Analysis of organophosphorus pesticides in vegetable samples by hollow fiber liquid phase microextraction coupled with gas chromatography-electron capture detection.

A method based on hollow fibre liquid phase microextraction (HF-LPME) coupled with gas chromatography electron capture detection (GC-ECD) has been developed for the determination of organophosphorus pesticides (OPPs) (chlorpyrifos and profenofos) in vegetable samples. In this method, a microsyringe...

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Main Authors: Sanagi, Mohd. Marsin, A. Ghani, Nurul Farhana Yanti, Miskam, Mazidatulakmam, Wan Ibrahim, Wan Aini, Aboul Enein, Hassan Y.
Format: Article
Published: Taylor and Francis Ltd. 2010
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Online Access:http://eprints.utm.my/id/eprint/22855/
http://dx.doi.org/10.1080/10826071003608850
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spelling my.utm.228552018-03-13T18:07:56Z http://eprints.utm.my/id/eprint/22855/ Analysis of organophosphorus pesticides in vegetable samples by hollow fiber liquid phase microextraction coupled with gas chromatography-electron capture detection. Sanagi, Mohd. Marsin A. Ghani, Nurul Farhana Yanti Miskam, Mazidatulakmam Wan Ibrahim, Wan Aini Aboul Enein, Hassan Y. Q Science (General) A method based on hollow fibre liquid phase microextraction (HF-LPME) coupled with gas chromatography electron capture detection (GC-ECD) has been developed for the determination of organophosphorus pesticides (OPPs) (chlorpyrifos and profenofos) in vegetable samples. In this method, a microsyringe needle with 1.5 cm polypropylene hollow fibre containing a volume of organic acceptor phase (n-dodecane) was immersed in an aqueous donor solution, and at the completion of extraction, the acceptor phase was withdrawn and transferred to GC-ECD for analysis. The effects of extraction solvent, volume of acceptor phase, and volume of donor phase were investigated. The optimized conditions for HF-LPME of the selected OPPs were n-dodecane as organic solvent, 11 mL of donor phase, and 3 µL of acceptor phase. The correlation coefficient (r2) of the calibration curves ranged from 0.998 to 0.999. The limits of detection (LOD) were between 0.099 and 0.128 µg/mL. The developed method provided excellent RSDs ranging from 0.54% to 8.00% and analyte recoveries ranging from 60.8% to 88.0%. This method was applied successfully for determination of organophosphorus pesticides in selected vegetables. Taylor and Francis Ltd. 2010-03 Article PeerReviewed Sanagi, Mohd. Marsin and A. Ghani, Nurul Farhana Yanti and Miskam, Mazidatulakmam and Wan Ibrahim, Wan Aini and Aboul Enein, Hassan Y. (2010) Analysis of organophosphorus pesticides in vegetable samples by hollow fiber liquid phase microextraction coupled with gas chromatography-electron capture detection. Journal of Liquid Chromatography & Related Technologies, 33 (5). 693 - 703. ISSN 1082-6076 http://dx.doi.org/10.1080/10826071003608850 DOI: 10.1080/10826071003608850
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic Q Science (General)
spellingShingle Q Science (General)
Sanagi, Mohd. Marsin
A. Ghani, Nurul Farhana Yanti
Miskam, Mazidatulakmam
Wan Ibrahim, Wan Aini
Aboul Enein, Hassan Y.
Analysis of organophosphorus pesticides in vegetable samples by hollow fiber liquid phase microextraction coupled with gas chromatography-electron capture detection.
description A method based on hollow fibre liquid phase microextraction (HF-LPME) coupled with gas chromatography electron capture detection (GC-ECD) has been developed for the determination of organophosphorus pesticides (OPPs) (chlorpyrifos and profenofos) in vegetable samples. In this method, a microsyringe needle with 1.5 cm polypropylene hollow fibre containing a volume of organic acceptor phase (n-dodecane) was immersed in an aqueous donor solution, and at the completion of extraction, the acceptor phase was withdrawn and transferred to GC-ECD for analysis. The effects of extraction solvent, volume of acceptor phase, and volume of donor phase were investigated. The optimized conditions for HF-LPME of the selected OPPs were n-dodecane as organic solvent, 11 mL of donor phase, and 3 µL of acceptor phase. The correlation coefficient (r2) of the calibration curves ranged from 0.998 to 0.999. The limits of detection (LOD) were between 0.099 and 0.128 µg/mL. The developed method provided excellent RSDs ranging from 0.54% to 8.00% and analyte recoveries ranging from 60.8% to 88.0%. This method was applied successfully for determination of organophosphorus pesticides in selected vegetables.
format Article
author Sanagi, Mohd. Marsin
A. Ghani, Nurul Farhana Yanti
Miskam, Mazidatulakmam
Wan Ibrahim, Wan Aini
Aboul Enein, Hassan Y.
author_facet Sanagi, Mohd. Marsin
A. Ghani, Nurul Farhana Yanti
Miskam, Mazidatulakmam
Wan Ibrahim, Wan Aini
Aboul Enein, Hassan Y.
author_sort Sanagi, Mohd. Marsin
title Analysis of organophosphorus pesticides in vegetable samples by hollow fiber liquid phase microextraction coupled with gas chromatography-electron capture detection.
title_short Analysis of organophosphorus pesticides in vegetable samples by hollow fiber liquid phase microextraction coupled with gas chromatography-electron capture detection.
title_full Analysis of organophosphorus pesticides in vegetable samples by hollow fiber liquid phase microextraction coupled with gas chromatography-electron capture detection.
title_fullStr Analysis of organophosphorus pesticides in vegetable samples by hollow fiber liquid phase microextraction coupled with gas chromatography-electron capture detection.
title_full_unstemmed Analysis of organophosphorus pesticides in vegetable samples by hollow fiber liquid phase microextraction coupled with gas chromatography-electron capture detection.
title_sort analysis of organophosphorus pesticides in vegetable samples by hollow fiber liquid phase microextraction coupled with gas chromatography-electron capture detection.
publisher Taylor and Francis Ltd.
publishDate 2010
url http://eprints.utm.my/id/eprint/22855/
http://dx.doi.org/10.1080/10826071003608850
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score 13.159267