首页> 外文期刊>Journal of Analytical Methods in Chemistry >Multiresidue Method for Quantification of Sulfonamides and Trimethoprim in Tilapia Fillet by Liquid Chromatography Coupled to Quadrupole Time-of-Flight Mass Spectrometry Using QuEChERS for Sample Preparation
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Multiresidue Method for Quantification of Sulfonamides and Trimethoprim in Tilapia Fillet by Liquid Chromatography Coupled to Quadrupole Time-of-Flight Mass Spectrometry Using QuEChERS for Sample Preparation

机译:通过液相色谱法与Quadrupole飞行时间质谱法测量罗非鱼内圆角在罗非鱼内圆角的多氟胺和三甲基吡啶的多雷替代方法使用QueChers进行样品制备

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摘要

A multiresidue method for detecting and quantifying sulfonamides (sulfapyridine, sulfamerazine, sulfathiazole, sulfamethazine, sulfadimethoxine, sulfamethoxazole, and sulfamethoxypyridazine) and trimethoprim in tilapia 7 llet (Oreochromis niloticus) using liquid chromatography coupled to mass spectrometry was developed and validated.. e sample preparation was optimized using the QuEChERS approach.. e chromatographic separation was performed using a C18 column and 0.1% formic acid in water and acetonitrile as the mobile phase in the isocratic elution mode. Method validation was performed based on the Commission Decision 2002/657/EC and Brazilian guideline.. e validation parameters evaluated were linearity (r = 0.99); limits of detection (LOD) and quanti 7 cation (LOQ), 1 ng center dot g(-1) and 5 ng center dot g(-1), respectively; intraday and interdays precision (CV lower than 19.4%).. e decision limit (CC alpha 102.6-120.0 ng center dot g(-1) and 70 ng center dot g(-1) for sulfonamides and trimethoprim, respectively) and detection capability (CC ss 111.7-140.1 ng center dot g(-1) and 89.9 ng center dot g(-1) for sulfonamides and trimethoprim, respectively) were determined. Analyses of tilapia 7 llet samples from 7 sh exposed to sulfamethazine through feed (incurred samples) were conducted in order to evaluate the method.. is new method was demonstrated to be fast, sensitive, and suitable for monitoring sulfonamides and trimethoprim in tilapia 7 llet in health surveillance programs, as well as to be used in pharmacokinetics and residue depletion studies.
机译:使用液相色谱法开发使用液相色谱法致荷拉皮脂(磺吡啶,磺胺嘧啶,磺胺嘧啶,磺胺甲嘧啶,磺胺甲嘧啶,磺胺甲嘧啶,磺胺甲嘧啶,磺胺甲苯胺,磺胺甲嘧啶,磺胺甲嘧啶,磺胺甲嘧啶,磺胺甲嘧啶,磺胺甲嘧嘧啶,磺胺甲嘧嘧啶)和三甲嘧啶。使用QueChers方法进行了优化..在水和乙腈中使用C18柱和0.1%甲酸在等离子洗脱模式下进行色谱分离。方法验证是根据委员会决定执行的2002/657 / EC和巴西指南。e验证参数评估为线性度(R> = 0.99);检测限(LOD)和Quanti 7阳离子(LOQ),1ng中心点G(-1)和5 ng中心点G(-1)分别;在内和中间的精度(CV低于19.4%).. E决策限制(CC alpha 102.6-120.0 Ng中心点G(-1)和70ng中心点G(-1)分别用于硫氧酰胺和Trimethoprim)和检测能力(分别为磺胺酰胺和三甲基吡啶的CC SS 111.7-140.1 NG中心点G(-1)和89.9 ng中心点G(-1)。通过进料(诱发样品)暴露于磺胺甲嘧啶的7 sh的罗非鱼7个Llet样品分析,以评估该方法..是新方法,证明是快速,敏感的,适用于罗非鱼7个Llet中的磺胺酰胺和三甲双胍。在卫生监测计划中,以及用于药代动力学和残留耗尽研究。

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