Determination of ethyl carbamate in wine by matrix modification-assisted headspace single-drop microextraction and gas chromatography–mass spectrometry technique

•A novel method for the determination of ethyl carbamate in wine has been established.•The application of matrix modification in single-drop microextraction is proposed.•Optimized the formulation of matrix modifiers.•Overcome the negative effect of water on the extraction of ethyl carbamate. A novel...

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Published inFood chemistry Vol. 373; no. Pt B; p. 131573
Main Authors Ma, Zexin, Zhao, Tingyong, Cui, Shiyao, Zhao, Xiaoning, Fan, Yong, Song, Jiangping
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 30.03.2022
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ISSN0308-8146
1873-7072
1873-7072
DOI10.1016/j.foodchem.2021.131573

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Abstract •A novel method for the determination of ethyl carbamate in wine has been established.•The application of matrix modification in single-drop microextraction is proposed.•Optimized the formulation of matrix modifiers.•Overcome the negative effect of water on the extraction of ethyl carbamate. A novel method for the analysis of ethyl carbamate in wine has been developed by coupling matrix modification-assisted headspace single-drop microextraction and gas chromatography-mass spectrometry (GC–MS) techniques. The method was developed by optimizing the matrix modifier and extraction parameters. The calibration method was followed by quantifying the internal isotope standard. The results suggested that the method was linear in the concentration range of 2–1000 ng/mL (R2 = 0.9996). The method presents a detection limit of 1.5 ng/mL, and the quantification limit is 5 ng/mL. The accuracy ranged between 94.9 and 99.9%, and the precision of the method was less than 5%. The method was applied for the detection of wine samples, and the results exhibited no significant difference when compared to the solid phase extraction method.
AbstractList A novel method for the analysis of ethyl carbamate in wine has been developed by coupling matrix modification-assisted headspace single-drop microextraction and gas chromatography-mass spectrometry (GC-MS) techniques. The method was developed by optimizing the matrix modifier and extraction parameters. The calibration method was followed by quantifying the internal isotope standard. The results suggested that the method was linear in the concentration range of 2-1000 ng/mL (R2 = 0.9996). The method presents a detection limit of 1.5 ng/mL, and the quantification limit is 5 ng/mL. The accuracy ranged between 94.9 and 99.9%, and the precision of the method was less than 5%. The method was applied for the detection of wine samples, and the results exhibited no significant difference when compared to the solid phase extraction method.A novel method for the analysis of ethyl carbamate in wine has been developed by coupling matrix modification-assisted headspace single-drop microextraction and gas chromatography-mass spectrometry (GC-MS) techniques. The method was developed by optimizing the matrix modifier and extraction parameters. The calibration method was followed by quantifying the internal isotope standard. The results suggested that the method was linear in the concentration range of 2-1000 ng/mL (R2 = 0.9996). The method presents a detection limit of 1.5 ng/mL, and the quantification limit is 5 ng/mL. The accuracy ranged between 94.9 and 99.9%, and the precision of the method was less than 5%. The method was applied for the detection of wine samples, and the results exhibited no significant difference when compared to the solid phase extraction method.
A novel method for the analysis of ethyl carbamate in wine has been developed by coupling matrix modification-assisted headspace single-drop microextraction and gas chromatography-mass spectrometry (GC-MS) techniques. The method was developed by optimizing the matrix modifier and extraction parameters. The calibration method was followed by quantifying the internal isotope standard. The results suggested that the method was linear in the concentration range of 2-1000 ng/mL (R  = 0.9996). The method presents a detection limit of 1.5 ng/mL, and the quantification limit is 5 ng/mL. The accuracy ranged between 94.9 and 99.9%, and the precision of the method was less than 5%. The method was applied for the detection of wine samples, and the results exhibited no significant difference when compared to the solid phase extraction method.
•A novel method for the determination of ethyl carbamate in wine has been established.•The application of matrix modification in single-drop microextraction is proposed.•Optimized the formulation of matrix modifiers.•Overcome the negative effect of water on the extraction of ethyl carbamate. A novel method for the analysis of ethyl carbamate in wine has been developed by coupling matrix modification-assisted headspace single-drop microextraction and gas chromatography-mass spectrometry (GC–MS) techniques. The method was developed by optimizing the matrix modifier and extraction parameters. The calibration method was followed by quantifying the internal isotope standard. The results suggested that the method was linear in the concentration range of 2–1000 ng/mL (R2 = 0.9996). The method presents a detection limit of 1.5 ng/mL, and the quantification limit is 5 ng/mL. The accuracy ranged between 94.9 and 99.9%, and the precision of the method was less than 5%. The method was applied for the detection of wine samples, and the results exhibited no significant difference when compared to the solid phase extraction method.
A novel method for the analysis of ethyl carbamate in wine has been developed by coupling matrix modification-assisted headspace single-drop microextraction and gas chromatography-mass spectrometry (GC–MS) techniques. The method was developed by optimizing the matrix modifier and extraction parameters. The calibration method was followed by quantifying the internal isotope standard. The results suggested that the method was linear in the concentration range of 2–1000 ng/mL (R² = 0.9996). The method presents a detection limit of 1.5 ng/mL, and the quantification limit is 5 ng/mL. The accuracy ranged between 94.9 and 99.9%, and the precision of the method was less than 5%. The method was applied for the detection of wine samples, and the results exhibited no significant difference when compared to the solid phase extraction method.
ArticleNumber 131573
Author Zhao, Tingyong
Ma, Zexin
Song, Jiangping
Cui, Shiyao
Zhao, Xiaoning
Fan, Yong
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Keywords Single drop microextraction
Ethyl carbamate
Substrate modification
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Snippet •A novel method for the determination of ethyl carbamate in wine has been established.•The application of matrix modification in single-drop microextraction is...
A novel method for the analysis of ethyl carbamate in wine has been developed by coupling matrix modification-assisted headspace single-drop microextraction...
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SubjectTerms Calibration
detection limit
Ethyl carbamate
food chemistry
Gas Chromatography-Mass Spectrometry
headspace analysis
isotopes
microextraction
Single drop microextraction
solid phase extraction
Substrate modification
Urethane - analysis
Wine - analysis
wines
Title Determination of ethyl carbamate in wine by matrix modification-assisted headspace single-drop microextraction and gas chromatography–mass spectrometry technique
URI https://dx.doi.org/10.1016/j.foodchem.2021.131573
https://www.ncbi.nlm.nih.gov/pubmed/34785112
https://www.proquest.com/docview/2598538786
https://www.proquest.com/docview/2636478202
Volume 373
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