Residual detection of naproxen, methyltestosterone and 17α-hydroxyprogesterone caproate in aquatic products by simple liquid-liquid extraction method coupled with liquid chromatography-tandem mass spectrometry

被引:9
作者
Zheng, Weijia [1 ]
Yoo, Kyung-Hee [1 ]
Choi, Jeong-Min [1 ]
Park, Da-Hee [1 ]
Kim, Seong-Kwan [1 ]
Kang, Young-Sun [1 ,2 ]
Abd El-Aty, A. M. [3 ,4 ]
Hacimuftuoglu, Ahmet [4 ]
Wang, Jing [5 ]
Shim, Jae-Han [6 ]
Shin, Ho-Chul [1 ]
机构
[1] Konkuk Univ, Dept Vet Pharmacol & Toxicol, Coll Vet Med, Seoul 143701, South Korea
[2] Konkuk Univ, Dept Biomed Sci & Technol, Seoul, South Korea
[3] Cairo Univ, Dept Pharmacol, Fac Vet Med, Giza 12211, Egypt
[4] Ataturk Univ, Med Fac, Dept Med Pharmacol, Erzurum, Turkey
[5] Chinese Acad Agr Sci, Inst Qual Standard & Testing Technol Agroprod, Key Lab Agroprod Qual & Safety, Beijing, Peoples R China
[6] Chonnam Natl Univ, Coll Agr & Life Sci, Nat Prod Chem Lab, Gwangju, South Korea
关键词
17 alpha-hydroxyprogesterone carproate; aquatic product; LC-MS/MS; methyltestosterone; naproxen; residue; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; ANABOLIC-STEROIDS RESIDUES; SOLID-PHASE EXTRACTION; QUANTITATIVE-DETERMINATION; PHARMACEUTICAL RESIDUES; MUSCLE-TISSUES; RAINBOW-TROUT; PRETERM BIRTH; ANIMAL MUSCLE; PERFORMANCE;
D O I
10.1002/bmc.4396
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In the present study, we aimed to develop a reliable screening method based on liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) for the detection and quantification of naproxen, methyltestosterone and 17 alpha-hydroxyprogesterone caproate residues. The target analytes were extracted from samples of eel, flatfish and shrimp using acetonitrile with 1% acetic acid, followed by liquid-liquid purification with n-hexane. Chromatographic separation was achieved on a reversed-phase analytical column using 0.1% formic acid containing 10 mm ammonium formate in distilled water (A) and methanol (B) as mobile phases. All the matrix-matched calibration curves were linear (R-2 >= 0.99) over the concentration range of the tested analytes. Recovery at three spiking levels (0.005, 0.01 and 0.02 mg/kg) ranged from 68 to 117% with intra- and inter-day precisions <10%. Five market samples for each matrix (eel, flatfish and shrimp) were collected and tested for method application. In summary, the proposed method is feasible to screen and quantify the analytes with high selectivity in aquatic food products meant for human consumption.
引用
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页数:9
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