Determination of widely used non-steroidal anti-inflammatory drugs in water samples by in situ derivatization, continuous hollow fiber liquid-phase microextraction and gas chromatography-flame ionization detector

被引:81
作者
Es'haghi, Z. [1 ,2 ]
机构
[1] Payame Noor Univ, Fac Sci, Dept Chem, Tehran, Iran
[2] Ferdowsi Univ Mashhad, Biotechnol Res Ctr, Mashhad, Iran
关键词
Continuous hollow fiber liquid-phase microextraction; Non-steroidal anti-inflammatory drugs; Water sample; Gas chromatography-flame ionization detector; CAPILLARY-ELECTROPHORESIS; CLOFIBRIC ACID; MASS-SPECTROMETRY; WASTE-WATER; SURFACE; PHARMACEUTICALS; QUANTIFICATION; DICLOFENAC; IBUPROFEN; RESIDUES;
D O I
10.1016/j.aca.2009.03.043
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The aim of this study was to develop an analytical procedure which allows the quantification of pharmaceuticals in water at the ng L-1 level. Hence, it is reported research on the application of a rapid, inexpensive and simple continuous hollow fiber liquid-phase micro extraction (CHF-LPME) for the pre-concentration and determination of non-steroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen (IBP), naproxen (NAP), and ketoprofen (KEP), in wastewater. In this method. a 2.50 cm end sealed piece of a polypropylene hollow fiber was immersed into the organic solvent, octanol. for 30 s. After solvent impregnation with the pores of the fiber, the excess amounts of solvent were removed from inside the fiber, and 4.0 mu L of octanol, as the acceptor phase, was injected into the fiber carefully. The fiber was settled using a microsyringe into a 10.0 mL. glass test tube, and 20.00 mL of the aqueous solution (the donor phase), was circulated by a pump around it. After analyte extraction for an optimized period of time (20 min), 2 mu L of the organic solvent was withdrawn into the microsyringe and injected into the CC-FID for further analysis. Finally, based oil the optimized analytical conditions, the method was linear in the range of 2.5-500 ng L-1. The limits of detection were 1-2 ng L-1. Repeatability of this method on an intra-day scale was 3.4-10.2% (RSD%). NSAIDs have been detected in several municipal wastewater samples, and the concentration range was 9.0-19.0 ng L-1. 0 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 88
页数:6
相关论文
共 30 条
[1]   Determination of drug residues in water by the combination of liquid chromatography or capillary electrophoresis with electrospray mass spectrometry [J].
Ahrer, W ;
Scherwenk, E ;
Buchberger, W .
JOURNAL OF CHROMATOGRAPHY A, 2001, 910 (01) :69-78
[2]   Determination of organochlorine pesticides in seawater using liquid-phase hollow fibre membrane microextraction and gas chromatography-mass spectrometry [J].
Basheer, C ;
Lee, HK ;
Obbard, JP .
JOURNAL OF CHROMATOGRAPHY A, 2002, 968 (1-2) :191-199
[3]   Occurrence of the pharmaceutical drug clofibric acid and the herbicide mecoprop in various Swiss lakes and in the North Sea [J].
Buser, HR ;
Muller, MD ;
Theobald, N .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (01) :188-192
[4]   Occurrence and fate of the pharmaceutical drug diclofenac in surface waters: Rapid photodegradation in a lake [J].
Buser, HR ;
Poiger, T ;
Muller, MD .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (22) :3449-3456
[5]   In-tube solid phase microextraction using a β-cyclodextrin coated capillary coupled to high performance liquid chromatography for determination of non-steroidal anti-inflammatory drugs in urine samples [J].
Fan, Y ;
Feng, YQ ;
Da, SL ;
Wang, ZH .
TALANTA, 2005, 65 (01) :111-117
[6]   Simultaneous analysis of neutral and acidic pharmaceuticals as well as related compounds by gas chromatography-tandem mass spectrometry in wastewater [J].
Gomez, M. J. ;
Agueera, A. ;
Mezcua, M. ;
Hurtado, J. ;
Mocholi, F. ;
Fernandez-Alba, A. R. .
TALANTA, 2007, 73 (02) :314-320
[7]   Determination of selected human pharmaceutical compounds in effluent and surface water samples by high-performance liquid chromatography-electrospray tandem mass spectrometry [J].
Hilton, MJ ;
Thomas, KV .
JOURNAL OF CHROMATOGRAPHY A, 2003, 1015 (1-2) :129-141
[8]   25,000-fold pre-concentration in a single step with liquid-phase microextraction [J].
Ho, Tung Si ;
Vasskog, Terje ;
Anderssen, Trude ;
Jensen, Einar ;
Rasmussen, Knut Einar ;
Pedersen-Bjergaard, Stig .
ANALYTICA CHIMICA ACTA, 2007, 592 (01) :1-8
[9]   Dynamic three-phase microextraction as a sample preparation technique prior to capillary electrophoresis [J].
Hou, L ;
Lee, HK .
ANALYTICAL CHEMISTRY, 2003, 75 (11) :2784-2789
[10]   Determination of non-steroidal anti-inflammatory drug (NSAIDs) residues in water samples [J].
Kosjek, T ;
Heath, E ;
Krbavcic, A .
ENVIRONMENT INTERNATIONAL, 2005, 31 (05) :679-685