About: Analytical evaluation of a high-throughput enzyme-linked immunosorbent assay for acrylamide determination in fried foods     Goto   Sponge   NotDistinct   Permalink

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  • The analytical performance and evaluation of a kit-based ELISA for the determination of acrylamide in fried potato and corn chip samples are described. The sample homogenate is subjected to clean-up using SPE, followed by analyte derivatization and ELISA detection. Accuracy, precision and linearity of the ELISA procedure have been validated using spiked samples. Analytical recovery ranged from 91.8% to 96.0% with coefficients of variation below 15%. Good linearity over a wide range of dilution and minimal assay drift was observed within a microtiter plate. IC50 value of the calibration curve was 110 ng/mL, with the limit of detection about 5 ng/mL and dynamic range from 10 to 1000 ng/mL. The high specificity of the ELISA was demonstrated by cross-reactivity study using 11 potential cross-reactants. A good correlation between the results obtained from the ELISA and GC-MS within the concentration range 120-1500 mu g/kg was found in the chip samples (r=0.992, n=120). The data demonstrate that the evaluated and validated ELISA has a potential utility in a quick, simple and reliable acrylamide screening analysis for the medium-and large-sized food companies, as well as for residue laboratories and the food industry dealing with improving the chemical safety of foods available to the consumer. (c) 2014 Elsevier B.V. All rights reserved.
  • The analytical performance and evaluation of a kit-based ELISA for the determination of acrylamide in fried potato and corn chip samples are described. The sample homogenate is subjected to clean-up using SPE, followed by analyte derivatization and ELISA detection. Accuracy, precision and linearity of the ELISA procedure have been validated using spiked samples. Analytical recovery ranged from 91.8% to 96.0% with coefficients of variation below 15%. Good linearity over a wide range of dilution and minimal assay drift was observed within a microtiter plate. IC50 value of the calibration curve was 110 ng/mL, with the limit of detection about 5 ng/mL and dynamic range from 10 to 1000 ng/mL. The high specificity of the ELISA was demonstrated by cross-reactivity study using 11 potential cross-reactants. A good correlation between the results obtained from the ELISA and GC-MS within the concentration range 120-1500 mu g/kg was found in the chip samples (r=0.992, n=120). The data demonstrate that the evaluated and validated ELISA has a potential utility in a quick, simple and reliable acrylamide screening analysis for the medium-and large-sized food companies, as well as for residue laboratories and the food industry dealing with improving the chemical safety of foods available to the consumer. (c) 2014 Elsevier B.V. All rights reserved. (en)
Title
  • Analytical evaluation of a high-throughput enzyme-linked immunosorbent assay for acrylamide determination in fried foods
  • Analytical evaluation of a high-throughput enzyme-linked immunosorbent assay for acrylamide determination in fried foods (en)
skos:prefLabel
  • Analytical evaluation of a high-throughput enzyme-linked immunosorbent assay for acrylamide determination in fried foods
  • Analytical evaluation of a high-throughput enzyme-linked immunosorbent assay for acrylamide determination in fried foods (en)
skos:notation
  • RIV/00027162:_____/14:#0001150!RIV15-MZE-00027162
http://linked.open...avai/riv/aktivita
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  • P(ED0006/01/01), Z(MZE0002716202)
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  • JUN
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  • 2888
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  • RIV/00027162:_____/14:#0001150
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  • Acrylamide; Screening method; ELISA kit; Validation; Chip samples; Food industry (en)
http://linked.open.../riv/klicoveSlovo
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  • NL - Nizozemsko
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  • [D6FB5E170AEB]
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  • Talanta
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  • 123
http://linked.open...iv/tvurceVysledku
  • Diblíková, Iva
  • Fránek, Milan
  • Rubio, D.
  • Rubio, F.
http://linked.open...ain/vavai/riv/wos
  • 000335616300021
http://linked.open...n/vavai/riv/zamer
issn
  • 0039-9140
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.talanta.2014.02.007
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