Rapid Determination of Tetracyclines in Drinking and Environmental Waters Using Fully Automatic Solid-Phase Extraction with Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry

• Published in: Molecules (Basel, Switzerland) Vol. 29; no. 12; p. 2921
• Main Authors: Zhang, Tongtong, Zhang, Xiangyang, Yu, Jiangmei, Hu, Hongmei, He, Pengfei, Li, Zhenhua, Fang, Yi, Li, Tiejun, Guo, Yuanming
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 19.06.2024; MDPI
• Subjects: Antibiotics; Aquaculture industry; automated solid-phase extraction; Automation; Chromatography; Chromatography, High Pressure Liquid - methods; Drinking water; Drinking Water - analysis; Drinking Water - chemistry; Ethylenediaminetetraacetic acid; isotope dilution; Limit of Detection; Mass spectrometry; Optimization; Oxytetracycline; Scientific imaging; Sea-water; Solid Phase Extraction - methods; Solvents; Tandem Mass Spectrometry - methods; tetracyclines; Tetracyclines - analysis; ultra-performance liquid chromatography–tandem mass spectrometry; Water; water matrix; Water Pollutants, Chemical - analysis; China; United States > US; automated solid-phase extraction; ultra-performance liquid chromatography–tandem mass spectrometry; isotope dilution; tetracyclines; water matrix
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules29122921

The abuse and irrational use of tetracyclines (TCs) in human medicine and animal husbandry has become a serious concern, affecting the ecological environment and human health. The aim of this study was to develop a sensitive and selective method using fully automatic solid-phase extraction coupled with ultra-performance liquid chromatography-tandem mass spectrometry for the determination of twelve TCs in water. Four isotope-labeled internal standards for TCs were used to correct matrix effects. Several parameters affecting extraction efficiency were systematically optimized, and the optimum experimental conditions found were 1.0 L water sample with 0.5 g/L Na EDTA (pH 3.0) extracted and enriched by CNW HLB cartridge and eluted by 4 mL of acetone:methanol ( / , 1:1). The enrichment factors were up to 798-1059 but only requiring about 60 min per six samples. Under the optimized conditions, the linearity of the method ranged from 0.2 to 100 μg/L for 12 TCs, the detection limits were as low as 0.01-0.15 ng/L, and the recoveries were in the range of 70%-118%, with relative standard deviations less than 15%. The developed method can be successfully utilized for the determination of 12 TCs in pure water, tap water, river water, and mariculture seawater. In summary, three and six TCs were detected in river water and mariculture seawater, respectively, with total concentrations of 0.074-0.520 ng/L (mean 0.248 ng/L) and 0.792-58.369 ng/L (12.629 ng/L), respectively. Tetracycline (TC) and oxytetracycline (OTC) were the dominant TCs in river water, while doxytetracycline (DXC) and OTC were dominant in mariculture seawater.