scholarly journals Rapid Determination of Fluoroquinolone Residues in Honey by a Microbiological Screening Method and Liquid Chromatography

2010 ◽  
Vol 93 (4) ◽  
pp. 1331-1339 ◽  
Author(s):  
Maki Kanda ◽  
Tomoto Kusano ◽  
Setsuko Kanai ◽  
Hiroshi Hayashi ◽  
Yoko Matushima ◽  
...  

Abstract A rapid and efficient method was developed for the simultaneous determination of seven fluoroquinolone (FQ) residues: norfloxacin, ciprofloxacin, danofloxacin, enrofloxacin, orbifloxacin, sarafloxacin, and difloxacin in honey. The samples were first screened with a microbiological method by using test plates made from metal-free purified agar seeded with Bacillus subtilis BGA. When a sample was found to contain FQ residues by using the microbiological method, it was analyzed by LC with fluorescence detection (LC/FL). FQs were extracted with Na2EDTA-McIlvaine buffer and purified by a dual SPE method in which a cation-exchange cartridge was connected to an anion-exchange cartridge. The overall recoveries of the seven FQs ranged from 70.0 to 92.1. The intra-assay and interassay CVs were 7.8 and 5.1, respectively. For the microbiological method, the LOD values ranged from 2 to 9 g/kg. For LC/FL, the LOQ values ranged from 2 to 7 g/kg. The developed method was used to analyze 70 honey samples. In 14 samples in which the microbiological method detected the presence of FQ residues, norfloxacin, ciprofloxacin, and enrofloxacin were identified by LC/FL.

2000 ◽  
Vol 83 (1) ◽  
pp. 17-19 ◽  
Author(s):  
Shozo Horii ◽  
Naoto Oku

Abstract A procedure was developed to determine nosiheptide residues in marketed meat and egg. Acetonitrile was used for the extraction, and the extract was partitioned with hexane to remove fat. The lower layer was reconstructed and quantitated by liquid chromatography using fluorescence detection at 357 nm excitation and 500 nm emission. The mobile phase consisted of 0.025% phosphoric acid–acetonitrile (50 + 50, v/v). Recoveries of nosiheptide from fortified samples ranged from 91.3 to 95.2% for swine muscle, 88.6 to 92.7% for chicken muscle, and 86.3 to 86.8% for egg. The method was used to monitor swine and chicken muscle and egg (20 samples each) in the market. Nosiheptide was not determined in all 60 samples.


2018 ◽  
Vol 35 (11) ◽  
pp. 2175-2182 ◽  
Author(s):  
Alberto Rico-Yuste ◽  
Lidia N. Gómez-Arribas ◽  
María Concepción Pérez-Conde ◽  
Javier L. Urraca ◽  
María Cruz Moreno-Bondi

2009 ◽  
Vol 92 (4) ◽  
pp. 1233-1240 ◽  
Author(s):  
Sarah E McMullen ◽  
Frank J Schenck ◽  
Victor A Vega

Abstract A simplified method for the extraction and determination of four fluoroquinolone (FQ) residues (ciprofloxacin, enrofloxacin, sarafloxacin, and difloxacin) in catfish is presented. In this method, the FQ residues were extracted with acidified acetonitrile, and the extract was defatted with dispersive C18 solid-phase extraction (SPE) sorbent or hexane. A portion of the extract was evaporated and reconstituted in the mobile phase. The quantitative determination was accomplished with LC-fluorescence detection (FLD), and the confirmation was by LC-MS/MS. Fortifications of catfish tissue were carried out at 0.5x, x, 2x, and 4x, where x = 5 ppb (U.S. Food and Drug Administration current regulatory target level). Recoveries for the LC/FLD determination of five replicates (for both cleanup routes) at each level ranged from 64 to 98, with RSD values <8. The method quantitation limits for all residues were <1 ng/g. The LC-MS/MS analysis of the same extracts confirmed all FQ residues at all levels. This method is an improvement over existing methodologies since additional cleanup steps, such as cation exchange SPE column cleanup, are not utilized. The C18 dispersive SPE method represents a novel cleanup approach for FQs in fish tissue.


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