2009Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca Animal Science and BiotechnologiesOpen access

Determination of Six Sulfonamide Residues in Honey by HPLC with Fluorescence Detection

Victorița Bonta, Liviu-Alexandru Marghitas, Daniel Severus Dezmirean, Otilia Bobiş

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Abstract

Six sulfonamides (sulfanilamide, sulfacetamide, sulfadiazine, sulfathiazole, sulfamethazine, sulfamethoxazole) were separated and quantified in honey of different botanic origin using an HPLC-fluorescence detection method. After the acidic hydrolysis, sulfonamides were extracted from honey with a mixture of acetonitrile and dichloromethane, further clean-up on a C18 SPE cartridge and pre-column derivatization with fluorescamine. LC separation was performed on a RP C8 column in gradient mode, in 30 min. The limit of detection was determined at 2µg/kg for sulfadiazine and sulfamethazine, 3µg/kg for sulfanilamide, sulfacetamide and sulfathiazole and 5µg/kg for sulfamethoxazole. The sample clean-up was efficient and recoveries of the analytes in spiked honeys ranged from 47 to 79%.

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What this paper is about

Six sulfonamides (sulfanilamide, sulfacetamide, sulfadiazine, sulfathiazole, sulfamethazine, sulfamethoxazole) were separated and quantified in honey of different botanic origin using an HPLC-fluorescence detection method. After the acidic hydrolysis, sulfonamides were extracted from honey with a mixture of acetonitrile and dichloromethane, further clean-up on a C18 SPE cartridge and pre-column derivatization with fluorescamine. LC separation was performed on a RP C8 column in gradient mode, in 30 min. The limit of detection was determined at 2µg/kg for sulfadiazine and sulfamethazine, 3µg/kg for sulfanilamide, sulfacetamide and sulfathiazole and 5µg/kg for sulfamethoxazole. The sample clean-up was efficient and recoveries of the analytes in spiked honeys ranged from 47 to 79%.

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Available abstract

Six sulfonamides (sulfanilamide, sulfacetamide, sulfadiazine, sulfathiazole, sulfamethazine, sulfamethoxazole) were separated and quantified in honey of different botanic origin using an HPLC-fluorescence detection method. After the acidic hydrolysis, sulfonamides were extracted from honey with a mixture of acetonitrile and dichloromethane, further clean-up on a C18 SPE cartridge and pre-column derivatization with fluorescamine. LC separation was performed on a RP C8 column in gradient mode, in 30 min. The limit of detection was determined at 2µg/kg for sulfadiazine and sulfamethazine, 3µg/kg for sulfanilamide, sulfacetamide and sulfathiazole and 5µg/kg for sulfamethoxazole. The sample clean-up was efficient and recoveries of the analytes in spiked honeys ranged from 47 to 79%.

Key concepts: Chromatography, Fluorescamine, Sulfadiazine, Sulfanilamide, Sulfamerazine, Chemistry, Sulfadimethoxine, Sulfadimidine

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