Repizo LM, Martinez LD, Olsina RA, Cerutti S, Raba J.
Anal Bioanal Chem. 2012 Jan;402(2):965-73.
A novel, simple, and rapid reversed-phase liquid chromatography-tandem mass spectrometric methodology was developed for the analysis of natamycin in wine samples. Natamycin was protonated to form singly charged ions in an electrospray positive ion mode. Data acquisition under MS/MS was achieved by applying multiple reaction monitoring (MRM) of three fragment ion transitions (666.3 → 648.2, 666.3 → 503.3, and 666.3 → 485.2) to provide a high degree of sensitivity and specificity. Chromatographic separation was performed on a rapid resolution column using a mobile phase consisting of an acetonitrile/water mixture with a total run time of 5.0 min. After only filtration as pretreatment, the sample was injected into the chromatographic system. The proposed method was validated in terms of selectivity, trueness, precision, decision limit (CCα), and detection capability (CCβ) according to 2002/657/EC Commission decision. The values for trueness, reported as bias (%), agreed with those established by the aforementioned document. Repeatability (intraday variability) values were 12.37% at a concentration of 1.0 μg L(-1) and 8.99-4.19% at concentrations between 2.5 and 10 μg L(-1). The overall within-laboratory (interday variability) reproducibility was 15.47% at a concentration of 1.0 μg L(-1), which was significantly lower than the indicative value reported in the EU decision. The results indicated that the proposed approach is a sensitive, fast, reproducible, and robust methodology suitable for the analysis of natamycin levels in wine samples.
http://pubs.rsc.org/en/Content/ArticleLanding/2011/AY/c0ay00330a nstituto de QuÃmica San Luis (CONICET-UNSL), Ãrea de QuÃmica AnalÃtica, Facultad de QuÃmica BioquÃmica y Farmacia, Universidad Nacional de San Luis, San Luis, Argentina.
United States
