Search results for "polymers"

showing 10 items of 3567 documents

Elastomeric Organosilicon Micronetworks

1997

Trifunctional methyltrimethoxysilane and bifunctional dimethyldimethoxysilane monomers were cocondensed in water in the presence of surfactant. Strictly spherical micronetworks of narrow size distribution were obtained for particle sizes 10 nm < R < 30 nm. By special “endcapping” reactions all reactive SiOH groups were removed quantitatively, and the resulting micronetworks become soluble in common organic solvents like toluene, THF, or chloroform. For contents of trifunctional monomer larger than 50 mol % the particles do not swell irrespective of the choice of the solvent, whereas for lower mole fractions of trimethoxysilane an increasing swelling ratio is observed. Below 2.5 mol % trifun…

Polymers and PlasticsMethyltrimethoxysilaneOrganic ChemistryMole fractionTolueneInorganic ChemistrySolventchemistry.chemical_compoundMonomerchemistryEndcappingPolymer chemistryMaterials ChemistryBifunctionalOrganosiliconMacromolecules
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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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Size-dependent knockdown potential of siRNA-loaded cationic nanohydrogel particles.

2014

To overcome the poor pharmacokinetic conditions of short double-stranded RNA molecules in RNA interference therapies, cationic nanohydrogel particles can be considered as alternative safe and stable carriers for oligonucleotide delivery. For understanding key parameters during this process, two different types of well-defined cationic nanohydrogel particles were synthesized, which provided nearly identical physicochemical properties with regards to their material composition and resulting siRNA loading characteristics. Yet, according to the manufacturing process using amphiphilic reactive ester block copolymers of pentafluorophenyl methacrylate (PFPMA) and tri(ethylene glycol)methyl ether m…

Polymers and PlasticsNanogelsBioengineeringEtherMethacrylateProtein Structure SecondaryPolyethylene GlycolsBiomaterialschemistry.chemical_compoundCationsAmphiphilePolymer chemistryMaterials ChemistryCopolymerHumansPolyethyleneimineParticle SizeRNA Small InterferingRNA Double-StrandedOligonucleotideCationic polymerizationHydrogelschemistryChemical engineeringGene Knockdown TechniquesEthylene glycolNanogelHeLa CellsBiomacromolecules
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Covalently Binding of Bovine Serum Albumin to Unsaturated Poly(Globalide-Co-ε-Caprolactone) Nanoparticles by Thiol-Ene Reactions.

2019

When nanoparticles (NPs) are introduced to a biological fluid, different proteins (and other biomolecules) rapidly get adsorbed onto their surface, forming a protein corona capable of giving to the NPs a new "identity" and determine their biological fate. Protein-nanoparticle conjugation can be used in order to promote specific interactions between living systems and nanocarriers. Non-covalent conjugates are less stable and more susceptible to desorption in biological media, which makes the development of engineered nanoparticle surfaces by covalent attachment an interesting topic. In this work, the surface of poly(globalide-co-e-caprolactone) (PGlCL) nanoparticles containing double bonds i…

Polymers and PlasticsNanoparticleBioengineering02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialschemistry.chemical_compoundLactonesMaterials ChemistryAnimalsHumansBovine serum albuminParticle SizeCaproateschemistry.chemical_classificationbiologyThiol-ene reactionBiomoleculeSerum Albumin Bovine021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryCovalent bondbiology.proteinNanoparticlesCattleNanocarriers0210 nano-technologyCaprolactoneBiotechnologyConjugateHeLa CellsMacromolecular bioscience
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HPMA-Based Nanoparticles for Fast, Bioorthogonal iEDDA Ligation

2019

Contains fulltext : 216143.pdf (Publisher’s version ) (Open Access) Fast and bioorthogonally reacting nanoparticles are attractive tools for biomedical applications such as tumor pretargeting. In this study, we designed an amphiphilic block copolymer system based on HPMA using different strategies to introduce the highly reactive click units 1,2,4,5-tetrazines (Tz) either at the chain end (Tz-CTA) or statistical into the hydrophobic block. This reactive group undergoes a rapid, bioorthogonal inverse electron-demand Diels-Alder reaction (iEDDA) with trans-cyclooctenes (TCO). Subsequently, this polymer platform was used for the preparation of different Tz-covered nanoparticles, such as micell…

Polymers and PlasticsNanoparticleBioengineeringFluorescence correlation spectroscopy02 engineering and technologyConjugated system010402 general chemistry01 natural sciencesMicelleArticleBiomaterialsAmphiphileMaterials ChemistryCopolymerBenzene DerivativesColloidsMicellesPretargetingAza CompoundsCycloaddition ReactionChemistryOther Research Radboud Institute for Health Sciences [Radboudumc 0]021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesCross-Linking ReagentsMethacrylatesNanoparticlesClick ChemistryBioorthogonal chemistry0210 nano-technology
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Pre- and post-modification of mixed cyclodextrin-calixarene co-polymers: A route towards tunability

2017

Various pre-modified and post-modified cyclodextrin-calixarene hyper-reticulated co-polymers were synthesized, fully characterized by different techniques (FT-IR, 13C{1H} CP-MAS and LGFS solid-state NMR, thermogravimetry, porosimetry), and tested to assess their absorption abilities as nanosponges. The construction of the polymer network was accomplished exploiting the well-known CuAAC reaction between two different heptakis-6-azido-β-cyclodextrins and two different propargyloxy-calix[4]arenes. Post-modification was aimed to achieve the presence of ionizable (acidic or basic) groups on the polymer framework. Sequestration tests towards two model pollutant molecules surprisingly showed that …

Polymers and PlasticsNanotechnology02 engineering and technology010402 general chemistryNanospongeSolid-state NMR01 natural sciencesCalixareneCiclodextrinsMaterials ChemistryMoleculeSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationCyclodextrinOrganic ChemistrySettore CHIM/06 - Chimica OrganicaPorosimetryPolymer021001 nanoscience & nanotechnology0104 chemical sciencesThermogravimetrySolid-state nuclear magnetic resonancechemistryChemical engineeringCalixareneAbsorption (chemistry)0210 nano-technologyCarbohydrate Polymers
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A Review of Bioplastics and Their Adoption in the Circular Economy

2021

The European Union is working towards the 2050 net-zero emissions goal and tackling the ever-growing environmental and sustainability crisis by implementing the European Green Deal. The shift towards a more sustainable society is intertwined with the production, use, and disposal of plastic in the European economy. Emissions generated by plastic production, plastic waste, littering and leakage in nature, insufficient recycling, are some of the issues addressed by the European Commission. Adoption of bioplastics–plastics that are biodegradable, bio-based, or both–is under assessment as one way to decouple society from the use of fossil resources, and to mitigate specific environmental risks …

Polymers and PlasticsNatural resource economics02 engineering and technologyReview010501 environmental sciences01 natural sciencesBioplasticbio-based plasticlcsh:QD241-441lcsh:Organic chemistrylife cycle assessmentmedia_common.cataloged_instanceProduction (economics)European unionLeakage (economics)Life-cycle assessmentbioeconomy0105 earth and related environmental sciencesmedia_commonCircular economyGeneral Chemistrybiodegradable plastic021001 nanoscience & nanotechnologysustainabilityWork (electrical)SustainabilityBusiness0210 nano-technologybioplasticPolymers
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Epicyanohydrin: Polymerization by Monomer Activation Gives Access to Nitrile-, Amino-, and Carboxyl-Functional Poly(ethylene glycol)

2015

Both homo- and copolymerization of the hitherto nonpolymerizable epoxide monomer epicyanohydrin (EPICH) with ethylene oxide (EO) have been studied, employing the monomer activation technique. Tetraoctylammonium bromide or tetrabutylammonium iodide was used as initiator combined with i-Bu3Al to activate the EPICH monomer. The EPICH content was varied from 4 to 16 mol %, yielding well-defined PEG-co-PEPICH copolymers with molecular weights Mn (SEC) ranging from 3700 to 8800 g mol–1. The nitrile groups of the resulting polyethers were further reduced or hydrolyzed to introduce amino, amide, or carboxyl groups at the polyether backbone, circumventing protecting group chemistry. Successful trans…

Polymers and PlasticsNitrileEthylene oxideOrganic ChemistryEpoxideInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationAmidePolymer chemistryMaterials ChemistryCopolymerTetraoctylammonium bromideMacromolecules
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Functionalization of Active Ester-Based Polymersomes for Enhanced Cell Uptake and Stimuli-Responsive Cargo Release

2016

Poly(2,3-dihydroxypropyl methacrylamide) (P(DHPMA))-based amphiphilic block copolymers have recently proven to form polymer vesicles (polymersomes). In this work, we further expand their potential by incorporating (i) units for pH-dependent disintegration into the hydrophobic membrane and (ii) mannose as targeting unit into the hydrophilic block. This last step relies on the use of an active ester prepolymer. We confirm the stability of the polymersomes against detergents like Triton X-100 and their low cytotoxicity. The incorporation of 2-(2,2-dimethyl-1,3-dioxolane-4-yl)ethyl methacrylate into the hydrophobic block (lauryl methacrylate) allows a pH-responsive disintegration for cargo rele…

Polymers and PlasticsOctoxynolPolymersMannoseBioengineering02 engineering and technology010402 general chemistryMethacrylate01 natural sciencesBiomaterialschemistry.chemical_compoundDrug Delivery SystemsAmphiphilePolymer chemistryMaterials ChemistryHumansMethacrylamidePrepolymerChemistryVesicleDioxolanesEstersHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesMembranePolymersomeBiophysicsMethacrylates0210 nano-technologyHydrophobic and Hydrophilic InteractionsBiomacromolecules
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Spectroscopic Studies of Oligonucleotide Adducts and Base Sequence Preference of Adducts Formed by the Stereoisomers of 7,8-Dihydroxy-9,10-epoxy-7,8,…

1996

Abstract 5′-d(CCTATAGATATCC) has been reacted with BPDE and the adducts derived from binding of BPDE to the exocyclic amino group of deoxyguanosine (dG) were studied with spectroscopic methods. The major dG-adducts of (+)- and (-)-anti-BPDE and a minor adduct of (+)-syn-BPDE showed the characteristics of trans-adducts. The major products formed with (+)- and (-)-syn-BPDE exhibit cis-adduct characteristics. Annealing of BPDE-modified oligonucleotides to complementary or partially complementary strands results in reduced fluorescence intensity in several cases and in others the intensity is markedly increased. These differences demonstrate that the adduct microenvironment is strongly influenc…

Polymers and PlasticsOligonucleotideStereochemistryOrganic ChemistryEpoxyPhotochemistryAdductchemistry.chemical_compoundchemistryDuplex (building)visual_artpolycyclic compoundsMaterials Chemistryvisual_art.visual_art_mediumPyreneDeoxyguanosineThermal stabilityBase sequencePolycyclic Aromatic Compounds
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