ELISA Kit for Peanut Protein Determination: Collaborative Study

A collaborative study in 10 laboratories was performed to validate an ELISA method developed for the quantitative determination of peanut protein in foods. The ELISA kit used for this study is based on rabbit polyclonal antibody. This kit does not produce any false-positive results or cross-reactivi...

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Published in:Journal of AOAC International Vol. 96; no. 5; pp. 1041 - 1047
Main Authors: LEXMAULOVA, Hana, GABROVSKA, Dana, IAMETTI, Stefania, DEL BARCO, Jorge Antonio Guisantes, MARTINEZ QUESADA, Jorge, PARDO, Esther Sunen, RESA, Idoia Postigo, TAKKINEN, Kristiina, LAUKKANEN, Marja-Leena, PIKNOVA, Lubica, LANGERHOLC, Tomaz, CENCIC, Avrelija, RYSOVA, Jana, BARSOVA, Soňa, CUHRA, Petr, PLICKA, Jan, STUMR, František, NETUSILOVA, Kateřina, BLAZKOVA, Martina, BULAWOVA, Hana, BRYCHTA, Josef, SUBRTOVA, Zdeňka, PAVELKA, Jiri
Format: Journal Article
Language:English
Published: Gaithersburg, MD AOAC International 01-09-2013
Oxford University Press
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Abstract A collaborative study in 10 laboratories was performed to validate an ELISA method developed for the quantitative determination of peanut protein in foods. The ELISA kit used for this study is based on rabbit polyclonal antibody. This kit does not produce any false-positive results or cross-reactivity with a broad range of peanut-free food matrixes. All participants obtained the peanut ELISA kit with standard operational procedures, a list of samples, the samples, and a protocol for recording test results. The study included 15 food samples. Three food matrix samples of zero peanut content showed peanut protein content lower than the first standard (0.10 mg/kg). Three samples with peanut declared as an ingredient revealed peanut protein content outside the calibration curve (absorbance was above the highest standard) in all laboratories, and three samples had the peanut content reported either above the highest standard or within the calibration curve, depending on the laboratory. Six samples with peanut declared as an ingredient gave the peanut protein content within the calibration curve. Only these six samples, together with a positive control sample (CS2), were used for statistical evaluation. The statistical tests (Cochran, Grubbs, and Mandel) and analysis of variance were used for the evaluation of the collaborative study results. Repeatability and reproducibility limits, as well as an LOQ (LOQcollaborative 0.22 mg peanut proteins/kg) and an LOD (LODcollaborative 0.07 mg peanut proteinslkg) for the kit were calculated.
AbstractList A collaborative study in 10 laboratories was performed to validate an ELISA method developed for the quantitative determination of peanut protein in foods. The ELISA kit used for this study is based on rabbit polyclonal antibody. This kit does not produce any false-positive results or cross-reactivity with a broad range of peanut-free food matrixes. All participants obtained the peanut ELISA kit with standard operational procedures, a list of samples, the samples, and a protocol for recording test results. The study included 15 food samples. Three food matrix samples of zero peanut content showed peanut protein content lower than the first standard (0.10 mg/kg). Three samples with peanut declared as an ingredient revealed peanut protein content outside the calibration curve (absorbance was above the highest standard) in all laboratories, and three samples had the peanut content reported either above the highest standard or within the calibration curve, depending on the laboratory. Six samples with peanut declared as an ingredient gave the peanut protein content within the calibration curve. Only these six samples, together with a positive control sample (CS2), were used for statistical evaluation. The statistical tests (Cochran, Grubbs, and Mandel) and analysis of variance were used for the evaluation of the collaborative study results. Repeatability and reproducibility limits, as well as an LOQ (LOQcollaborative 0.22 mg peanut proteins/kg) and an LOD (LODcollaborative 0.07 mg peanut proteinslkg) for the kit were calculated.
A collaborative study in 10 laboratories was performed to validate an ELISA method developed for the quantitative determination of peanut protein in foods. The ELISA kit used for this study is based on rabbit polyclonal antibody. This kit does not produce any false-positive results or cross-reactivity with a broad range of peanut-free food matrixes. All participants obtained the peanut ELISA kit with standard operational procedures, a list of samples, the samples, and a protocol for recording test results. The study included 15 food samples. Three food matrix samples of zero peanut content showed peanut protein content lower than the first standard (0.10 mg/kg). Three samples with peanut declared as an ingredient revealed peanut protein content outside the calibration curve (absorbance was above the highest standard) in all laboratories, and three samples had the peanut content reported either above the highest standard or within the calibration curve, depending on the laboratory. Six samples with peanut declared as an ingredient gave the peanut protein content within the calibration curve. Only these six samples, together with a positive control sample (CS2), were used for statistical evaluation. The statistical tests (Cochran, Grubbs, and Mandel) and analysis of variance were used for the evaluation of the collaborative study results. Repeatability and reproducibility limits, as well as an LOQ (LOQcollaborative 0.22 mg peanut proteins/kg) and an LOD (LODcollaborative 0.07 mg peanut proteins/kg) for the kit were calculated.
A collaborative study in 10 laboratories was performed to validate an ELISA method developed for the quantitative determination of peanut protein in foods. The ELISA kit used for this study is based on rabbit polyclonal antibody. This kit does not produce any false-positive results or cross-reactivity with a broad range of peanut-free food matrixes. All participants obtained the peanut ELISA kit with standard operational procedures, a list of samples, the samples, and a protocol for recording test results. The study included 15 food samples. Three food matrix samples of zero peanut content showed peanut protein content lower than the first standard (0.10 mg/kg). Three samples with peanut declared as an ingredient revealed peanut protein content outside the calibration curve (absorbance was above the highest standard) in all laboratories, and three samples had the peanut content reported either above the highest standard or within the calibration curve, depending on the laboratory. Six samples with peanut declared as an ingredient gave the peanut protein content within the calibration curve. Only these six samples, together with a positive control sample (CS2), were used for statistical evaluation. The statistical tests (Cochran, Grubbs, and Mandel) and analysis of variance were used for the evaluation of the collaborative study results. Repeatability and reproducibility limits, as well as an LOQ ([LOQ.sub.collaborative] 0.22 mg peanut proteins/kg) and an LOD ([LOD.sub.collaborative] 0.07 mg peanut proteins/kg) for the kit were calculated.
Audience Academic
Author RYSOVA, Jana
BRYCHTA, Josef
BLAZKOVA, Martina
PLICKA, Jan
BARSOVA, Soňa
PAVELKA, Jiri
STUMR, František
BULAWOVA, Hana
TAKKINEN, Kristiina
IAMETTI, Stefania
LEXMAULOVA, Hana
GABROVSKA, Dana
MARTINEZ QUESADA, Jorge
CENCIC, Avrelija
LAUKKANEN, Marja-Leena
LANGERHOLC, Tomaz
SUBRTOVA, Zdeňka
DEL BARCO, Jorge Antonio Guisantes
PIKNOVA, Lubica
CUHRA, Petr
PARDO, Esther Sunen
RESA, Idoia Postigo
NETUSILOVA, Kateřina
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  givenname: Jorge Antonio Guisantes
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  organization: Czech Agriculture and Food Inspection Authority, Za Opravnou, 150 00, Praha 5, Czech Republic
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  surname: PLICKA
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  organization: Immunotech, Ltd, Radiová 1, 102 27 Praha 10, Czech Republic
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  givenname: František
  surname: STUMR
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  organization: SEDIUM RD, Ltd, Plemenářský podnik 29, 530 03 Pardubice-Nemošice, Czech Republic
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  givenname: Kateřina
  surname: NETUSILOVA
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  surname: BLAZKOVA
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  organization: Institute of Chemical Technology, Technická 5, 166 28 Praha 6, Czech Republic
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  givenname: Hana
  surname: BULAWOVA
  fullname: BULAWOVA, Hana
  organization: State Veterinary Institute, Rantířovská 93, 586 05 Jihlava, Czech Republic
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  givenname: Josef
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  givenname: Jiri
  surname: PAVELKA
  fullname: PAVELKA, Jiri
  organization: Ekocentrum Ovalab, Ltd, Martinovská 3248, 732 08, Ostrava-Martinov, Czech Republic
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Protein
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Snippet A collaborative study in 10 laboratories was performed to validate an ELISA method developed for the quantitative determination of peanut protein in foods. The...
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SubjectTerms Analysis
Arachis - chemistry
Biological and medical sciences
Cooperative Behavior
Enzyme-linked immunosorbent assay
Enzyme-Linked Immunosorbent Assay - methods
Fundamental and applied biological sciences. Psychology
Limit of Detection
Plant Proteins - analysis
Reagent Kits, Diagnostic
Title ELISA Kit for Peanut Protein Determination: Collaborative Study
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