Literature DB >> 20817191

Coacervative microextraction ultrasound-assisted back-extraction technique for determination of organophosphates pesticides in honey samples by gas chromatography-mass spectrometry.

Ariel R Fontana1, Alejandra B Camargo, Jorgelina C Altamirano.   

Abstract

Coacervative microextraction ultrasound-assisted back-extraction technique (CME-UABE) is proposed for the first time for extracting and preconcentrating organophosphates pesticides (OPPs) from honey samples prior to gas chromatography-mass spectrometry (GC-MS) analysis. The extraction/preconcentration technique is supported on the micellar organized medium based on non-ionic surfactant. To enable coupling the proposed technique with GC, it was required to back extract the analytes into hexane. Several variables including, surfactant type and concentration, equilibration temperature and time, matrix modifiers, pH and buffers nature were studied and optimized over the relative response of the analytes. The best working conditions were as follows: an aliquot of 10 mL 50 gL(-1) honey blend solution was conditioned by adding 100 μL 0.1 molL(-1) hydrochloric acid (pH 2) and finally extracted with 100 μL Triton X-114 100 gL(-1) at 85°C for 5 min using CME technique. Under optimal experimental conditions, the enrichment factor (EF) was 167 and limits of detection (LODs), calculated as three times the signal-to-noise ratio (S/N=3), ranged between 0.03 and 0.47 ngg(-1). The method precision was evaluated over five replicates at 1 ngg(-1) with RSDs ≤ 9.5%. The calibration graphs were linear within the concentration range of 0.3-1000 ngg(-1) for chlorpirifos; and 1-1000 ngg(-1) for fenitrothion, parathion and methidathion, respectively. The coefficients of correlation were ≥ 0.9992. Validation of the methodology was performed by standard addition method at two concentration levels (2 and 20 ngg(-1)). The recoveries were ≥ 90%, indicating satisfactory robustness of the methodology, which could be successfully applied for determination of OPPs in honey samples of different Argentinean regions. Two of the analyzed samples showed levels of methidathion ranged between 1.2 and 2.3 ngg(-1).
Copyright © 2010. Published by Elsevier B.V.

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Year:  2010        PMID: 20817191     DOI: 10.1016/j.chroma.2010.08.021

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  5 in total

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Journal:  Mikrochim Acta       Date:  2022-01-05       Impact factor: 5.833

Review 2.  Cloud point extraction coupled with back extraction: a green methodology in analytical chemistry.

Authors:  Shivpoojan Kori
Journal:  Forensic Sci Res       Date:  2019-09-18

3.  Pesticide Residues in Honey from the Major Honey Producing Forest Belts in Ghana.

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Journal:  J Environ Public Health       Date:  2017-08-16

4.  Detection of Diazinon Residue in Honey and Honey Bee (Apis mellifera) in Bandar-Abbas and Meshkinshahr, Iran.

Authors:  Fatemeh Bagheri; Hassan Vatandoost; Mansoureh Shayeghi; Yavar Rassi; Ahmad Ali Hanafi-Bojd; Abbas Rahimi-Foroushani; Alireza Razavi; Fatemeh Nikpour
Journal:  J Arthropod Borne Dis       Date:  2019-06-24       Impact factor: 1.198

5.  Organochlorine Pesticides in Honey and Pollen Samples from Managed Colonies of the Honey Bee Apis mellifera Linnaeus and the Stingless Bee Scaptotrigona mexicana Guérin from Southern, Mexico.

Authors:  Jovani Ruiz-Toledo; Rémy Vandame; Ricardo Alberto Castro-Chan; Rosa Patricia Penilla-Navarro; Jaime Gómez; Daniel Sánchez
Journal:  Insects       Date:  2018-05-10       Impact factor: 2.769

  5 in total

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