Search results for "Biomaterial"

showing 10 items of 1350 documents

Acid—base properties of azo dyes in the presence of surfactants

1991

Abstract The changes in the acid—base properties of an azo dye produced by the presence of surfactants, at surfactant concentrations below and above the CMC, are quantitatively described using a simple model and spectrophotometric and potentiometric measurements. The azo dye formed by aniline and N -(1-naphthyl)-ethylenediamine, and the surfactants sodium dodecyl sulphate, Triton X-100 and N -cetylpyridinium chloride (NCPC) are used. The protonation constants of the free and surfactant-bound dye species, the binding constant of the protonated and unprotonated forms of the dye, and the average aggregation number of the dye—NCPC aggregates are evaluated.

chemistry.chemical_classificationAggregation numberBase (chemistry)Potentiometric titrationInorganic chemistryProtonationCetylpyridinium chlorideBinding constantSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryAnilinechemistryPulmonary surfactantJournal of Colloid and Interface Science
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Copolymers sensitive to temperature and pH in water and in water+oil mixtures: A DSC, ITC and volumetric study

2011

Block copolymer micelles are receiving an increasing interest because of the variety of structures and the possibilities to tune them by changing external and internal parameters achieving the desired properties for a specific purpose. We have investigated the acid/base behavior, self-assembling and solubilization ability towards polar oils of star-like copolymers named Tetronics. They are composed of branched four-arms each one consisting of two blocks made of EO and PO units linked to the diethylenediamine group, which confers pH response ability. The copolymers T1107 and T90R4 were studied with a sequential and reverse architecture. The thermodynamics of the acid/base equilibrium was stu…

chemistry.chemical_classificationAqueous solutionBase (chemistry)ChemistryCopolymers DSC ITC solubilizationMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsColloid and Surface ChemistryDifferential scanning calorimetryMolar volumeChemical engineeringPulmonary surfactantCopolymerOrganic chemistryMacromoleculeJournal of Colloid and Interface Science
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Transfer of Some Alkyl Substituted Ferrocenes from Water to Cationic Surfactant Micelles Studied by Kinetic Method

1994

Abstract Binding of ferrocene and its 1,1′-dimethyl and n -butyl derivatives to dodecyl and tetradecyltrimethylammonium nitrate micellar aggregates has been studied at 20.0°C and ionic strength 0.02 tool dm -3 by examining the micellar retarding effects on the rates of iron(III) oxidation of these substrates. Solubilization of the ferrocenes in the cationic micellar phase increases as the substrate hydrophobic character increases and, to a lesser extent, as the surfactant hydrocarbon chain length becomes longer. The critical micelle concentrations of the surfactants used and the incremental free energy of transfer of methylene groups of both the substrate and the surfactant from the aqueous…

chemistry.chemical_classificationAqueous solutionChemistryInorganic chemistryCationic polymerizationMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryPulmonary surfactantFerroceneIonic strengthMethyleneAlkylJournal of Colloid and Interface Science
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Enthalpies of Mixing of Some Primary Hydrogenated and Fluorinated Alcohols and Sodium Dodecanoate Aqueous Solutions

1993

Abstract The enthalpies of transfer from water to the surfactant solutions ΔH(W → W + S) of some hydrogenated and fiuorinated alkanols and of sodium dodecanoate NaL were determined. In the premicellar region the measurements were carried out as functions of both the additive and the surfactant concentrations in order to evaluate the interaction parameters between the additive and the surfactant molecules. It is shown that in this region, pair, triplet, and quadruplet interaction parameters between unlike solute molecules contribute to ΔH(W → W + S). Within the large uncertainty with which these parameters are determined because of the very narrow surfactant and alcohol concentration interva…

chemistry.chemical_classificationAqueous solutionDistribution constantEnthalpyConcentration effectSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsPropanolchemistry.chemical_compoundColloid and Surface ChemistrychemistryPulmonary surfactantPhysical chemistryOrganic chemistryAlkylHexanolJournal of Colloid and Interface Science
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Polyaspartamide-graft- Polymethacrylate Nanoparticles for Doxorubicin Delivery

2011

A new PHEA-IB-PMANa + copolymer has been synthesized and its pH-induced self-assembly has been investigated in an aqueous medium. PHEA-IB-PMANa + formed nanoparticles with diameters from 25 to 50 nm upon protonation of the carboxylic acid moieties dislocated along the grafted polymethacrylate sodium salt side chains. The physico-chemical characterization of the nanoparticles was performed using light scattering, zeta-potential measurements, SEM, and AFM. Doxorubicin-loaded nanoparticles were prepared and drug release profiles were evaluated under conditions mimicking physiological media. A biological characterization was carried out by testing the cytotoxicity on Caco-2 cells, and cellular …

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsChemistryCarboxylic acidNanoparticleBioengineeringProtonationBiomaterialsPolymer chemistryMaterials ChemistrySide chainCopolymerDrug carrierCytotoxicityBiotechnologyMacromolecular Bioscience
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Thermal diffusion of dextran in aqueous solutions in the absence and the presence of urea.

2006

The Ludwig-Soret effect was studied for aqueous solutions of dextran in the temperature range 15T55 degrees C taking into account the effect of the addition of urea. In the absence of urea, the Soret coefficient S(T) changes sign; it is positive for T45.0 degrees C but negative for T45.0 degrees C. The positive sign of S(T) means that the dextran molecules migrate toward the cold side of the fluid; this behavior is typical for polymer solutions, whereas a negative sign indicates the macromolecules move toward the hot side. The addition of urea to the aqueous solution of dextran rises S(T) and reduces the inversion temperature. For 2 M urea the change in the sign of S(T) is observed at T = 2…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsChemistryHydrogen bondAnalytical chemistryTemperatureThermodynamicsWaterBioengineeringDextransPolymerAtmospheric temperature rangeThermal diffusivityBiomaterialsDiffusionSolutionschemistry.chemical_compoundDextranMaterials ChemistryUreaUreaMacromoleculeBiomacromolecules
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Synergy of Axial and Point Chirality to Construct Helical N -Heterotriangulene-Based Supramolecular Polymers

2018

chemistry.chemical_classificationAtropisomerMaterials science010405 organic chemistryRenewable Energy Sustainability and the EnvironmentEnergy Engineering and Power TechnologyCooperativity010402 general chemistry01 natural sciencesHelicity0104 chemical sciencesBiomaterialsSupramolecular polymerschemistryChemical physicsMaterials ChemistryPoint (geometry)Chirality (chemistry)ChemNanoMat
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Radioactive labeling of defined HPMA-based polymeric structures using [18F]FETos for in vivo imaging by positron emission tomography.

2009

During the last decades polymer-based nanomedicine has turned out to be a promising tool in modern pharmaceutics. The following article describes the synthesis of well-defined random and block copolymers by RAFT polymerization with potential medical application. The polymers have been labeled with the positron-emitting nuclide fluorine-18. The polymeric structures are based on the biocompatible N-(2-hydroxypropyl)-methacrylamide (HPMA). To achieve these structures, functional reactive ester polymers with a molecular weight within the range of 25,000-110,000 g/mol were aminolyzed by 2-hydroxypropylamine and tyramine (3%) to form (18)F-labelable HPMA-polymer precursors. The labeling procedure…

chemistry.chemical_classificationBiodistributionAcrylamidesFluorine RadioisotopesPolymers and PlasticsPolymersRadical polymerizationSize-exclusion chromatographyRadiochemistryBioengineeringChain transferPolymerPolymerizationRatsBiomaterialsPolymerizationchemistryIsotope LabelingPositron-Emission TomographyPolymer chemistryMaterials ChemistryAnimalsReversible addition−fragmentation chain-transfer polymerizationPreclinical imagingBiotransformationBiomacromolecules
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Cell Adhesive and Antifouling Polyvinyl Chloride Surfaces Via Wet Chemical Modification

2012

Polyvinyl chloride (PVC) is one of the most frequently used polymers for the manufacturing of medical devices. Limitations for its usage are based upon unfavorable surface properties of the polymer including its hydrophobicity and lack of functionalities in order to increase its versatility. To address this issue, wet chemical modification of PVC was performed through surface amination using the bifunctional compound ethylene diamine. The reaction was conducted in order to achieve maximum surface amination while leaving the bulk material unaffected. The initial activation step was characterized by means of various methods including contact angle measurements, colorimetric amine quantificati…

chemistry.chemical_classificationBiomedical EngineeringMedicine (miscellaneous)Chemical modificationBioengineeringGeneral MedicinePolymerBiomaterialsContact angleGel permeation chromatographyPolyvinyl chloridechemistry.chemical_compoundchemistryChemical engineeringPolymer chemistrySurface modificationAdhesiveWettingArtificial Organs
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Inverted Solution Processable OLEDs Using a Metal Oxide as an Electron Injection Contact.

2007

A new type of bottom-emission electroluminescent device is described in which a metal oxide is used as the electron-injecting contact. The preparation of such a device is simple. It consists of the deposition of a thin layer of a metal oxide on top of an indium tin oxide covered glass substrate, followed by the solution processing of the light-emitting layer and subsequently the deposition of a high-workfunction (air-stable) metal anode. This architecture allows for a low-cost electroluminescent device because no rigorous encapsulation is required. Electroluminescence with a high brightness reaching 5700 cd m–2 is observed at voltages as low as 8 V, demonstrating the potential of this new a…

chemistry.chemical_classificationBrightnessMaterials sciencebusiness.industryOxideFísicaPolymerElectroluminescenceCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsIndium tin oxideBiomaterialschemistry.chemical_compoundchemistryElectrochemistryOLEDOptoelectronicsbusinessMaterialsVoltageDiodeAdvanced Functional Materials
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