In this liquid-chromatographic method for determination of urinary oxalate, interfering compounds in the urinary samples were eliminated before chromatography by passage through a preparative C18 mini-column (Sep-pak cartridge, Waters Associates). In the reversed-phase system tetrabutyl ammonium was included as a counter ion to enhance the retention of oxalate. The H of the mobile phase was kept low (2.00) to avoid precipitation of calcium oxalate. This method is faster and significantly more precise than the colorimetric method we currently use.
CITATION STYLE
Larsson, L., Libert, B., & Asperud, M. (1982). Determination of urinary oxalate by reversed-phase ion-pair “high-performance” liquid chromatography. Clinical Chemistry, 28(11), 2272–2274. https://doi.org/10.1093/clinchem/28.11.2272
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