A capillary electrophoretic (CE) assay for oxalate has been applied to the
quantitative determination of free oxalate in amniotic fluid. Indirect abso
rbance detection of oxalate is accomplished with a chromate-based backgroun
d electrolyte modified with ethylenediaminetetraacetic acid (EDTA). Detecti
on interference due to the presence of high levels (approximate to 4 mg/ml)
of inorganic chloride is eliminated through a direct sample clean-up proce
dure based on cation (Ag+-form) resins. Separation interference from amniot
ic fluid proteins is prevented through the use of a simple aqueous-based di
lution procedure. This method for the determination of oxalate in amniotic
fluid provides precision of approximate to 5% relative standard deviation (
RSD). Within-day precisions for the oxalate response and migration time are
better than 3% RSD and 1% RSD, respectively. Between-day precisions for th
e oxalate response and migration time are better than 6% RSD and 3% RSD, re
spectively. The analytical recovery of oxalate (1000 ng/ml) spiked into amn
iotic fluid was better than 96%. The limit of detection (LOD) for the metho
d is approximate to 100 ng/ml oxalate. This method also shows promising res
ults for the determination of oxalate in human blood plasma samples. (C) 20
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