Josefa Tolosa

Dr. Josefa Tolosa

Department of Preventive Medicine and Public Health, Food Sciences, Toxicology and Forensic Medicine, Laboratory of Toxicology, University of Valencia; Burjassot, 46100 Valencia, Spain
orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 November 2014 in Journal of Agricultural and Food Chemistry
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Journal Article
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Josefa TolosaJosefa Tolosa
Josefa Tolosa
GFGuillermina Font
Guillermina Font
JMJordi Mañes
Jordi Mañes
EGEmilia FERRER GARCIA
Emilia FERRER GARCIA


1 June 2019 in Food and Chemical Toxicology
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Journal Article
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DCDionisia Carballo
Dionisia Carballo
Josefa TolosaJosefa Tolosa
Josefa Tolosa
EGEmilia FERRER GARCIA
Emilia FERRER GARCIA
HBHouda Berrada
Houda Berrada

14 June 2019 in Toxins
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Journal Article
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Ana Juan-GarciaAna Juan-Garcia
Ana Juan-Garcia
Josefa TolosaJosefa Tolosa
Josefa Tolosa
Cristina Juan GarcíaCristina Juan García
Cristina Juan García
María José RuizMaría José Ruiz
María José Ruiz
Mycotoxins are produced by a number of fungal genera spp., for example, Aspergillus, Penicillium, Alternaria, Fusarium, and Claviceps. Beauvericin (BEA) and Ochratoxin A (OTA) are present in various cereal crops and processed grains. This goal of this study was to determine their combination effect in HepG2 cells, presented for the first time. In this study, the type of interaction among BEA and OTA through an isobologram method, cell cycle disturbance by flow cytometry, and genotoxic potential by in vitro micronucleus (MN) assay following the TG 487 (OECD, 2016) of BEA and OTA individually and combined in HepG2 cells are presented. Cytotoxic concentration ranges studied by the MTT assay over 24, 48, and 72 h were from 0 to 25 µM for BEA and from 0 to 100 µM for OTA, while BEA + OTA combinations were at a 1:10 ratio from 3.4 to 27.5 µM. The toxicity observed for BEA was higher than for OTA at all times assayed; additive and synergistic effects were detected for their mixtures. Cell cycle arrest in the G0/G1 phase was detected for OTA and BEA + OTA treatments in HepG2 cells. Genotoxicity revealed significant effects for BEA, OTA, and in combinations underlining the importance of studying real exposure scenarios of chronic exposure to mycotoxins.

9 February 2017 in Toxins
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Journal Article
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Josefa TolosaJosefa Tolosa
Josefa Tolosa
GGGiulia Graziani
Giulia Graziani
AGAnna Gaspari
Anna Gaspari
DCDonato Chianese
Donato Chianese
EGEmilia FERRER GARCIA
Emilia FERRER GARCIA
Alberto RitieniAlberto Ritieni
Alberto Ritieni
A simple and rapid multi‐mycotoxin method for the determination of 17 mycotoxins simultaneously is described in the present survey on durum and soft wheat pasta samples. Mycotoxins included in the study were those mainly reported in cereal samples: ochratoxin‐A (OTA), aflatoxin B1 (AFB1), zearalenone (ZON), deoxynivalenol (DON), 3‐and 15‐acetyl‐deoxynivalenol (3‐AcDON and 15‐AcDON), nivalenol (NIV), neosolaniol (NEO), fusarenon‐X, (FUS‐X), T‐2 toxin (T‐2) and HT‐2 toxin (HT‐2), fumonisin B1 and B2 (FB1 and FB2), and four emerging mycotoxins: three enniatins (ENA, ENA1, and ENB), and beauvericin (BEA). Twenty‐nine samples were analyzed to provide an overview on mycotoxin presence: 27 samples of durum wheat pasta, and two samples of baby food. Analytical results concluded that trichothecenes showed the highest incidence, mainly DON, NIV, and HT‐2 toxin, followed by ZON and ENB, while NEO, FUS‐X, OTA, AFB1, and FUM were not detected in any sample. The highest contents corresponded to ENB and ranged from 91.15μg/kg to 710.90 μg/kg.

1 September 2013 in Food Control
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Journal Article
Closed access
Josefa TolosaJosefa Tolosa
Josefa Tolosa
GFGuillermina Font
Guillermina Font
JMJordi Mañes
Jordi Mañes
EGEmilia FERRER GARCIA
Emilia FERRER GARCIA