Search results for "cross-linking"

showing 10 items of 91 documents

CROSSLINKED HYALURONAN WITH A PROTEIN-LIKE POLYMER: NOVEL BIORESORBABLE FILMS FOR BIOMEDICAL APPLICATIONS

2007

In this work, novel hydrogel films based on hyaluronan (HA) chemically crosslinked with the alpha,beta-poly(N-2-hydroxyethyl) (2-aminoethylcarbamate)-D,L-aspartamide (PHEA-EDA) were produced by solution casting method. The goal was to exploit both the biological key role of HA in tissue repair and regeneration, and the versatility of a synthetic protein-like polymer as the PHEA-EDA, in order to obtain biomaterials with physicochemical and biological properties suitable for a clinical use. By varying the molar ratio between the PHEA-EDA amino groups and HA carboxyl groups, three different films were obtained and characterized. Particularly FTIR, swelling, hydrolysis, and enzymatic degradatio…

Materials scienceCell SurvivalBiomedical EngineeringTetrazolium SaltsBiomaterialsHydrolysischemistry.chemical_compoundTissue engineeringCoated Materials BiocompatibleHyaluronidaseNephelometry and TurbidimetryPolymer chemistryHyaluronic acidSpectroscopy Fourier Transform InfraredmedicineCell AdhesionPolyaminesHumansHyaluronic AcidAspartameSkinchemistry.chemical_classificationWound HealingHydrolysisMetals and AlloysProteinsCalorimetry IndirectHydrogelsPolymerTrypan BlueFibroblastsThiazolesCross-Linking ReagentschemistryChemical engineeringHYDROGELS HYALURONIC ACIDSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSelf-healing hydrogelsCeramics and CompositesTrypan blueSwellingmedicine.symptommedicine.drug
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Fibrin-chitosan composite substrate for in vitro culture of chondrocytes

2013

The aim of this study was to develop a biocompatible monolayer substrate based on fibrin and chitosan for in vitro culture of chondrocytes. Fibrin-chitosan composite substrates combined the proved cell adhesion properties of fibrin with the hydrophilicity and poor adhesion capacity of chitosan. Chitosan microspheres were produced by coacervation method, agglomerated within a fibrin network and subsequently crosslinked with genipin. The composite substrate was stable for 28 days of culture due to the high crosslinking density. Human chondrocytes cultured on the composite substrate were viable during the culture period. At the end of culture time (28 days) the composite substrate showed low c…

Materials scienceCell SurvivalComposite numberBiomedical EngineeringCell Culture Techniquesmacromolecular substancesFibrinBiomaterialsChitosanchemistry.chemical_compoundChondrocytesHumansIridoidscompositefibrinCell adhesionCell ShapeCells Culturedbiologytechnology industry and agricultureMetals and AlloysSubstrate (chemistry)AdhesionDNAChondrogenesisExtracellular MatrixmicrospheresCross-Linking ReagentschemistryMAQUINAS Y MOTORES TERMICOSCeramics and Compositesbiology.proteinBiophysicsGenipinchitosanBiomedical engineeringchondrocyte redifferentiation
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Comparative evaluation of the swelling and degrees of cross-linking in three organic gel packings for SEC through some geometric parameters.

2003

Abstract The size exclusion chromatographic (SEC) behavior of five solvent/polymer systems in three organic column packings based on polystyrene/divinylbenzene (PS/DVB) copolymer, TSK-Gel H HR , μ-styragel and TSK-Gel H XL , has been compared. All the packings offer similar characteristics (pore size, particle size and efficiency) but some differences have been found when eluting the same systems. The different elution behavior observed in both polymeric gels has been analyzed in terms of their swelling and cross-linking degrees and of the fractal parameters. From the Universal Calibration plots, values of the chromatographic partition coefficient, K p , have been obtained and using some eq…

Materials scienceMacromolecular SubstancesSize-exclusion chromatographyBiophysicsAnalytical chemistryMolecular ConformationBiochemistryFractal dimensionchemistry.chemical_compoundMaterials TestingmedicineOrganic ChemicalsParticle SizeViscositySolvationDivinylbenzenePartition coefficientEquipment Failure AnalysisCross-Linking ReagentschemistryVolume fractionCalibrationChromatography GelParticle sizeSwellingmedicine.symptomGelsPorosityJournal of biochemical and biophysical methods
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Nanostructuring with a crosslinkable discotic material.

2007

A high-yielding synthesis afforded a hexa-peri-hexabenzocoronene carrying acrylate units at the end of six attached alkyl spacers. The polymerization of these acrylate moieties could be initiated with thermal energy and through direct photoactivation without the addition of a photoinitiator. This allowed the organization of the liquid-crystalline material to be fixed in either the crystalline state or the mesophase, which preserved the organization in the respective phase. The use of a focused synchrotron beam permitted selected regions of a thin film to be rendered insoluble. After "developing" the film in this lithographic process by dissolving the soluble, unpolymerized material, defined…

Materials scienceMacromolecular SubstancesSurface PropertiesMolecular ConformationBiomaterialschemistry.chemical_compoundPhase (matter)Polymer chemistryMaterials TestingNanotechnologyGeneral Materials ScienceParticle SizeAlkylchemistry.chemical_classificationTitaniumAcrylateMesophaseGeneral ChemistryLiquid CrystalsNanostructuresMembraneCross-Linking ReagentsPolymerizationchemistryAcrylatesMesoporous materialCrystallizationPhotoinitiatorBiotechnologySmall (Weinheim an der Bergstrasse, Germany)
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Comparative performance of electrospun collagen nanofibers cross-linked by means of different methods.

2009

[EN] Collagen, as the major structural protein of the extracellular matrix in animals, is a versatile biomaterial of great interest in various engineering applications. Electrospun nanofibers of collagen are regarded as very promising materials for tissue engineering applications because they can reproduce the morphology of the natural bone but have as a drawback a poor structural consistency in wet conditions. In this paper, a comparative study between the performance of different cross-linking methods such as a milder enzymatic treatment procedure using transglutaminase, the use of N-[3-(dimethylamino)propyl]-N¿-ethylcarbodiimide hydrochloride/ N-hydroxysuccinimide, and genipin, and the u…

Materials scienceNanofibersExtracellular matrixBiomaterialschemistry.chemical_compoundBiopolymersTissue engineeringCell Line TumorUltraviolet lightmedicineHumansNanotechnologyGeneral Materials ScienceComposite materialAminesNucleic acid structureCell ProliferationOsteoblastsTransglutaminasesTissue EngineeringTemperatureBiomaterialOsteoblastElectrochemical TechniquesElectrospinningFibersmedicine.anatomical_structureCross-Linking ReagentschemistryChemical engineeringNanofiberBone SubstitutesGenipinMicroscopy Electron ScanningCollagenACS applied materialsinterfaces
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Off-Resonant Optical Excitation of Gold Nanorods: Nanoscale Imprint of Polarization Surface Charge Distribution

2011

International audience; We report on the nanoscale optical characterization of gold nanorods irradiated out of their plasmonic resonance. Our approach is based on the reticulation of a photopolymerizable formulation locally triggered by enhanced electromagnetic fields. The tiny local field enhancement stems from the surface polarization charges associated with the electric field discontinuity at the metal/dielectric interface. This allows us to get a nanoscale signature of the spatial distribution of the surface charge density in metallic nanoparticles irradiated off-resonance.

Materials sciencesurface charge densityAnalytical chemistryPhysics::Optics02 engineering and technologyDielectric010402 general chemistry01 natural sciencesplasmonicspolymer cross-linkingElectric fieldoptical properties of metal nanoparticlesGeneral Materials ScienceSurface chargePhysical and Theoretical ChemistryPolarization (electrochemistry)ComputingMilieux_MISCELLANEOUSPlasmonbusiness.industryCharge density[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology0104 chemical sciences[ CHIM.POLY ] Chemical Sciences/Polymers[CHIM.POLY]Chemical Sciences/Polymers[ CHIM.MATE ] Chemical Sciences/Material chemistrypolymerizationOptoelectronicsNanorodnanorods0210 nano-technologybusinessExcitationThe Journal of Physical Chemistry Letters
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A novel bio-orthogonal cross-linker for improved protein/protein interaction analysis

2015

International audience; The variety of protein cross-linkers developed in recent years illustrates the current requirement for efficient reagents optimized for mass spectrometry (MS) analysis. To date, the most widely used strategy relies on commercial cross-linkers that bear an isotopically labeled tag and N-hydroxysuccinimid-ester (NHS-ester) moieties. Moreover, an enrichment step using liquid chromatography is usually performed after enzymatic digestion of the cross-linked proteins. Unfortunately, this approach suffers from several limitations. First, it requires large amounts of proteins. Second, NHS-ester cross-linkers are poorly efficient because of their fast hydrolysis in water. Fin…

Models MolecularAzidesMolecular Sequence DataPeptide[CHIM.THER]Chemical Sciences/Medicinal ChemistryMass spectrometry01 natural sciencesMass SpectrometryAnalytical ChemistryProtein–protein interaction03 medical and health sciencesHydrolysis[CHIM.ANAL]Chemical Sciences/Analytical chemistryProtein Interaction MappingHumansOrganic chemistryAmino Acid SequenceProtein Interaction MapsCross linker030304 developmental biologychemistry.chemical_classification0303 health sciencesRigid coreEnzymatic digestionChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistry010401 analytical chemistryHSC70 Heat-Shock ProteinsParkinson Disease[CHIM.CATA]Chemical Sciences/CatalysisCombinatorial chemistry0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCross-Linking ReagentsReagentalpha-SynucleinCarbamates[CHIM.CHEM]Chemical Sciences/CheminformaticsChromatography Liquid
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2,8-Diazido-ATP — a short-length bifunctional photoaffinity label for photoaffinity cross-linking of a stable F1 in ATP synthase (from thermophilic b…

1995

Abstract To demonstrate the direct interfacial position of nucleotide binding sites between subunits of proteins we have synthesized the bifunctional photoaffinity label 2,8-diazidoadenosine 5′-triphosphate (2,8-DiN3ATP). UV irradiation of the F1-ATPase (TF1) from the thermophilic bacterium PS3 in the presence of 2,8-DiN3ATP results in a nucleotide-dependent inactivation of the enzyme and in a nucleotide-dependent formation of α-β crosslinks. The results confirm an interfacial localization of all the nucleotide binding sites on TF1.

Models MolecularAzidesNucleotide binding siteLightStereochemistryImmunoblottingBiophysicsDirect interfacial localizationShort lengthBiochemistry8-azidoadenosine 5'-triphosphatechemistry.chemical_compoundAdenosine TriphosphateStructural BiologyGeneticsNucleotide binding sitesBifunctionalMolecular BiologyThermophilic bacterium PS3Photoaffinity cross-linkingchemistry.chemical_classificationATP synthasebiologyBacteriaThermophileAffinity LabelsCell BiologyProton-Translocating ATPasesEnzymeCross-Linking ReagentsBiochemistrychemistrybiology.proteinF1-ATPase: Short-length bifunctional photoaffinity labelFEBS Letters
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Combining reactive triblock copolymers with functional cross-linkers: A versatile pathway to disulfide stabilized-polyplex libraries and their applic…

2017

Therapeutic nucleic acids such as pDNA hold great promise for the treatment of multiple diseases. These therapeutic interventions are, however, compromised by the lack of efficient and safe non-viral delivery systems, which guarantee stability during blood circulation together with high transfection efficiency. To provide these desired properties within one system, we propose the use of reactive triblock copolypept(o)ides, which include a stealth-like block for efficient shielding, a hydrophobic block based on reactive disulfides for cross-linking and a cationic block for complexation of pDNA. After the complexation step, bifunctional cross-linkers can be employed to bio-reversibly stabiliz…

Models MolecularLysisEndosomePolymersPharmaceutical ScienceNanotechnology02 engineering and technologyGene delivery010402 general chemistryCleavage (embryo)Transfection01 natural sciencesCell Linechemistry.chemical_compoundMiceVaccines DNAAnimalsHumansDisulfidesBifunctionalCationic polymerizationGene Transfer TechniquesTransfection021001 nanoscience & nanotechnology0104 chemical sciencesCross-Linking ReagentschemistryBiophysicsNucleic acid0210 nano-technologyPlasmidsJournal of controlled release : official journal of the Controlled Release Society
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Lhca5 interaction with plant photosystem I

2006

AbstractIn the outer antenna (LHCI) of higher plant photosystem I (PSI) four abundantly expressed light-harvesting protein of photosystem I (Lhca)-type proteins are organized in two heterodimeric domains (Lhca1/Lhca4 and Lhca2/Lhca3). Our cross-linking studies on PSI-LHCI preparations from wildtype Arabidopsis and pea plants indicate an exclusive interaction of the rarely expressed Lhca5 light-harvesting protein with LHCI in the Lhca2/Lhca3-site. In PSI particles with an altered LHCI composition Lhca5 assembles in the Lhca1/Lhca4 site, partly as a homodimer. This flexibility indicates a binding-competitive model for the LHCI assembly in plants regulated by molecular interactions of the Lhca…

Models MolecularPhotosystem IArabidopsisLight-Harvesting Protein ComplexesBiophysicsPhotosystem IBiochemistrychemistry.chemical_compoundLight harvesting complex IStructural BiologyArabidopsisGeneticsMolecular BiologyLhca5Molecular interactionsPhotosystem I Protein ComplexbiologyArabidopsis ProteinsPeasWild typefood and beveragesArabidopsis ProteinsCell BiologyLight-Harvesting Protein Complexesbiology.organism_classificationCrystallographychemistryChlorophyllBiophysicsLight-harvesting complex ICross-linkingFEBS Letters
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