2018
DOI: 10.1007/s12161-018-1150-0
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Use of 2-Naphthalenethiol for Derivatization and Determination of Acrylamide in Potato Crisps by High-Performance Liquid Chromatographic with Fluorescence Detection

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Cited by 12 publications
(8 citation statements)
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“…Acrylamide determination was carried out by chemical derivatization, using 2-naphthalenethiol as a derivatization reagent, followed by HPLC separation and quantification with fluorescence detection [30]. In brief, 3 g of potato crisps were homogenized with 30 mL of deionized water and then defatted with hexane.…”
Section: Methodsmentioning
confidence: 99%
“…Acrylamide determination was carried out by chemical derivatization, using 2-naphthalenethiol as a derivatization reagent, followed by HPLC separation and quantification with fluorescence detection [30]. In brief, 3 g of potato crisps were homogenized with 30 mL of deionized water and then defatted with hexane.…”
Section: Methodsmentioning
confidence: 99%
“…Profiting from the catalytic action of n -butylamine, the developed thiol-ene click derivatization has the features of simplicity and efficiency, and is suitable for labeling acrylamide with low-concentration level. Some mercapto compounds were also reported to label acrylamide for UV or MS detection, such as 2-mercaptobenzoic acid, 2-naphthalenthiol, and so on. However, these derivatization reactions usually required longer time (1–3 h) and were inefficient, thus resulting in lower sensitivity for subsequent analysis. Then it can be deduced that the developed derivatization method in this study has universal significance for analogous thiol-ene click reactions.…”
Section: Resultsmentioning
confidence: 99%
“…Accuracy of the proposed methods was determined by comparison to an HPLC-FLD established methodology and the results were compared using a Student paired t-test. 26,32 The results obtained using the uorescence quenching methodology differs from the HPLC-FLD data. On the other hand, there is no signicant difference between the results obtained by the uorescence recovery methodology (2N-TQDs).…”
Section: Methods Validationmentioning
confidence: 99%
“…2N (the nucleophile) reacts with acrylamide (the electrophile) in a Michael addition obtaining 3-(naphthalen-2-ylthio)propenamide, the latter compound does not participate in the PET process, recovering the emission signal quenched by 2N. 26 Recovery of the process has been described previously by Liu et al on CuInS 2 , in the system the emission signal of QDs is quenched by Cu 2+ due to a PET process and aer the addition of biothiols, a complex between Cu(II) and biothiols is formed, the complex does not participate in the PET process resulting in the recovery of the emission signal of QDs. 27 TEM images of TQDs were recorded in the presence of AA (Fig.…”
Section: Acrylamide Sensingmentioning
confidence: 99%