General approach for the analysis of various alkaloid classes using capillary electrophoresis and capillary electrophoresis mass spectrometry

被引:60
作者
Unger, M
Stockigt, D
Belder, D
Stockigt, J
机构
[1] MAX PLANCK INST KOHLENFORSCH,ABT MASSENSPEKTROMETRIE,D-45470 MULHEIM,GERMANY
[2] UNIV MAINZ,INST PHARM,LEHRSTUHL PHARMAZEUT BIOL,D-55099 MAINZ,GERMANY
[3] MAX PLANCK INST KOHLENFORSCH,ABT CHROMATOG & ELEKTROPHORESE,D-45470 MULHEIM,GERMANY
关键词
electrophoretic mobility; buffer composition; alkaloids; ZONE ELECTROPHORESIS; ELECTROSPRAY-IONIZATION; LIQUID-CHROMATOGRAPHY; SEPARATION; INTERFACE; PROTEINS;
D O I
10.1016/S0021-9673(96)01013-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The analysis of various alkaloid classes employing capillary electrophoresis (CE) and on-line combined CE-mass spectrometry (CE-MS) is described. A CE method is presented for the analysis of alkaloids without derivatisation or purification. The separation of four different groups of alkaloids consisting of monoterpenoid indole alkaloids, protoberberines/benzophenanthridines, beta-carboline alkaloids, and isoquinolines from poppy by free zone capillary electrophoresis has been obtained using a 1:1 mixture of 100 mmol l(-1) ammonium acetate (pH 3.1) and acetonitrile. The influence of alkaloid structure on the electrophoretic mobility is discussed. The CE-MS reconstructed total ion current (RIC) of the indole- and the opium-type standard alkaloids shows a decreased signal-to-noise ratio compared to CE using only UV detection. As expected the single-ion traces (or individual mass traces) of the [M+H](+) ions show higher signal-to-noise ratios than the RIC. The electrospray MS data of the alkaloids are dominated by the protonated molecules and the Na+-, and K+-adducts. They display the typical pattern resulting from cluster formation or doubly charged species.
引用
收藏
页码:263 / 276
页数:14
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