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This article introduces the high performance liquid chromatography method to determine the residues of oxytetracycline, tetracycline and chlortetracycline in livestock and poultry meat (according to GB/T5009.
116-2003)
.
1.
Principle
The sample is extracted, filtered by a microporous membrane, and injected directly, separated by reversed-phase chromatography, detected by ultraviolet detector, and quantified compared with the standard.
The peak sequence is oxytetracycline , tetracycline , and chlortetracycline
.
Standard addition method quantification
Calculate as follows:
In the formula, X——the antibiotic content in the sample, mg/kg
m 1 ——The quality of the antibiotic measured in the sample solution, ug
m 2 ——the mass of the sample, g
2.
Chromatographic conditions
Chromatographic column: 0DS-C18 (5um) 6.
2mm × 15cm; detection wavelength: 355nm; sensitivity: 0.
002 AUFS; column temperature: room temperature; flow rate: 1.
0 mL/min; injection volume: 10 uL; mobile phase: acetonitrile + 0.
01mol/ L sodium dihydrogen phosphate solution ( adjust pH 2.
5 with 30% nitric acid solution)=35+65, degas with ultrasonic for 10min before use
.
3.
Tips
This method is suitable for the determination of oxytetracycline, tetracycline, and chlortetracycline residues in various livestock and poultry meats
.
The detection limit was 0.