Isolation and identification of the Amanita muscaria and Amanita pantherina toxins in human urine
Jazyk angličtina Země Švédsko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
18987593
PII: NEL290508A27
Knihovny.cz E-zdroje
- MeSH
- Amanita chemie MeSH
- amanitiny moč MeSH
- extrakce na pevné fázi MeSH
- hmotnostní spektrometrie s elektrosprejovou ionizací MeSH
- indikátory a reagencie MeSH
- inhibitory syntézy nukleových kyselin moč MeSH
- kyselina ibotenová moč MeSH
- lidé MeSH
- muscimol moč MeSH
- muskarin moč MeSH
- rozpouštědla MeSH
- vysokoúčinná kapalinová chromatografie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- amanitiny MeSH
- indikátory a reagencie MeSH
- inhibitory syntézy nukleových kyselin MeSH
- kyselina ibotenová MeSH
- muscimol MeSH
- muskarin MeSH
- rozpouštědla MeSH
OBJECTIVES: Ibotenic acid, muscimol and muscarine were recognized as responsible for psychotropic effects of A. muscaria and A. pantherina. Demand for their specific and sensitive identification and quantitation in biological material lead to effort to develop reliable analytical method, but satisfactory solution is still lacking. Presented article describes liquid chromatography-mass spectrometry method suitable for isolation and identification of principal toxins of A. muscaria and A. pantherina in urine. METHODS AND RESULTS: Dedicated liquid chromatography-mass spectrometry method is reported. Technique consists of an extraction of analytes on Strata X-CW and Discovery SCX SPE cartridges and separation is achieved using a Gemini C18 column (150 mm x 2.0 mm, 5 micron) and 8 mM heptafluorobutyric acid as mobile phase. Detection at m/z 159 for ibotenic acid, m/z 115 for muscimol and m/z 174 for muscarine was used. Retention times and LODs are 2.6 min and 50 ng.ml-1 for ibotenic acid, 4.6 min and 40 ng.ml-1 for muscimol and 14.2 min and 3 ng.ml-1 for muscarine. CONCLUSION: A sensitive and specific liquid chromatography-mass spectrometry assay was developed for analysis of principal toxins of A. muscaria and A. pantherina in urine. Method was found to be sufficiently sensitive and specific for analysis of urine of intoxicated patients.