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The effect of signal suppression and mobile phase composition on the simultaneous analysis of multiple classes of acidic/neutral pharmaceuticals and personal care products in surface water by solid-phase extraction and ultra performance liquid chromatography-negative electrospray tandem mass spectrometry
被引:120
作者:
Kasprzyk-Hordern, Barbara
[1
]
Dinsdale, Richard M.
[1
]
Guwy, Alan J.
[1
]
机构:
[1] Univ Glamorgan, Sustainable Environm Res Ctr, Pontypridd CF37 1DL, M Glam, Wales
来源:
关键词:
pharmaceuticals and personal care products;
ultra performance liquid chromatograpby-tandem mass spectrometry;
solid-phase extraction;
multi-residue method;
ion suppression;
mobile-phase additives;
D O I:
10.1016/j.talanta.2007.08.037
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Anew multi-residue method for the determination of 25 acidic/neutral pharmaceuticals (antibiotics, anti-inflammatory/analgesics, lipid regulating agents, diuretics, triazides, H2-receptor antagonists, cardiac glicozides and angiotensin II antagonists) and personal care products (sunscreen agents and preservatives) in surface water with the usage of a new technique: ultra performance liquid chromatography-negative electrospray tandem mass spectrometry (lJPLC-MS/MS) was developed and validated. The novel UPLC system with 1.7 mu m particle-packed column allowed for good resolution of analytes with the application of low mobile phase flow rates (0.05 mL min(-1)) and short retention times (from 4.7 min to 13.3 min) delivering a fast and cost-effective multi-residue method. SPE with the usage of Oasis MCX strong cation-exchange mixed-mode polymeric sorbent was chosen for sample clean-up and concentration. The influence of mobile-phase composition, matrix assisted ion suppression and SPE recovery on the sensitivity of the method was identified and quantified. The instrumental limits of quantification varied from 0.2 mu g L-1 to 30 mu g L-1. The method limits of quantification were at low nanogram per litre levels and ranged from 0.3 ng L-1 to 30 ng L-1. The instrumental and method intra-day and inter-day repeatabilities were on average less than 5%. The method was successfully applied for the determination of PPCPs in River Taff. Thirteen compounds were determined in river water at levels ranging from a single to a few hundred nanograms per litre. Among them were ten pharmaceuticals (aspirin, salicylic acid, ketoprofen, naproxen, diclofenac, ibuprofen, mefenamic acid, furosemide, sulfasalazine and valsartan) and three personal care products (methyl- and ethylparaben and 4-benzophenone). (c) 2007 Elsevier B.V. All rights reserved.
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页码:1299 / 1312
页数:14
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