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  • Determination of methylbenzoquate in premixes and animal feeds using liquid chromatography with fluorescence detection.

Determination of methylbenzoquate in premixes and animal feeds using liquid chromatography with fluorescence detection.

Journal of AOAC International (2005-07-09)
Michal Dousa, Karel Lemr, Zdenek Stránský
ZUSAMMENFASSUNG

A rapid analytical procedure was developed and tested for routine identification and quantification of methylbenzoquate in feeds by liquid chromatography (LC). The ground feed samples were extracted using methanol-water (80 + 20, v/v) at 65 degrees-70 degrees C in a water bath for premixes and in dichloromethane at 45 degrees C in a water bath for final feeds, respectively. The extract of final feeds was cleaned using solid-phase extraction on silica columns. Both the final feed and premix extracts were analyzed by reversed-phase LC on a NovaPak C18 column (3.9 x 150 mm; 4 microm) with methanol-acetonitrile-water-phosphoric acid (340 + 350 + 308 + 2, v/v) as mobile phase. Fluorescence detection was performed at excitation and emission wavelengths of 265 and 390 nm, respectively. Alternatively, post-column addition of sulfuric acid solution was used to decrease the determination limit. The recovery of methylbenzoquate, in a concentration range of 0.5-10 mg/kg, was 105.0 +/- 7.3%. The limit of quantitation, based on a signal-to-noise ratio of 10:1, was 48 microg/kg. The developed LC method was tested in an interlaboratory study. The interlaboratory repeatibility for both samples ranged from 7.1 to 10.6%; the interlaboratory reproducibility ranged from 11.7 to 15.2%. With the post-column addition of sulfuric acid, the limit of quantification was decreased by a factor of 50. Overall, the developed method is highly selective and can be used in routine analysis.

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Nechinat, VETRANAL®, analytical standard