4.6 Article

Trace determination of prohibited acrylamide in cosmetic products by vortex-assisted reversed-phase dispersive liquid-liquid microextraction and liquid chromatography-tandem mass spectrometry

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JOURNAL OF CHROMATOGRAPHY A
卷 1687, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.chroma.2022.463651

关键词

Acrylamide; Cosmetic products; Liquid chromatography-mass spectrometry; Reversed-phase dispersive liquid-liquid; microextraction

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This study presents an analytical method for the determination of residual acrylamide in cosmetic products. The method involves vortex-assisted reversed-phase dispersive liquid-liquid microextraction (VA-RP-DLLME) using water as extraction solvent, followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) for detection. The method shows good analytical features, including high linearity, low limits of detection and quantification, and good repeatability. It is effective, simple, and fast, and can easily determine trace levels of acrylamide in cosmetic products, making it useful for quality control purposes.
An analytical method for the determination of residual acrylamide in cosmetic products containing po-tential acrylamide-releasing ingredients is presented. The method is based on vortex-assisted reversed -phase dispersive liquid-liquid microextraction (VA-RP-DLLME) to extract and preconcentrate acrylamide by using water as extraction solvent taking advantage the highly polar behavior of this analyte, followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) for its determination. Under optimized conditions (5 mL toluene as supporting solvent, 50 mu L of water as extraction solvent, 1 min for vortex ex-traction time) the method was properly validated obtaining good analytical features (linearity up to 20 ng mL -1, method limits of detection and quantification of 0.51 and 1.69 ng g -1, respectively, enrichment factor of 52, and good repeatability (RSD < 4.1%)). The proposed analytical method was applied to the determination of acrylamide in commercial samples that were weighed and dispersed in the minimum quantity of methanol (50 mu L) by vortex stirring before applying the VA-RP-DLLME procedure. Through the pretreatment of the sample and the use of acrylamide-d3 as surrogate, the matrix effect was overcome, obtaining good relative recovery values (88-108%). The proposed method has shown efficacy, simplicity, and speed, and it allows the determination of acrylamide at trace levels easily, which could make it very useful for companies in the quality control of cosmetic products containing potential acrylamide-releasing ingredients to fulfill the safety limits imposed by European Regulation.(c) 2022 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )

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