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http://krishi.icar.gov.in/jspui/handle/123456789/39112
Title: | Validation of a QuEChERS-based gas chromatographic method for analysis of pesticide residues in Cassia angustifolia (senna) |
Other Titles: | Not Available |
Authors: | Vandana Tripathy, Ajoy Saha, Dilipkumar J Patel, BB Basak, Paresh G Shah, Jitendra Kumar |
ICAR Data Use Licennce: | http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf |
Author's Affiliated institute: | ICAR-DMAPR |
Published/ Complete Date: | 2016-08-02 |
Project Code: | Not Available |
Keywords: | Gas chromatograph, organochlorine, organophosphorus, pesticides residues, senna, QuEChERS |
Publisher: | Taylor & Francis |
Citation: | Vandana Tripathy, Ajoy Saha, Dilipkumar J. Patel, B. B. Basak, Paresh G. Shah & Jitendra Kumar (2016) Validation of a QuEChERS-based gas chromatographic method for analysis of pesticide residues in Cassia angustifolia (senna), Journal of Environmental Science and Health, Part B, 51:8, 508-518, DOI: 10.1080/03601234.2016.1170544 |
Series/Report no.: | Not Available; |
Abstract/Description: | A simple multi-residue method based on modified QuEChERS (Quick, Easy, Cheap, Effective, Rugged and Safe) approach was established for the determination of 17 organochlorine (OC), 15 organophosphorous (OP) and 7 synthetic pyrethroid (SP) pesticides in an economically important medicinal plant of India, Senna (Cassia angustifolia), by gas chromatography coupled to electron capture and flame thermionic detectors (GC/ECD/FTD) and confirmation of residues was done on gas chromatograph coupled with mass spectrometry (GC-MS). The developed method was validated by testing the following parameters: linearity, limit of detection (LOD), limit of quantification (LOQ), matrix effect, accuracy–precision and measurement uncertainty; the validation study clearly demonstrated the suitability of the method for its intended application. All pesticides showed good linearity in the range 0.01–1.0 μg mL−1 for OCs and OPs and 0.05–2.5 μg mL−1 for SPs with correlation coefficients higher than 0.98. The method gave good recoveries for most of the pesticides (70–120%) with intra-day and inter-day precision < 20% in most of the cases. The limits of detection varied from 0.003 to 0.03 mg kg−1, and the LOQs were determined as 0.01-0.049 mg kg−1. The expanded uncertainties were <30%, which was distinctively less than a maximum default value of ±50%. The proposed method was successfully applied to determine pesticide residues in 12 commercial market samples obtained from different locations in India. |
Description: | Not Available |
ISSN: | Not Available |
Type(s) of content: | Research Paper |
Sponsors: | ICAR |
Language: | English |
Name of Journal: | Journal of Environmental Science and Health Part B-Pesticides Food Contaminants and Agricultural Was |
NAAS Rating: | 7.7 |
Volume No.: | 51 |
Page Number: | 508-518 |
Name of the Division/Regional Station: | Division of Soil Science and Agricultural Chemistry |
Source, DOI or any other URL: | https://doi.org/10.1080/03601234.2016.1170544 |
URI: | http://krishi.icar.gov.in/jspui/handle/123456789/39112 |
Appears in Collections: | HS-DMAPR-Publication |
Files in This Item:
File | Description | Size | Format | |
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11 JES & H Part B 2016 Vol 0 1-11-2.pdf | 764.06 kB | Adobe PDF | View/Open |
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