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采用 Q-Exactive Orbitrap 高分辨精确质量质谱法单次运行快速极性切换法测定废水中的 30 种药物和个人护理产品。

A single run, rapid polarity switching method for determination of 30 pharmaceuticals and personal care products in waste water using Q-Exactive Orbitrap high resolution accurate mass spectrometry.

机构信息

School of Geography, Earth, and Environmental Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom; Department of Analytical Chemistry, Faculty of Pharmacy, Assiut University, 71526 Assiut, Egypt.

School of Geography, Earth, and Environmental Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.

出版信息

J Chromatogr A. 2019 Mar 15;1588:68-76. doi: 10.1016/j.chroma.2018.12.033. Epub 2018 Dec 21.

Abstract

The analytical capability of the UPLC-Q Exactive™ Orbitrap MS was exploited for simultaneous determination of 30 acidic and basic PPCPs in a single run, using rapid polarity switching of the electrospray ionisation source. Full scan MS mode at resolution of 35,000 FWHM, Automatic gain control (AGC) target of 1E6 ions at injection time of 50 ms provided the optimum parameters for high sensitivity, together with sufficient data points per peak (≥15) for improved reproducibility. In addition to chromatographic retention times, method selectivity was achieved via applying high resolution accurate mass with low mass tolerance filter (<5 ppm) for identification of each target compound. Six-point linear calibration curves (R > 0.95) were established for all target analytes over a concentration range of 1-1500 ng/ml. Good results were obtained for method accuracy (% recovery = 76-104%), inter- and intra-day precision (relative standard deviation <15%) at 3 concentration levels. Instrumental detection and quantification limits ranged from (0.02-1.21 ng/ml) and (0.07-4.05 ng/ml), respectively. While optimised MS/MS analysis through parallel reaction monitoring (PRM) mode provided slightly higher sensitivity, Full scan MS mode allowed for higher mass resolution (selectivity), more data points per peak (reproducibility) and more importantly, the potential for post-acquisition screening of non-target compounds. Following solid phase extraction (SPE) of target analytes, the method was successfully applied to provide first data on PPCPs occurrence in effluent and surface water samples (n = 10) from Egypt. Moreover, screening for non-target compounds revealed the presence of bisphenol A, which was further confirmed via matching with an authentic standard. Overall, this study provides first insight into the high analytical capabilities of the Q-Exactive™ Orbitrap platform for both targeted/non-targeted analysis of PPCPs in environmental matrices.

摘要

UPLC-Q Exactive™ Orbitrap MS 的分析能力得到了利用,通过电喷雾离子源的快速极性切换,在单次运行中同时测定 30 种酸性和碱性 PPCPs。在全扫描 MS 模式下,分辨率为 35,000 FWHM,注入时间为 50 ms 时的自动增益控制 (AGC) 目标为 1E6 离子,为提高灵敏度提供了最佳参数,同时每个峰的峰点数(≥15)也足够,提高了重现性。除了色谱保留时间外,还通过应用高分辨率精确质量和低质量容限过滤器(<5 ppm)来实现方法选择性,以鉴定每个目标化合物。所有目标分析物在 1-1500 ng/ml 的浓度范围内建立了 6 点线性校准曲线(R>0.95)。在 3 个浓度水平下,方法的准确度(%回收率=76-104%)、日内和日间精密度(相对标准偏差<15%)均得到了良好的结果。仪器检测限和定量限范围分别为(0.02-1.21 ng/ml)和(0.07-4.05 ng/ml)。虽然通过平行反应监测(PRM)模式优化的 MS/MS 分析提供了稍高的灵敏度,但全扫描 MS 模式允许更高的质量分辨率(选择性)、每个峰更多的峰点数(重现性),更重要的是,在采集后有潜力筛选非目标化合物。在目标分析物固相萃取(SPE)后,该方法成功地应用于提供埃及废水和地表水样品(n=10)中 PPCPs 存在情况的首批数据。此外,非目标化合物的筛选显示出双酚 A 的存在,并用与真实标准相匹配进一步证实了这一点。总的来说,本研究首次深入了解了 Q-Exactive™Orbitrap 平台在环境基质中对 PPCPs 的靶向/非靶向分析的高分析能力。

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