Application of the Mechanical High-Pressure Method Combined with High-Performance Liquid Chromatography–Tandem Mass Spectrometry for Determination of Veterinary Drug Residues in Incurred Chicken and Rabbit Muscle Tissues

2019 ◽  
Vol 82 (3) ◽  
pp. 415-421 ◽  
Author(s):  
MINGXIA LIU ◽  
ZHEN WANG ◽  
XIANGJUN LI ◽  
XIAOGANG CHU ◽  
YALEI DONG ◽  
...  

ABSTRACTRapid sample preparation is a key step in the field of food safety. A mechanical high-pressure method using a laboratory-made meat press machine was first introduced in this study to process the incurred muscle samples of chicken and rabbit. By applying high pressure to animal muscle, the meat juice was obtained. After extraction and purification, veterinary drug residues in the juice were qualitatively and quantitatively analyzed by using high-performance liquid chromatography–tandem mass spectrometry. The sample press conditions and extraction solvents were optimized. Under the optimal conditions, all veterinary drug residues, including tetracycline, enrofloxacin, clenbuterol, ampicillin, lincomycin, erythromycin, and sulfadiazine, in the incurred samples were detected. The residual concentration of drugs in samples obtained by using the mechanical high-pressure method can reach up to 94.0% of that obtained by using the common homogenization method, suggesting that drug residues exist in the tissue juice, which justifies the use of the mechanical high-pressure method. Moreover, with the mechanical high-pressure method, the sample preparation time was shortened by five times, and the consumption of the extraction solvent was reduced by 50%, relative to the homogenization method.

2016 ◽  
Vol 10 (4) ◽  
pp. 1063-1077 ◽  
Author(s):  
Flávia Lada Degaut Pontes ◽  
João Cleverson Gasparetto ◽  
Thais Martins Guimarães de Francisco ◽  
Heloise Calzado Goetzke ◽  
Letícia Paula Leonart ◽  
...  

2021 ◽  
Vol 64 (1) ◽  
Author(s):  
Eunjung Kim ◽  
Hyunjin Park ◽  
Sihyun Park ◽  
Jangduck Choi ◽  
Hae Jung Yoon ◽  
...  

AbstractThe objective of this study was to optimize the analytical method for multi-class veterinary drug residues of 64 compounds in fishery products. Several compounds from veterinary drugs are banned or unauthorized in fishery products according to the Korean Food Code. Samples were extracted using acetonitrile/water (4:1, v/v) and the clean-up step was carried out by adding octadecylsilane and acetonitrile-saturated hexane. The target compounds were confirmed and quantified using liquid chromatography–tandem mass spectrometry (LC–MS/MS). The proposed method was validated according to the CODEX guidelines (CAC/GL-71), and most target compounds were found to be in acceptable quantities under the requirements of the validation guidelines. The recovery of analytes was typically in the 60–120% range, and precision, expressed as the coefficient of variation was less than 31% at all levels of concentration. The limit of quantification ranged from 0.03 to 3 μg kg−1 in the fishery products. Moreover, the application of the proposed method to 96 real samples demonstrated that no drug residues exceeded the Korean maximum residue limits (MRLs). This evaluation method provides reliable identification and quantification of multi-class veterinary drugs in fishery products and can be an efficient means to inspect drugs currently banned or not approved for aquaculture in Korea.


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