Search results for "AROMA"

showing 10 items of 1006 documents

Inter-individual retronasal aroma release variability during cheese consumption: Role of food oral processing

2014

The aim of our study was to explain inter-individual differences on in vivo aroma release during cheese consumption by oral physiological parameters. To reach this objective, 34 subjects were recruited. Their salivary flow, oral volume and velum opening were determined. Six cheddar-based melted cheeses with different fat levels and firmness were flavoured with nonan-2-one.(NO) and ethyl propanoate (EP). During their consumption (free protocol), in vivo retro nasal aroma release was followed by Atmospheric Pressure Chemical lonisation-Mass Spectrometry (APCI-MS). Chewing activity was evaluated by electromyography recordings. Bolus saliva content, mouth-coating, and bolus rheology were also d…

Salivainter individual variability030309 nutrition & dieteticsFat content[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionFood consumption03 medical and health scienceschemistry.chemical_compound0404 agricultural biotechnologyBolus (medicine)[SDV.IDA]Life Sciences [q-bio]/Food engineeringin vivo aroma releaseAroma compoundFood scienceAromaNo release2. Zero hunger0303 health sciencesfood oral processingbiologyChemistry[ SDV.IDA ] Life Sciences [q-bio]/Food engineeringEthyl propanoatefood and beverages04 agricultural and veterinary sciencesbiology.organism_classification040401 food sciencemouth coating[SDV.AEN]Life Sciences [q-bio]/Food and Nutritionmodel cheesesFood Sciencechewing activity
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Molecular mechanisms of aroma persistence: From noncovalent interactions between aroma compounds and the oral mucosa to metabolization of aroma compo…

2021

International audience; The present study aims to reveal the molecular mechanisms underlying aroma persistence, as it plays a major role in food appreciation and quality. A multidisciplinary approach including ex vivo experiments using a novel model of oral mucosa and saliva as well as in vivo dynamic instrumental and sensory experiments was applied. Ex vivo results showed a reduction in aroma release between 7 and 86% in the presence of the thin layer of salivary proteins covering the oral mucosa (mucosal pellicle). This reduction was explained by hydrophobic interactions involving the mucosal pellicle and by the ability of oral cells and saliva to metabolize specific aroma compounds. The …

Salivaproton transfer reaction-mass spectrometry (PTR-MS)Thin layeraroma perception01 natural sciencesdynamic sensory evaluationAnalytical ChemistryPersistence (computer science)0404 agricultural biotechnologyIn vivomedicine[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyOral mucosaSalivary Proteins and PeptidesSalivaAromaVolatile Organic CompoundsbiologyChemistry010401 analytical chemistryMouth Mucosafood and beveragesafter-odour04 agricultural and veterinary sciencesGeneral Medicinebiology.organism_classification040401 food science0104 chemical sciencesmedicine.anatomical_structureBiochemistrymucosal pelliclearoma releaseOdorantsSalivary Proteins[SDV.AEN]Life Sciences [q-bio]/Food and NutritionEx vivoFood Science
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The role of saliva in aroma release and perception

2017

Aroma perception is an important factor driving food acceptance. Volatile organic compounds (VOCs) are released from the food matrix and then reach the receptors located in the nasal cavity, leading to their perception. These steps are closely dependent on the physicochemical properties of the volatile compounds and the food matrix, but also on human physiology. Among the different physiological parameters involved, the literature reports that saliva has various effects on VOCs and therefore appears as a major actor impacting the perception of aroma. This article reviews how saliva takes part in aroma release, considering both in vitro and in vivo approaches, and how it may affect perceptio…

Salivavolatile organic compound[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritionmedia_common.quotation_subjectsalivary proteinsprotéine salivaireAnalytical Chemistry0404 agricultural biotechnologyPerceptionvolatile organic compoundsHumansflaveurFood sciencesaliveAromamedia_commonenzymatic reactionAffect perceptionMolecular interactionssalivabiologyChemistryenzymatic conversioncomposé organique volatilFood acceptancefood and beverages04 agricultural and veterinary sciencesGeneral MedicineHuman physiologymucinslibération d'arômeinteractionsbiology.organism_classification040401 food scienceflavourBiochemistryaroma releaseOdorantsréaction enzymatiquePerceptionIndirect impact[SDV.AEN]Life Sciences [q-bio]/Food and NutritionFood Science
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The influence of automobile exhausts on mutagenicity of soils: contamination with, fractionation, separation, and preliminary identification of mutag…

2000

To test the assumption that automobile exhausts contribute to soil mutagenicity, two soils with low levels of mutagenic activities were exposed to traffic exhausts at a heavily charged junction of German motorways (Autobahnen) for 3, 7, 10, 13, 17, 21, and 26 weeks. Indeed, in the presence of a metabolic activation system from rat liver (S9), an average increase of 8 and 9 (4 and 12) revertants per gram per week was found in Salmonella typhimurium TA 98 (TA 100). In the absence of S9, meaningful measurements were impossible on account of a concurrent dose dependent increase of toxicity. No correlation between the increase of mutagenicity and the contents of polycyclic aromatic hydrocarbons …

Salmonella typhimuriumHealth Toxicology and MutagenesisSister chromatid exchangeMutagenBone Marrow CellsFractionationmedicine.disease_causeAmes testchemistry.chemical_compoundMiceGermanyGeneticsmedicineAnimalsHumansSoil PollutantsLymphocytesPolycyclic Aromatic HydrocarbonsBiotransformationCells CulturedVehicle EmissionsFluorenesChromatographyMicronucleus TestsPyrenesMutagenicity TestsTolueneRatsSolventchemistryMicronucleus testMicrosomes LiverSolventsPyreneSister Chromatid ExchangeMutagensMutation research
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Degradation of heterocyclic aromatic amines in oil under storage and frying conditions and reduction of their mutagenic potential.

2007

Heterocyclic aromatic amines (HAA) were systematically studied concerning their partition behavior in water/oil-systems and their thermostability in different animal derived fats and vegetable oils. Partitioning of IQx-compounds and PhIP in water/oil systems was found to depend on the polarity defined by the molecular structure and on the pH-value of the aqueous phase. In particular, beta-carbolines norharman and harman showed a significant strong lipophilic character at alkaline pH. After heating in frying fats at 130 degrees C, contents of IQx compounds and PhIP were reduced by more than 40% and after heating at 180 degrees C less than 10% of the HAA initial concentration was recovered. B…

Salmonella typhimuriumHot TemperatureMutagenToxicologymedicine.disease_causeLipid oxidationHeterocyclic CompoundsmedicineOrganic chemistryPlant OilsCookingAminesThermostabilitychemistry.chemical_classificationDose-Response Relationship DrugMolecular StructureMutagenicity TestsAqueous two-phase systemAromatic amineWaterGeneral MedicineDietary FatschemistryHeterocyclic compoundDegradation (geology)Oxidation-ReductionGenotoxicityFood ScienceMutagensFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association
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Heteroaromatic Inhibitors of the Astacin Proteinases Meprin α, Meprin β and Ovastacin Discovered by a Scaffold-Hopping Approach.

2020

Abstract Astacin metalloproteinases, in particular meprins α and β, as well as ovastacin, are emerging drug targets. Drug‐discovery efforts have led to the development of the first potent and selective inhibitors in the last few years. However, the most recent compounds are based on a highly flexible tertiary amine scaffold that could cause metabolic liabilities or decreased potency due to the entropic penalty upon binding to the target. Thus, the aim of this study was to discover novel conformationally constrained scaffolds as starting points for further inhibitor optimization. Shifting from flexible tertiary amines to rigid heteroaromatic cores resulted in a boost in inhibitory activity. …

ScaffoldTertiary amineStereochemistryCell SurvivalAntineoplastic Agentsscaffold hoppingMatrix metalloproteinaseScaffold hoppinghydroxamate01 natural sciencesBiochemistryHydrocarbons AromaticmetalloproteinasesStructure-Activity RelationshipmeprinVery Important PaperDrug DiscoveryTumor Cells CulturedHumansProtease InhibitorsGeneral Pharmacology Toxicology and PharmaceuticsAminesPharmacologyDose-Response Relationship DrugMolecular StructureFull Paper010405 organic chemistryChemistryOrganic ChemistryMetalloendopeptidasesFull PapersovastacinRecombinant Proteinsheteroaromatics0104 chemical sciences010404 medicinal & biomolecular chemistryMetalloproteasesMolecular MedicineAstacinDrug Screening Assays AntitumorSelectivityChemMedChem
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X-ray and DFT-calculated structures of a vanadyl Schiff base complex: (methanol-κO)[2-methoxy-6-({2-[(2-oxido-3-methoxybenzylidene)amino]benzyl}imino…

2012

The central VVatom in the title mononuclear oxovanadium complex, [VO(C23H20N2O4)(CH3OH)]·H2O, has a distorted octahedral coordination. Two N atoms and two O atoms of the Schiff base define the base of the bipyramid and two O atoms are in the apical positions, one from vanadyl and the second from methanol. Density functional theory (DFT) calculations were performed for the title complex and its ligand to compare their geometry in the solid and gas phases. Additional analyses were made of the changes in the geometry of the ligand during complex formation. The HOMA (harmonic oscillator model of aromaticity) descriptor of π-electron delocalization was calculated to estimate the aromaticity of t…

Schiff baseStereochemistryLigandAromaticityGeneral MedicineCrystal structureGeneral Biochemistry Genetics and Molecular BiologyBipyramidchemistry.chemical_compoundCrystallographyDelocalized electronchemistryDensity functional theoryBenzeneActa Crystallographica Section C Crystal Structure Communications
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A vanadyl Schiff base complex: {2,2'-[1,1'-(o-phenylenedinitrilo)bis(ethan-1-yl-1-ylidene)]diphenolato}oxovanadium(IV).

2011

The green crystals of the title compound, [V(C(22)H(18)N(2)O(2))O], represent a mononuclear oxovanadium complex. The central V(IV) centre has a distorted square-pyramidal coordination. Two N atoms and two O atoms of the Schiff base ligand define the base of the pyramid, and the oxide O atom is in the apical position. Density functional theory (DFT) calculations were performed to analyse the changes in the geometry of the ligand during the complex formation. The most significant changes are observed in the values of the torsion angles in the vicinity of the donor N atoms. The HOMA index (Harmonic Oscillator Model of Aromaticity) has been calculated to compare the aromaticity of the benzene r…

Schiff baseStereochemistryOxideAromaticityGeneral MedicineCrystal structureOxovanadium IVGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundCrystallographychemistryAtomDensity functional theoryBenzeneActa crystallographica. Section C, Crystal structure communications
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Photocatalytic oxidation of 4-methoxybenzyl alcohol to p-anisaldehyde in a fixed bed continuous reactor,

2008

Selective oxidation TiO2 Aromatic alcohol Aromatic aldehyde Fixed bed reactor
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Home-prepared anatase, rutile, and brookite TiO2 catalysts for selective photocatalytic oxidation of p-methoxybenzyl alcohol in water: reactivity and…

2008

Selective oxidation TiO2 Rutile Brookite Aromatic alcohol ATR-FTIR analysis
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