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A highly sensitive sandwich ELISA for the determination of glycomacropeptide to detect liquid whey in raw milk
Milk processing industries and distributors have problems with adulteration of liquid milk by the addition of bovine cheese whey. Recently, the detection of fraudulent manipulation of milk with whey has focused on the identification of glycomacropeptide (GMP). Current non-immunological methods to de...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362802/ https://www.ncbi.nlm.nih.gov/pubmed/22662290 http://dx.doi.org/10.1007/s13594-011-0052-3 |
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author | Chávez, Norma A. Jauregui, Juan Palomares, Laura A. Macías, Karla E. Jiménez, Mariela Salinas, Eva |
author_facet | Chávez, Norma A. Jauregui, Juan Palomares, Laura A. Macías, Karla E. Jiménez, Mariela Salinas, Eva |
author_sort | Chávez, Norma A. |
collection | PubMed |
description | Milk processing industries and distributors have problems with adulteration of liquid milk by the addition of bovine cheese whey. Recently, the detection of fraudulent manipulation of milk with whey has focused on the identification of glycomacropeptide (GMP). Current non-immunological methods to detect GMP in dairy products are expensive and time-consuming or have low sensitivity. In this study, a novel sandwich enzyme-linked immunosorbent assay (ELISA) for the detection and quantification of whey in raw milk was developed, using a polyclonal rabbit anti-GMP antibody. Calibration curves were constructed by analyzing raw milk standards containing different known concentrations of liquid cheese whey (0.02–20%). The method had a detection limit of 0.047% (v/v) and a quantification limit of 0.14% (v/v). The antibody showed high specificity and no cross-reaction with milk components (other than κ-casein) and was successful in detecting GMP in dairy commercial products. The recovery ratio was between 95.62% and 113.88% for all matrices tested. The intra-assay and interassay coefficients of variation were <6% and <7%, respectively. Finally, it can be stored for 3 months in the form of a ready-to-use kit, while maintaining its accuracy and reproducibility. |
format | Online Article Text |
id | pubmed-3362802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-33628022012-05-31 A highly sensitive sandwich ELISA for the determination of glycomacropeptide to detect liquid whey in raw milk Chávez, Norma A. Jauregui, Juan Palomares, Laura A. Macías, Karla E. Jiménez, Mariela Salinas, Eva Dairy Sci Technol Original Paper Milk processing industries and distributors have problems with adulteration of liquid milk by the addition of bovine cheese whey. Recently, the detection of fraudulent manipulation of milk with whey has focused on the identification of glycomacropeptide (GMP). Current non-immunological methods to detect GMP in dairy products are expensive and time-consuming or have low sensitivity. In this study, a novel sandwich enzyme-linked immunosorbent assay (ELISA) for the detection and quantification of whey in raw milk was developed, using a polyclonal rabbit anti-GMP antibody. Calibration curves were constructed by analyzing raw milk standards containing different known concentrations of liquid cheese whey (0.02–20%). The method had a detection limit of 0.047% (v/v) and a quantification limit of 0.14% (v/v). The antibody showed high specificity and no cross-reaction with milk components (other than κ-casein) and was successful in detecting GMP in dairy commercial products. The recovery ratio was between 95.62% and 113.88% for all matrices tested. The intra-assay and interassay coefficients of variation were <6% and <7%, respectively. Finally, it can be stored for 3 months in the form of a ready-to-use kit, while maintaining its accuracy and reproducibility. Springer-Verlag 2012-01-18 2012 /pmc/articles/PMC3362802/ /pubmed/22662290 http://dx.doi.org/10.1007/s13594-011-0052-3 Text en © INRA and Springer-Verlag, France 2012 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Paper Chávez, Norma A. Jauregui, Juan Palomares, Laura A. Macías, Karla E. Jiménez, Mariela Salinas, Eva A highly sensitive sandwich ELISA for the determination of glycomacropeptide to detect liquid whey in raw milk |
title | A highly sensitive sandwich ELISA for the determination of glycomacropeptide to detect liquid whey in raw milk |
title_full | A highly sensitive sandwich ELISA for the determination of glycomacropeptide to detect liquid whey in raw milk |
title_fullStr | A highly sensitive sandwich ELISA for the determination of glycomacropeptide to detect liquid whey in raw milk |
title_full_unstemmed | A highly sensitive sandwich ELISA for the determination of glycomacropeptide to detect liquid whey in raw milk |
title_short | A highly sensitive sandwich ELISA for the determination of glycomacropeptide to detect liquid whey in raw milk |
title_sort | highly sensitive sandwich elisa for the determination of glycomacropeptide to detect liquid whey in raw milk |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362802/ https://www.ncbi.nlm.nih.gov/pubmed/22662290 http://dx.doi.org/10.1007/s13594-011-0052-3 |
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