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Detection and quantitation of additions of soybean proteins in cured-meat products by perfusion reversed-phase high-performance liquid chromatography

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Authors
Criado, Mónica; Castro Rubio, FlorentinaUniversity of Alcalá Author; García Ruiz, CarmenUniversity of Alcalá Author; García López, María ConcepciónUniversity of Alcalá Author; Marina Alegre, María LuisaUniversity of Alcalá Author
Identifiers
Permanent link (URI): http://hdl.handle.net/10017/1330
DOI: 10.1002/jssc.200500011
ISSN: 1615-9306
Publisher
John Wiley & Sons
Date
2005
Affiliation
Universidad de Alcalá. Departamento de Química Analítica e Ingeniería Química
Funders
The authors thank the Comunidad Autónoma de Madrid (Spain) for project 07G/0025/2003. Dr. C. García-Ruiz also thanks the Ministerio de Ciencia y Tecnolog a for her contract from the Ramón y Cajal program (RYC-2003-001). F. Castro-Rubio thanks the Ministerio de Educación y Ciencia (Spain) for her predoctoral grant.
Bibliographic citation
Journal of Separation Science, 2005, v. 28, p. 987-995
Keywords
Soybean proteins
Cured-meat products
Perfusion reversed-phase high-performance liquid chromatography
Project
07G/0025/2003 (Comunidad de Madrid)
RYC2003-001 (Ministerio de Ciencia y Tecnología)
Document type
info:eu-repo/semantics/article
Version
info:eu-repo/semantics/publishedVersion
Publisher's version
http://dx.doi.org/10.1002/jssc.200500011
Rights
(c) WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, 2005
Access rights
info:eu-repo/semantics/openAccess
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Abstract
Perfusion liquid chromatography has been applied in this work to the determination of soybean proteins in commercially available cured meat products, enabling the detection of additions of soybean proteins in cured meat products to which the addition of these vegetable proteins is forbidden and the quantitation of soybean proteins in cured meat products to which the addition of these proteins is allowed up to a certain limit. The analytical methodology is based on a sample treatment (fat extraction and soybean protein solubilization) prior to chromatographic analysis. Fat extraction with acetone and soybean protein solubilization with a buffer solution at basic pH (pH 10 or 9) were necessary to obtain selective and sensitive conditions. Use of water-acetonitrile-trifluoroacetic acid or water-tetrahydrofuran-trifluoroacetic acid linear binary gradients at a flow rate of 3 mL/min, a temperature of 50 degrees C, and UV detection at 280 nm enabled chromatographic analysis of soybean proteins in cured meat products in less than 3 min.
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