TY - JOUR
T1 - Determination of oxytetracycline, tetracycline and chloramphenicol antibiotics in animal feeds using subcritical water extraction and high performance liquid chromatography
AU - Wang, Linling
AU - Yang, Hai
AU - Zhang, Chunwei
AU - Mo, Yulin
AU - Lu, Xiaohua
PY - 2008
Y1 - 2008
N2 - A rapid analytical method for the determination of oxytetracycline (OTC), tetracycline (TC) and chloramphenicol (CAP) antibiotics in animal feeds has been developed based on subcritical water extraction (SWE) without further sample clean-up followed by high performance liquid chromatography (HPLC) with ultraviolet (UV) detection. On extracting target antibiotics from spiked samples, the efficiency of the water extraction device was evaluated in terms of pH and volume of the extractant, temperature and time of the static extraction. The best extraction conditions were obtained by using 5.5mL of water adjusted to pH 2 with hydrochloric acid as the extractant at 100°C with 5-min static extraction. After filtration, 20μL of the aqueous extract was directly injected into the HPLC column. Recoveries between 82.1% and 90.0% with relative standard deviations ranging between 1.6% and 4.8% were achieved from spiked animal feed samples by using this method. Compared with the traditional ultrasonic extraction, this procedurewas remarkablymore efficient in extracting OTC, TC and CAP, simpler to perform, and there was no use of toxic organic solvents.
AB - A rapid analytical method for the determination of oxytetracycline (OTC), tetracycline (TC) and chloramphenicol (CAP) antibiotics in animal feeds has been developed based on subcritical water extraction (SWE) without further sample clean-up followed by high performance liquid chromatography (HPLC) with ultraviolet (UV) detection. On extracting target antibiotics from spiked samples, the efficiency of the water extraction device was evaluated in terms of pH and volume of the extractant, temperature and time of the static extraction. The best extraction conditions were obtained by using 5.5mL of water adjusted to pH 2 with hydrochloric acid as the extractant at 100°C with 5-min static extraction. After filtration, 20μL of the aqueous extract was directly injected into the HPLC column. Recoveries between 82.1% and 90.0% with relative standard deviations ranging between 1.6% and 4.8% were achieved from spiked animal feed samples by using this method. Compared with the traditional ultrasonic extraction, this procedurewas remarkablymore efficient in extracting OTC, TC and CAP, simpler to perform, and there was no use of toxic organic solvents.
KW - chromatography
KW - oxytetracycline
UR - http://handle.uws.edu.au:8081/1959.7/550553
U2 - 10.1016/j.aca.2008.01.026
DO - 10.1016/j.aca.2008.01.026
M3 - Article
SN - 0003-2670
VL - 619
SP - 54
EP - 58
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
IS - 1
ER -