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Multiresidue Method for the Rapid Determination of Pesticide Residues in Tea Using Ultra Performance Liquid Chromatography Orbitrap High Resolution Mass Spectrometry and In-Syringe Dispersive Solid Phase Extraction

[Image: see text] A method based on in-syringe dispersive solid phase extraction (IS-D-SPE) and ultra performance liquid chromatography Orbitrap high resolution mass spectrometry for the multiresidue analysis of 117 pesticides in tea was developed. Full scan mode was acquired over an m/z range of 10...

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Detalles Bibliográficos
Autores principales: Chen, Hongping, Gao, Guanwei, Chai, Yunfeng, Ma, Guicen, Hao, Zhenxia, Wang, Chen, Liu, Xin, Lu, Chengyin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044959/
https://www.ncbi.nlm.nih.gov/pubmed/30023756
http://dx.doi.org/10.1021/acsomega.7b00863
Descripción
Sumario:[Image: see text] A method based on in-syringe dispersive solid phase extraction (IS-D-SPE) and ultra performance liquid chromatography Orbitrap high resolution mass spectrometry for the multiresidue analysis of 117 pesticides in tea was developed. Full scan mode was acquired over an m/z range of 100–800 with Orbitrap resolution at 70000, followed by full scan/dd-MS(2) mode for confirmation. The identification criteria of retention time and mass accuracy tolerance was ±0.20 min and ±5.0 ppm, respectively. MS/MS fragment ions obtained dd-MS(2) were necessary to identify the pesticides with the same molecular mass weight. The IS-D-SPE technique involved a mixture of 200 mg PSA, 100 mg C18, and 15 mg multiwalled carbon nanotubes for the cleanup of tea matrix. Good linearity (R(2) > 0.99) for 117 pesticides was obtained. Satisfactory recoveries in the range of 70–120% were obtained for 105 pesticides, while intraday and interday precisions were below 20%. Limits of quantification were generally 10 μg kg(–1). Finally, this method was employed to analyze 117 pesticides in 70 tea samples.