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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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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 |
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author | Chen, Hongping Gao, Guanwei Chai, Yunfeng Ma, Guicen Hao, Zhenxia Wang, Chen Liu, Xin Lu, Chengyin |
author_facet | Chen, Hongping Gao, Guanwei Chai, Yunfeng Ma, Guicen Hao, Zhenxia Wang, Chen Liu, Xin Lu, Chengyin |
author_sort | Chen, Hongping |
collection | PubMed |
description | [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. |
format | Online Article Text |
id | pubmed-6044959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60449592018-07-16 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 Chen, Hongping Gao, Guanwei Chai, Yunfeng Ma, Guicen Hao, Zhenxia Wang, Chen Liu, Xin Lu, Chengyin ACS Omega [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. American Chemical Society 2017-09-18 /pmc/articles/PMC6044959/ /pubmed/30023756 http://dx.doi.org/10.1021/acsomega.7b00863 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Chen, Hongping Gao, Guanwei Chai, Yunfeng Ma, Guicen Hao, Zhenxia Wang, Chen Liu, Xin Lu, Chengyin 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 |
title | 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 |
title_full | 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 |
title_fullStr | 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 |
title_full_unstemmed | 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 |
title_short | 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 |
title_sort | 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 |
url | 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 |
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