A Fully Automatic HPLC–CAD–DAD Method Coupled with ASE and Online SPE for Simultaneous Determination of Seven Antibiotics in Bio-Matrices

Qian, Zhou; Wang, Nan; Zhu, Lihua; Tang, Heqing

doi:10.1007/s10337-015-2986-8

Cited by 5 publications

(1 citation statement)

References 31 publications

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“…At present, the analytical methods for antibiotics in animal food mainly include liquid chromatography (LC) (Zhou et al, 2015), liquid chromatography tandem triple quadrupole mass spectrometry (LC-MS/MS) (Guidi et al, 2018) and liquid chromatography hybrid quadrupole time-of-flight mass spectrometry (LC-QToFMS) (Ki et al, 2019). An LC method is always equipped with fluorescence detector which has the disadvantage of lower sensitivity and poorer qualitative ability.…”

Section: Introductionmentioning

confidence: 99%

Screening of 49 antibiotic residues in aquatic products using modified QuEChERS sample preparation and UPLC-QToFMS analysis

Gao

Zhang

Huang

et al. 2021

PeerJ Analytical Chemistry

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A precise analytical method was established for rapid screening of 49 antibiotic residues in aquatic products by ultra-high performance liquid chromatography-quadrupole time of flight mass spectrometry (UPLC-QToFMS). The quick, easy, cheap, effective, rugged and safe (QuEChERS) process was refined for effective sample preparation. The homogenized samples of aquatic products were extracted with 3% acetic acid in acetonitrile, salted out with anhydrous magnesium sulfate and sodium chloride, and cleaned up by octadecylsilane (C18) and primary-secondary amine (PSA) powder. Then, the purified samples were separated on a BEH C18 column using 0.1% formic acid and methanol as mobile phases by gradient elution, detected by MS under positive Electron Spray Ionization (ESI+) mode. The linear range of matrix-matched calibration curve was 1–100 μg/L for each compound with the correlation coefficients in the range of 0.9851–0.9999. The recoveries of target antibiotics at the different spiked levels ranged from 60.2% to 117.9% except for lincomycin hydrochloride, whereas relative standard deviations (RSDs) were between 1.6% and 14.0% except for sulfaguanidine in grass Carp, Penaeus vannamei and Scylla serrata matrices. The limits of detection (LODs) (S/N = 3) for the analytes were 0.05–2.40 μg/kg, 0.08–2.00 μg/kg and 0.10–2.27 μg/kg and the limits of quantification (LOQs) (S/N = 10) were 0.16–8.00 μg/kg, 0.25–6.66 μg/kg and 0.32–7.56 μg/kg in grass Carp, Penaeus vannamei and Scylla serrata, respectively. The method was successfully applied to grass Carp, Penaeus vannamei and Scylla serrata, demonstrating its ability for the determination of multi-categories antibiotic residues in aquatic products.

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Section: Introductionmentioning

confidence: 99%