Search results for "Chromatography-mass spectrometry"

showing 10 items of 332 documents

Oxidation of melatonin by oxoferryl hemoglobin: A mechanistic study

2002

Reaction of melatonin with the hypervalent iron centre of oxoferryl hemoglobin, produced in aqueous solution from methemoglobin and H2O2, has been investigated at 37 degrees C and pH 7.4, by absorption spectroscopy. The reaction results in reduction of the oxoferryl moiety with formation of a heme-ferric containing hemoprotein. Stopped-flow spectrophotometric measurements provide evidence that the reduction of oxoferryl-Hb by melatonin is first-order in oxoferryl-Hb and first-order in melatonin. The bimolecular reaction constant at pH 7.4 and 37 degrees C is 112 +/- 1.0 M(-1) s(-1). Two major oxidation products from melatonin have been found by gas chromatography-mass spectroscopy: the cycl…

HemeproteinMagnetic Resonance SpectroscopyTime FactorsKynuraminePhotochemistryBiochemistryMethemoglobinGas Chromatography-Mass SpectrometryMelatoninHemoglobinsReaction rate constantmedicineAnimalsMethemoglobinMelatoninIndole testCyclic compoundChemistryOxidesGeneral MedicineHydrogen PeroxideKineticsYield (chemistry)CattleSpectrophotometry UltravioletHemoglobinChlorineOxidation-Reductionmedicine.drug
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Effect of fat nature and aroma compound hydrophobicity on flavor release from complex food emulsions.

2004

Complex food emulsions containing either hydrogenated palm kernel oil (vegetable fat) or anhydrous milk fat (animal fat) were flavored by using different aroma compounds. The fats differed by their fatty acid and triacylglycerol compositions and by their melting behavior, while the aroma compounds (ethyl butanoate, ethyl hexanoate, methyl hexanoate, mesifurane, linalool, diacetyl, cis-3-hexen-1-ol, and gamma-octalactone) differed by their hydrophobicity. Application of differential scanning calorimetry to fat samples in bulk and emulsified forms indicated differences in the ratio of solid-to-liquid between temperatures ranging from 10 to 35 degrees C. Solid-phase microextraction coupled wit…

Hot TemperatureChemical Phenomena030309 nutrition & dieteticsPalm OilGas Chromatography-Mass Spectrometry03 medical and health scienceschemistry.chemical_compound0404 agricultural biotechnology[SDV.IDA]Life Sciences [q-bio]/Food engineeringAroma compoundAnimalsPlant OilsFood scienceAromaFlavorComputingMilieux_MISCELLANEOUSTriglycerideschemistry.chemical_classification0303 health sciencesAnimal fatChromatographybiologyChemistryChemistry PhysicalFatty Acidsfood and beveragesEthyl hexanoateFatty acid04 agricultural and veterinary sciencesGeneral Chemistry[SDV.IDA] Life Sciences [q-bio]/Food engineeringbiology.organism_classification040401 food scienceDiacetylDietary FatsLipidsMilkFoodEmulsionOdorantsEmulsionsGeneral Agricultural and Biological SciencesHydrophobic and Hydrophilic InteractionsJournal of agricultural and food chemistry
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Stabilization of a nutraceutical omega-3 fatty acid by encapsulation in ultrathin electrosprayed zein prolamine.

2010

Docosahexaenoic acid (DHA) is a long chain polyunsaturated fatty acid of the omega-3 series (omega-3), which exerts strong positive influences on human health. The target of this study was the stabilization by encapsulation of this bioactive ingredient in zein ultrathin capsules produced by electrospraying. The zein ultrathin DHA encapsulation was observed by ATR-FTIR spectroscopy to be more efficient against degradation under both ambient conditions and in a confined space (so-called headspace experiment). In the latter case, that more closely simulates a sealed food packaging situation, the bioactive DHA was considerably more stable. By fitting the degradation data to a specific auto-deco…

Hot TemperatureDocosahexaenoic AcidsZeinPhenylpropanolamineGas Chromatography-Mass SpectrometryIngredientNutraceuticalNanocapsulesFatty Acids Omega-3Spectroscopy Fourier Transform InfraredOmega 3 fatty acidchemistry.chemical_classificationAldehydesVolatile Organic CompoundsChromatographyfood and beveragesFatty acidHumidityElectrochemical TechniquesFood packagingKineticschemistryModels ChemicalDocosahexaenoic acidPlant proteinTasteDietary SupplementsFood TechnologyOxidation-ReductionFood SciencePolyunsaturated fatty acidHalf-LifeJournal of food science
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Analysis of furan in coffee of different provenance by head-space solid phase microextraction gas chromatography-mass spectrometry: effect of brewing…

2009

A simple, sensitive and accurate method for the analysis of furan in roasted coffee has been used based on headspace-solid-phase micro-extraction (HS-SPME) coupled to gas chromatography-mass spectrometry (GC-MS). The extraction was performed using 75-microm carboxen/polydimethylsiloxane fiber. Ionic strength, extraction time and temperature, and desorption time were assessed as the most important parameters affecting the HS-SPME procedure and d(4)-furan was used as the internal standard. The linearity range was in the range 0.0075-0.486 ng g(-1); the LOD and LOQ calculated using the signal-to-noise ratio approach were 0.002 and 0.006 ng g(-1), respectively. The inter- and intra-day precisio…

Hot TemperatureSettore CHIM/10 - Chimica Degli AlimentiFood HandlingfuranHealth Toxicology and MutagenesisAnalytical chemistryFood ContaminationToxicologyMass spectrometrySolid-phase microextractionCoffeeGas Chromatography-Mass SpectrometryBeverageschemistry.chemical_compoundbrewing procedures; coffee; furan; SPME-GC/MSFuranFuransSolid Phase MicroextractionSPME-GC/MSChromatographybusiness.industryExtraction (chemistry)Public Health Environmental and Occupational HealthGeneral ChemistryGeneral MedicinechemistryIonic strengthCarcinogensbrewing procedureBrewingGas chromatographyGas chromatography–mass spectrometrybusinessFood ScienceFood additivescontaminants. Part A, Chemistry, analysis, control, exposurerisk assessment
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Thermal degradation and isomerisation kinetics of triolein studied by infrared spectrometry and GC–MS combined with chemometrics

2008

Authors version of article published in the journal: Chemistry and Physics of Lipids Published version available on Science Direct: http://dx.doi.org/10.1016/j.chemphyslip.2008.12.002 Triolein, a triglyceride containing oleic acid as the only acid moiety in the glyceride molecules has been isothermally treated at 280,300,and 325 degrees C in glass vials under nitrogen atmosphere. The products formed during the thermal treatment at each temperature have been analysed both by infrared spectrometry and GC-MS. The CC-MS analysis was performed after derivatisation of the fatty acids into their methyl esters (FAMEs). Chemometric tools were used in determining the concentrations of the main produc…

Hot TemperatureSpectrophotometry Infraredmedicine.diagnostic_testChemistryOrganic ChemistryKineticsAnalytical chemistryInfrared spectroscopyCell BiologyBiochemistryGas Chromatography-Mass SpectrometryChemometricsVDP::Mathematics and natural science: 400::Basic biosciences: 470::Biochemistry: 476Kineticschemistry.chemical_compoundIsomerismSpectrophotometrymedicinelipids (amino acids peptides and proteins)TrioleinGas chromatography–mass spectrometryMolecular BiologyIsomerizationTrioleinChemistry and Physics of Lipids
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A new potential toxaphene congener: synthesis, GC/EI-MS study, crystal structure, NMR analysis, and ab initio calculations of 3-endo,5-endo-dichloro-…

2001

Abstract A new potential toxaphene congener 3- endo ,5- endo -dichloro-7,7-bis-chloromethyl-4-dichloromethyl-tricyclo[2.2.1.0 2,6 ]heptane 2 has been isolated from reaction mixture obtained by the chlorination of 2- exo ,10,10-trichlorobornane 1 . The X-ray structural analysis of 2 revealed an unusual tricyclic structure, where the two chlorine atoms occupying endo -positions are in close spatial proximity with each other and near to the neighbouring CHCl 2 group. Further, it revealed that the symmetry of the molecule is distorted. The 1 H and 13 C NMR spectra of 2 have been assigned by means of 1 H, 1 H d ouble- q uantum f iltered co rrelation s pectroscop y (DQF COSY), PFG 1 H, 13 C HMQC …

InsecticidesMagnetic Resonance SpectroscopyEnvironmental EngineeringHealth Toxicology and MutagenesisAnalytical chemistryAb initioCrystal structureGas Chromatography-Mass Spectrometrychemistry.chemical_compoundAb initio quantum chemistry methodsEnvironmental ChemistryMoleculeToxapheneHeptaneChemistryTemperaturePublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryModels TheoreticalCarbon-13 NMRPollutionCrystallographyProton NMRMass spectrumEnvironmental PollutantsChemosphere
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Steady-state levels of retinal 24S-hydroxycholesterol are maintained by glial cells intervention after elevation of intraocular pressure in the rat

2012

Purpose: Our previous studies suggested that CYP46A1 and 24S-hydroxycholesterol. (24SOH) may be associated with glaucoma. Loss of CYP46A1-expressing retinal. ganglion cells is involved in the activation of glia, and therefore possibly in the. disbalance of cholesterol. In this context, the purpose of our present work was to. emphasize the glial and longitudinal CYP46A1 expression after an interventional. glaucoma-related stress triggered by elevated intraocular pressure (IOP). Methods: Sprague–Dawley rats were submitted to laser photocoagulation of the. trabecular meshwork, limbus and episcleral veins in one eye to induce elevated IOP. Rats were euthanized at days 3, 14, 30 and 60 (n = 10 p…

Intraocular pressuregenetic structures[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionGlaucomacholesterol homeostasisRats Sprague-Dawleychemistry.chemical_compound0302 clinical medicineHomeostasis0303 health sciencesGeneral MedicineAnatomyGanglionmedicine.anatomical_structureCytokinesIntercellular Signaling Peptides and Proteinsmedicine.symptomNeurogliamedicine.medical_specialtyBlotting WesternContext (language use)BiologyGas Chromatography-Mass SpectrometryRetina03 medical and health sciencesOphthalmologyGlial Fibrillary Acidic ProteinCholesterol 24-HydroxylasemedicineAnimalsIntraocular Pressure030304 developmental biologyRetinaRetinalmedicine.diseaseHydroxycholesterolseye diseasesRatsDisease Models AnimalOphthalmologyglaucomagliosisGliosischemistrySteroid Hydroxylases030221 ophthalmology & optometryOcular HypertensionMuller cellTrabecular meshworksense organs[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
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Volatile constituents of aerial parts of two Mediterranean species of Inula: Inula crithmoides L. and I. verbascifolia (Willd.) Hausskn. (Asteraceae)

2014

Inula crithmoides L. grows along the Mediterranean coasts and is used as an edible vegetable as the young leaves or shoots are eaten raw, cooked or pickled. Inula verbascifolia (Willd.) Hausskn. is a quite localised species growing mainly along the Adriatic Sea coasts. In this study the volatile components of the aerial part of both species are described. Gas chromatography and gas chromatography mass spectrometry analysis showed the presence of 41 components in I. crithmoides and 75 compounds in I. verbascifolia, respectively, and a very different profile in the composition of the two species. The chemotaxonomy of I. crithmoides, by comparison with other data reported in the literature, is…

Inula crithmoidesMediterranean climateInula crithmoidePlant ScienceAsteraceaeBiochemistryGas Chromatography-Mass Spectrometryessential oilAnalytical ChemistryBotanyVegetablesOils VolatileInulabiologyMediterranean RegionOrganic ChemistrySettore CHIM/06 - Chimica OrganicaAsteraceaebiology.organism_classificationchemotaxonomyItalyChemotaxonomyShootGas chromatographyInulaInula verbascifoliaGas chromatography–mass spectrometry
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Chemical composition of the essential oil from the aerial parts of Ononis reclinata L. (Fabaceae) grown wild in Sicily

2016

In the present study, the chemical composition of the essential oil from aerial parts of Ononis reclinata L., a species not previously investigated, collected in Sicily was evaluated by GC and Gas chromatography-Mass spectrometry. The main components of O. reclinata were menthone (43.6%), isopimpinellin (38.4%) and pulegone (11.2%). The comparison with other studied oils of genus Ononis showed a peculiar and characteristic profile.

IsopimpinellinChromatography GasmenthoneFlowersPlant ScienceBiology01 natural sciencesBiochemistryPlant StemGas Chromatography-Mass SpectrometryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundGenuslawOnonisBotanyOils VolatileOnoniSicilyChemical compositionEssential oilpulegoneOnonis reclinataPlant Stems010405 organic chemistryOrganic ChemistryFabaceaeFabaceaeisopimpinellinPlant Components Aerialbiology.organism_classificationMenthone0104 chemical sciencesPlant Leavesvolatile component010404 medicinal & biomolecular chemistrychemistryChromatography GaFlowerOnonisPlant LeavePulegoneNatural Product Research
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Evaluation of furanocoumarins from seeds of the wild parsnip (Pastinaca sativa L. s.l.).

2018

Abstract Although the wild parsnip (Pastinaca sativa L. s.l.) fruits are known to contain linear and angular furanocoumarins, the individual components of the seeds have not been fully identified and quantitated, and, in the case of immature seeds, reported. In view of this, the main furanocoumarin compounds were extracted using pyridine, and were isolated using semi-preparative high-performance liquid chromatography. The structural elucidation of isolated compounds was done based on detailed spectral analysis conducted by liquid chromatography–electrospray ionization–mass spectrometry (LC–ESI/MS), 1H and 13C NMR and, where possible, by gas chromatography–mass spectrometry (GC–MS). The quan…

IsopimpinellinSpectrometry Mass Electrospray IonizationClinical BiochemistryWild parsnip030226 pharmacology & pharmacy01 natural sciencesBiochemistryBergaptenGas Chromatography-Mass SpectrometryAnalytical Chemistry03 medical and health scienceschemistry.chemical_compoundFuranocoumarin0302 clinical medicinefoodLimit of DetectionFurocoumarinsmedicinePastinacaPastinacaChromatography High Pressure LiquidChromatographyApiaceaebiologyImperatorinMethoxsalen010401 analytical chemistryReproducibility of ResultsCell BiologyGeneral Medicinebiology.organism_classificationfood.food0104 chemical scienceschemistrySeedsLinear Modelsmedicine.drugJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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