A Rapid High-performance Liquid Chromatography-Tandem Mass Spectrometric Method for Determination of 4 Fluoroquinolones Residues in Fish Meat
LI Gui-sheng
Abstract
LI Gui-sheng
Abstract
A high-performance liquid chromatography-tandem mass spectrometric (HPLC-MS/MS) method was developed for the simultaneous determination of 4 fluoroquinolone antibiotic residues in fish meat. In the method, analytes were extracted with acidified acetonitrile, cleaned up with n-hexane, concentrated to dryness under nitrogen, redissolved in 1 mL of mixed solution of acetonitrile and 1% formic acid (1:9, V/V), separated on a RP-HPLC column, detected by HPLC-MS/MS with positive electrospray ionization (ESI+) in multiple reaction monitoring (MRM) mode, and quantified using an external standard method. The standard curves for all analytes exhibited good linearity over the concentration range of 2 - 40 μg/kg with correlation coefficients (r2) beyond 0.997. The recoveries of 4 fluoroquinolone antibiotics in fish meat samples spiked at concentration levels of 4, 10 μg/kg and 20 μg/kg ranged from 79.9% to 98.1%, with relative standard deviations between 2.7% and 8.7%. The limits of detection (LOD) and limits of quantification (LOQ) of the developed method were in the ranges of 0.1 - 0.4 μg/kg and 0.3 - 1.0 μg/kg, respectively. This method is characterized by simplicity, rapidity, high sensitivity, good reproducibility and better selectivity, and therefore can be used for identification and determination of fluoroquinolones in fish meat.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
A high-performance liquid chromatography-tandem mass spectrometric (HPLC-MS/MS) method was developed for the simultaneous determination of 4 fluoroquinolone antibiotic residues in fish meat. In the method, analytes were extracted with acidified acetonitrile, cleaned up with n-hexane, concentrated to dryness under nitrogen, redissolved in 1 mL of mixed solution of acetonitrile and 1% formic acid (1:9, V/V), separated on a RP-HPLC column, detected by HPLC-MS/MS with positive electrospray ionization (ESI+) in multiple reaction monitoring (MRM) mode, and quantified using an external standard method. The standard curves for all analytes exhibited good linearity over the concentration range of 2 - 40 μg/kg with correlation coefficients (r2) beyond 0.997. The recoveries of 4 fluoroquinolone antibiotics in fish meat samples spiked at concentration levels of 4, 10 μg/kg and 20 μg/kg ranged from 79.9% to 98.1%, with relative standard deviations between 2.7% and 8.7%. The limits of detection (LOD) and limits of quantification (LOQ) of the developed method were in the ranges of 0.1 - 0.4 μg/kg and 0.3 - 1.0 μg/kg, respectively. This method is characterized by simplicity, rapidity, high sensitivity, good reproducibility and better selectivity, and therefore can be used for identification and determination of fluoroquinolones in fish meat.
Key concepts: Chromatography, Chemistry, High-performance liquid chromatography, Formic acid, Detection limit, Selected reaction monitoring, Electrospray ionization, Reproducibility