Search results for "release"

showing 10 items of 602 documents

Enzyme-Responsive Intracellular Controlled Release Using Nanometric Silica Mesoporous Supports Capped with "Saccharides"

2010

The synthesis of new capped silica mesoporous nanoparticles for on-command delivery applications is described. The gate-like functional hybrid systems consisted of nanoscopic MCM-41-based materials functionalized on the pore outlets with different “saccharide” derivatives and a dye contained in the mesopores. A series of hydrolyzed starch products as saccharides were selected. The mesoporous silica nanoparticles S1, S2, and S3 containing the grafted starch derivatives Glucidex 47, Gludicex 39, and Glucidex 29 were synthesized. Additionally, for comparative purposes solid S4 containing lactose was prepared. Delivery studies in pure water in the presence of pancreatin or -D-galactosidase were…

INGENIERIA DE LA CONSTRUCCIONMaterials scienceTECNOLOGIA DE ALIMENTOSSwineStarchIntracellular SpaceCarbohydratesGatecarbohydratesGeneral Physics and AstronomyNanoparticleMesoporousKluyveromycesHydrolysischemistry.chemical_compoundAdsorptionQUIMICA ORGANICAgateAnimalsHumansOrganic chemistryGeneral Materials ScienceDrug CarriersQUIMICA INORGANICAGeneral EngineeringMesoporous silicaSilicon Dioxidebeta-GalactosidaseControlled releaseNanostructuresIntracellular controlled releaseMesoporous organosilicaenzymechemistryChemical engineeringEnzymeDelayed-Action Preparationsintracellular controlled releaseLLC-PK1 CellsAdsorptionMesoporous materialmesoporousPorosityHeLa Cells
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Enzyme-Mediated Controlled Release Systems by Anchoring Peptide Sequences on Mesoporous Silica Supports

2011

[EN] Gated community: Peptides anchored to the surface of silica mesoporous supports by a valid procedure act as gatekeepers. In this way, "zero release" supports that selectively deliver the cargo in the presence of a suitable peptidase are obtained (see picture, red spheres: cargo, colored chains: peptides). © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

INGENIERIA DE LA CONSTRUCCIONPeptide sequencesStereochemistryPeptide hydrolaseMolecular Sequence DataAnchoringPeptideCatalysisRutheniumArticleAmino acid sequenceNanoparticleQUIMICA ORGANICACoordination ComplexesControlled release systemsSilicon dioxideControlled releaseOrganic chemistryMolecular geneticsValenciachemistry.chemical_classificationbiologyQUIMICA INORGANICAMesoporous supportSilicaGeneral ChemistryGeneral MedicineMesoporous silicaMolecular gatesbiology.organism_classificationControlled releaseMesoporous materialsChemistryKineticsEnzymeMetabolismchemistryMesoporous SilicaPeptide HydrolasesPeptideNanoparticlescontrolled releasePeptidesPorosityCoordination compoundmolecular gatesPeptide HydrolasesAngewandte Chemie
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Poly(N-isopropylacrylamide)-gated Fe3O4/SiO2 core shell nanoparticles with expanded mesoporous structures for the temperature triggered release of ly…

2015

Core-shell nanoparticles comprised of Fe3O4 cores and a mesoporous silica shell with an average expanded pore size of 6.07 nm and coated with a poly(N-isopropylacrylamide) (PNIPAM) layer (CS MSNs EP PNIPAM) were prepared and characterized. The nanoparticles was loaded with (Ru(bipy)3 2+) dye or an antibacterial enzyme, lysozyme, to obtain CS MSNs EP PNIPAM Ru(bipy)3 2+ and CS MSNs EP PNIPAM Lys, respectively. The lysozyme loading was determined to be 160 mg/g of nanoparticle. It was seen that Ru(bipy)3 2+ and lysozyme release was minimal at a room temperature of 25 ºC while at physiological temperature (37 º C), abrupt release was observed. The applicability of the CS MSNs EP PNIPAM Lys was…

INGENIERIA DE LA CONSTRUCCIONSilicon dioxideAcrylic ResinsBiomedical EngineeringNanoparticleBioengineeringchemistry.chemical_compoundPNIPAMQUIMICA ORGANICAColloid and Surface ChemistryBacillus cereusBIOQUIMICA Y BIOLOGIA MOLECULARNanotechnologyFerrous CompoundsPhysical and Theoretical ChemistryChemical PhysicsChromatographybiologyProtein deliveryQUIMICA INORGANICATemperatureTriggered releaseSurfaces and InterfacesGeneral MedicineChemical EngineeringMesoporous silicaSilicon Dioxidebiology.organism_classificationAnti-Bacterial AgentsMicrococcus luteuschemistryDrug deliveryPoly(N-isopropylacrylamide)NanoparticlesMuramidaseLysozymePore expansionMesoporous materialMicrococcus luteusPorosityMesoporous silicaPhysical Chemistry (incl. Structural)BiotechnologyNuclear chemistryColloids and Surfaces B: Biointerfaces
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Stability of different mesoporous silica particles during an in vitro digestion

2016

Mesoporous silica materials have the ability to entrap drugs, nutrients and functional biomolecules and can be able to act as smart delivery systems capable to control and target the release of their cargo in a particular part of the gastrointestinal tract when administrated orally. However, the aptness of these encapsulation supports in in vivo oral controlled release relies on their chemical stability through the digestive tube. In this context, we have evaluated the stability of four different mesoporous silica particles, frequently used as encapsulating supports, during an in vitro digestion process comprising buccal, stomach and intestinal phases. Results showed that after 4 h of diges…

INGENIERIA DE LA CONSTRUCCIONTECNOLOGIA DE ALIMENTOSNanoparticle02 engineering and technology010402 general chemistryElectron Microscopy Service of the UPV01 natural sciencesMesoporous silica particlesQUIMICA ORGANICAQUIMICA ANALITICAOrganic chemistryMoietyGeneral Materials ScienceAmine-functionalizationchemistry.chemical_classificationChemistryBiomoleculeQUIMICA INORGANICAIn vitro digestionGeneral ChemistryBuccal administrationMesoporous silica021001 nanoscience & nanotechnologyCondensed Matter PhysicsControlled release0104 chemical sciencesChemical engineeringMechanics of MaterialsSurface modificationChemical stability0210 nano-technologyStabilityMicroporous and Mesoporous Materials
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PREPARATION AND IN VITRO CHARACTERIZATION OF NEW HYDROGELS BASED ON INULIN AND ALPHA,BETA-POLYASPARTYLHYDRAZIDE FOR COLONIC DRUG DELIVERY

2008

INULIN POLYASPARTYLHYDRAZIDE DRUG RELEASE HYDROGELS
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Exemples de QSAR sur des coefficients de partage

2005

National audience

IOTA-CARAGEENAN[SPI.GPROC] Engineering Sciences [physics]/Chemical and Process EngineeringQSARQSPRAROMA RELEASE[SDV.IDA]Life Sciences [q-bio]/Food engineering[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process Engineering[SDV.IDA] Life Sciences [q-bio]/Food engineeringPARTITION COEFFICIENTINTERACTIONHEADSCAPE ANALYSISGELSComputingMilieux_MISCELLANEOUS
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Understanding fat, proteins and saliva impact on aroma release from flavoured ice-creams

2017

Publication également référencée sous le numéro WOS:000437803400018; The release profile of fourteen aroma compounds was studied in ice cream samples varying in fat and protein, both in level and type. In vitro aroma release was monitored by solid phase micro-extraction gas chromatography using an innovative saliva reactor, which imitated human chewing under temperature control. The results showed that the effect of the fat type on aroma release was smaller than that of fat level. Ice creams with low fat level released more hydrophobic aroma compounds than ice creams with high fat level. At low fat level more aroma compounds were released from ice creams with lower protein content. At high …

Ice creamSalivaChromatography GasFood chemistrySolid-phase microextractionAnalytical Chemistry0404 agricultural biotechnologySaliva reactorPhase (matter)fatHumansFood scienceAromaVolatile Organic CompoundsGas chromatographysalivaChromatographybiologyChemistrySaltingProteinsfood and beverages04 agricultural and veterinary sciencesGeneral MedicineSolid phase microextractionbiology.organism_classificationLipids040401 food scienceFlavoring Agents[SDV.AEN] Life Sciences [q-bio]/Food and NutritionAroma releaseice-creamSalting outGas chromatographyprotein[SDV.AEN]Life Sciences [q-bio]/Food and NutritionFood Science
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Impaired Binding to Junctophilin-2 and Nanostructural Alteration in CPVT Mutation

2021

Rationale: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare disease, manifested by syncope or sudden death in children or young adults under stress conditions. Mutations in the Ca 2+ release channel/RyR2 (type 2 ryanodine receptor) gene account for about 60% of the identified mutations. Recently, we found and described a mutation in RyR2 N-terminal domain, RyR2 R420Q . Objective: To determine the arrhythmogenic mechanisms of this mutation. Methods and Results: Ventricular tachycardias under stress conditions were observed in both patients with catecholaminergic polymorphic ventricular tachycardia and knock-in mice. During action potential recording (by patch-clamp in …

Ile de francePhysiologyCPVT030204 cardiovascular system & hematologyArticle03 medical and health sciences0302 clinical medicineaction potential[SDV.MHEP.CSC]Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular systemPolitical sciencejunctophilinryanodine receptormedia_common.cataloged_instanceHumansEuropean union610 Medicine & health030304 developmental biologymedia_common0303 health sciencescalciumRyanodine Receptor Calcium Release ChannelRyR2musculoskeletal systemSarcoplasmic ReticulumDeath Sudden Cardiaccalcium induced calcium releaseGain of Function Mutationcardiomyocyte calcium handlingcardiovascular systemventricular tachycardiamutationCardiology and Cardiovascular MedicineHumanities
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Quantitative studies of the secretion of complement component C3 by resident, elicited and activated macrophages. Comparison with C2, C4 and lysosoma…

1982

To quantitate the secretion of complement component C3 by guinea pig peritoneal macrophages an enzyme-linked immunosorbent assay was developed. C3 secretion was studied in resident, elicited and activated macrophages and compared with release of hemolytically active C2 and C4, as well as the lysosomal enzyme β-D-2-acetamido-2-deoxyglucosidase. Resident macrophages secreted about 6 ng C3/106 cells/h into culture supernatants over a period of 12 h. Corynebacterium parvum-activated cells were found to secrete 3 times that amount at nearly constant rates. There was a stepwise increase in secretion of functional C2 and C4 when comparing resident, elicited and activated macrophages; secretion was…

ImmunologyEnzyme releaseGuinea PigsCorynebacteriumEnzyme-Linked Immunosorbent AssayHemolysisGuinea pigAcetylglucosaminidaseImmunology and AllergyAnimalsHumansSecretionPropionibacterium acnesSerum Albuminchemistry.chemical_classificationbiologyMacrophagesComplement C4Complement C3Complement C2Macrophage Activationbiology.organism_classificationMolecular biologyKineticsEnzymechemistryCell culture supernatantLysosomesEuropean journal of immunology
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Environmental impact of antifouling technologies: state of art and perspectives

2001

1. Marine fouling affects most man-made surfaces temporarily or permanently immersed in the sea, resulting in significant (or substantial) economic costs. Intense research is aimed at preventing or reducing fouling. 2. The most widespread solution to avoid fouling formation is to make surfaces unsuitable for settlers, coating them with antifouling (AF) paints containing toxic compounds. Most AF agents (e.g. tributyltin, (TBT)) have undesirable effects on non-target species, including commercially important organisms. 3. To date, the use of TBT in AF paints has been restricted (but not prohibited) in a number of countries and new biocides are in use. 4. The environmental problems posed to ma…

ImposexBiocidefoulingEcologyFoulingimposexantifouling (AF)foul-release coatingsAquatic ScienceToxicologyBiofoulingchemistry.chemical_compoundchemistryEnvironmental protectionbiomonitoringTributyltinEnvironmental scienceEnvironmental impact assessmentantifouling (AF) ablative copper AF biomonitoring fouling foul-release coatings imposex TBT-based AFablative copper AFNature and Landscape ConservationTBT-based AF
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