The apphcatlon of the chemdummescence system oxahc acid-fluorescer-peroxy compound-carbodnnude to bmchenucal analyst m prow solvents IS described By measunng the mtegrated chennlummescence enussion generated by the above reactlon, very low concentrations of oxalate (down to 10 nmol I-') can be deter
Determination of urinary oxalic acid and of oxalate pool size by stable isotope dilution
β Scribed by D.E. Duggan; R.W. Walker; R.M. Noll; W.J.A. VandenHeuvel
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- English
- Weight
- 395 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0003-2697
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β¦ Synopsis
An isotope dilution procedure for oxalate based upon [1,2-'T,]oxalic acid is described. For routine determinations of urinary concentration, a known quantity of sodium [1,2-1 'Tloxalate is admixed with the sample, total oxalate precipitated as the calcium salt, and converted by BF, catalysis to di-n-propyl esters for mass-spectrometric analysis. Selective ion monitoring provides 12C:13C ratios directly, thus precluding the necessity for quantitative recovery at any step of the rapid, single-tube assay. Following a bolus injection of sodium [1,2JT]oxalate, whole body oxalate pools and their turnover rates can be determined by sequential sampling of urine. Biosynthetic rates calculated from the product of pool size and turnover are in excellent agreement with urinary excretion rates, confirming directly that urinary oxalate is a quantitative index of biosynthesis.
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