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Determination of urinary triclosan by stir bar sorptive extraction and thermal desorption-gas chromatography-mass spectrometry
被引:32
|作者:
Kawaguchi, Migaku
[1
]
Ito, Rie
[1
]
Honda, Hidehiro
[1
]
Endo, Naoyuki
[1
]
Okanouchi, Noriya
[1
]
Saito, Koichi
[1
]
Seto, Yasuo
[2
]
Nakazawa, Hiroyuki
[1
]
机构:
[1] Hoshi Univ, Fac Pharmaceut Sci, Dept Analyt Chem, Shinagawa Ku, Tokyo 1428501, Japan
[2] Natl Res Inst Police Sci, Kashiwa, Chiba 2770882, Japan
来源:
关键词:
Triclosan;
Urine sample;
Stir bar sorptive extraction (SBSE);
Thermal desorption (TD);
Gas chromatography-mass spectrometry (GC-MS);
D O I:
10.1016/j.jchromb.2008.10.008
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
We have developed an analytical method for the determination of urinary 5-cliloro-2-(2,4-dichlorophenoxy)phenol (triclosan), which utilizes stir bar sorptive extraction (SBSE) and thermal desorption (TD)-gas chromatography-mass spectrometry (GC-MS). Human urine sample is deconjugated by treatment with P-glucuronidase and sulfatase. A stir bar coated with polydimethylsiloxane (PDMS) is added to the urine sample in a vial and the sample is stirred for 60min at room temperature (25 degrees C). Then, the PDMS stir bar is subjected to TD-GC-MS. The detection limit of triclosan is 0.05 ngmL(-1). The method shows linearity over the calibration range (0.1-10ng mL(-1)) and the correlation coefficient (r) is higher than 0.993 for triclosan standard solution. The average recoveries of triclosan in human urine sample are 102.8-113.1% (RSD: 2.4-6.7%). This simple, sensitive, and selective analytical method may be used in the determination of trace amounts of triclosan in human urine samples. (c) 2008 Elsevier B.V. All rights reserved.
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页码:577 / 580
页数:4
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