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建立并验证超高效液相色谱-四极杆飞行时间质谱(MS 模式)法,用于定量检测欧洲鲈鱼可食肌肉组织中 20 种抗菌药物残留。

Development and validation of an ultra performance liquid chromatography-quadrupole time of flight-mass spectrometry (in MS mode) method for the quantitative determination of 20 antimicrobial residues in edible muscle tissue of European sea bass.

机构信息

Institute of Marine Biology, Biotechnology and Aquaculture, Hellenic Centre for Marine Research, Agios Kosmas, Hellenikon, 16777 Athens, Greece; Laboratory of Analytical Chemistry, Department of Chemistry, Aristotle University of Thessaloniki, GR-54 124 Thessaloniki, Greece.

Laboratory of Analytical Chemistry, Department of Chemistry, Aristotle University of Thessaloniki, GR-54 124 Thessaloniki, Greece.

出版信息

J Chromatogr A. 2018 Nov 9;1575:40-48. doi: 10.1016/j.chroma.2018.09.017. Epub 2018 Sep 9.

Abstract

A UPLC-QTOF-MS method for the simultaneous determination of 20 veterinary drug residues and metabolites (tetracyclines, quinolones, sulfonamides and diaminopyrimidines) in edible muscle plus skin tissue of European sea bass (Dicentrarchus Labrax) was developed. For the identification of analytes a positive electrospray ionization quadropole time-of flight mass spectrometer operating in MS mode (UPLC-QTOF-MS) was used. MS mode provides high chromatographic resolution and accurate mass measurements in both MS and MS/MS modes simultaneously in a single run. Separation was achieved on a UPLC BEH C18 (50 mm × 2.1 mm, 1.7 μm) column in a gradient elution program of 10 min. Examined antibiotics were isolated easily after a simple solid-liquid extraction procedure with acidic acetonitrile (0.1% v/v formic acid) and NaEDTA 0.1 M. Recovery rates from muscle plus skin tissue ranged from 93.8% to 107.5% for all targeted compounds. The detection limits and the limits of quantification ranged from 2.22 to 15.00 μg/kg, and from 6.67 to 45.46 μg/kg, respectively. The developed method was validated in terms of selectivity, matrix effect, linearity, accuracy, precision, stability and sensitivity, CCα and CCβ according to European Union Decision 2002/657/EC. The proposed method was applied for the analysis of contaminated fish samples after in feed administration of danofloxacin mesylate.

摘要

建立了一种 UPLC-QTOF-MS 方法,用于同时测定欧洲鲈鱼(Dicentrarchus Labrax)可食肌肉加皮组织中的 20 种兽药残留及其代谢物(四环素类、喹诺酮类、磺胺类和二氨基嘧啶类)。为了鉴定分析物,使用正电喷雾电离四极杆飞行时间质谱仪(UPLC-QTOF-MS)在 MS 模式下操作。MS 模式在单次运行中同时提供高色谱分辨率和 MS 和 MS/MS 模式下的准确质量测量。在 UPLC BEH C18(50mm×2.1mm,1.7μm)柱上,采用 10min 的梯度洗脱程序进行分离。经过简单的酸性乙腈(0.1%v/v 甲酸)和 NaEDTA 0.1M 固相萃取程序后,很容易从肌肉加皮组织中分离出被检测的抗生素。所有目标化合物的肌肉加皮组织回收率均在 93.8%至 107.5%之间。检测限和定量限范围分别为 2.22 至 15.00μg/kg 和 6.67 至 45.46μg/kg。根据欧盟 2002/657/EC 号决定,该方法在选择性、基质效应、线性、准确性、精密度、稳定性和灵敏度、CCα 和 CCβ 方面进行了验证。该方法应用于甲磺酸达氟沙星经饲料给药后污染鱼样的分析。

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