KRISHI
ICAR RESEARCH DATA REPOSITORY FOR KNOWLEDGE MANAGEMENT
(An Institutional Publication and Data Inventory Repository)
"Not Available": Please do not remove the default option "Not Available" for the fields where metadata information is not available
"1001-01-01": Date not available or not applicable for filling metadata infromation
"1001-01-01": Date not available or not applicable for filling metadata infromation
Please use this identifier to cite or link to this item:
http://krishi.icar.gov.in/jspui/handle/123456789/1553
Title: | Multiresidue analysis of multiclass pesticides and polyaromatic hydrocarbons in fatty fish by gas chromatography tandem mass spectrometry and evaluation of matrix effect. |
Other Titles: | Not Available |
Authors: | Niladri S. Chatterjee, Sagar Utture, Kaushik Banerjee, Ahammed Shabeer T.P., Narayan Kamble, Suseela Mathew , and K. Ashok Kumar |
Published/ Complete Date: | 2015-09-08 |
Project Code: | Not Available |
Keywords: | Fatty fish, Pesticide residues, Polyaromatic hydrocarbons, Sample preparation, Gas chromatography mass spectrometry, Matrix effect |
Publisher: | Not Available |
Citation: | Niladri S. Chatterjee, Sagar Utture, Kaushik Banerjee, Ahammed Shabeer T.P., Narayan Kamble, Suseela Mathew , and K. Ashok Kumar. 2016. Multiresidue analysis of multiclass pesticides and polyaromatic hydrocarbons in fatty fish by gas chromatography tandem mass spectrometry and evaluation of matrix effect. Food Chem. 196: 1-8. |
Series/Report no.: | Not Available; |
Abstract/Description: | This paper reports a selective and sensitive method for multiresidue determination of 119 chemical residues including pesticides and polyaromatic hydrocarbons (PAH) in high fatty fish matrix. The novel sample preparation method involved extraction of the target analytes from homogenized fish meat (5 g) in acetonitrile (15 mL, 1% acetic acid) after three-phase partitioning with hexane (2 mL) and the remaining aqueous layer. An aliquot (1.5 mL) of the acetonitrile layer was aspirated and subjected to two-stage dispersive solid phase extraction (dSPE) cleanup and the residues were finally estimated by gas chromatography mass spectrometry with selected reaction monitoring (GC–MS/MS). The co-eluted matrix components were identified on the basis of their accurate mass by GC with quadrupole time of flight MS. Addition of hexane during extraction and optimized dSPE cleanup significantly minimized the matrix effects. Recoveries at 10, 25 and 50 lg/kg were within 60–120% with associated precision, RSD < 11%. |
Description: | Not Available |
ISSN: | Not Available |
Type(s) of content: | Research Paper |
Sponsors: | Not Available |
Language: | English |
Name of Journal: | Food Chemisrty |
NAAS Rating: | 12.31 |
Volume No.: | 196 |
Page Number: | 1-8 |
Name of the Division/Regional Station: | Not Available |
Source, DOI or any other URL: | http://dx.doi.org/10.1016/j.foodchem.2015.09.014 |
URI: | http://krishi.icar.gov.in/jspui/handle/123456789/1553 |
Appears in Collections: | HS-NRCG-Publication |
Files in This Item:
There are no files associated with this item.
Items in KRISHI are protected by copyright, with all rights reserved, unless otherwise indicated.