Search results for "STAR"

showing 10 items of 4285 documents

Retention of aroma compounds in starch matrices: competitions between aroma compounds toward amylose and amylopectin

2002

International audience; The retention of three aroma compounds-isoamyl acetate, ethyl hexanoate, and linalool--from starch-containing model food matrices was measured by headspace analysis, under equilibrium conditions. We studied systems containing standard or waxy corn starch with one or two aroma compounds. The three studied aroma compounds interact differently: ethyl hexanoate and linalool form complexes with amylose, and isoamyl acetate cannot. However, in systems containing one aroma compound, we observed with both starches a significant retention of the three molecules. These results indicate that amylopectin could play a role in the retention of aroma. In systems containing two arom…

Chemical PhenomenaStarchAcyclic MonoterpenesIsoamyl acetate01 natural sciencesBinding CompetitiveZea mayschemistry.chemical_compound0404 agricultural biotechnologyPentanolsamyloseAmylose[CHIM.ANAL]Chemical Sciences/Analytical chemistry[SDV.IDA]Life Sciences [q-bio]/Food engineeringAroma compoundOrganic chemistryamylopectinCaproatesAromaWaxy corncomplexesbiologyChemistry Physicalflavor retention010401 analytical chemistryEthyl hexanoatefood and beveragesStarch04 agricultural and veterinary sciencesGeneral Chemistryinteractionsbiology.organism_classification040401 food science0104 chemical scienceschemistryFoodAmylopectinOdorantsMonoterpenesStarch pasteGeneral Agricultural and Biological Sciencescompetition[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
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Influence of Physicochemical Interactions between Amylose and Aroma Compounds on the Retention of Aroma in Food-like Matrices

2002

In food matrices, where starch is often used as a gelling or texturing agent, the occurrence of amylose-aroma complexes and their effect on the release of aroma compounds are difficult to determine. Indeed, thick or gelled systems are known to reduce the diffusion rate of flavor molecules, resulting in an increase of retention. Moreover, interactions between aroma compounds and matrix components might increase the retention of aroma compounds. The complexing behavior of three aroma compounds with amylose was studied by DSC and X-ray diffraction to determine the relative importance of these two factors. Their interaction properties were different: two of them formed complexes, and the third …

Chemical PhenomenaStarchAmylopectinOrganolepticZea mays01 natural scienceschemistry.chemical_compoundViscosity0404 agricultural biotechnologyX-Ray DiffractionAmylose[SDV.IDA]Life Sciences [q-bio]/Food engineeringOrganic chemistryMoleculeComputingMilieux_MISCELLANEOUSAromaFlavorSolanum tuberosumCalorimetry Differential ScanningbiologyChemistry PhysicalViscosity010401 analytical chemistryfood and beveragesStarch04 agricultural and veterinary sciencesGeneral Chemistry[SDV.IDA] Life Sciences [q-bio]/Food engineeringbiology.organism_classification040401 food science0104 chemical scienceschemistryFoodAmylopectinOdorantsThermodynamicsAmyloseGeneral Agricultural and Biological SciencesGelsJournal of Agricultural and Food Chemistry
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Formulation strategy towards minimizing viscosity mediated negative food effect on disintegration and dissolution of immediate release tablets.

2017

Food induced viscosity can delay disintegration and subsequent release of API from solid dosage form which may lead to severe reduction in the bioavailability of BCS type III compounds. Formulations of such tablets need to be optimized in view of this postprandial viscosity factor. In this study, three super disintegrants, croscarmellose sodium (CCS), cross-linked polyvinylpolypyrrolidone (CPD), and sodium starch glycolate (SSG) were assessed for their efficiency under simulated fed state. Tablets containing these disintegrants were compressed at 10 and 30 KN, while taking lactose as a soluble filler. In addition to other compendial tests, disintegration force of these formulations was meas…

Chemistry PharmaceuticalPharmaceutical ScienceLactose02 engineering and technology030226 pharmacology & pharmacyDosage formExcipients03 medical and health sciencesViscosity0302 clinical medicineDrug DiscoverySodium Starch GlycolateImmediate releaseDissolutionPharmacologyFOOD EFFECTChemistryViscosityOrganic Chemistryfood and beveragesPovidoneStarch021001 nanoscience & nanotechnologyBioavailabilityChemical engineeringSolubilityFoodCarboxymethylcellulose Sodium0210 nano-technologyFederal stateTabletsDrug development and industrial pharmacy
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Molecular Stark-effect spectroscopy of Prodan and Laurdan in different solvents and electric dipole moments in their equilibrated ground and Franck–C…

2007

Abstract The results from electrooptical absorption measurements (EOAM) on the ground and excited Franck–Condon state dipole moments of Prodan and Laurdan in 1,4-dioxane and cyclohexane are presented. The ground and excited Franck–Condon state electric dipole moments as well as the respective transition moment of both probes are parallel. The electric dipole moments of Prodan and Laurdan in the ground state in cyclohexane and 1,4-dioxane have values within the range (15.7–16.5) × 10 −30  C m. On optical excitation the dipole moments increase by (42.1–49.5) × 10 −30  C m. The obtained results are compared with the values of the dipole moments of Prodan and Laurdan determined by other methods.

ChemistryGeneral Chemical EngineeringTransition dipole momentGeneral Physics and AstronomyGeneral ChemistryPhotochemistrysymbols.namesakeDipolechemistry.chemical_compoundStark effectExcited statesymbolsAtomic physicsSpectroscopyGround stateLaurdanExcitationJournal of Photochemistry and Photobiology A: Chemistry
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Electric field induced alignment-orientation conversion in diatomic molecules: analysis and observation for NaK

1999

This article reports the observation of the molecular fluorescence circularity under irradiation with linearly polarised light. This alignment-orientation conversion phenomenon arises as a result of partial transformation from alignment of the ensemble of 1 P state molecular angular momenta into their orientation under the effect of non-linear dc Stark effect. Circularity rate up to 0.12 was observed in D 1 P! X 1 S fluorescence of 23 Na 39 K molecules in agreement with the theoretically predicted value.

ChemistryOrganic ChemistryFluorescenceDiatomic moleculeAnalytical ChemistryInorganic Chemistrysymbols.namesakeStark effectOrientation (geometry)Electric fieldsymbolsMoleculeIrradiationAtomic physicsSpectroscopyNAKJournal of Molecular Structure
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Studies of rotational level Λ-doubling by rf-optical double resonance spectroscopy: application to NaK D1Π

1997

Abstract We report here the application of optical-radio frequency double resonance spectroscopy for individual rotational levels of the NaK D 1 Π state. Lambda doubling constant q values for five ν′, J ′ levels are obtained. These data are combined with measurements of dc e - f Stark-mixing-induced changes in optical spectra, and the electric dipole moment d p in the D 1 Π state is determined.

ChemistryOrganic ChemistryTransition dipole momentAnalytical chemistryResonanceLambdaAnalytical ChemistryInorganic Chemistrysymbols.namesakeDipoleElectric dipole momentStark effectsymbolsAtomic physicsSpectroscopySpectroscopyNAKJournal of Molecular Structure
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Poly(glycolide) multi-arm star polymers: Improved solubility via limited arm length.

2010

Due to the low solubility of poly(glycolic acid) (PGA), its use is generally limited to the synthesis of random copolyesters with other hydroxy acids, such as lactic acid, or to applications that permit direct processing from the polymer melt. Insolubility is generally observed for PGA when the degree of polymerization exceeds 20. Here we present a strategy that allows the preparation of PGA-based multi-arm structures which significantly exceed the molecular weight of processable oligomeric linear PGA (<1000 g/mol). This was achieved by the use of a multifunctional hyperbranched polyglycerol (PG) macroinitiator and the tin(II)-2-ethylhexanoate catalyzed ring-opening polymerization of gly…

ChemistryPGAOrganic Chemistryblock copolymerhyperbranchedDegree of polymerizationstar polymerGraftingFull Research PaperLactic acidlcsh:QD241-441Polyesterchemistry.chemical_compoundChemistrypolyglycerollcsh:Organic chemistryPolymerizationPolymer chemistryCopolymerlcsh:QpolyesterSolubilitylcsh:Sciencepoly(glycolide)Glycolic acidBeilstein journal of organic chemistry
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Photoinduced optical anisotropy in organic molecular films controlled by an electric field

1993

Abstract The photoinduced reorientation of dye molecules in molecular films on solid substrates has been controlled with external dc electric fields, leading to solid state structures, which are macroscopically polar, temporally stable at room temperature, and well-defined at the molecular level. A simulation based on the excitation-driven rotational diffusion of the molecules in the potential of their neighbors yielded a realistic model and indicated a collective character of the process. This shows that we are close to a quantitative comprehension of the molecular interactions within these films.

Chemistrybusiness.industryGeneral Physics and AstronomyRotational diffusionCondensed Matter::Materials Sciencesymbols.namesakeOpticsStark effectChemical physicsElectric fieldMolecular filmsymbolsPolarMoleculePhysical and Theoretical ChemistryThin filmbusinessAnisotropyChemical Physics Letters
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Hypothermic preservation of lung allograft inhibits cytokine-induced chemoattractant-1, endothelial leucocyte adhesion molecule, vascular cell adhesi…

2007

Summary Organ dysfunction is a major clinical problem after lung transplantation. Prolonged cold ischaemia and reperfusion injury are believed to play a central role in this complication. The influence of cold preservation on subsequent warm reperfusion was studied in an isolated, ventilated and perfused rat lung. Rat lungs were flushed with cold Perfadex-solution and stored at 4°C for different time periods. Thereafter lungs were perfused and ventilated for up to 3 h. Physiological parameters, production of inflammatory mediators and leucocyte infiltration were measured before and after perfusion. Lungs subjected to a cold ischaemia time of up to 6 h showed stable physiological conditions …

ChemokinePathologymedicine.medical_specialtymedicine.medical_treatmentImmunologyIntercellular Adhesion Molecule-1Vascular Cell Adhesion Molecule-1Blood PressurePulmonary EdemaPulmonary ArteryBasic ImmunologyHypothermia InducedmedicineImmunology and AllergyAnimalsRespiratory systemRats WistarLungChemokine CCL2LungbiologyCell adhesion moleculemedicine.diseaseIntercellular Adhesion Molecule-1RatsEndothelial stem cellCytokinemedicine.anatomical_structureReperfusion InjuryImmunologybiology.proteinLeukocytes MononuclearTissue PreservationInflammation MediatorsE-SelectinReperfusion injuryCell Adhesion MoleculesLung Transplantation
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Sensitivity of the Cherenkov Telescope Array to spectral signatures of hadronic PeVatrons with application to Galactic Supernova Remnants

2023

The local Cosmic Ray (CR) energy spectrum exhibits a spectral softening at energies around 3~PeV. Sources which are capable of accelerating hadrons to such energies are called hadronic PeVatrons. However, hadronic PeVatrons have not yet been firmly identified within the Galaxy. Several source classes, including Galactic Supernova Remnants (SNRs), have been proposed as PeVatron candidates. The potential to search for hadronic PeVatrons with the Cherenkov Telescope Array (CTA) is assessed. The focus is on the usage of very high energy $\gamma$-ray spectral signatures for the identification of PeVatrons. Assuming that SNRs can accelerate CRs up to knee energies, the number of Galactic SNRs whi…

Cherenkov Telescope ArrayGamma rays: generalstatistical [methods]energy spectrumFOS: Physical sciencesVHESettore FIS/05 - Astronomia E Astrofisicacosmic raysMethods: data analysissupernovadata analysis [methods][PHYS.PHYS.PHYS-INS-DET]Physics [physics]/Physics [physics]/Instrumentation and Detectors [physics.ins-det]Cosmic raysInstrumentation and Methods for Astrophysics (astro-ph.IM)Cherenkov Telescope Arra ; alactic Supernova Remnants ; PeVatrons ;Methods: statisticalgalactic PeVatronsHigh Energy Astrophysical Phenomena (astro-ph.HE)emission spectrum) supernovae: general [(stars]Astronomy and AstrophysicssensitivityobservatoryGalactic PeVatronscosmic radiationspectralgalaxyhadron(Stars:) supernovae: generalAstrophysics - High Energy Astrophysical PhenomenaAstrophysics - Instrumentation and Methods for Astrophysics[PHYS.ASTR]Physics [physics]/Astrophysics [astro-ph]statisticalgeneral [gamma rays]signature
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