Search results for "Biocompatible Material"

showing 10 items of 290 documents

New hyaluronic acid based brush copolymers synthesized by atom transfer radical polymerization.

2013

Abstract In this work, an efficient method for the synthesis of hyaluronic acid based brush copolymers using atom transfer radical polymerization (ATRP) has been reported. At first, two different hyaluronic acid (HA) based macroinitiators have been prepared and then they have been used for the polymerization via ATRP of hydrophilic or hydrophobic molecules carrying vinyl portions. In particular, by linking 2-bromo-2-methylpropionic acid (BMP) to the primary hydroxyl groups of tetrabutyl ammonium salt of HA (HA–TBA) or to amino groups of the ethylenediamino derivative of HA–TBA (HA–TBA–EDA), two macroinitiators (HA–TBA–BMP and HA–TBA–EDA–BMP) have been obtained. Then they have been used for …

Polymers and PlasticsChemistryAtom-transfer radical-polymerizationPolymersOrganic ChemistrySize-exclusion chromatographyBiocompatible MaterialsChemistry Techniques SyntheticMethacrylateEthylenediaminesPolymerizationMolecular Weightchemistry.chemical_compoundLiving free-radical polymerizationPolymerizationPolymer chemistryMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationHyaluronic AcidPropionatesEthylene glycolCarbohydrate polymers
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From Polymers to Functional Biomaterials.

2017

Polymers and PlasticsChemistryPolymersMEDLINEBioengineeringBiocompatible Materials02 engineering and technologyComputational biology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesModels Biological0104 chemical sciencesBiomaterialsDrug Delivery SystemsMaterials ChemistryAnimalsHumansNanoparticlesRNA Interference0210 nano-technologyBiotechnologyIntroductory Journal ArticleMacromolecular bioscience
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Synthesis of multiarm star poly(glycerol)-block-poly(2-hydroxyethyl methacrylate).

2006

Well-defined multiarm star block copolymers poly(glycerol)-b-poly(2-hydroxyethyl methacrylate) (PG-b-PHEMA) with an average of 56, 66, and 90 PHEMA arms, respectively, have been prepared by atom transfer radical polymerization (ATRP) of HEMA in methanol by a core-first strategy. The hyperbranched macroinitiators employed were prepared on the basis of well-defined hyperbranched polyglycerol by esterification with 2-bromoisobutyryl bromide. Polydispersites M(w)/M(n) of the new multiarm stars were in the range of 1.11-1.82. Unexpectedly, with the combination of CuCl/CuBr(2)/2,2'-bipyridyl as catalyst, the polymerization conversion can be driven to maximum values of 79%. The control of CuCl cat…

Polymers and PlasticsMolecular StructureAtom-transfer radical-polymerizationMacromolecular SubstancesPolymersDispersityBioengineeringSolution polymerizationBiocompatible MaterialsMethacrylateCatalysisCatalysisPolyethylene GlycolsBiomaterialschemistry.chemical_compoundKineticschemistryPolymerizationModels ChemicalBromidePolymer chemistryMaterials ChemistryCopolymerMethacrylatesBiomacromolecules
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Joining Two Natural Motifs: Catechol-Containing Poly(phosphoester)s.

2017

Numerous catechol-containing polymers, including biodegradable polymers, are currently heavily discussed for modern biomaterials. However, there is no report combining poly(phosphoester)s (PPEs) with catechols. Adhesive PPEs have been prepared via acyclic diene metathesis polymerization. A novel acetal-protected catechol phosphate monomer was homo- and copolymerized with phosphoester comonomers with molecular weights up to 42000 g/mol. Quantitative release of the catechols was achieved by careful hydrolysis of the acetal groups without backbone degradation. Degradation of the PPEs under basic conditions revealed complete and statistical degradation of the phosphotri- to phosphodiesters. In …

Polymers and PlasticsPolymersCatecholsBioengineeringBiocompatible Materials02 engineering and technology010402 general chemistry01 natural sciencesFerric CompoundsPhosphatesPolymerizationBiomaterialschemistry.chemical_compoundPolymer chemistryMaterials ChemistryOrganic chemistrychemistry.chemical_classificationCatecholTissue EngineeringHydrolysisAcetalEstersPolymer021001 nanoscience & nanotechnologyBiodegradable polymer0104 chemical sciencesMonomerchemistryPolymerizationPhosphodiester bondNanoparticles0210 nano-technologyGelsAcyclic diene metathesisBiomacromolecules
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HPMA copolymers as surfactants in the preparation of biocompatible nanoparticles for biomedical application.

2012

In this work we describe the application of amphiphilic N-(2-hydroxypropyl)methacrylamide (HPMA)-based copolymers as polymeric surfactants in miniemulsion techniques. HPMA-based copolymers with different ratios of HPMA (hydrophilic) to laurylmethacrylate (LMA; hydrophobic) units were synthesized by RAFT polymerization and postpolymerization modification. The amphiphilic polymers can act as detergents in both the miniemulsion polymerization of styrene and the miniemulsion process in combination with solvent evaporation, which was applied to polystyrene and polylactide. Under optimized conditions, monodisperse colloids can be prepared. The most promising results could be obtained by using the…

Polymers and PlasticsPolymersPolyestersDispersityBioengineeringBiocompatible MaterialsPolymerizationBiomaterialschemistry.chemical_compoundSurface-Active AgentsPolymer chemistryAmphiphileMaterials ChemistryCopolymerMethacrylamideHumansReversible addition−fragmentation chain-transfer polymerizationColloidsMicroscopy ConfocalChemistryMiniemulsionPolymerizationMethacrylatesNanoparticlesPolystyreneHydrophobic and Hydrophilic InteractionsHeLa CellsBiomacromolecules
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Cationic Copolymerization of 3,3-Bis(hydroxymethyl)oxetane and Glycidol: Biocompatible Hyperbranched Polyether Polyols with High Content of Primary H…

2015

The cationic ring-opening copolymerization of 3,3-bis(hydroxymethyl)oxetane (BHMO) with glycidol using different comonomer ratios (BHMO content from 25 to 90%) and BF3OEt2 as an initiator has been studied. Apparent molecular weights of the resulting hyperbranched polyether copolymers ranged from 1400 to 3300 g mol(-1) (PDI: 1.21-1.48; method: SEC, linear PEG standards). Incorporation of both comonomers is evidenced by MALDI-TOF mass spectroscopy. All hyperbranched polyether polyols with high content of primary hydroxyl groups portray good solubility in water, which correlates with an increasing content of glycerol units. Detailed NMR characterization was employed to elucidate the copolymer …

Polymers and PlasticsPropanolsProton Magnetic Resonance SpectroscopyComonomerGlycidolCationic polymerizationBiocompatible MaterialsBioengineeringOxetanePolymerizationBiomaterialschemistry.chemical_compoundchemistryPolymerizationEthers CyclicCationsSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationPolymer chemistryMaterials ChemistryCopolymerEpoxy CompoundsOrganic chemistryHydroxymethylCarbon-13 Magnetic Resonance SpectroscopySolubilityBiomacromolecules
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Poly(Ethylene Glycol) Dimethacrylates with Cleavable Ketal Sites: Precursors for Cleavable PEG-Hydrogels.

2017

The authors introduce poly(ethylene glycol) (PEG) based macromonomers containing acid-labile ketal moieties as well as terminal methacrylate units that are amenable to radical polymerization. The synthesis of PEGs of different molecular weights (ranging from 2000 to 13 000 g mol-1 with polydispersities <1.15) with a central ketal unit (PEG-ketal-diol) and their conversion to PEG-ketal-dimethacrylates (PEG-ketal-DMA) is introduced. Degradation rates of both PEG-ketal-diols and PEG-ketal-DMA are investigated by in situ 1 H NMR kinetic studies in deuterated phosphate buffer. Hydrogels containing 0, 5, or 10 wt% of PEG-ketal-DMA and 100, 95, or 90 wt% of PEG-DMA, respectively, are synthesized a…

Polymers and PlasticsRadical polymerizationBioengineeringBiocompatible Materialsmacromolecular substances02 engineering and technology010402 general chemistryMethacrylate01 natural sciencesHydrogel Polyethylene Glycol DimethacrylatePolymerizationBiomaterialschemistry.chemical_compoundPEG ratioPolymer chemistryMaterials ChemistryMolecular massChemistryHydrolysistechnology industry and agricultureHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesMolecular WeightKineticsDrug deliverySelf-healing hydrogelsProton NMR0210 nano-technologyEthylene glycolBiotechnologyMacromolecular bioscience
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Prospective Cancer Therapies Using Stimuli‐Responsive DNA Nanostructures

2021

Financial support by the Emil Aaltonen Foundation, the Sigrid Jusélius Foundation, the Magnus Ehrnrooth Foundation, Academy of Finland (grants no. 317042 and 331151), the Jane and Aatos Erkko Foundation and the Vilho, Yrjö and Kalle Väisälä Foundation of the Finnish Academy of Science and Letters is gratefully acknowledged Nanostructures based on DNA self-assembly present an innovative way to address the increasing need for target-specific delivery of therapeutic molecules. Currently, most of the chemotherapeutics being used in clinical practice have undesired and exceedingly high off-target toxicity. This is a challenge in particular for small molecules, and hence, developing robust and ef…

Polymers and PlasticsStimuli responsiveComputer scienceAptameraptamersBioengineeringNanotechnologyAntineoplastic Agents02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialsDrug Delivery Systemsstimuli-based drug deliveryDna nanostructuresNeoplasmsDNA nanotechnologyMaterials ChemistryDNA origamiHumansDNA nanotechnologyimmunostimulationchemotherapeuticsfungiDNA021001 nanoscience & nanotechnologyBiocompatible materialSmall molecule3. Good health0104 chemical sciencesNanostructuresDrug deliveryDNA origami0210 nano-technologyBiotechnology
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Minimalism in radiation synthesis of biomedical functional nanogels.

2012

A scalable, single-step, synthetic approach for the manufacture of biocompatible, functionalized micro- and nanogels is presented. In particular, poly(N-vinyl pyrrolidone)-grafted-(aminopropyl)methacrylamide microgels and nanogels were generated through e-beam irradiation of PVP aqueous solutions in the presence of a primary amino-group-carrying monomer. Particles with different hydrodynamic diameters and surface charge densities were obtained at the variance of the irradiation conditions. Chemical structure was investigated by different spectroscopic techniques. Fluorescent variants were generated through fluorescein isothiocyanate attachment to the primary amino groups grafted to PVP, to …

Polymers and PlasticsSurface PropertiesBioengineeringBiocompatible MaterialsElectronsConjugated systemBiomaterialschemistry.chemical_compoundMicePolymer chemistryMaterials ChemistryMethacrylamideAnimalsBovine serum albuminParticle SizeCells CulturedBioconjugationbiologyChemistryNanogel engineering e-beam irradiation bio-hybrid materials nanomedicine poly(N-vinyl-pyrrolidoneCombinatorial chemistryMice Inbred C57BLMonomerDrug deliverybiology.proteinNanomedicineNanoparticlesSettore CHIM/07 - Fondamenti Chimici Delle TecnologieGelsNanogelBiomacromolecules
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Synthesis of Novel Folic Acid-Functionalized Biocompatible Block Copolymers by Atom Transfer Radical Polymerization for Gene Delivery and Encapsulati…

2005

Two synthetic routes to folic acid (FA)-functionalized diblock copolymers based on 2-(methacryloyloxy)- ethyl phosphorylcholine [MPC] and either 2-(dimethylamino)ethyl methacrylate [DMA] or 2-(diisopropylamino) ethyl methacrylate [DPA] were explored. The most successful route involved atom transfer radical polymerization (ATRP) of MPC followed by the tertiary amine methacrylate using a 9-fluorenylmethyl chloroformate (Fmoc)-protected ATRP initiator. Deprotection of the Fmoc groups produced terminal primary amine groups, which were conjugated with FA to produce two series of novel FA-functionalized biocompatible block copolymers. Nonfunctionalized MPC-DMA diblock copolymers have been previou…

Polymers and PlasticsTertiary aminePolymersDrug CompoundingBiocompatible MaterialsBioengineeringChloroformateConjugated systemMethacrylateBiomaterialschemistry.chemical_compoundFolic AcidPolymer chemistryMaterials ChemistryCopolymerPOLYMER SYNTHESIS ATRPDrug CarriersMolecular StructureAtom-transfer radical-polymerizationGenetic TherapyHydrogen-Ion ConcentrationEnd-groupchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug carrierHydrophobic and Hydrophilic InteractionsBiomacromolecules
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