## Abstract A method for the quantitative determination of major antidepressants in aqueous matrices by CE using ESI‐MS is presented. Several aqueous, nonaquoeus, and mixed aqueous/organic solvent BGEs including inorganic and organic acids were investigated with respect to their suitability for the
Capillary electrophoresis with inductively coupled plasma-mass spectrometric and electrospray time of flight mass spectrometric detection for the determination of arsenic species in fish samples
✍ Scribed by Björn Meermann; Marc Bartel; Andy Scheffer; Stefan Trümpler; Uwe Karst
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 356 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0173-0835
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
CE was coupled to inductively coupled plasma MS (ICP‐MS) and ESI‐MS to identify and quantify the arsenic species arsenobetaine (AsB), arsenite (As^III^), arsenate (As^V^), and dimethylarsinic acid (DMA). A GC‐flame ionization detector (FID)‐based German standard method and ICP‐MS were used for validation of the data obtained for arsenobetaine and total arsenic, respectively. LODs obtained with the CE‐ESI‐TOF‐MS method were 1.0×10^−7^ M for AsB, 5.0×10^−7^ M for DMA, and 1.0×10^−6^ M for As^III^ and As^V^. For the CE‐ICP‐MS method, LODs were 8.5×10^−8^ M for AsB, 9.5×10^−8^ M for DMA, 9.3×10^−8^ M for As^III^, and 6.2×10^−8^ M for As^V^. While CE‐ICP‐MS provided high sensitivity and better reproducibility for quantitative measurements, CE‐ESI‐MS with a TOF mass analyzer proved to be valuable for species identification. With this setup, fish samples were prepared and analyzed and the obtained data were successfully validated with the independent methods.
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