0000000000246659

AUTHOR

Maria Jose Ruiz

0000-0003-4174-6688

showing 12 related works from this author

Bioaccessibility and bioavailability of fumonisin B2 and its reaction products with isothiocyanates through a simulated gastrointestinal digestion sy…

2014

Abstract Fumonisins (FBs) are toxins produced mainly by the molds Fusarium verticillioides (also known as Fusarium moniliforme) and Fusarium proliferatum. These mycotoxins are contaminants of wheat, maize, maize-based foods and other grains worldwide. Isothiocyanates (ITCs) are natural compounds produced by the enzymatic hydrolysis of glucosinolates, which are found in plants of the Brassicaceae family. The use of ITCs as food preservatives has been extensively researched. In this study, allyl (AITC), phenyl (PITC) and benzyl isothiocyanates (BITC) fumigation systems (500 μL/L) were employed to reduce FB2 levels naturally produced in bread by Gibberella moniliformis CECT 2987. Reaction prod…

FusariumFumonisin B2PreservativebiologyFusarium proliferatumbiology.organism_classificationBioavailabilitychemistry.chemical_compoundchemistryEnzymatic hydrolysisFood scienceMycotoxinFood ScienceBiotechnologyFood contaminantFood Control
researchProduct

Formation of fumonisin B(1)-glucose reaction product, in vitro cytotoxicity, and lipid peroxidation on kidney cells.

2010

Fumonisin B(1) (FB(1)) content in corn products decreases during the heating process in foods containing reducing sugars, mainly because of the formation of N-(carboxymethyl)fumonisin B(1). In this study, a rapid method has been developed for the determination of both compounds in corn products using a high-speed blender, Ultra-Turrax, for solvent extraction and liquid chromatography-tandem mass spectrometry. The kinetics of FB(1) degradation and the formation of the Maillard adduct were studied in a model system constituted by corn bread spiked with FB(1) and heated at 160, 180, and 200 degrees C for 3, 6, 10, 15, and 20 min. FB(1) decreased from 0.96 to 0.3 mg/kg and N-(carboxymethyl)fumo…

Neutral redFood HandlingKidneyFumonisinsZea maysLipid peroxidationsymbols.namesakechemistry.chemical_compoundfumonisinFumonisinChlorocebus aethiopskidney cellAnimalsIC50Vero CellsFumonisin B1ChromatographyChemistryfood and beveragesGeneral ChemistryCarbohydrateMalondialdehydeMaillard reactionKineticsGlucosesymbolsLipid PeroxidationGeneral Agricultural and Biological SciencesJournal of agricultural and food chemistry
researchProduct

Isolation, purification, LC–MS/MS characterization and reactive oxygen species induced by fumonisin B1 in VERO cells

2010

Fumonisins are mycotoxins produced by Fusarium verticillioides that commonly contaminate maize and maize products. The present work shows the results of a comparative study of three different fermentation's techniques (solid and liquid medium of corn and a solid agarized medium) for the production of fumonisins B-1, B-2 and B-3 with strains of F. verticillioides. The solid medium of corn was the most effective in the production of fumonisins, being Fumonisin B-1 the one produced with higher concentration, so the extract obtained by solid fermentation process was used for FB1 purification. Fumonisins characterization and quantification were performed with reversed-phase high-performance liqu…

FusariumEXTRACTIONVERTICILLIOIDESCULTURESToxicologyFumonisinsMECHANISMSchemistry.chemical_compoundFUSARIUM-MONILIFORMEFusariumTandem Mass SpectrometryLiquid chromatography–mass spectrometryDichlorofluoresceinChlorocebus aethiopsFumonisinAnimalsOXIDATIVE STRESSMycotoxinVero CellsChromatography High Pressure LiquidPROLIFERATUMFumonisin B1ChromatographyMYCOTOXINSbiologyfood and beveragesGeneral MedicineReference StandardsFluoresceinsbiology.organism_classificationCulture MediaDNA-DAMAGEchemistryFermentationVero cellFermentationOCHRATOXINReactive Oxygen SpeciesFood ScienceFood and Chemical Toxicology
researchProduct

Comparative cytotoxicity study of enniatins A, A1, A2, B, B1, B4 and J3 on Caco-2 cells, Hep-G2 and HT-29

2011

Abstract Enniatins (ENs) are ionophoric, phytotoxic, antihelminthic, and antibiotic compounds of hexadepsipeptidic structure produced by several strains of Fusarium spp. The cytotoxicity effect of the ENs A, A 1 , A 2 , B, B 1 , B 4 and J 3 was compared on three tumor cell lines, the human epithelial colorectal adenocarcinoma (Caco-2), the human colon carcinoma (HT-29), and the human liver carcinoma (Hep-G2). The endpoint evaluated was the mitochondrial integrity by using the MTT assays, after 24 and 48 h of incubation. The IC 50 value for EN A 2 on Caco-2 cells, after 24 h exposure, was 18.7 ± 4.5 μM and decrease to 2.6 ± 0.7 μM at 48 h of incubation. However, ENs A, A 1 , B 1 and B 4 exer…

StereochemistryGeneral MedicineBiologyToxicologyMolecular biologyHep G2Caco-2Cell cultureToxicityCytotoxic T cellMTT assayCytotoxicityIncubationFood ScienceFood and Chemical Toxicology
researchProduct

Study of the potential toxicity of enniatins A, A(1), B, B(1) by evaluation of duodenal and colonic bioavailability applying an in vitro method by Ca…

2010

Abstract The bioavailability of the minor Fusarium mycotoxins enniatins (ENs) utilizing an in vitro method which allows the simulation of the small and large intestine tracts has been studied. This method, based on the application of the Caco-2 cells grown alone or in symbiosis with several strains characteristics of the gastrointestinal tract, has permitted to simulate the duodenal and colonic intestinal compartments, respectively. The duodenal bioavailability expressed as absorption value after 4 h of exposure, ranged from 57.7 to 76.8% for EN A, from 68.8 to 70.2% for EN A1, from 65.0 to 67.0% for EN B, and from 62.2 to 65.1% for EN B1. Colonic bioavailability after 48 h of incubation ra…

FusariumColonDuodenumBiological AvailabilityAbsorption (skin)PharmacologyToxicologyRisk AssessmentFusariumDepsipeptidesToxicity TestsmedicineHumansLarge intestineIncubationGastrointestinal tractbiologyChemistryMycotoxinsbiology.organism_classificationIn vitroBioavailabilitymedicine.anatomical_structureIntestinal AbsorptionCaco-2Caco-2 CellsToxicon : official journal of the International Society on Toxinology
researchProduct

Isolation and purification of enniatins A, A1, B, B1, produced by Fusarium tricinctum in solid culture, and cytotoxicity effects on Caco-2 cells

2010

Enniatins (ENs) are antibiotic compounds of hexadepsipeptidic structure produced by several strains of Fusarium spp. The ENs A, A(1), B, B-1 were purified from extracts of Fusarium tricinctum grown on a solid medium of corn, by a low pressure liquid chromatography (LPLC) on reverse phase of Amberlite XAD-7 followed by semipreparative LC. The purity and the structure of the isolated compounds were confirmed by LC-MS/MS. The technique of the purification of the fungal extract enabled complete separation of the ENs A, A(1), B, B-1 with a mean purity of 97% for all the compounds. The cytoxicity of the ENs was tested in the cell lines of human origin (epithelial colorectal adenocarcinoma cells, …

FusariumMagnetic Resonance SpectroscopySTRESSSTATE FERMENTATIONToxicologyFUSAPROLIFERINFusariumTandem Mass SpectrometryDepsipeptidesBEAUVERICINHumansMTT assayCytotoxicityIC50AVENACEUMANALOGSChromatographybiologyChemistryFungi imperfectiFUNGUS VERTICILLIUM-HEMIPTERIGENUMbiology.organism_classificationIn vitroCaco-2Cell cultureMK1688Caco-2 CellsLIQUID-CHROMATOGRAPHYMAIZEChromatography LiquidToxicon
researchProduct

Antibacterial activity of the enniatin B, produced by Fusarium tricinctum in liquid culture, and cytotoxic effects on Caco-2 cells.

2011

The enniatins (ENs) are bioactive compounds of hexadepsipeptidic structure produced by several strains of Fusarium sp. The EN B was purified from extracts of Fusarium tricinctum growth on liquid culture of potato dextrose broth (PDB), using a semipreparative liquid chromatography (LC) followed by an analytical LC. The purity and the structure of the isolated compound were confirmed by the determination of the extinction coefficient and with electrospray ionization-mass spectrometry (ESI-MS) study. The pure fraction of EN B was utilized to determine the antibiotic effects on several bacterial strains that are considered normally pathogens of the intestinal tract: Escherichia coli, Enterococc…

FusariumSpectrometry Mass Electrospray IonizationShigella dysenteriaeCell SurvivalHealth Toxicology and MutagenesisCell Culture TechniquesMicrobial Sensitivity TestsToxicologymedicine.disease_causeMicrobiologyListeria monocytogenesFusariumDepsipeptidesmedicineHumansYersinia enterocoliticaEscherichia colibiologyDose-Response Relationship DrugCell DifferentiationClostridium perfringensbiology.organism_classificationLipidsAnti-Bacterial AgentsCulture MediaSalmonella entericaCaco-2 CellsEnterococcus faeciumToxicology mechanisms and methods
researchProduct

Study of the cytotoxic activity of beauvericin and fusaproliferin and bioavailability in vitro on Caco-2 cells.

2010

Abstract Beauvericin (BEA) is a cyclohexadepsipeptide mycotoxin which has insecticidal properties and produces cytotoxic effects in mammalian cells. Fusaproliferin (FUS) is a mycotoxin that has toxic activity against brine shrimp, insect cells, and teratogenic effects on chicken embryos. The aim of this study was to determine the cytotoxicity of BEA and FUS in human epithelial colorectal adenocarcinoma HT-29 and Caco-2 cells, the transepithelial transport and the bioavailability using Caco-2 cells as a simulated in vitro gastrointestinal model of the human intestinal epithelium. The inhibitory concentration (IC 50 ) evidenced by BEA in the Caco-2 cells was 24.6 and 12.7 μM at 24 and 48 h ex…

Cell SurvivalTerpenesBiological AvailabilityGeneral MedicinePharmacologyBiologyToxicologyIntestinal epitheliumIn vitroBeauvericinBioavailabilitychemistry.chemical_compoundInhibitory Concentration 50chemistryCaco-2DepsipeptidesCytotoxic T cellHumansCaco-2 CellsDrug Screening Assays AntitumorCytotoxicityMycotoxinFood ScienceChromatography LiquidFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association
researchProduct

Bioaccessibility of Enniatins A, A1, B, and B1 in Different Commercial Breakfast Cereals, Cookies, and Breads of Spain

2013

Fusarotoxins enniatins (ENs) can represent a potential risk as natural contaminants of cereal commodities. However, only their bioaccessible fraction can exert a toxicity. The purpose of this study was to determine the ENs A, A₁, B, and B₁ bioaccessibility added in 1.5 and 3.0 μmol/g concentrations in breakfast cereals, cookies, and breads using a simulated in vitro gastrointestinal extraction model. Bioaccessibility values ranged between 40.4 ± 1.9 and 79.9 ± 2.8%. The lower values were 50.1, 40.4, 43.9, and 46.3% in wheat bran with fibers, and the higher values were 79.9, 64.2, 69.8, and 73.6% in white loaf bread for the ENs A, A₁, B, and B₁, respectively. Food composition, compounds stru…

BranChemistryPotential riskFood composition dataGeneral ChemistryFood scienceGeneral Agricultural and Biological SciencesDigestionIntestinal absorptionFood contaminantJournal of Agricultural and Food Chemistry
researchProduct

Study of the potential toxicity of commercial crispy breads by evaluation of bioaccessibility and bioavailability of minor Fusarium mycotoxins

2011

Abstract Enniatins (ENs) are bioactive compounds produced by the secondary metabolism of several Fusarium strains and known to have several biological activities, such as acting as enzyme inhibitors, antifungal and antibacterial agents, and immunomodulatory substances. This study has investigated the ENs bioaccessibility, spiked in commercial wheat crispy bread at 1.5 and 3.0 μmol/g concentrations, their transepithelial transport and bioavailability using Caco-2 cells as a model of the human intestinal epithelium. The content (%) of the four ENs contained in the gastric fluid has resulted variable from 69% to 91%, considering the two concentrations assayed. The mean bioaccessibility data fo…

FusariumBiological AvailabilityFood ContaminationAbsorption (skin)Toxicologychemistry.chemical_compoundFusariumDepsipeptidesHumansFood scienceSecondary metabolismMycotoxinTriticumchemistry.chemical_classificationbiologyGastric fluidBiological TransportBreadGeneral MedicineMycotoxinsbiology.organism_classificationBioavailabilityEnzymechemistryEnvironmental chemistryCaco-2 CellsFood SciencePotential toxicityFood and Chemical Toxicology
researchProduct

Production, purification, and mass spectrometry characterization of the cyclohexadepsipeptide enniatin J3and study of the cytoxicity on differentiate…

2011

The enniatins (EN) are bioactive compounds of hexadepsipeptidic structure produced by several strains of Fusarium spp. The enniatin J3 (EN J3) was purified from extracts of Fusarium solani growth on solid medium of kamut, using semipreparative liquid chromatography (LC) followed by an analytical LC. The purity and the structure of the isolated compound were confirmed by electrospray ionization-mass spectrometry study-linear ion trap (ESI-MS-LIT). The pure fraction of EN J3 was utilized to study the cytotoxicity on differentiated and undifferentiated Caco-2 cells. The use of both chromatographic techniques allowed us to produce and purify 50 mg of EN J3 completely characterized with the tech…

FusariumElectrosprayChromatographybiologyChemistryHealth Toxicology and Mutagenesisbiology.organism_classificationMass spectrometryPollutionEnvironmental ChemistryMTT assayIon trapEnniatinCytotoxicityFusarium solaniToxicological & Environmental Chemistry
researchProduct

Dar malas noticias. Grupo de Enfermería (4)

2012

Vídeo perteneciente a la asignatura de Psicología del Grado de Enfermería donde se demuestra la competencia en habilidades de comunicación para manejar situaciones difíciles.

3211 Ciències Médiques
researchProduct