Rapid and simple pretreatment of human body fluids using electromembrane extraction across supported liquid membrane for capillary electrophoretic determination of lithium

被引:65
|
作者
Strieglerova, Lenka [1 ]
Kuban, Pavel [1 ]
Bocek, Petr [1 ]
机构
[1] Acad Sci Czech Republic, Inst Analyt Chem, Vvi, CZ-60200 Brno, Czech Republic
关键词
Biological samples; Capacitively coupled contactless conductivity detection; Capillary electrophoresis; Electromembrane extraction; Sample pretreatment; CONTACTLESS CONDUCTIVITY DETECTION; ATOMIC-ABSORPTION-SPECTROMETRY; ZONE-ELECTROPHORESIS; BIOLOGICAL SAMPLES; ELECTROKINETIC MIGRATION; PHASE MICROEXTRACTION; MASS-SPECTROMETRY; TRACE LITHIUM; WHOLE-BLOOD; NITRIC-ACID;
D O I
10.1002/elps.201000620
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Electromembrane extraction was used for simultaneous sample cleanup and preconcentration of lithium from untreated human body fluids. The sample of a body fluid was diluted 100 times with 0.5 mM Tris solution and lithium was extracted by electromigration through a supported liquid membrane composed of 1-octanol into 100 mM acetic acid acceptor solution. Matrix compounds, such as proteins, red blood cells, and other high-molecular-weight compounds were efficiently retained on the supported liquid membrane. The liquid membrane was anchored in pores of a short segment of a polypropylene hollow fiber, which represented a low cost, single use, disposable extraction unit and was discarded after each use. Acceptor solutions were analyzed using capillary electrophoresis with capacitively coupled contactless conductivity detection (CE-C(4)D) and baseline separation of lithium was achieved in a background electrolyte solution consisting of 18 mM L-histidine and 40 mM acetic acid at pH 4.6. Repeatability of the electromembrane extraction-CE-C(4)D method was evaluated for the determination of lithium in standard solutions and real samples and was better than 0.6 and 8.2% for migration times and peak areas, respectively. The concentration limit of detection of 9 nM was achieved. The developed method was applied to the determination of lithium in urine, blood serum, blood plasma, and whole blood at both endogenous and therapeutic concentration levels.
引用
收藏
页码:1182 / 1189
页数:8
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