CAS Key Laboratory of Urban Pollutant Conversion, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021, China.
Anal Methods. 2021 Jan 28;13(3):299-310. doi: 10.1039/d0ay02022b.
A convenient, effective, and low-cost method was developed for the determination of 38 pharmaceuticals and personal care products (PPCPs), including 19 antibiotics in surface water samples by lyophilization combined with liquid chromatography-tandem quadrupole mass spectrometry (LC-MS/MS). The components of the extraction solvent, the volume of the water sample, and the volume of extraction solvent were successively optimized. The analytes in 80 mL water samples were concentrated by lyophilization, eluted effectively by the solvent of 2 mL acetonitrile, 2 mL acetone, and 2 mL ultrapure water. The method detection limits ranged from 0.02 ng L-1 (caffeine) to 0.17 μg L-1 (glibenclamide). The recoveries of 30 analytes ranged from 40.0% (sulfaguanidine) to 124.4% (flumequine). The relative standard deviations of all analytes were below 21% except ciprofloxacin (29%). The performance of the optimized method was comparable to the solid phase extraction and ultrasonic extraction method with much less consumption of labor, organic solvent, and consumables. The developed method was successfully applied to surface river water, reservoir water, and effluent of the wastewater treatment plant.
建立了一种简便、高效、低成本的方法,用于测定地表水中的 38 种药物和个人护理产品(PPCPs),包括 19 种抗生素,采用冻干法结合液相色谱-串联四极杆质谱法(LC-MS/MS)进行分析。优化了萃取溶剂的组成、水样的体积和萃取溶剂的体积。80 mL 水样中的分析物经冻干浓缩,用 2 mL 乙腈、2 mL 丙酮和 2 mL 超纯水的混合溶剂有效洗脱。方法检出限范围为 0.02ng L-1(咖啡因)至 0.17μg L-1(格列本脲)。30 种分析物的回收率范围为 40.0%(磺胺脒)至 124.4%(氟甲喹)。除环丙沙星(29%)外,所有分析物的相对标准偏差均低于 21%。与固相萃取和超声萃取方法相比,优化方法的性能相当,但消耗的劳动力、有机溶剂和消耗品要少得多。该方法已成功应用于地表河水、水库水和污水处理厂的出水。