Simultaneous determination of oxalate, citrate and sulfate in children's plasma with ion chromatography

被引:45
作者
Hoppe, B
Kemper, MJ
Hvizd, MG
Sailer, DE
Langman, CB
机构
[1] Univ Childrens Hosp, Div Pediat Nephrol, Hamburg, Germany
[2] Dionex Chem Corp, Westmont, IL USA
[3] Northwestern Univ, Childrens Mem Hosp, Div Pediat Nephrol, Chicago, IL 60614 USA
关键词
mineral metabolism; nephrolithiasis; primary hyperoxaluria; children; nephrocalcinosis;
D O I
10.1046/j.1523-1755.1998.00891.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
To improve our understanding of both diagnosis and treatment of diseases of oxalate metabolism, we first set out Lo establish a new ion-chromatographic method to determine normal plasma levels of oxalate, citrate and sulfate from single plasma samples. In 50 infants and children (23 girls, 27 boys, aged 0.2 to 17 years) with normal renal function, blood was drawn in Li-heparin tubes, placed on ice and preserved immediately with 40 mu l 1 M HCl/ml plasma in two ultracentrifugation steps. For measurement, plasma was injected onto an ion chromatography system with NaOH as the mobile phase. and then run as a linear gradient from 5 mM to 52.5 mM over 21 minutes. Analysis yielded measurable and reproducible oxalate (6.43 +/- 1.06 mu M/liter), citrate (79.3 +/- 27.4 mu M/liter) and sulfate 235.0 +/- 85.3 mu M/liter) levels. without any age and gender specific differences. The least detectable plasma oxalate level was < 0.3 mu M with a high reliability and reproducibility (coefficient of variance 1.95 to 4.75%). In conclusion, we established a reproducible, precise method to determine the relevant plasma anions involved in mineral metabolism, which heretofore have not been easily measurable. Studies of diseases of oxalate and citrate metabolism are ongoing on the basis of the normal plasma values achieved this study.
引用
收藏
页码:1348 / 1352
页数:5
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