Search results for "Acrylate"

showing 10 items of 554 documents

Beads of Acryloylated Polyaminoacidic Matrices Containing 5-Fluorouracil for Drug Delivery

2002

Spherical polymeric microparticles have been prepared by a reverse phase suspension polymerization technique. The starting polymer was alpha,beta-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA), partially derivatized with glycidylmethacrylate (GMA). PHEA-GMA copolymer (PHG) was crosslinked in the presence of N,N'-dimethylacrylamide (DMAA) or N,N'-ethylenebisacrylamide (EBA). 5-fluorouracil was incorporated into PHG-DMAA or PHG-EBA beads both during and after the crosslinking process. Swelling studies revealed a high affinity toward aqueous medium, influenced by the presence of 5-fluorouracil. The in vitro release study showed that the release rate depends on the chemical structure of the beads…

Antimetabolites AntineoplasticMaterials scienceChemical structurePharmaceutical Sciencemacromolecular substancesExcipientsDrug Delivery SystemsPhase (matter)Polymer chemistryCopolymermedicineParticle Sizechemistry.chemical_classificationCalorimetry Differential ScanningAqueous mediumdigestive oral and skin physiologytechnology industry and agricultureProteinsHydrogelsGeneral MedicinePolymerHydrogen-Ion ConcentrationMicrospheresMolecular WeightKineticsCross-Linking ReagentsAcrylateschemistryDrug deliveryMicroscopy Electron ScanningIndicators and ReagentsSuspension polymerizationFluorouracilSwellingmedicine.symptomDrug Delivery
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Folate-mediated targeting of polymeric conjugates of gemcitabine.

2005

The synthesis of two new macromolecular prodrugs for active tumor targeting was set up. Gemcitabine (2'-deoxy-2',2'-difluorocytidine) was conjugated to alpha,beta-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA) through succinyl or diglycolyl hydrolysable spacers. The targeting agent folic acid was attached to the macromolecular backbone through the aminocaproic spacer. The two conjugates [PHEA-(5'-succinylgemcitabine)-1'-carboxypentyl-folamide and PHEA-(5'-diglycolyl-gemcitabine)-1'-carboxypentyl-folamide], were purified and extensively characterised by spectroscopic (UV, IR and NMR) and chromatographic analyses to determine the correct chemical structure, the purity degree and the reaction yi…

Antimetabolites AntineoplasticTime FactorsStereochemistryCell SurvivalpolyaspartamideChemical structurePharmaceutical ScienceReceptors Cell SurfaceConjugated systemDeoxycytidineDrug Delivery SystemsFolic AcidCell Line Tumorfolate-mediated targetingExtracellularHumansProdrugsIncubationPolyhydroxyethyl MethacrylateDrug CarriersDose-Response Relationship DrugChemistrypolymeric conjugateFolate Receptors GPI-AnchoredSuccinatesHydrogen-Ion ConcentrationGemcitabineIn vitroBiochemistryCell cultureCarrier ProteinsMacromoleculeConjugateInternational journal of pharmaceutics
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Functionalization of Crosslinked Vesicles by Co-Self-Assembly of a Gelable Diblock Copolymer and Mercaptosilane

2008

Herein, a convenient and general method to simultaneously fix and functionalize polymeric vesicles with sulphydryl groups by the co-self-assembly of poly(ethylene oxide)-block-poly[3-(triethoxysilyl)propyl methacrylate] (PEO-b-PTESPMA) and 3-mercaptopropyltrialkoxysilane in an aqueous solution is reported. The presence of sulphydryl groups across the vesicle membrane has been confirmed by using an energy-filtered technique during TEM analysis and by capturing Au nanoparticles.

Aqueous solutionMaterials sciencePolymers and PlasticsEthylene oxideVesicleOrganic ChemistryNanoparticleMethacrylatechemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerSurface modificationSelf-assemblyMacromolecular Rapid Communications
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Multiarm star polyglycerol-block-poly(HEMA) as a versatile precursor for the preparation of micellar nanocapsules with different properties

2007

Well-defined multiarm star polymer with hyperbranched polyglycerol as core and poly(2-hydroxyethyl methacrylate) (PHEMA) as arms were used as precursor for the preparation of inverted and aqueous micellar nanocapsules. The partial modification of the hydroxyl groups of PHEMA arms with aliphatic chains led to the formation of inverted micellar nanocapsules. The hydrophilic dye encapsulation capacity of the inverted micelles can be enhanced significantly by transforming the inner hydroxyl groups of PHEMA arms into quaternized amine groups. The modification of the outer and inner hydroxyl groups of PHEMA arms with polyethylene glycol acid chloride and pivaloyl chloride, respectively, resulted …

Aqueous solutionPolymers and PlasticsChemistryGeneral Chemical Engineeringtechnology industry and agricultureChemical modificationGeneral ChemistryPolyethylene glycolMethacrylateBiochemistryMicelleNanocapsuleschemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerEnvironmental ChemistryAmine gas treatingReactive and Functional Polymers
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Determination of the glass transition temperature of poly(cyclohexyl acrylate) from oxygen permeability measurements

1993

Abstract The glass transition temperature ( T g ) of poly(cyclohexyl acrylate) (PCA) has been obtained from measurements of the oxygen permeability ( P = 0.60 barrers, T g = 23.5 ± 2.0°C) using a potentiostatic electrochemical sensor, and from the oxygen diffusion coefficient ( D = 0.12 × 10 −8 cm 2 s −1 , T g = 24.0 ± 1.8°C) by the time-lag method. A T g of 25 ± 1°C was found by differential scanning calorimetry and a T g of 25.0 ± 3.5°C was obtained from the specific volume by dilatometry. The fractional free volume ( v f ) at T g is 0.020 ± 0.002, which is slightly below (∼ 20%) most glassy polymers. A linear correlation has been observed between ln D and the reciprocal of v f , which su…

Arrhenius equationAcrylatePolymers and PlasticsDiffusionOrganic ChemistryAnalytical chemistrychemistry.chemical_elementActivation energyOxygensymbols.namesakeOxygen permeabilitychemistry.chemical_compoundDifferential scanning calorimetrychemistryPolymer chemistryMaterials ChemistrysymbolsGlass transitionPolymer
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Solidification behavior of the theta system 2-propanol/poly(n-butyl methacrylate) I. Influences of thermoreversible gelation on stationary flow

1994

Zero shear viscosities, η0, were determined by means of a magnetoviscometer for melts of poly(n-butyl methacrylate) (M = 8.7 to 450 kg/mol, T =53.5 to 200°C) and for concentrated solutions of the highest molecular weight sample in isopropanol (T = 34.8 to 131.5 °C). Master curves can be constructed in both cases if the reference temperature is set proportional to the gelation temperature of the particular fluid. Special intersegmental interactions (eventually leading to thermoreversible gelation) can above all be felt in η0 (T) and in M c , the critical molecular weight determined in plots of log η0 vs. log M. As the temperature is lowered, the behavior changes from WLF to Arrhenius, and M …

Arrhenius equationMaterials scienceTheta solventThermodynamicsCondensed Matter PhysicsMethacrylatePoly n-butyl methacrylatePropanolShear (sheet metal)symbols.namesakechemistry.chemical_compoundchemistryPolymer chemistrysymbolsStationary flowGeneral Materials ScienceGlass transitionRheologica Acta
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1981

The anionic polymerization of tert-butyl methacrylate (TBMA) in tetrahydrofuran, using Na+ and Cs+ as counterions proceeds without side reactions even at room temperature. The resulting molecular weight distributions are nearly monodisperse (Mw/Mn ⩽ 1,01). The rate constants for the propagation of ion pairs were measured in the range from + 15 to −100°C. The Arrhenius plots are linear, but different for the two counterions, resulting in the following numerical values for the frequency exponent A and the activation energy Ea: A = 8,5 and Ea = 7,2 kcal/mol = 30 kJ/mol for Na+; A = 9,5 and Ea = 5,6 kcal/mol = 23 kJ/mol for Cs+. The difference between the counterions, which is in contrast to th…

Arrhenius equationsymbols.namesakechemistry.chemical_compoundAnionic addition polymerizationReaction rate constantchemistryPolymerizationSteric factorPolymer chemistrysymbolsActivation energyMethyl methacrylateTetrahydrofuranDie Makromolekulare Chemie
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HPMA-Based Nanocarriers for Effective Immune System Stimulation.

2019

The selective activation of the immune system using nanoparticles as a drug delivery system is a promising field in cancer therapy. Block copolymers from HPMA and laurylmethacrylate-co-hymecromone-methacrylate allow the preparation of multifunctionalized core-crosslinked micelles of variable size. To activate dendritic cells (DCs) as antigen presenting cells, the carbohydrates mannose and trimannose are introduced into the hydrophilic corona as DC targeting units. To activate DCs, a lipophilic adjuvant (L18-MDP) is incorporated into the core of the micelles. To elicit an immune response, a model antigen peptide (SIINFEKL) is attached to the polymeric nanoparticle-in addition-via a click rea…

AzidesPolymers and PlasticsOvalbuminPolymersMannoseBioengineering02 engineering and technology010402 general chemistry01 natural sciencesMicelleBiomaterialschemistry.chemical_compoundDrug Delivery SystemsAntigenAdjuvants ImmunologicMaterials ChemistryHumansParticle SizeAntigen-presenting cellMicellesMannanChemistryDendritic Cells021001 nanoscience & nanotechnologyPeptide Fragments0104 chemical sciencesImmune SystemDrug deliveryBiophysicsMethacrylatesNanoparticlesClick ChemistryNanocarriers0210 nano-technologyHydrophobic and Hydrophilic InteractionsMannose receptorBiotechnologyMacromolecular bioscience
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1986

The terpolymerization of the three monomers (3-vinyl phenylazo)methylmalodinitrile (1), (3-vinyl phenylazo)phenylsulfid (2) or 1-(3-vinylphenylazo)-1,1′-diphenyl methylacetate (3) with methyl methacrylate and butanediol-1,4-dimethyacrylate leads to networks in which the thermolabile azo groups remain intact. Both, the azo monomer and the crosslinking agent are essentially quantitatively incorporated into the network before the conversion of the third monomer is complete. The networks have been characterized in terms of their swelling in benzene, chlorobenzene, and methacrylonitrile. Die Terpolymerisation der drei Monomeren (3-Vinylphenylazo)-methylmalodinitril (1), (3-Vinylphenylazo)phenyls…

Azo polymerchemistry.chemical_compoundMonomerchemistryChlorobenzeneMethacrylonitrilePolymer chemistryGeneral Materials ScienceMethyl methacrylateThermolabileGraftingAngewandte Makromolekulare Chemie
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Cycloaddition reactions of 3-vinylthiophen

1987

Abstract Cycloaddition reactions between 3-vinylthiophen and the dienophiles maleic anhydride, methyl acrylate, dimethyl acetylene - dicarboxylate, and methyl propiolate give products including methyl benzo[b]thiophen-7-carboxylate (11) and its dihydroderivative (10), the 6,7-dicarboxylic acid (3), its dimethyl ester (7) and dihydroester (6); the naphtho[a,b]dithiophen (14), and the novel ethano bridged benzo[b]thiophen (15).

Bicyclic moleculeMethyl propiolateOrganic ChemistryMaleic anhydrideNuclear magnetic resonance spectroscopyBiochemistryMedicinal chemistryDimethyl esterCycloadditionchemistry.chemical_compoundAcetylenechemistryDrug DiscoveryOrganic chemistryMethyl acrylateTetrahedron
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