Nonaqueous capillary electrophoresis with indirect electrochemical detection

被引:0
|
作者
Matysik, FM
Marggraf, D
Gläser, P
Broekaert, JAC
机构
[1] Univ Leipzig, Inst Analyt Chem, D-04103 Leipzig, Germany
[2] Univ Hamburg, Inst Anorgan & Angew Chem, D-2000 Hamburg, Germany
关键词
acetonitrile; amperometry; electroactive complexes; indirect electrochemical detection; nonaqueous capillary electrophoresis;
D O I
10.1002/1522-2683(200211)23:21<3711::AID-ELPS3711>3.0.CO;2-Z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nonaqueous capillary electrophoresis (NACE) which makes use of organic solvents in place of conventional aqueous electrophoresis buffers is gaining increasing importance among modern separation techniques. Recently, it has been shown that amperometric detection in conjunction with acetonitrile-based NACE offers an extended accessible potential range and an enhanced long-term stability of the amperometric responses generated at solid electrodes. The present contribution takes advantage of the latter aspect to develop reliable systems for NACE with indirect electrochemical detection (IED). In this context, several compounds such as (ferrocenylmethyl)trimethylammonium perchlorate, tris(1,10-phenanthroline)cobalt(III) perchlorate and bis(1,4,7-triazacyclononane)nickel(II) perchlorate were studied regarding their suitability to act as electroactive buffer additives for IED in NACE. The performance characteristics for the respective buffer systems were evaluated. Tetraalkylammonium perchlorates served as model compounds for the optimization of the NACE-IED system. Target analytes choline and acetylcholine could easily be separated and determined by means of NACE-IED. In the case of a buffer system containing 10(-4) M tris(1,10-phenanthroline)cobalt(III) perchlorate the limits of detection were 2.5 x 10(-7) M and 4.6 x 10(-7) M for choline and acetylcholine, respectively. With the elaborated analytical procedure choline could be determined in pharmaceutical preparations.
引用
收藏
页码:3711 / 3717
页数:7
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