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-μm 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.
CITATION STYLE
Miller, M. E., Cosgriff, J. M., & Schwartz, R. H. (1985). Anion-exchange chromatography to determine the concentration of chloride in sweat for diagnosis of cystic fibrosis. Clinical Chemistry, 31(10), 1715–1716. https://doi.org/10.1093/clinchem/31.10.1715
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