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Elsevier, Talanta, (88), p. 330-337, 2012

DOI: 10.1016/j.talanta.2011.10.049

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Simultaneous determination of four synthesized metabolites of mequindox in urine samples using ultrasound-assisted dispersive liquid–liquid microextraction combined with high-performance liquid chromatography

Journal article published in 2012 by Jiaheng Zhang, Haixiang Gao, Bing Peng ORCID, Yubo Li, Songqing Li, Zhiqiang Zhou
This paper is available in a repository.
This paper is available in a repository.

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Abstract

Talanta j o u r n a l h o m e p a g e : w w w . e l s e v i e r . c o m / l o c a t e / t a l a n t a Simultaneous determination of four synthesized metabolites of mequindox in urine samples using ultrasound-assisted dispersive liquid–liquid microextraction combined with high-performance liquid chromatography: Ultrasound-assisted dispersive liquid–liquid microextraction High-performance liquid chromatography Mequindox Metabolite Urine sample a b s t r a c t A novel pretreatment method termed ultrasound-assisted dispersive liquid–liquid microextraction (UADLLME) coupled with high-performance liquid chromatography-ultraviolet detector (HPLC-UV) was applied for the detection of four synthesized metabolites of mequindox in pig urine samples. A total vol-ume of 200 ␮L of methanol (dispersant) and 60 ␮L of 1,1,2,2-tetrachloroethane (extract) were injected into 5.0 mL of urine sample and then emulsified by ultrasound treatment for 4 min to form a cloudy solution. The effect of several factors on the recovery of each metabolite was investigated by a fitting derivation method for the first time. Under optimum conditions, the method yields a linear calibration curve in the concentration range from 0.5 to 500 ␮g/L and a limit of detection (LOD) of 0.16–0.28 ␮g/L for target analytes. The recoveries ranged from 72.0% to 91.3% with a relative standard deviation (RSD) of less than 5.2%. The enrichment factors for the four compounds ranged from 75 to 95. Two pig urine samples were successfully analyzed using the proposed method.