Simultaneous determination of mushroom toxins α-amanitin, β-amanitin and muscarine in human urine by solid-phase extraction and ultra-high-performance liquid chromatography coupled with ultra-high-resolution TOF mass spectrometry
Language English Country Ireland Media print-electronic
Document type Journal Article
PubMed
25916793
DOI
10.1016/j.forsciint.2015.04.007
PII: S0379-0738(15)00153-X
Knihovny.cz E-resources
- Keywords
- Liquid chromatography, Mass spectrometry, Mushroom toxins, Solid-phase extraction,
- MeSH
- Amanitins urine MeSH
- Chromatography, Liquid methods MeSH
- Solid Phase Extraction MeSH
- Mass Spectrometry methods MeSH
- Humans MeSH
- Limit of Detection MeSH
- Adolescent MeSH
- Muscarine urine MeSH
- Mushroom Poisoning diagnosis urine MeSH
- Aged, 80 and over MeSH
- Forensic Toxicology MeSH
- Check Tag
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Amanitins MeSH
- Muscarine MeSH
This paper presents a method for the simultaneous determination of α-amanitin, β-amanitin and muscarine in human urine by solid-phase extraction (SPE) and ultra-high-performance liquid chromatography coupled with ultra-high-resolution TOF mass spectrometry. The method can be used for a diagnostics of mushroom poisonings. Different SPE cartridges were tested for sample preparation, namely hydrophilic modified reversed-phase (Oasis HLB) and polymeric weak cation phase (Strata X-CW). The latter gave better results and therefore it was chosen for the subsequent method optimization and partial validation. In the course of validation, limits of detection, linearity, intraday and interday precisions and recoveries were evaluated. The obtained LOD values of α-amanitin and β-amanitin were 1ng/mL and of muscarine 0.09ng/mL. The intraday and interday precisions of human urine spiked with α-amanitin (10ng/mL), β-amanitin (10ng/mL) and muscarine (1ng/mL) ranged from 6% to 10% and from 7% to 13%, respectively. The developed method was proved to be a relevant tool for the simultaneous determination of the studied mushroom toxins in human urine after mushroom poisoning.
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