Analytical Method Development for the Determination of Α-Endosulfan and Bifenthrin Pesticide Residues in Tea

The development of analytical method for the determination of α-endosulfan and bifenthrin residues in tea has been done. The complex matrices and also the pigment were the challenge in doing quantification of the pesticide residues in tea matrices. In order to get appropriate analysis method for the...

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Main Authors: Dyah Styarini, Andreas Andreas, Y. Susanto Ridwan, Retno Yusiasih
Format: Article
Language:English
Published: Department of Chemistry, Universitas Gadjah Mada 2014-03-01
Series:Indonesian Journal of Chemistry
Subjects:
Online Access:https://jurnal.ugm.ac.id/ijc/article/view/21262
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author Dyah Styarini
Andreas Andreas
Y. Susanto Ridwan
Retno Yusiasih
author_facet Dyah Styarini
Andreas Andreas
Y. Susanto Ridwan
Retno Yusiasih
author_sort Dyah Styarini
collection DOAJ
description The development of analytical method for the determination of α-endosulfan and bifenthrin residues in tea has been done. The complex matrices and also the pigment were the challenge in doing quantification of the pesticide residues in tea matrices. In order to get appropriate analysis method for the determination of pesticide residues in tea, the modification was done in the analytical method for the determination of organochlorine multiresidue in non fat matrices: seasoning and spicy that is published by Directorate General of Food Crops, Directorate of Food Plant Protection. The modification was done particularly in clean-up step to remove the interferences from the extract of tea matrices such as the pigment that usually interfere the measurement with Gas Chromatography (GC). The result showed that the MDL value for both analytes were 0.5 ng/g that were much lower than MRLs. The percent recovery obtained from the method was 78.58 and 90.19% for α-endosulfan and bifenthrin, respectively. The precision of the analysis method for both analytes were good since the % RSD values were below than the Horwitz’s value that was 19.18% at spiking level concentration of 300 ng/g.
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spelling doaj.art-9091612333c04d9497e396a6feb16b4c2022-12-21T19:11:16ZengDepartment of Chemistry, Universitas Gadjah MadaIndonesian Journal of Chemistry1411-94202460-15782014-03-01141122110.22146/ijc.2126214360Analytical Method Development for the Determination of Α-Endosulfan and Bifenthrin Pesticide Residues in TeaDyah Styarini0Andreas Andreas1Y. Susanto Ridwan2Retno Yusiasih3Division of Analytical Chemistry and Standard, Research Center for Chemistry, Indonesian Institute of Sciences, Komplek Puspiptek, Serpong, Tangerang, Banten 15314Division of Analytical Chemistry and Standard, Research Center for Chemistry, Indonesian Institute of Sciences, Jl. Cisitu-Sangkuriang, Bandung 40135Division of Analytical Chemistry and Standard, Research Center for Chemistry, Indonesian Institute of Sciences, Jl. Cisitu-Sangkuriang, Bandung 40135Division of Analytical Chemistry and Standard, Research Center for Chemistry, Indonesian Institute of Sciences, Jl. Cisitu-Sangkuriang, Bandung 40135The development of analytical method for the determination of α-endosulfan and bifenthrin residues in tea has been done. The complex matrices and also the pigment were the challenge in doing quantification of the pesticide residues in tea matrices. In order to get appropriate analysis method for the determination of pesticide residues in tea, the modification was done in the analytical method for the determination of organochlorine multiresidue in non fat matrices: seasoning and spicy that is published by Directorate General of Food Crops, Directorate of Food Plant Protection. The modification was done particularly in clean-up step to remove the interferences from the extract of tea matrices such as the pigment that usually interfere the measurement with Gas Chromatography (GC). The result showed that the MDL value for both analytes were 0.5 ng/g that were much lower than MRLs. The percent recovery obtained from the method was 78.58 and 90.19% for α-endosulfan and bifenthrin, respectively. The precision of the analysis method for both analytes were good since the % RSD values were below than the Horwitz’s value that was 19.18% at spiking level concentration of 300 ng/g.https://jurnal.ugm.ac.id/ijc/article/view/21262α-endosulfanbifenthrinGC-ECDteapesticide
spellingShingle Dyah Styarini
Andreas Andreas
Y. Susanto Ridwan
Retno Yusiasih
Analytical Method Development for the Determination of Α-Endosulfan and Bifenthrin Pesticide Residues in Tea
Indonesian Journal of Chemistry
α-endosulfan
bifenthrin
GC-ECD
tea
pesticide
title Analytical Method Development for the Determination of Α-Endosulfan and Bifenthrin Pesticide Residues in Tea
title_full Analytical Method Development for the Determination of Α-Endosulfan and Bifenthrin Pesticide Residues in Tea
title_fullStr Analytical Method Development for the Determination of Α-Endosulfan and Bifenthrin Pesticide Residues in Tea
title_full_unstemmed Analytical Method Development for the Determination of Α-Endosulfan and Bifenthrin Pesticide Residues in Tea
title_short Analytical Method Development for the Determination of Α-Endosulfan and Bifenthrin Pesticide Residues in Tea
title_sort analytical method development for the determination of α endosulfan and bifenthrin pesticide residues in tea
topic α-endosulfan
bifenthrin
GC-ECD
tea
pesticide
url https://jurnal.ugm.ac.id/ijc/article/view/21262
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AT ysusantoridwan analyticalmethoddevelopmentforthedeterminationofaendosulfanandbifenthrinpesticideresiduesintea
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