Publication: Multiresidue analysis of pesticides in fruits and vegetables using solid-phase extraction and gas chromatographic methods
dc.citedby | 19 | |
dc.contributor.author | Lal A. | en_US |
dc.contributor.author | Tan G. | en_US |
dc.contributor.author | Chai M. | en_US |
dc.contributor.authorid | 24172476100 | en_US |
dc.contributor.authorid | 7202393048 | en_US |
dc.contributor.authorid | 24172523100 | en_US |
dc.date.accessioned | 2023-12-29T07:56:46Z | |
dc.date.available | 2023-12-29T07:56:46Z | |
dc.date.issued | 2008 | |
dc.description.abstract | A new extraction and cleanup procedure with gas chromatography was developed for the sensitive determination of acephate, dimethoate, malathion, diazinon, quinalphos, chlorpyrifos, profenofos, ?-endosulfan, ?-endosulfan, chlorothalonil and carbaryl using 1-chloro-4-fluorobenzene as an internal standard in fruits and vegetables. Several extracting and eluting solvents for solid-phase extraction were investigated. The overall extracting solvent with a mixture of acetone:ethyl acetate:hexane (10:80:10, v/v/v) and a eluting solvent of 5% acetone in hexane used with the RPC18 cartridge gave the best recovery for all of the investigated pesticides, and minimized the interference from co-extractants. Under the optimal extraction and clean-up conditions, recoveries of 85 - 99% with RSD < 5.0% (n = 3) for most of the pesticides at the 0.02-0.5 mg/kg level were obtained. The limit of detection was between 0.005-0.01 mg/kg and the limit of quantification was 0.01 mg/kg. This analytical procedure was characterized with high accuracy and acceptable sensitivity to meet requirements for monitoring pesticides in crops. 2008 � The Japan Society for Analytical Chemistry. | en_US |
dc.description.nature | Final | en_US |
dc.identifier.doi | 10.2116/analsci.24.231 | |
dc.identifier.epage | 236 | |
dc.identifier.issue | 2 | |
dc.identifier.scopus | 2-s2.0-43049173768 | |
dc.identifier.spage | 231 | |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-43049173768&doi=10.2116%2fanalsci.24.231&partnerID=40&md5=1813a11d3b288c8943709722a447b7f4 | |
dc.identifier.uri | https://irepository.uniten.edu.my/handle/123456789/30963 | |
dc.identifier.volume | 24 | |
dc.pagecount | 5 | |
dc.publisher | Japan Society for Analytical Chemistry | en_US |
dc.source | Scopus | |
dc.sourcetitle | Analytical Sciences | |
dc.subject | Chromatography, Gas | |
dc.subject | Food Analysis | |
dc.subject | Food Contamination | |
dc.subject | Fruit | |
dc.subject | Pesticides | |
dc.subject | Reproducibility of Results | |
dc.subject | Sensitivity and Specificity | |
dc.subject | Solid Phase Extraction | |
dc.subject | Time Factors | |
dc.subject | Vegetables | |
dc.subject | Acetone | |
dc.subject | Chromatographic analysis | |
dc.subject | Fruits | |
dc.subject | Gas chromatography | |
dc.subject | Hexane | |
dc.subject | Insecticides | |
dc.subject | Phase separation | |
dc.subject | Solvents | |
dc.subject | Vegetables | |
dc.subject | pesticide | |
dc.subject | Analytical procedure | |
dc.subject | Chromatographic methods | |
dc.subject | Fruits and vegetables | |
dc.subject | Internal standards | |
dc.subject | Limit of detection | |
dc.subject | Limit of quantifications | |
dc.subject | Multi-residue analysis | |
dc.subject | Solid-phase extraction | |
dc.subject | article | |
dc.subject | chemistry | |
dc.subject | food analysis | |
dc.subject | food contamination | |
dc.subject | fruit | |
dc.subject | gas chromatography | |
dc.subject | instrumentation | |
dc.subject | methodology | |
dc.subject | reproducibility | |
dc.subject | sensitivity and specificity | |
dc.subject | solid phase extraction | |
dc.subject | time | |
dc.subject | vegetable | |
dc.subject | Extraction | |
dc.title | Multiresidue analysis of pesticides in fruits and vegetables using solid-phase extraction and gas chromatographic methods | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication |