman Partisil SAX 10-microns column, an isocratic phosphate-buffered mobile phase, and ultraviolet detection at 200 nm. The sweat chloride concentrations of 10 individuals with cystic fibrosis ranged from 101 to 131 mmol/L (mean 111, SD 9 mmol/L). For 11 controls the values ranged from 13 to 54 mmol/L (mean 28, SD 11 mmol/L). We conclude that the procedure is reliable for the diagnosis of cystic fibrosis.
对于囊性纤维化的诊断,我们使用“Macroduct汗液采集系统”(Wescor)采集汗液样本,并采用阴离子交换色谱法测定其氯化物含量。该色谱系统由一根Whatman Partisil SAX 10微米柱、等度磷酸盐缓冲流动相和200nm波长的紫外检测组成。10例囊性纤维化患者的汗液氯化物浓度范围为101至131mmol/L(平均111,标准差9mmol/L)。11例对照者的值范围为13至54mmol/L(平均28,标准差11mmol/L)。我们得出结论,该方法对于囊性纤维化的诊断是可靠的。