Determination of Chlormequat and Mepiquat Residues in Seeding Cultivation Using Accelerated Solvent Extraction-Solid phase Extraction/Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry
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Determination of Chlormequat and Mepiquat Residues in Seeding Cultivation Using Accelerated Solvent Extraction-Solid phase Extraction/Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry
Vol. 31, Issue 5, Pages: 559-563(2012)
作者机构:
1. 新疆农业大学食品科学与药学学院
2. 新疆出入境检验检疫局技术中心
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Determination of Chlormequat and Mepiquat Residues in Seeding Cultivation Using Accelerated Solvent Extraction-Solid phase Extraction/Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry. [J]. 31(5):559-563(2012)
DOI:
Determination of Chlormequat and Mepiquat Residues in Seeding Cultivation Using Accelerated Solvent Extraction-Solid phase Extraction/Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry. [J]. 31(5):559-563(2012)DOI:
Determination of Chlormequat and Mepiquat Residues in Seeding Cultivation Using Accelerated Solvent Extraction-Solid phase Extraction/Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry
A method for the determination of chlormequat and mepiquat residues in samples from seeding cultivation products was established by accelerated solvent extraction-solid-phase extraction coupled with ultra-performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS).The samples were extracted with ASE 200 system and cleaned up with weak cation exchange(CBA) column.The identifications of chlormequat and mepiquat were performed on a HILIC column packed with 5 μm particles under isocratic LC conditions by using 0.1% formic acid in 20 mmol/L ammonium acetate(A) and acetonitrile(B)( VA∶VB=40∶60).The quantification of analytes was achieved by using electrospray ionization under positive ion mode(ESI+) with multiple reaction monitoring(MRM).The result indicated that the calibration curves were linear in the range of 0.2-10 μg/kg for both compounds.The average recoveries at spiked concentration levels of 2,5,10 μg/kg ranged from 77% to 111% with relative standard deviations of 5.6%-21.7%.The limits of detection were 0.02 μg/kg and the limits of quantitation were 0.1 μg/kg for both compounds.The established method was simple,rapid,sensitive and specific,and was suitable for the identification and quantification of chlormequat and mepiquat residues in seeding cultivation.
关键词
育苗基质固相萃取加速溶剂萃取矮壮素助状素超高效液相色谱-串联质谱法
Keywords
seeding cultivationsolid-phase extractionaccelerated solvent extractionchlormequatmepiquatultra-performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS)
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