首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development of a subcritical water extraction approach for trace analysis of chloramphenicol, thiamphenicol, florfenicol, and florfenicol amine in poultry tissues
【24h】

Development of a subcritical water extraction approach for trace analysis of chloramphenicol, thiamphenicol, florfenicol, and florfenicol amine in poultry tissues

机译:亚临界水萃取方法的开发,用于家禽组织中的氯霉素,甲砜霉素,氟苯尼考和氟苯尼考胺的痕量分析

获取原文
获取原文并翻译 | 示例
           

摘要

Subcritical water extraction was investigated as a novel and alternative technology for the separation of trace amounts of chloramphenicol, thiamphenicol, florfenicol and its major metabolite florfenicol amine from poultry tissues and its results were compared with those of conventional shaking extraction, ultrasonic extraction, and pressurized liquid extraction. Decreasing the polarity of water by successively increasing the extraction temperature from 50 degrees C to 200 degrees C at the moderate pressure enabled selective, highly effective extractions to be performed. Rapid quantification of the target compounds was carried out by ultra-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry (UPLC-ESI-MS/MS). The critical parameters of subcritical water extraction such as solvent modifier, temperature, pressure, extraction time, and static cycles were varied with control. The optimized extraction procedures using subcritical water as extraction solvent, were carried out on a pressurized liquid extractor operated at 150 degrees C and 100 bar, applying two static cycles for 3 min. Average recoveries of the four analytes from fortified samples ranged between 86.8% and 101.5%, with relative standard deviations (RSDs) lower than 7.7%. The limits of detection (LODs) and quantification (LOQs) for the target compounds were in the ranges of 0.03-0.5 mu g kg(-1) and 0.1-2.0 mu g kg(-1), respectively. The proposed method is fast, sensitive, water-based thus more environmental acceptable, making it a suitable replacement for conventional organic solvent extraction in veterinary drug residue analysis. (C) 2015 Elsevier B.V. All rights reserved.
机译:研究亚临界水萃取是一种从禽类组织中分离痕量氯霉素,甲砜霉素,氟苯尼考及其主要代谢物氟苯尼考胺的新型替代技术,并将其结果与常规摇动萃取,超声萃取和加压液体的结果进行了比较。萃取。通过在适度的压力下将萃取温度从50摄氏度连续提高到200摄氏度来降低水的极性,可以进行选择性,高效的萃取。通过超高效液相色谱结合电喷雾电离串联质谱分析法(UPLC-ESI-MS / MS)对目标化合物进行快速定量。亚临界水萃取的关键参数(如溶剂改性剂,温度,压力,萃取时间和静态循环)随控制而变化。使用亚临界水作为萃取溶剂的优化萃取程序在压力为150℃,压力为100 bar的液体萃取器上进行,两次静态循环持续3分钟。强化样品中四种分析物的平均回收率介于86.8%和101.5%之间,相对标准偏差(RSD)低于7.7%。目标化合物的检出限(LOD)和定量限(LOQ)分别在0.03-0.5μg kg(-1)和0.1-2.0μgkg(-1)范围内。所提出的方法是快速,灵敏的,水基的,因此更能被环境接受,使其成为兽药残留分析中常规有机溶剂萃取的合适替代品。 (C)2015 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号