Ultrasound-assisted emulsification microextraction based on a solidified floating organic droplet for the rapid determination of 19 antibiotics as environmental pollutants in hospital drainage and Gomti river water

被引:30
|
作者
Jha, Rakesh Roshan [1 ,2 ]
Singh, Nivedita [3 ,5 ]
Kumari, Rupender [4 ]
Patel, Devendra Kumar [1 ,2 ]
机构
[1] CSIR IITR, Analyt Chem Lab, Regulatory Toxicol Grp, Vishvigyan Bhawan,31,Mahatma Gandhi Marg, Lucknow 226001, Uttar Pradesh, India
[2] Acad Sci & Innovat Res AcSIR, CSIR IITR Campus, Lucknow, Uttar Pradesh, India
[3] BBD Univ, Babu Banarasi Das BBD Coll Dent Sci, Dept Biochem, Lucknow, Uttar Pradesh, India
[4] CFSL, Toxicol Div, Kolkata, India
[5] CSIR IITR, Syst Toxicol, Lucknow, Uttar Pradesh, India
关键词
antibiotics; microextraction; pollution; river water; PERFORMANCE LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; PHASE MICROEXTRACTION; WASTE-WATER; HUMAN HEALTH; VETERINARY ANTIBIOTICS; AQUATIC ENVIRONMENT; RISK-ASSESSMENT; DRINKING-WATER; SURFACE WATERS;
D O I
10.1002/jssc.201700170
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Antibiotics that are used excessively and disposed of improperly are categorized as emerging pollutants. The determination of micropollutants in water with an accurate and precise method is always a big challenge. Hence, a simple, rapid, sensitive, economical and almost eco-friendly method is proposed for the quantitative determination of 19 antibiotics. The proposed method, ultrasound-assisted emulsification microextraction and solidified floating organic droplet coupled with liquid chromatography and triple quadrupole mass spectrometry, has only a 3 min chromatographic run time for the determination of the 19 antibiotics. We report for the first time the use of the developed method for the quantitative determination of the antibiotics in waste water samples with better results in terms of higher sensitivity, cost-effectiveness, better detection limits and a greener approach compared to the earlier reported methods. The limits of detection and quantification were in the range of 0.003-0.236 and 0.013-0.834 mu g/L, respectively, with good linearity in the concentration range of 0.01-64.0 mu g/L. The correlation coefficient was >= 0.987-0.99 for each analyte. The developed method has been successfully applied for the determination of antibiotics in water samples.
引用
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页码:2694 / 2702
页数:9
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