National Institute for Alternative Technologies of Detection, Toxicological Evaluation and Removal of Micropollutants and Radioactives (INCT-DATREM), Institute of Chemistry, São Paulo State University, P.O. Box 355, Araraquara, SP, 14800-060, Brazil.
College of Veterinary Medicine, Department of Physiological Sciences, University of Florida, P.O. Box 490, Gainesville, FL, 32601, USA.
Anal Bioanal Chem. 2021 Aug;413(20):5147-5160. doi: 10.1007/s00216-021-03481-7. Epub 2021 Jun 26.
An automated method was developed using on-line solid-phase extraction (SPE) as a sample preparation step, coupled to liquid chromatography-tandem mass spectrometry (LC-MS/MS), for determination of pharmaceutical compounds in wastewater samples at nanograms per liter to micrograms per liter concentration levels. This method is suitable for use in routine analysis, especially in environmental applications, avoiding cross-contamination and requiring minimal sample handling. Results can be obtained rapidly, with a chromatographic run time of only 24 min (including sample preparation and chromatographic analysis). Using a 50 μL injection volume, the method was validated according to international guidelines, considering parameters included in terms of method detection (MDL) and quantification limit (MQL), linearity, inter-day and intra-day precisions, and matrix effects. Assessment of chromatographic efficiency considered peak resolution and asymmetry, and carryover was evaluated to ensure analytical reliability and the ability to reuse the SPE cartridge. The intra- and inter-day precisions were lower than 10 and 17%, respectively. The MDL values ranged from 1×10 to 1 μg L, while the MQL values were from 0.001 to 3 μg L. Matrix effects were minimized by isotope dilution calibration. Application of the method to 20 wastewater samples showed that caffeine was the most frequently detected compound, with the highest concentration of 715 μg L, while other pharmaceutical compounds were detected in fewer samples and at lower concentrations (up to 8.51 μg L).
开发了一种自动化方法,使用在线固相萃取(SPE)作为样品制备步骤,与液相色谱-串联质谱(LC-MS/MS)联用,用于测定纳克/升至微克/升浓度水平的废水中的药物化合物。该方法适用于常规分析,特别是在环境应用中,可避免交叉污染,所需样品处理最少。结果可快速获得,色谱运行时间仅为 24 分钟(包括样品制备和色谱分析)。使用 50 μL 的进样体积,根据国际指南对方法进行了验证,考虑了方法检测限(MDL)和定量限(MQL)、线性、日间和日内精密度以及基质效应等参数。评估色谱效率时考虑了峰分辨率和不对称性,并评估了交叉污染以确保分析可靠性和能够重复使用 SPE 卡。日内和日间精密度分别低于 10%和 17%。MDL 值范围为 1×10 至 1 μg L,而 MQL 值范围为 0.001 至 3 μg L。通过同位素稀释校准最小化了基质效应。该方法应用于 20 个废水样品,结果表明咖啡因是最常检测到的化合物,浓度最高达 715 μg L,而其他药物化合物在较少的样品中以较低的浓度(高达 8.51 μg L)检测到。