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采用反相高效液相色谱法分离后,用碘叠氮检测系统测定尿液中的甲巯咪唑。

Determination of methimazole in urine with the iodine-azide detection system following its separation by reversed-phase high-performance liquid chromatography.

作者信息

Zakrzewski Robert

机构信息

Department of Instrumental Analysis, University of Łódź, Lodz, Poland.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Jun 15;869(1-2):67-74. doi: 10.1016/j.jchromb.2008.05.021. Epub 2008 May 16.

Abstract

The iodine-azide detection system to determine methimazole following its separation by RP-HPLC is described in this paper. The reaction between iodine and azide ions induced by methimazole was applied as a post-column reaction detection system. Neither extraction nor preconcentration of the sample was necessary. The methimazole standards added to normal urine show that the response of the detector, set at 350 nm (corresponding to unreacted iodine in the post-column iodine-azide reaction), was linear within the concentration range 2-10 nmol/mL of urine. The relative standard deviation values for precision and recovery within the calibration range were from 0.3 to 3.2% and from 97 to 102%, respectively. Limits of detection (LOD) and quantitation (LOQ) were 1 and 2 nmol/mL of urine, respectively. The method was applied to the separation and determination of patient urine samples and the analytical results were satisfactory.

摘要

本文描述了一种通过反相高效液相色谱(RP-HPLC)分离后测定甲巯咪唑的碘-叠氮化物检测系统。甲巯咪唑引发的碘与叠氮离子之间的反应被用作柱后反应检测系统。样品无需萃取或预浓缩。添加到正常尿液中的甲巯咪唑标准品表明,设置在350 nm(对应柱后碘-叠氮化物反应中未反应的碘)的检测器响应在尿液浓度范围2-10 nmol/mL内呈线性。校准范围内精密度和回收率的相对标准偏差值分别为0.3%至3.2%和97%至102%。检测限(LOD)和定量限(LOQ)分别为1 nmol/mL和2 nmol/mL尿液。该方法应用于患者尿液样品的分离和测定,分析结果令人满意。

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