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采用简单液液萃取法结合液相色谱-串联质谱法对水产品中萘普生、甲基睾酮和己酸17α-羟基孕酮进行残留检测。

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.

作者信息

Zheng Weijia, Yoo Kyung-Hee, Choi Jeong-Min, Park Da-Hee, Kim Seong-Kwan, Kang Young-Sun, Abd El-Aty A M, Hacımüftüoğlu Ahmet, Wang Jing, Shim Jae-Han, Shin Ho-Chul

机构信息

Department of Veterinary Pharmacology and Toxicology, College of Veterinary Medicine, Konkuk University, Seoul, Republic of Korea.

Department of Biomedical Science and Technology, Konkuk University, Seoul, Republic of Korea.

出版信息

Biomed Chromatogr. 2019 Jan;33(1):e4396. doi: 10.1002/bmc.4396. Epub 2018 Oct 17.

Abstract

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 17α-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  ≥ 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.

摘要

在本研究中,我们旨在开发一种基于液相色谱-串联质谱联用(LC-MS/MS)的可靠筛选方法,用于检测和定量萘普生、甲基睾酮和己酸17α-羟基孕酮残留量。目标分析物用含1%乙酸的乙腈从鳗鱼、比目鱼和虾的样品中提取,然后用正己烷进行液-液净化。在反相分析柱上进行色谱分离,以蒸馏水中含10 mM甲酸铵的0.1%甲酸(A)和甲醇(B)作为流动相。所有基质匹配校准曲线在测试分析物的浓度范围内呈线性(R≥0.99)。在三个加标水平(0.005、0.01和0.02 mg/kg)下的回收率为68%至117%,日内和日间精密度<10%。收集了每种基质(鳗鱼、比目鱼和虾)的五个市售样品并进行方法应用测试。总之,所提出的方法对于筛选和定量供人类食用的水产食品中的分析物具有高选择性,是可行的。

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