毛细管区带电泳测定尿17-羟皮质类固醇

目的 :应用高效毛细管区带电泳 (CZE)技术分离和检测人尿内 1 7-羟类皮质类固醇 (1 7-OHCS) ,以解决微色谱柱 -分光光度测定尿 1 7-OHCS时 ,多酚类化合物对测定的干扰。方法 :标本用活性高岭土吸附尿内色素 ,以茶碱作内标 ,中性苯乙烯 -二乙烯苯树脂微色谱柱吸附尿中 1 7-OHCS。乙醇解吸附 ,采用毛细管区带电泳进一步分离并测定。结果 :运用CZE法分离了人尿 1 7-OHCS ,皮质醇浓度在 2～ 5 0mg .L- 1 范围内具有良好的线性关系 (r=0 .994) ,方法平均回收率 96 .1 7% ,日内及日间CV均小于 5 % ,最低检测限度为 0 .3mg .L- 1 。结论 :与微色谱柱 -分光光度法相比 ,CZE法检测尿内 1 7-OHCS无干扰 ,方法简便、快速、可靠。

Determination of 17-hydroxycorticosteroid by capillary zone elec trophoresis

Objective To detect and dissociate 17-hydroxycorticosteroids(17-OHCS) in urine by using high performance capillary zone electrophoresis(CZE) so as to solve the problem that phenolic compounds interfere with the determination of urine 17-OHCS by chromatographic-spectrophotometry. Methods Pigments were absorbed from samples by activated kaolin in which the internal standard was theophyline. Urine 17-OHCS was absorbed by neutral styrene-divinylbenzene resin. Thus pigments and phenolic compounds were separated roughly. Then 17-OHCS was washed down by alcohol and separated and detected by capillary zone electrophoresis . Results Urinary 17- OHCS was separated succussfully. Urinary 17-OHCS had a good linearity in the range of 2～50 mg.L -1 (r= 0.994). The average recovery rate was 96.17%. The relative standard deviation was less than 5%. The consistence detection limit was 0.3 mg.L -1 . Conclusions Compared with chromatographic- spectrophotometry, the high performance capillary electrophoresis has much less interference and is more simple, rapid, and accurate.