Search results for "solution"

showing 10 items of 5638 documents

Measurement of cloud point temperature in polymer solutions

2013

Polymer solutions Phase separation Phase diagram
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The apparently anomalous effects of surfactants on interfacial tension in the IBA/water system near its upper critical solution temperature

2016

We studied the effect of anionic, cationic, and nonionic surfactants on the interfacial tension between the two phases of the isobutyric acid/water system using spinning drop tensiometry. It has been found that interfacial tension decreases with increasing concentration of the surfactant in the case of sodium dodecyl sulfate (SDS) and of dodecyltrimethylammonium chloride (DTAC). However, in the case of Triton X-100 an increase of surfactant concentration leads to an increase of the interfacial tension. Such results are consistent with the upper critical solution temperature (UCST) in the presence of these surfactants: the UCST decreases with increasing SDS and DTAC concentrations while it i…

Polymers and Plastics02 engineering and technology01 natural sciencesSpinning drop tensiometry010305 fluids & plasmasIsobutyric acidSurface tensionchemistry.chemical_compoundColloid and Surface ChemistryPulmonary surfactantUpper critical solution temperature0103 physical sciencesPolymer chemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistrySodium dodecyl sulfateSettore CHIM/02 - Chimica FisicaChemistryDrop (liquid)Cationic polymerizationUpper critical solution temperature (UCST)021001 nanoscience & nanotechnologyChemical engineering0210 nano-technologyInterfacial tensionColloid and Polymer Science
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Crosslinked α,β-Polyasparthydrazide Micromatrices for Controlled Release of Anticancer Drugs

1995

The preparation of new hydrogels by the reaction of α,β- polyasparthydrazide and glutaraldehyde is reported. A different crosslinking degree was obtained by varying the ratio crosslinking agent/polymer which influenced the swelling behavior of the gel. 5-Fluorouracil, was incorporated into the matrices during the crosslinking reaction and in vitro release studies were performed in simulated gastric juice (pH 1.1) and pH 7.4 buffer solution. The hydrogels prepared were chemically stable in the dissolution media. The observed data show the potential application of these new matrices for peroral administration of anticancer agents.

Polymers and Plastics0206 medical engineeringBioengineeringmacromolecular substances02 engineering and technologyBiomaterialschemistry.chemical_compoundPolymer chemistryMaterials ChemistrymedicineDissolutionchemistry.chemical_classificationtechnology industry and agriculturePolymerBuffer solution021001 nanoscience & nanotechnology020601 biomedical engineeringControlled releaseIn vitrochemistrySelf-healing hydrogelsGlutaraldehydeSwellingmedicine.symptom0210 nano-technologyNuclear chemistryJournal of Bioactive and Compatible Polymers
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Tamoxifen-loaded polymeric micelles: preparation, physico-chemical characterization and in vitro evaluation studies.

2004

Several samples of polymeric micelles, formed by amphiphilic derivatives of PHEA, obtained by grafting into polymeric backbone of PEGs and/or hexadecylamine groups (PHEA-PEG-C(16) and PHEA-C(16)) and containing different amount of Tamoxifen, were prepared. All Tamoxifen-loaded polymeric micelles showed to increase drug water solubility. TEM studies provided evidence of the formation of supramolecular core/shell architectures containing drug, in the nanoscopic range and with spherical shape. Samples with different amount of encapsulated Tamoxifen were subjected to in vitro cytotoxic studies in order to evaluate the effect of Tamoxifen micellization on cell growth inhibition. All samples of T…

Polymers and PlasticsAntineoplastic Agents HormonalPolymersSupramolecular chemistryBioengineeringMicellePolyethylene GlycolsBiomaterialsPlasmaDrug Delivery SystemsTamoxifen polymeric micelles polyaspartammideAmphiphileMaterials ChemistryOrganic chemistryHumansMicellesAqueous solutionMolecular StructureChemistryHydrogen-Ion ConcentrationTamoxifenMembraneSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliveryLiberationDrug carrierPeptidesBiotechnologyNuclear chemistryMacromolecular bioscience
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Polysaccharide-Based pH-Responsive Nanocapsules Prepared with Bio-Orthogonal Chemistry and Their Use as Responsive Delivery Systems.

2020

Bio-orthogonal reactions have become an essential tool to prepare biomaterials; for example, in the synthesis of nanocarriers, bio-orthogonal chemistry allows circumventing common obstacles related to the encapsulation of delicate payloads or the occurrence of uncontrolled side reactions, which significantly limit the range of potential payloads to encapsulate. Here, we report a new approach to prepare pH-responsive nanocarriers using dynamic bio-orthogonal chemistry. The reaction between a poly(hydrazide) crosslinker and functionalized polysaccharides was used to form a pH-responsive hydrazone network. The network formation occurred at the interface of aqueous nanodroplets in miniemulsion …

Polymers and PlasticsBioengineeringNanotechnologyBiocompatible Materials02 engineering and technology010402 general chemistryHydrazidePolysaccharide01 natural sciencesNanocapsulesArticleBiomaterialschemistry.chemical_compoundNanocapsulesPolysaccharidesMaterials Chemistrychemistry.chemical_classificationAqueous solutionChemistrytechnology industry and agricultureHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesMiniemulsionNanocarriers0210 nano-technologyBiomacromolecules
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Kinetic Analysis of “Living” Polymerization Systems Exhibiting Slow Equilibria. 3. “Associative” Mechanism of Group Transfer Polymerization and Ion P…

1996

The averages of the molecular weight distribution are derived for a “living” polymerization process which proceeds via active and “dormant” species and where the active species are formed by addition of a catalyst to a “dormant” species. Such a mechanism is applicable to group transfer and “living” cationic polymerizations (assuming that ion pairs are formed exclusively in the latter case). Both equilibrium and nonequilibrium initial conditions are used for the calculation. The results are very similar to those obtained for degenerative transfer (i.e., direct exchange of activity between active and “dormant” species). The dominating parameter is β = k2/(kpI0), where k2 and kp are the rate c…

Polymers and PlasticsBulk polymerizationChemistryOrganic ChemistryDispersityRadical polymerizationCationic polymerizationSolution polymerizationInorganic ChemistryPolymerizationPolymer chemistryMaterials ChemistryLiving polymerizationIonic polymerizationMacromolecules
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Supramolecular Assemblies Based on Complexes of Nonionic Amphiphilic Cyclodextrins and a meso-Tetra(4- sulfonatophenyl)porphine Tributyltin(IV) Deriv…

2013

Amphiphilic cyclodextrin (ACyD) provides water-soluble and adaptable nanovectors by modulating the balance between the hydrophobic and hydrophilic chains at both CyD sides. This work aimed to design nanoassemblies based on nonionic and hydrophilic ACyD (SC6OH) for the delivery of a poor-water-soluble organotin(IV)-porphyrin derivative [(Bu3Sn)4TPPS] to melanoma cancer cells. To characterize the porphyrin derivatives under simulated physiological conditions, a speciation was performed using complementary techniques. In aqueous solution (≤ 20 μM), (Bu3Sn)4TPPS primarily exists as a monomer (2 in Figure 1), as suggested by the low static anisotropy (ρ ≈ 0.02) with a negligible formation of por…

Polymers and PlasticsCell SurvivalSurface PropertiesPotentiometric titrationSupramolecular chemistryAntineoplastic AgentsBioengineeringBiomaterialsStructure-Activity RelationshipSurface-Active Agentschemistry.chemical_compoundDrug Delivery SystemsAmphiphilePolymer chemistryTumor Cells CulturedMaterials ChemistryHumansOrganic chemistryParticle SizeMelanomaMELANOMA porphyrins organotin(IV)Cell Proliferationchemistry.chemical_classificationCyclodextrinsAqueous solutionCell DeathDose-Response Relationship DrugMolecular StructureCyclodextrinPorphyrinNanomedicineMonomerchemistrySettore CHIM/03 - Chimica Generale E InorganicaDrug Screening Assays AntitumorTrialkyltin CompoundsDrug carrier
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Mechanism of Anionic Polymerization of (Meth)acrylates in the Presence of Aluminium Alkyls IV. Formation of a Co-ordinative Polymer Network via the L…

1996

The polymerization of methyl methacrylate in the presence of aluminium alkyls in toluene deviates from conventional kinetics. This results predominantly from the formation and precipitation of a co-ordinative polymer gel or network. Due to the lower reactivity and accessibility of the living chains in the gel, they are regarded as ’dormant’ and thus the concentration of active species decreases during polymerization. The network formation occurs via co-ordination of the living aluminate chain end group with in-chain ester carbonyl groups. Part of the chains are deactivated by a termination process but they are free of cyclic β-ketoesters which would result from the common ’back-biting’ reac…

Polymers and PlasticsChemistryAluminateSolution polymerizationPoly(methyl methacrylate)End-groupchemistry.chemical_compoundAnionic addition polymerizationPolymerizationvisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumLiving polymerizationLiving anionic polymerizationPolymer Journal
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Influence of End Groups on the Stimulus-Responsive Behavior of Poly[oligo(ethylene glycol) methacrylate] in Water

2010

The influence of the chemical structure of both end groups onto the lower critical solution temperature (LCST) of poly[oligo(ethylene glycol) monomethyl ether methacrylate] (POEGMA) in water was systematically investigated. POEGMA of Mn = 3550 g/mol and Mw/Mn = 1.14 prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization was equipped with two different functional end groups in a one-step postpolymerization reaction combining activated esters, functional amines, and functional methane thiosulfonates. As end groups, n-propyl, n-hexadecyl, di(n-octadecyl), poly(ethylene glycol)-550 (PEG), 1H,1H-perfluorononyl, azobenzene, and trimethylethylammonium groups were system…

Polymers and PlasticsChemistryOrganic ChemistryChain transferLower critical solution temperatureMicelleInorganic ChemistryHydrophobic effectEnd-groupchemistry.chemical_compoundPolymerizationAzobenzenePolymer chemistryMaterials ChemistryEthylene glycolMacromolecules
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Ring-opening polymerization of lactides using heterobimetallic yttrocene complexes

1999

Structurally characterized, chiral heterobimetallic yttrocene derivatives Li[Y(η 5 :η 1 -C 5 R 4 Si-Me 2 NCH 2 CH 2 OMe) 2 ] (R = Me, H) have been shown to be active in the controlled ring-opening polymerization of L-lactide to give poly(L-lactide)s with high molecular weights and moderately narrow molecular weight distributions (M w /M n < 1.50). Both transesterification and racemization appear to be less prominent. 'H NMR spectroscopic tetrad analysis of copolymers prepared using a mixture of L- and D-lactide demonstrates the absence of any preference for one enantiomer during the polymerization.

Polymers and PlasticsChemistryOrganic ChemistrySolution polymerizationCondensed Matter PhysicsRing-opening polymerizationchemistry.chemical_compoundPolymerizationPolymer chemistryMaterials ChemistryProton NMRCopolymerPhysical and Theoretical ChemistryEnantiomerMetalloceneRacemizationMacromolecular Chemistry and Physics
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