Chinese Journal of Chromatography ›› 2013, Vol. 31 ›› Issue (1): 15-21.DOI: 10.3724/SP.J.1123.2012.09015

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Simultaneous determination of 18 pharmaceuticals and personal care products in surface water by ultra-high performance liquid chromatography-tandem mass spectrometry

ZHU Saichang1, WANG Jing2, SHAO Weiwei2, CHEN Hong1*   

  1. 1. Department of Environmental Engineering, College of Environmental and Resource Science of Zhejiang University, Hangzhou 310058, China; 2. Zhejiang Environmental Monitoring Center, Hangzhou 310058, China
  • Received:2012-09-10 Revised:2012-10-16 Online:2013-01-28 Published:2013-01-21

Abstract: An analytical method has been developed and validated for the simultaneous determination of 18 pharmaceuticals and personal care products (PPCPs), including antibiotics (trimethoprim, erythromycin•2H2O, norfloxacin, ofloxacin, pencilline G, penicillin V potassium salt, cephalexin and sulfamethoxazole), β-bloker (atenolol), anophelifuge (N,N-diethyl-3-methylbenzoylamide, DEET), antiepileptics (carbamazepine), central nervous system stimulant (caffeine), lipid modifying agent (clofibric acid), non-steroidal anti-inflammatory drugs (ibuprofen, naproxen and diclofenac sodium salt) and antimicrobial agents (triclosan and triclocarban). The detection and qualification of the target compounds were performed by ultra-high performance liquid chromatography-tandem mass spectrometry. The optimized mobile phases were methanol as organic phase, 0.3% (v/v) formic acid-5 mmol/L ammonium acetate for positive electrospray ionization (ESI+) and 5 mmol/L ammonium acetate for ESI- as inorganic phase. Water samples were concentrated by solid phase extraction at 2 mL/min, and all the target PPCPs were efficiently extracted at pH 7. The extracted PPCPs were eluted by the mixture of methanol and acetonitrile (1:1, v/v). The average recoveries of the target compounds in the spiked pure water samples ranged from 53.9%-112%. The average recoveries of the target compounds ranged from 45.1%-156.6% with the relative standard deviations ranged from 2.4%-15.7%, in the surface water samples spiked at 100 ng/L. The surface water samples collected from Yu Hangtang River in Hangzhou were detected. The results showed that nine PPCPs were detected including caffeine that reached a maximum concentration of 550.7 ng/L. It proved that this analytical method is reliable and acceptable.

Key words: pharmaceuticals and personal care products, surface water, solid phase extraction (SPE), ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS)