Department of Chemistry and Biochemistry, Florida International University, 3000 NE 151 Street, Biscayne Bay Campus Marine Sciences Building, MSB356, North Miami, FL 33181, USA.
Anal Bioanal Chem. 2013 Jul;405(18):5953-64. doi: 10.1007/s00216-013-6863-8. Epub 2013 Mar 14.
An online solid-phase extraction and liquid chromatography in combination with tandem mass spectrometry method was developed for the simultaneous determination of 31 antibiotics in drinking water, surface water and reclaimed waters. The developed methodology requires small sample volume (10 mL), very little sample preparation and total sample run time was 20 min. An Ion Max API heated electrospray ionization source operated in the positive mode with two selected reaction monitoring transitions was used per antibiotic for positive identity and quantification performed by the internal standard approach, to correct for matrix effects and any losses in the online extraction step. Method detection limits were in the range of 1.2-9.7, 2.2-15, 5.5-63 ng/L in drinking water, surface water and reclaimed waters, respectively. The method accuracy in matrix spiked samples ranged from 50-150% for the studied antibiotics. The applicability of the method was demonstrated using various environmental and reclaimed water matrices. Erythromycin was detected in more than 85% of the samples in all matrices (28-414, n.d.-199, n.d.-66 ng/L in reclaimed, river and drinking waters respectively). The other frequently detected antibiotics in reclaimed waters were nalidixic acid, clarithromycin, azithromycin, trimethoprim, and sulfamethoxazole.
建立了一种在线固相萃取和液相色谱串联质谱法,用于同时测定饮用水、地表水和再生水中的 31 种抗生素。所建立的方法需要小体积的样品(10mL),很少的样品制备,总样品运行时间为 20 分钟。采用 Ion Max API 加热电喷雾电离源,在正模式下,每个抗生素使用两个选择的反应监测转换,进行阳性鉴定和内标法定量,以校正基质效应和在线提取步骤中的任何损失。方法检测限分别为 1.2-9.7、2.2-15 和 5.5-63ng/L,在饮用水、地表水和再生水中。在基质加标样品中,该方法的准确度在研究的抗生素的 50-150%之间。该方法的适用性通过各种环境和再生水基质得到了证明。在所有基质中(再生水、河流和饮用水中分别为 28-414、n.d.-199 和 n.d.-66ng/L),红霉素在超过 85%的样品中被检出。在再生水中经常检测到的其他抗生素有萘啶酸、克拉霉素、阿奇霉素、甲氧苄啶和磺胺甲恶唑。