Multiresidue determination of 375 organic contaminants including pesticides, polychlorinated biphenyls and polyaromatic hydrocarbons in fruits and vegetables by gas chromatography–triple quadrupole mass spectrometry with introduction of semi-quantification approach

Banerjee, Kaushik; Utture, Sagar C.; Dasgupta, Soma; Kandaswamy, Chandrasekar; Pradhan, Saswati; Kulkarni, Sunil Jayant; Adsule, Pandurang G.

doi:10.1016/j.chroma.2012.10.066

Cited by 72 publications

(33 citation statements)

References 13 publications

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“…25 We removed 49 pesticides before method validation began. Some were removed due to low sensitivity (e.g., azinphos methyl oxon, phorate sulfoxide, and pyridate).…”

mentioning

confidence: 99%

Multiresidue Pesticide Analysis of Botanical Dietary Supplements Using Salt-out Acetonitrile Extraction, Solid-Phase Extraction Cleanup Column, and Gas Chromatography–Triple Quadrupole Mass Spectrometry

Hayward

Wong

Shi³

et al. 2013

Anal. Chem.

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Dietary supplements form an increasing part of the American diet, yet broadly applicable multiresidue pesticide methods have not been evaluated for many of these supplements. A method for the analysis of 310 pesticides, isomers, and pesticide metabolites in dried botanical dietary supplements has been developed and validated. Sample preparation involved acetonitrile:water added to the botanical along with anhydrous magnesium sulfate and sodium chloride for extraction, followed by cleanup with solid-phase extraction using a tandem cartridge consisting of graphitized carbon black (GCB) and primary-secondary amine sorbent (PSA). Pesticides were measured by gas chromatography-tandem mass spectrometry. Accuracy and precision were evaluated through fortifications of 24 botanicals at 10, 25, 100, and 500 μg/kg. Mean pesticide recoveries and relative standard deviations (RSDs) for all botanicals were 97%, 91%, 90%, and 90% and 15%, 10%, 8%, and 6% at 10, 25, 100, and 500 μg/kg, respectively. The method was applied to 21 incurred botanicals. Quinoxyfen was measured in hops (100-620 μg/kg). Tetraconazole (48 μg/kg), tetramethrin (15 μg/kg), methamidophos (50 μg/kg), and chlorpyrifos (93 μg/kg) were measured in licorice, mallow, tea, and tribulus, respectively. Quintozene, its metabolites and contaminants (pentachloroaniline, pentachlorobenzene, pentachloroanisole, and pentachlorothioanisole and hexachlorobenzene and tecnazene, respectively), with hexachlorocyclohexanes and DDT were identified in ginseng sources along with azoxystrobin, diazinon, and dimethomorph between 0.7 and 2800 μg/kg. Validation with these botanicals demonstrated the extent of this method's applicability for screening 310 pesticides in a wide array of botanical dietary supplements.

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“…25 We removed 49 pesticides before method validation began. Some were removed due to low sensitivity (e.g., azinphos methyl oxon, phorate sulfoxide, and pyridate).…”

mentioning

confidence: 99%

Multiresidue Pesticide Analysis of Botanical Dietary Supplements Using Salt-out Acetonitrile Extraction, Solid-Phase Extraction Cleanup Column, and Gas Chromatography–Triple Quadrupole Mass Spectrometry

Hayward

Wong

Shi³

et al. 2013

Anal. Chem.

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“…Matrix-matched standards calibration is a good option for quantification of analytes affected by matrix effects, and it has been widely applied in PRA of food commodities. 8,9,17,22,[27][28][29][30][31]57,59 Cervera et al 48 studied the matrix effect of several food matrices (orange, nectarine, spinach, raisin, paprika, cabbage, pear, rice, legume and 20 gherkin) comparing the response of reference standards prepared in solvent with the response of matrix-matched standards. Most of the pesticides showed an evident signal enhancement in the presence of matrix, and matrix-matched calibration using relative responses to an internal standard was required for the correct quantification of compounds.…”

Section: Gc-ms/ms Applications In Food Analysismentioning

confidence: 99%

The role of GC-MS/MS with triple quadrupole in pesticide residue analysis in food and the environment

et al. 2013

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“…Acephate was determined in vegetables by a QuEChERS method (X. Wang et al 2013), solid phase extraction (Banerjee et al 2012), and gel permeation chromatography (Specht and Tillkes 1985), gas chromatography-mass spectrometry (X. Wang et al 2013;Banerjee et al 2012), and gas chromatography with flame photometric detection (Specht and Tillkes 1985).…”

Section: Analysis Of Vegetablesmentioning

confidence: 99%

“…Several purification procedures have also been reported, including the quick, easy, cheap, effective, rugged, and safe (QuEChERS) method (X. Wang et al 2013), solid phase extraction (SPE) (Banerjee et al 2012), and gel permeation chromatography (GPC) (Specht and Tillkes 1985;Andersson, and Pålsheden 1991). However, these methods have some disadvantages.…”

Section: Introductionmentioning

confidence: 98%

“…Some methods have been reported, such as liquid chromatography-mass spectrometry (MS) (Mol, Dam, and Steijger 2003), liquid chromatography with ultraviolet detection (Rodríguez-Gonzalo, Sánchez-Martín, and Sánchez-Camazano 1991), gas chromatography-mass spectrometry (X. Wang et al 2013;Banerjee et al 2012), and gas chromatography with flame photometric detection (Specht and Tillkes 1985). Prior to the determination of acephate, extraction and preconcentration are usually necessary.…”

Section: Introductionmentioning

confidence: 99%

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Determination of Acephate in Vegetables by Magnetic Molecularly Imprinted Polymer Isolation Coupled with High-Performance Liquid Chromatography

2014

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Magnetic molecularly imprinted polymers based on carbon nanotubes were prepared and characterized by infrared spectrometry, transmission electron microscopy, and vibrating sample magnetometry and were employed for the isolation of acephate from cabbage, spinach, lettuce, leeks, and celery. Kinetic and recognition studies were carried out in order to investigate the adsorption properties of the polymers. During the application process, the acephate extracted from vegetables was purified with the magnetic molecularly imprinted polymers and determined by high performance liquid chromatography with an ultraviolet detector. The recoveries of acephate at three fortified concentrations (0.015, 0.15, and 1.5 mg kg À1 ) were between 89.2% and 93.4%. The limits of detection and quantification of acephate were 0.0025 and 0.0077 mg kg À1 , respectively. The linear dynamic range was from 0.01 to 5 mg kg À1 . The relative standard deviations of intra-and inter-day precision were 1.1% to 5.9% and 2.7% to 6.4%, respectively. The developed method was demonstrated to be rapid and selective for the extraction and determination of acephate in vegetables.

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Multiresidue determination of 375 organic contaminants including pesticides, polychlorinated biphenyls and polyaromatic hydrocarbons in fruits and vegetables by gas chromatography–triple quadrupole mass spectrometry with introduction of semi-quantification approach

Cited by 72 publications

References 13 publications

Multiresidue Pesticide Analysis of Botanical Dietary Supplements Using Salt-out Acetonitrile Extraction, Solid-Phase Extraction Cleanup Column, and Gas Chromatography–Triple Quadrupole Mass Spectrometry

Multiresidue Pesticide Analysis of Botanical Dietary Supplements Using Salt-out Acetonitrile Extraction, Solid-Phase Extraction Cleanup Column, and Gas Chromatography–Triple Quadrupole Mass Spectrometry

The role of GC-MS/MS with triple quadrupole in pesticide residue analysis in food and the environment

Determination of Acephate in Vegetables by Magnetic Molecularly Imprinted Polymer Isolation Coupled with High-Performance Liquid Chromatography

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