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Multi-dye residue analysis of triarylmethane, xanthene, phenothiazine and phenoxazine dyes in fish tissues by ultra-performance liquid chromatography-tandem mass spectrometry

Onderzoeksoutput: Bijdrage aan tijdschriftA1: Web of Science-artikelOnderzoekpeer review

Auteurs

Externe Organisaties

  • Scientific Institute of Public Health, Food, Medicines and Consumer Safety, Chemical Residues and Contaminants, Juliette Wytsmanstraat 14, 1050 Brussel, Belgium.
  • Scientific Institute of Public Health, Food, Medicines and Consumer Safety, Chemical Residues and Contaminants, Juliette Wytsmanstraat 14, 1050 Brussel, Belgium. Electronic address: Tim.Reyns@wiv-isp.be.

Details

Originele taal-2Engels
TijdschriftJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
Volume953-954
Pagina's (van-tot)92-101
Aantal pagina's10
StatusGepubliceerd - 2014

Abstract

Beside the possible illegal use of malachite green in aquaculture, other familiar dyes could also been applied by fraudulent producers due to their antiseptic and antibacterial activity. In this contribution, a new sensitive multi-residue method was developed to determine triarylmethane, xanthene, phenothiazine and phenoxazine dyes in fish by ultra-performance liquid chromatography-tandem mass spectrometry. Samples were extracted with acetonitrile, followed by an oxidation step using 2,3-dichloro-5,6-dicyanobenzoquinone. Further clean-up was performed by tandem solid phase extraction using weak and strong cation exchange cartridges. Extracts were analysed by UPLC-MS(n) operating in the positive electrospray ionisation mode (ESI+). The fourteen dyes were separated within only 12min on a C18 BEH column using 1mM ammonium acetate in water at pH 4.5 and acetonitrile as mobile phases at a flowrate of 0.4mLmin(-1). The presented method was validated as defined by the European Union and scientific literature. Good linearity (R ≥0.99 and goodness-of-fit (g) ≤10%) was achieved over the tested concentration range (0.25-2ngg(-1)). Limit of quantification was 0.25ngg(-1) for all dyes, with a signal-to-noise ratio of at least 10/1. This is at least 5 to 10 times lower than previous published methods. Limits of detection were all

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  • Reyns_etal_2014_JChromatogrB

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