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 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: Hana surname: LEXMAULOVA fullname: LEXMAULOVA, Hana organization: ELISA Development, Ltd, 412 01 Velké Žernoseky 186, Czech Republic – sequence: 2 givenname: Dana surname: GABROVSKA fullname: GABROVSKA, Dana organization: Food Research Institute Prague, Radiová 7, 102 31 Praha 10, Czech Republic – sequence: 3 givenname: Stefania surname: IAMETTI fullname: IAMETTI, Stefania organization: Universitâ degli studi di Milano, DISMA, Via Celoria2, Milano, Italy – sequence: 4 givenname: Jorge Antonio Guisantes surname: DEL BARCO fullname: DEL BARCO, Jorge Antonio Guisantes organization: University of the Basque Country, Faculty of Pharmacy, Paseo de la Universidad 7, Vitoria-Gasteiz, Basque Country, Spain – sequence: 5 givenname: Jorge surname: MARTINEZ QUESADA fullname: MARTINEZ QUESADA, Jorge organization: University of the Basque Country, Faculty of Pharmacy, Paseo de la Universidad 7, Vitoria-Gasteiz, Basque Country, Spain – sequence: 6 givenname: Esther Sunen surname: PARDO fullname: PARDO, Esther Sunen organization: University of the Basque Country, Faculty of Pharmacy, Paseo de la Universidad 7, Vitoria-Gasteiz, Basque Country, Spain – sequence: 7 givenname: Idoia Postigo surname: RESA fullname: RESA, Idoia Postigo organization: University of the Basque Country, Faculty of Pharmacy, Paseo de la Universidad 7, Vitoria-Gasteiz, Basque Country, Spain – sequence: 8 givenname: Kristiina surname: TAKKINEN fullname: TAKKINEN, Kristiina organization: VTT Technical Research Centre of Finland, PO Box 1000, Espoo, Finland – sequence: 9 givenname: Marja-Leena surname: LAUKKANEN fullname: LAUKKANEN, Marja-Leena organization: VTT Technical Research Centre of Finland, PO Box 1000, Espoo, Finland – sequence: 10 givenname: Lubica surname: PIKNOVA fullname: PIKNOVA, Lubica organization: Food Research Institute, Priemyselna 4, Bratislava, Slovakia – sequence: 11 givenname: Tomaz surname: LANGERHOLC fullname: LANGERHOLC, Tomaz organization: University of Maribor, Pivola 10, 2311 Hoče, Slovenia – sequence: 12 givenname: Avrelija surname: CENCIC fullname: CENCIC, Avrelija organization: University of Maribor, Pivola 10, 2311 Hoče, Slovenia – sequence: 13 givenname: Jana surname: RYSOVA fullname: RYSOVA, Jana organization: Food Research Institute Prague, Radiová 7, 102 31 Praha 10, Czech Republic – sequence: 14 givenname: Soňa surname: BARSOVA fullname: BARSOVA, Soňa organization: Czech Agriculture and Food Inspection Authority, Za Opravnou, 150 00, Praha 5, Czech Republic – sequence: 15 givenname: Petr surname: CUHRA fullname: CUHRA, Petr organization: Czech Agriculture and Food Inspection Authority, Za Opravnou, 150 00, Praha 5, Czech Republic – sequence: 16 givenname: Jan surname: PLICKA fullname: PLICKA, Jan organization: Immunotech, Ltd, Radiová 1, 102 27 Praha 10, Czech Republic – sequence: 17 givenname: František surname: STUMR fullname: STUMR, František organization: SEDIUM RD, Ltd, Plemenářský podnik 29, 530 03 Pardubice-Nemošice, Czech Republic – sequence: 18 givenname: Kateřina surname: NETUSILOVA fullname: NETUSILOVA, Kateřina organization: SEDIUM RD, Ltd, Plemenářský podnik 29, 530 03 Pardubice-Nemošice, Czech Republic – sequence: 19 givenname: Martina surname: BLAZKOVA fullname: BLAZKOVA, Martina organization: Institute of Chemical Technology, Technická 5, 166 28 Praha 6, Czech Republic – sequence: 20 givenname: Hana surname: BULAWOVA fullname: BULAWOVA, Hana organization: State Veterinary Institute, Rantířovská 93, 586 05 Jihlava, Czech Republic – sequence: 21 givenname: Josef surname: BRYCHTA fullname: BRYCHTA, Josef organization: State Veterinary Institute, Rantířovská 93, 586 05 Jihlava, Czech Republic – sequence: 22 givenname: Zdeňka surname: SUBRTOVA fullname: SUBRTOVA, Zdeňka organization: Ekocentrum Ovalab, Ltd, Martinovská 3248, 732 08, Ostrava-Martinov, Czech Republic – sequence: 23 givenname: Jiri surname: PAVELKA fullname: PAVELKA, Jiri organization: Ekocentrum Ovalab, Ltd, Martinovská 3248, 732 08, Ostrava-Martinov, Czech Republic |
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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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