Search results for "Phenyl isothiocyanate"

showing 4 items of 4 documents

Isocratic high-performance liquid chromatographic determination of tryptophan in infant formulas.

1996

The application to infant formulas of a method for tryptophan determination by isocratic HPLC with UV detection at 254 nm, after derivatization with phenyl isothiocyanate, was studied. Protein was hydrolysed by barium hydroxide at 120 degrees C for 8 h, followed by derivatization with phenyl isothiocyanate, HPLC and UV detection at 254 nm. The optimum chromatographic conditions (pH, ionic strength of elution solvent and eluent ratio) were established. The analytical parameters (linearity, precision, accuracy of derivatization and limits of detection and quantification) were determined. The values obtained demonstrated that the method is useful for determining the tryptophan content of infan…

AcetatesBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryBarium hydroxidechemistry.chemical_compoundColumn chromatographyIsothiocyanatesHumansDerivatizationChromatography High Pressure LiquidAcetic AcidDetection limitChromatographyPhenyl isothiocyanateElutionOrganic ChemistryOsmolar ConcentrationTryptophanInfant NewbornTryptophanInfantGeneral MedicineHydrogen-Ion ConcentrationchemistrySolventsInfant FoodThiocyanatesJournal of chromatography. A
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A chemical approach for the reduction of beauvericin in a solution model and in food systems.

2014

Abstract Beauvericin (BEA) is a bioactive compound produced by the secondary metabolism of several Fusarium strains with a strong antibacterial, antifungal, and insecticidal activities. This study evaluated the reduction of BEA added at 25 mg/kg in phosphate buffer saline (PBS) solutions at pH of 4, 7 and 10, or to different cereal products (kernels and flours) by the bioactive compounds phenyl isothiocyanate (PITC) and benzyl isothiocyanate (BITC). The concentration of the mycotoxin was evaluated using liquid chromatography coupled to the diode array detector (LC-DAD). In solution, BEA reduction ranged from 9% to 94% on a time-dependent fashion and lower pH levels resulted in higher BEA re…

FusariumChromatographybiologyBenzyl isothiocyanatePhenyl isothiocyanatefood and beveragesFood ContaminationGeneral MedicineModels TheoreticalToxicologybiology.organism_classificationBeauvericinBioactive compoundchemistry.chemical_compoundchemistryChromatography detectorDepsipeptidesSecondary metabolismMycotoxinOxidation-ReductionFood ScienceChromatography LiquidFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association
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Study of the chemical reduction of the fumonisins toxicity using allyl, benzyl and phenyl isothiocyanate in model solution and in food products

2012

Abstract Fumonisins (FBs) are bioactive compounds produced by several strains of Fusarium spp. which contain a polyketide structure similar to sphinganine. These mycotoxins contain a free amino group that could work as an electron donor and react with the electrophile carbon present within the isothiocyanate (ITC) group. The objective of this study was to determine the effect of ITCs (allyl, benzyl and phenyl) on the stability of FB 1 , FB 2 and FB 3 . Firstly, PBS solutions at three pH levels (4, 7 and 9) were prepared and added with pairs of one FB (1 mg/L) plus one ITC (1 mg/L). Then, gaseous ITC was used to fumigate corn kernels and corn flour contaminated with FBs produced by Gibberell…

FusariumSpectrometry Mass Electrospray IonizationTime FactorsFood HandlingElectrospray ionizationFood ContaminationElectron donorToxicologyMass spectrometryTandem mass spectrometryFumonisinsZea maysPoisonschemistry.chemical_compoundDrug StabilityIsothiocyanatesTandem Mass SpectrometryMycotoxinChromatography High Pressure LiquidDecontaminationChromatographybiologyPhenyl isothiocyanateHydrogen-Ion Concentrationbiology.organism_classificationchemistryFumigationIsothiocyanateFood MicrobiologyToxicon
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Antifungal activity of gaseous allyl, benzyl and phenyl isothiocyanate in vitro and their use for fumonisins reduction in bread

2013

Abstract Fumonisins (FBs) are toxins produced mainly by the molds Fusarium verticillioides (synonym Fusarium moniliforme ) and Fusarium proliferatum . These mycotoxins are contaminants of wheat, maize, maize-based foods and other grains worldwide. FB 1 , the most abundant and toxic metabolite, is known to cause a range of species-specific toxic responses. It has been associated with a high incidence of esophageal cancer in the Transkei region of South Africa and some provinces of China. In addition, FB 1 has been declared a class 2B carcinogen or “possibly carcinogenic to humans”. Isothiocyanates (ITCs) are natural compounds produced by enzymatic conversion of metabolites called glucosinola…

FusariumbiologyPhenyl isothiocyanateMetabolitefood and beveragesFusarium proliferatumbiology.organism_classificationAntimicrobialchemistry.chemical_compoundchemistryFumonisinOrganic chemistryFood scienceMycotoxinMyceliumFood ScienceBiotechnologyFood Control
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