Determination of Sulfamethoxazole,N-acetyl Sulfamethoxazole and Trimethoprim Residues in Fish Tissues by Ultra-high Performance Liquid Chromatography with Modified QuEChERS
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Determination of Sulfamethoxazole,N-acetyl Sulfamethoxazole and Trimethoprim Residues in Fish Tissues by Ultra-high Performance Liquid Chromatography with Modified QuEChERS
刘永涛, 韩刚, 宋金龙, 董靖, 胥宁, 杨移斌, 杨秋红, 艾晓辉. Determination of Sulfamethoxazole,N-acetyl Sulfamethoxazole and Trimethoprim Residues in Fish Tissues by Ultra-high Performance Liquid Chromatography with Modified QuEChERS[J]. 2019, 38(8): 973-978.
DOI:
刘永涛, 韩刚, 宋金龙, 董靖, 胥宁, 杨移斌, 杨秋红, 艾晓辉. Determination of Sulfamethoxazole,N-acetyl Sulfamethoxazole and Trimethoprim Residues in Fish Tissues by Ultra-high Performance Liquid Chromatography with Modified QuEChERS[J]. 2019, 38(8): 973-978.DOI: doi:10.3969/j.issn.1004-4957.2019.08.012.
Determination of Sulfamethoxazole,N-acetyl Sulfamethoxazole and Trimethoprim Residues in Fish Tissues by Ultra-high Performance Liquid Chromatography with Modified QuEChERS
An ultra high performance liquid chromatographic(UPLC) method was established for the rapid determination of sulfamethoxazole(SMZ)
N acetyl sulfamethoxazole(N-ac-SMZ) and trimethoprim(TMP) in fish tissues
including muscle and skin in natural proportions
liver
kidney
gill and plasma.Samples of muscle and skin in natural proportions
liver
kidney and gill tissues of fish were prepared using the modified QuEChERS
and plasma sample was prepared by a liquid-liquid extraction procedure.The analytes were separated on an Acquity UPLC-BEH C18 column(2.1 mm×100 mm,1.7 μm) with methanol and water containing 0.1%acetic acid as mobile phases
at a detection wavelength of 270 nm
using an absorbent minus median baseline filter(MBF) in data acquisition mode.The external standard method was used for quantitation.Results showed that there were good linear relationships for SMZ
N ac-SMZ and TMP in the range of 0.05-10 mg/L with correlation coefficients(r2) not less than 0.998 9.The detection limits and quantitation limits for the analytes in fish tissues were 25 μg/kg and 50 μg/kg
respectively.Recoveries for the target compounds at spiked levels of 0.05-2.00 mg/kg were between 68.2%and 97.3%with relative standard deviations of 1.7%-13%.The method is simple
accurate and highly sensitive
and is suitable for the residue determination
pharmacokinetic and tissue distribution study of SMZ
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