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URI permanente desta comunidadehttps://thoth.dti.ufv.br/handle/123456789/3352

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2012 - 20132

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Autor: search.filters.author.Cruz, Marcus Henrique Campino de laTem arquivos: Sim

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    Comparison of high performance liquid chromatography with fluorescence detector and with tandem mass spectrometry methods for detection and quantification of ochratoxin a in green and roasted coffee beans
    (Instituto de Tecnologia do Paraná - Tecpar, 2013-11) Bandeira, Raquel Duarte da Costa Cunha; Uekane, Thais Matsue; Cunha, Carolina Passos da; Rodrigues, Janaina Marques; Cruz, Marcus Henrique Campino de la; Godoy, Ronoel Luiz de Oliveira; Fioravante, Andreia de Lima
    Two analytical methods for the determination and confirmation of ochratoxin A (OTA) in green and roasted coffee samples were compared. Sample extraction and clean-up were based on liquid–liquid phase extraction and immunoaffinity column. The detection of OTA was carried out with the high performance liquid chromatography (HPLC) combined either with fluorescence detection (FLD), or positive electrospray ionization (ESI+) coupled with tandem mass spectrometry (MS–MS). The results obtained with the LC-ESI-MS/MS were specific and more sensitive, with the advantages in terms of unambiguous analyte identification, when compared with the HPLC-FLD.
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    Development and validation of a method for detection and quantification of ochratoxin A in green coffee using liquid chromatography coupled to mass spectrometry
    (Sociedade Brasileira de Ciência e Tecnologia de Alimentos, 2012-10) Bandeira, Raquel Duarte da Costa Cunha; Uekane, Thaís Matsue; Cunha, Carolina Passos da; Cunha, Valnei Smarçaro da; Rodrigues, Janaína Marques; Godoy, Ronoel Luiz de Oliveira; Cruz, Marcus Henrique Campino de la
    A method using Liquid Chromatography Tanden Mass Spectrometry (LC-MS/MS) with matrix-matched calibration curve was developed and validated for determining ochratoxin A (OTA) in green coffee. Linearity was found between 3.0 and 23.0 ng.g –1 . Mean recoveries ranged between 90.45% and 108.81%; the relative standard deviation under repeatability and intermediate precision conditions ranged from 5.39% to 9.94% and from 2.20% to 14.34%, respectively. The limits of detection and quantification were 1.2 ng.g –1 and 3.0 ng.g –1 , respectively. The method developed was suitable and contributed to the field of mycotoxin analysis, and it will be used for future production of the Certified Reference Material (CRM) for OTA in coffee.