Chiral Separation of Clenbuterol Stereoisomer by Ultrahigh Performance Convergence Chromatography and Its Application in Residue Determination of Swine Urine
Scientific Papers|更新时间:2023-02-13
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Chiral Separation of Clenbuterol Stereoisomer by Ultrahigh Performance Convergence Chromatography and Its Application in Residue Determination of Swine Urine
Journal of Instrumental AnalysisVol. 40, Issue 12, Pages: 1758-1764(2021)
ZHANG Wen-hua,HOU Jian-bo,RONG Jie-feng,et al.Chiral Separation of Clenbuterol Stereoisomer by Ultrahigh Performance Convergence Chromatography and Its Application in Residue Determination of Swine Urine[J].Journal of Instrumental Analysis,2021,40(12):1758-1764.
ZHANG Wen-hua,HOU Jian-bo,RONG Jie-feng,et al.Chiral Separation of Clenbuterol Stereoisomer by Ultrahigh Performance Convergence Chromatography and Its Application in Residue Determination of Swine Urine[J].Journal of Instrumental Analysis,2021,40(12):1758-1764. DOI: 10.19969/j.fxcsxb.21070206.
Chiral Separation of Clenbuterol Stereoisomer by Ultrahigh Performance Convergence Chromatography and Its Application in Residue Determination of Swine Urine
An ultrahigh performance convergence chromatography(UPC,2,) was established for the separation of two kinds of clenbuterol stereoisomers,which was applied to the residue analysis of swine urine samples.The experimental conditions,including back pressures,types of constant volume reagents,gradient elution conditions and types of purification columns were optimized.The best experimental conditions were as follows:the back pressure:13.8 MPa,constant volume reagent:heptane,gradient elution condition:gradient 3,purification column:PCX column.The swine urine samples were extracted with ethyl acetate,then purified on a cation exchange solid phase extraction column.The separation of two clenbuterol stereoisomers was performed on a CHIRALPAK IA-3(4.6 mm × 100 mm,3 µm) chiral column by gradient elution,with supercritical carbon dioxide and 10 mol/L ammonium acetate-methanol(0.5∶99.5,by volume) as mobile phases at a flow rate of 2.0 mL/min.The detection wavelenth for photo-diode array detector(PDAD) was set at 241 nm.Results showed that the linear ranges for two clenbuterol stereoisomers were between 50 µg/L and 10 000 µg/L,with corelation coefficients greater than 0.999 8.The limits of quantitation(,S/N ,= 10) for (+)-clenbuterol and (-)-clenbuterol were both 1.0 µg/L.The recoveries at three spiked levels of 1.0,5.0,20.0 µg/L ranged from 76.4% to 94.5%,with relative standard deviations(RSD) of 3.6%-6.6%.The method was used to detect standard clenbuterol racemates and 20 swine urine samples.Results showed that clenbuterol racemates contained two kinds of clenbuterol stereoisomers,i.e.(+)-clenbuterol and(-)-clenbuterol.The contents of (+)-clenbuterol and (-)-clenbuterol were 5.6 mg/L and 5.5 mg/L,respectively. The content ratio of(+)-clenbuterol and (-)-clenbuterol in standard clenbuterol raceme complied with the ratio reported in literature.Two kinds of clenbuterol stereoisomers were undetected in 20 swine urine samples.With the characteristics of rapid analysis,good separation effect,good reproducibility and less consumption of organic solvent,this method is applicable for the determination of clenbuterol stereoisomer content in swine urine samples.It provides a scientific support for the development and use of chiral drugs as well as the formulation of relevant regulations.
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Department of Chemistry and Chemical Engineering,Yunnan Normal University
Zhejiang Academy of Science and Technology for Inspection and Quarantine