Fast determination of harmala alkaloids in edible algae by capillary electrophoresis mass spectrometry

被引:19
作者
Tascon, Marcos [1 ]
Benavente, Fernando [3 ]
Sanz-Nebot, Victoria M. [3 ]
Gagliardi, Leonardo G. [1 ,2 ]
机构
[1] Univ Nacl La Plata, LIDMA, RA-1900 Buenos Aires, DF, Argentina
[2] Consejo Nacl Invest Cient & Tecn, Ctr Invest & Desarrollo Tecnol Pinturas CIDEPINT, CIC, RA-1900 Buenos Aires, DF, Argentina
[3] Univ Barcelona, Dept Quim Analat, Nutr & Food Safety Res Inst INSA, E-08028 Barcelona, Spain
关键词
Capillary electrophoresis; Mass spectrometry; MS-MS; Undaria pinnatifida; Harmala alkaloids; Validation; BETA-CARBOLINES NORHARMAN; MS; SEPARATION; PLASMA; IDENTIFICATION; METABOLITES; AYAHUASCA; PEPTIDES; HARMINE; URINE;
D O I
10.1007/s00216-015-8579-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The use of algae as a foodstuff is rapidly expanding worldwide from the East Asian countries, where they are also used for medical care. Harmala alkaloids (HAlk) are a family of bioactive compounds found in the extracts of some plants, including wakame (Undaria pinnatifida), an edible marine invasive algae. HAlks are based on a characteristic beta-carboline structure with at least one amino ionizable group. In this work, we report the successful separation of a mixture of six HAlks (harmine, harmaline, harmol, harmalol, harmane, and norharmane) by capillary electrophoresis ion-trap mass spectrometry (CE-IT-MS) in less than 8 min. Optimum separation in fused-silica capillaries and detection sensitivity in positive-ion mode were achieved using a background electrolyte (BGE) with 25 mmol L-1 ammonium acetate (pH 7.8) and 10 % (v/v) methanol, and a sheath liquid with 60:40 (v/v) isopropanol-water and 0.05 % (v/v) formic acid. The separation method was validated in terms of linearity, limits of detection and quantification, repeatability, and reproducibility. Later, a sample pretreatment was carefully optimized to determine HAlks in commercial wakame samples with excellent recovery and repeatability. For the complex wakame extracts, the MS-MS fragmentation patterns of the different HAlks were useful to ensure a reliable identification. The complete procedure was validated using the standard-addition calibration method, determining matrix effects on the studied compounds. Harmalol, harmine, and harmaline were naturally present in the samples and were quantified at very low concentrations, ranging from 7 to 24 mu g kg(-1) dry algae.
引用
收藏
页码:3637 / 3645
页数:9
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