Search results for "Polymers."

showing 10 items of 3543 documents

Ligand-Binding Cooperativity Effects in Polymer-Protein Conjugation.

2019

We present an electron paramagnetic resonance (EPR) spectroscopic characterization of structural and dynamic effects that stem from post-translational modifications of bovine serum albumin (BSA), an established model system for polymer-protein conjugation. Beyond the typical drug delivery and biocompatibility aspect of such systems, we illustrate the causes that alter internal dynamics and therefore functionality in terms of ligand-binding to the BSA protein core. Uptake of the paramagnetic fatty acid derivative 16-doxyl stearic acid by several BSA-based squaric acid macroinitiators and polymer-protein conjugates was studied by EPR spectroscopy, aided by dynamic light scattering (DLS) and z…

Ethylene GlycolPolymers and PlasticsPolymersBioengineeringCooperativity02 engineering and technology010402 general chemistryLigands01 natural scienceslaw.inventionPolyethylene GlycolsBiomaterialsCyclic N-Oxideschemistry.chemical_compoundDrug Delivery SystemsDynamic light scatteringlawMaterials ChemistryZeta potentialBovine serum albuminElectron paramagnetic resonanceBinding SitesbiologyElectron Spin Resonance SpectroscopySerum Albumin Bovine021001 nanoscience & nanotechnologyLigand (biochemistry)Dynamic Light Scattering0104 chemical scienceschemistrybiology.proteinBiophysicsSurface modificationMethacrylates0210 nano-technologyEthylene glycolBiomacromolecules
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Relationship between the structure of amphiphilic copolymers and their ability to disturb lipid bilayers.

2005

Nonionic amphiphiles and particularly block copolymers of ethylene oxide and propylene oxide (Pluronics) cause pronounced chemosensitization of tumor cells that exhibit multiple resistance to antineoplastic drugs. This effect is due to inhibition of P-glycoprotein (P-gp) responsible for drug efflux. It was suggested that the inhibition of P-gp might be due to changes in its lipid surrounding. Indeed, high dependence of P-gp activity on the membrane microviscosity was demonstrated [Regev et al. (1999) Eur. J. Biochem. 259, 18-24], suggesting that the ability of Pluronics to affect the P-gp activity is mediated by their effect on the membrane structure. We have found recently that adsorption …

Ethylene OxideGlycerolFree RadicalsPolymersLipid BilayersPoloxamerBiochemistryPermeabilityPolyethylene GlycolsMicroviscositychemistry.chemical_compoundStructure-Activity RelationshipAmphiphilePolymer chemistryCopolymerAnimalsHexanesLipid bilayerLiposomeEthylene oxideWaterMembranes ArtificialPoloxamerMembranechemistryDoxorubicinLiposomesBiophysicsPhosphatidylcholinesEpoxy CompoundsCattleAdsorptionBiochemistry
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From an epoxide monomer toolkit to functional PEG copolymers with adjustable LCST behavior.

2011

The lower critical solution temperature (LCST) behavior of novel poly(ethylene glycol) (PEG)-based copolymers bearing multiple functional groups, obtained by anionic ring-opening (co)polymerization (AROP), has been investigated. Variable comonomer ratios of ethylene oxide (EO) and the corresponding oxiranes isopropylidene glyceryl glycidyl ether (IGG), ethoxyl vinyl glycidyl ether (EVGE), allyl glycidyl ether (AGE), or N,N-dibenzyl amino glycidyl (DBAG), particularly designed to implement functional groups at the PEG backbone, were found to influence the LCST behavior. Sharp transitions from translucent to opaque solutions, comparable to other well-established stimuli-responsive polymers, w…

Ethylene OxideMaterials scienceHot TemperaturePolymers and PlasticsPolymersAllyl glycidyl etherpolyethersEpoxideLower critical solution temperaturePolymerizationPolyethylene Glycolschemistry.chemical_compoundPolymer chemistrycopolymersMaterials ChemistryCopolymerPoly(Ethylene Glycol) CopolymersSide-ChainsAqueous-SolutionEthylene oxideComonomerstimuli-sensitiveOrganic ChemistryPegchemistryPolymerizationGlycidolLcstEthylene glycolHydrophobic and Hydrophilic InteractionsMacromolecular rapid communications
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Polystyrene nanoparticles in the presence of (ethylene oxide)13(propylene oxide)30(ethylene oxide)13, N,N-dimethyloctylamine-N-oxide and their mixtur…

2008

Polystyrene nanoparticles were synthesized by emulsion polymerization of styrene. They were functionalized using the conventional surfactant N,N-dimethyloctylamine-N-oxide (ODAO), the tri-block copolymer (ethylene oxide)13(propylene oxide)30(ethylene oxide)13 (L64) and their mixtures. To this purpose, dynamic light scattering and calorimetric experiments were carried out and provided information consistent to each other. The L64 adsorption is Langmuir-type in the copolymer dilute regime and generates complex structures at larger concentrations. In the region where ODAO is in the unimeric state, the adsorption process is cooperative leading to hemi-micelle formation at the polystyrene nanopa…

Ethylene OxideMaterials scienceLightSurface PropertiesOxideGeneral Physics and AstronomyEmulsion polymerizationCalorimetryTRIBLOCK COPOLYMERSStyrenechemistry.chemical_compoundDynamic light scatteringAQUEOUS-SOLUTIONSPolymer chemistryCopolymerScattering RadiationPropylene oxideSURFACTANTSPhysical and Theoretical ChemistryStyreneEthylene oxideLAPONITE CLAYWaterOxidesOctanesHEAT-CAPACITIESSolutionsBLOCK-COPOLYMERSLATEXchemistryChemical engineeringNanoparticlesPolystyrenesMASS-ACTION MODELTHERMODYNAMIC PROPERTIESAdsorptionPolystyrenePhys. Chem. Chem. Phys.
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“Dumb” pH-Independent and Biocompatible Hydrogels Formed by Copolymers of Long-Chain Alkyl Glycidyl Ethers and Ethylene Oxide

2020

The formation and rheological properties of hydrogels based on amphiphilic ABA triblock polyether copolymers are described, relying solely on the hydrophobic interaction of long-chain alkyl glycidyl ether (AlkGE)- based A-blocks that are combined with a hydrophilic poly(ethylene glycol) (PEG) midblock. Via anionic ring-opening copolymerization (AROP), ethylene oxide (EO) and long-chain alkyl glycidyl ethers (AlkGEs) were copolymerized, using deprotonated poly(ethylene glycol) (PEG) macroinitiators (Mn of 10, 20 kg mol-1). The polymerization afforded amphiphilic ABA triblock copolymers with molar masses in the range of 21-32 kg mol-1 and dispersities (Đ) of Đ = 1.07-1.17. Kinetic studies rev…

Ethylene OxidePolymers and PlasticsPolymersBioengineering02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene GlycolsBiomaterialsHydrophobic effectchemistry.chemical_compoundAmphiphilePolymer chemistryMaterials ChemistryCopolymerAlkylchemistry.chemical_classificationEthylene oxidetechnology industry and agricultureHydrogelsHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesKineticschemistryPolymerizationSelf-healing hydrogelsEpoxy Compounds0210 nano-technologyEthylene glycolBiomacromolecules
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Convenient Access to α‐Amino‐ω‐Hydroxyl Heterobifunctional PEG and PPO via a Sacrificial Hexahydro‐Triazine Star Strategy

2019

The anionic ring opening polymerizations of ethylene oxide (EO) and propylene oxide (PO) are performed by using 1,3,5-triethanol hexahydro-1,3,5-triazine (TrAz) as a "sacrificial" trifunctional initiator. Well-defined three-arm star polymers are obtained with a narrow molecular weight distribution (M w /M n < 1.1). Molecular weights range from 3-15 kg mol-1 . Since these star polymers possess an acid-labile hexahydro-triazine core, acidic hydrolysis leads to cleavage of the arms. This gives access to well-defined α-amino-ω-hydroxyl heterobifunctional poly(ethylene glycol) (PEG) and poly(propylene oxide) (PPO) in the molecular weight range of 1-5 kg mol-1 and low dispersity M w /M n < 1.1. T…

Ethylene OxidePolymers and PlasticsPolymersDispersity02 engineering and technologyPolyethylene glycol010402 general chemistry01 natural sciencesPolymerizationchemistry.chemical_compoundPolyolPolymer chemistryMaterials ChemistryPropylene oxideTriazinechemistry.chemical_classificationEthylene oxideTriazinesOrganic Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMolecular WeightchemistryPropylene GlycolsMolar mass distributionEpoxy Compounds0210 nano-technologyEthylene glycolMacromolecular Rapid Communications
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Long-Chain Alkyl Epoxides and Glycidyl Ethers: An Underrated Class of Monomers.

2020

Long-chain epoxides and specifically alkyl glycidyl ethers represent a class of highly hydrophobic monomers for anionic ring-opening polymerization (AROP), resulting in apolar aliphatic polyethers. In contrast, poly(ethylene glycol) is known for its high solubility in water. The combination of hydrophobic and hydrophilic monomers in block and statistical copolymerization reactions enables the synthesis of amphiphilic polyethers for a wide range of purposes, utilizing micellar interactions in aqueous solutions, e.g., viscosity enhancement of aqueous solutions, formation of supramolecular hydrogels, or for polymeric surfactants. Controlled polymerization of these highly hydrophobic long-chain…

Ethylene OxidePolymers and PlasticsPolymersEpoxide02 engineering and technologyPoloxamer010402 general chemistry01 natural sciencesPolymerizationchemistry.chemical_compoundSurface-Active AgentsAmphiphileMaterials ChemistryCopolymerAlkylMicelleschemistry.chemical_classificationEthylene oxideChemistryOrganic Chemistrytechnology industry and agriculture021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesMonomerPolymerizationEpoxy Compounds0210 nano-technologyEthylene glycolHydrophobic and Hydrophilic InteractionsMacromolecular rapid communications
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Polymerization of Ethylene Oxide, Propylene Oxide, and Other Alkylene Oxides: Synthesis, Novel Polymer Architectures, and Bioconjugation.

2015

The review summarizes current trends and developments in the polymerization of alkylene oxides in the last two decades since 1995, with a particular focus on the most important epoxide monomers ethylene oxide (EO), propylene oxide (PO), and butylene oxide (BO). Classical synthetic pathways, i.e., anionic polymerization, coordination polymerization, and cationic polymerization of epoxides (oxiranes), are briefly reviewed. The main focus of the review lies on more recent and in some cases metal-free methods for epoxide polymerization, i.e., the activated monomer strategy, the use of organocatalysts, such as N-heterocyclic carbenes (NHCs) and N-heterocyclic olefins (NHOs) as well as phosphazen…

Ethylene OxidePolymersEpoxide02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationchemistry.chemical_compoundPolymer chemistryCopolymerOrganic chemistryPropylene oxideEthylene oxideMolecular StructureCationic polymerizationOxidesGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesAnionic addition polymerizationchemistryPolymerizationAlkynesCoordination polymerizationEpoxy Compounds0210 nano-technologyChemical reviews
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Preparation and characterization of dummy-template molecularly imprinted polymers as potential sorbents for the recognition of selected polybrominate…

2018

The main aim of this work was to conduct the preliminary/basic research concerning the preparation process of a new dummy molecularly imprinted polymer (DMIP) materials. Developed DMIPs were proposed as a sorption material in solid-phase extraction (SPE) technique for recognition of selected low mass polybrominated diphenyl ethers (PBDEs) – PBDE-47 and PBDE-99. Four new DMIPs were synthesized employing bulky polymerization technique by application of structural analogue of low mass PBDEs - 4,4′-Dihydroxydiphenyl ether, as a dummy template. The DMIPs and corresponding non-imprinted polymers were prepared using different functional monomers: methacrylic acid; methyl methacrylate and different…

Ethylene glycol dimethacrylatebasic laboratory studiesPBDE010501 environmental sciences01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundsorption materials characteristicPolybrominated diphenyl ethersEnvironmental Chemistrysolid-phase extractionFourier transform infrared spectroscopySpectroscopy0105 earth and related environmental scienceschemistry.chemical_classification010401 analytical chemistryMolecularly imprinted polymerSorptionPolymer0104 chemical scienceschemistryMethacrylic acidPolymerizationmolecularly imprinted polymersNuclear chemistryAnalytica chimica acta
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Über die Stabilität Von Copolymeren aus 1,3,5-Trioxan mit verschiedenen Lactonen

1976

Der thermische Abbau von Copolymeren aus 1,3,5-Trioxan und den Lactonen β-Propiolacton (3-Propanolid), Pivalolacton (2,2-Dimethyl-3-propanolid) und e-Caprolacton (6-Hexanolid) wurde untersucht. Der langsame und vollstandige Abbau der Copolymeren wird zuruckgefuhrt auf 1 eine statistische acidolytische Kettenspaltung durch Carboxyl-Endgruppen, 2 die Abspaltung von Acrylsaure an den sauren Endgruppen, 3 die statistische Kettenspaltung durch Pyrolyse von Esterbindungen vor allem in Sequenzen aus mehreren β-Propiolactonbausteinen. Die Teilreaktionen (1) und (2) konnen durch Zusatz von Butandiol-Diglycidylather-(1,4-Bis(2,3-epoxypropoxy)butan) oder N-(2-Naphthyl)anilin oder von Epoxiden stark ve…

Ethylene oxideChain scissionPolymers and PlasticsChemistrychemistry.chemical_compoundReaction rate constantAnilineColloid and Surface ChemistryButanediolPolymer chemistryCopolymerMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryAcrylic acidColloid and Polymer Science
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