Determination of Selected Pesticide Residues in River Water Using SBSE Technique

The analytical procedure based on stir‑bar sorptive extraction technique, for the determination of selected pesticide residues (diazinon, malathion, cyprodinyl, penconazole, fludioxonyl, pyriproxyfen, boscalid, pyraclostrobin) is described. Analysis was performed using the commercial TwisterTM stir...

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Main Author: Andrea Purdešová
Format: Article
Language:English
Published: Mendel University Press 2017-01-01
Series:Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis
Subjects:
Online Access:https://acta.mendelu.cz/65/5/1595/
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spelling doaj-2d983f3df104493ebf945bc5d63d9b872020-11-24T22:31:23ZengMendel University PressActa Universitatis Agriculturae et Silviculturae Mendelianae Brunensis1211-85162464-83102017-01-016551595159910.11118/actaun201765051595Determination of Selected Pesticide Residues in River Water Using SBSE TechniqueAndrea Purdešová0Slovak University of Technology, Faculty of Chemical and Food Technology, Institute of Analytical Chemistry, Radlinského 9, 812 37 Bratislava, Slovak RepublicThe analytical procedure based on stir‑bar sorptive extraction technique, for the determination of selected pesticide residues (diazinon, malathion, cyprodinyl, penconazole, fludioxonyl, pyriproxyfen, boscalid, pyraclostrobin) is described. Analysis was performed using the commercial TwisterTM stir bar for sorptive extraction. It consists of a 2.0‑cm‑long glass‑encapsulated magnetic stir bar externally coated with PDMS. The extracts were off‑line analyzed using fast GC‑MS in SIM mode. Optimized conditions were established as follows concerning extraction time, stirring speed, aqueous medium characteristics (ionic strength and polarity) respectively: 120 min (700 rpm), addition of 4 g of sodium chloride, no addition of methanol as organic modifier, and 30 min ultrasonic desorption in acetonitrile. Recoveries ranged from 38 % to 58 % (RSD < 15 %, n = 6). Validated limits of quantification in matrix were between 1.6 ngL−1 and 548.8 ngL−1, depending on the compound.https://acta.mendelu.cz/65/5/1595/Fast gas chromatography‑mass spectrometrywaterpesticideselectron ionizationSBSE
collection DOAJ
language English
format Article
sources DOAJ
author Andrea Purdešová
spellingShingle Andrea Purdešová
Determination of Selected Pesticide Residues in River Water Using SBSE Technique
Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis
Fast gas chromatography‑mass spectrometry
water
pesticides
electron ionization
SBSE
author_facet Andrea Purdešová
author_sort Andrea Purdešová
title Determination of Selected Pesticide Residues in River Water Using SBSE Technique
title_short Determination of Selected Pesticide Residues in River Water Using SBSE Technique
title_full Determination of Selected Pesticide Residues in River Water Using SBSE Technique
title_fullStr Determination of Selected Pesticide Residues in River Water Using SBSE Technique
title_full_unstemmed Determination of Selected Pesticide Residues in River Water Using SBSE Technique
title_sort determination of selected pesticide residues in river water using sbse technique
publisher Mendel University Press
series Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis
issn 1211-8516
2464-8310
publishDate 2017-01-01
description The analytical procedure based on stir‑bar sorptive extraction technique, for the determination of selected pesticide residues (diazinon, malathion, cyprodinyl, penconazole, fludioxonyl, pyriproxyfen, boscalid, pyraclostrobin) is described. Analysis was performed using the commercial TwisterTM stir bar for sorptive extraction. It consists of a 2.0‑cm‑long glass‑encapsulated magnetic stir bar externally coated with PDMS. The extracts were off‑line analyzed using fast GC‑MS in SIM mode. Optimized conditions were established as follows concerning extraction time, stirring speed, aqueous medium characteristics (ionic strength and polarity) respectively: 120 min (700 rpm), addition of 4 g of sodium chloride, no addition of methanol as organic modifier, and 30 min ultrasonic desorption in acetonitrile. Recoveries ranged from 38 % to 58 % (RSD < 15 %, n = 6). Validated limits of quantification in matrix were between 1.6 ngL−1 and 548.8 ngL−1, depending on the compound.
topic Fast gas chromatography‑mass spectrometry
water
pesticides
electron ionization
SBSE
url https://acta.mendelu.cz/65/5/1595/
work_keys_str_mv AT andreapurdesova determinationofselectedpesticideresiduesinriverwaterusingsbsetechnique
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