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固相萃取和高效液相色谱-质谱/质谱法优化水中抗生素分析。

Optimization of antibiotic analysis in water by solid-phase extraction and high performance liquid chromatography-mass spectrometry/mass spectrometry.

机构信息

Department of Applied Science, London South Bank University, London, UK.

出版信息

Anal Chim Acta. 2012 Jun 20;731:32-9. doi: 10.1016/j.aca.2012.04.021. Epub 2012 Apr 25.

DOI:10.1016/j.aca.2012.04.021
PMID:22652262
Abstract

This paper describes the development of an optimized method based on solid-phase extraction (SPE) followed by liquid chromatography-electrospray ionization tandem mass spectrometry (LC-MS/MS) for the simultaneous analysis of ten antibiotic compounds including tetracyclines, sulfonamides, macrolides and quinolones. LC-MS/MS sensitivity has been optimized by alterations to both LC and MS operations. Of the two high resolution columns tested, Waters Symmetry C(18) endcapped and Agilent Zorbax Bonus-RP, the latter was found to show better performance in producing sharp peaks and clear separation for most of the target compounds. Optimization of the MS fragmentation collision and cone energy enhanced the peak areas of the target analytes. The recovery of the target compounds from water samples was most efficient on Waters Oasis HLB SPE cartridge, while methanol was shown to be the most suitable solvent for desorbing the compounds from SPE. In addition, acidification of samples prior to SPE was shown to enhance the recovery of the compounds. To ensure a satisfactory recovery, the flow rate through SPE should be maintained at ≤10 mL min(-1). The method was successfully applied to the analysis of antibiotics from environmental water samples, with concentrations being <LOD in tap water, between <LOD to 28 ng L(-1) in river water and between <LOD to 230 ng L(-1) in sewage effluent.

摘要

本文描述了一种基于固相萃取(SPE)的优化方法的开发,该方法随后采用液相色谱-电喷雾串联质谱(LC-MS/MS)对包括四环素、磺胺类、大环内酯类和喹诺酮类在内的十种抗生素化合物进行同时分析。通过对 LC 和 MS 操作的改变,优化了 LC-MS/MS 的灵敏度。在所测试的两个高分辨率柱中,Waters Symmetry C(18) 端封和 Agilent Zorbax Bonus-RP,后者在产生尖锐峰和大多数目标化合物的清晰分离方面表现出更好的性能。优化 MS 碎裂碰撞和锥形能量增强了目标分析物的峰面积。从水样中提取目标化合物的最佳回收率是在 Waters Oasis HLB SPE 小柱上,而甲醇则被证明是从 SPE 中洗脱化合物的最适宜溶剂。此外,在 SPE 之前对样品进行酸化被证明可以提高化合物的回收率。为了确保令人满意的回收率,SPE 的流速应保持在≤10 mL min(-1)。该方法成功应用于环境水样中抗生素的分析,自来水中的浓度低于检测限,河水中的浓度在<LOD 到 28 ng L(-1)之间,污水中的浓度在<LOD 到 230 ng L(-1)之间。

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