Search results for "Poly(ethylene glycol)"

showing 10 items of 337 documents

Amphiphilic Copolymers Based on Poly[(hydroxyethyl)-d,l-aspartamide]: A Suitable Functional Coating for Biocompatible Gold Nanostars

2013

Novel amphiphilic copolymers have been synthesized based on a biocompatible poly(hydroxyethylaspartamide) (PHEA) backbone, bearing both anchoring groups for gold nanoparticles, such as thiols and disulfide, and conjugable moieties, such as amino groups, the latter as points suitable for appending further functional agents. The strategy was to functionalize α,β-poly[(N-2- hydroxyethyl)-d,l-aspartamide] (PHEA) with PEG2000-NH2 and with ethylenediamine (EDA) obtaining a partially pegylated copolymer with a large number of pendant primary amino groups. A fraction of the latter was conjugated with molecules bearing terminal thiol moieties such as 12-mercaptododecanoic acid (MDA) and disulfide gr…

Polymers and PlasticsCell SurvivalMetal NanoparticlesBioengineeringEthylenediamineengineering.materialConjugated systemPolyethylene GlycolsBiomaterialsSurface-Active Agentschemistry.chemical_compoundCoated Materials BiocompatibleCoatingCell Line TumorMaterials TestingAmphiphilePolymer chemistryMaterials ChemistryCopolymerHumansMoleculePoly(hydroxyethyl)-DL-aspartamideParticle Sizechemistry.chemical_classificationAmphiphilic copolymersgold nanostarlipoic acidEthylenediamineschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoColloidal goldThiolengineeringGoldPeptidesgold nanoparticleBiomacromolecules
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Effect of Core-Crosslinking on Protein Corona Formation on Polymeric Micelles.

2021

Most nanomaterials acquire a protein corona upon contact with biological fluids. The magnitude of this effect is strongly dependent both on surface and structure of the nanoparticle. To define the contribution of the internal nanoparticle structure, protein corona formation of block copolymer micelles with poly(N-2-hydroxypropylmethacrylamide) (pHPMA) as hydrophilic shell, which are crosslinked-or not-in the hydrophobic core is comparatively analyzed. Both types of micelles are incubated with human blood plasma and separated by asymmetrical flow field-flow fractionation (AF4). Their size is determined by dynamic light scattering and proteins within the micellar fraction are characterized by…

Polymers and PlasticsChemical PhenomenaLightPolymersNanoparticleBioengineeringProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesMicelleMass SpectrometryPolyethylene GlycolsBiomaterialsCorona (optical phenomenon)PlasmaDynamic light scatteringMaterials ChemistryCopolymerHumansScattering RadiationChromatography High Pressure LiquidMicellesGel electrophoresisChemistry021001 nanoscience & nanotechnologyBlood proteins0104 chemical sciencesNanostructuresCross-Linking ReagentsBiophysicsProtein CoronaAdsorption0210 nano-technologyHydrophobic and Hydrophilic InteractionsBiotechnologyMacromolecular bioscience
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Aminal Protection of Epoxide Monomer Permits the Introduction of Multiple Secondary Amine Moieties at Poly(ethylene glycol).

2019

In contrast to acetal groups, aminal moieties are almost unknown in polymer chemistry. The aminal-protected isopropyl-hexahydro-pyrimidine glycidyl amine (PyGA) for the anionic ring-opening polymerization (AROP) is introduced. The monomer is prepared in a two-step synthesis and can be polymerized in a well-controlled manner under AROP conditions. Several poly(ethylene glycol) block and triblock copolymers are synthesized in a molecular weight range from 2 700 to 11 400 g mol-1 with up to 11 mol% PyGA. The molecular weight distributions are monomodal with low dispersity (Đ = Mw /Mn ) below 1.2. After the polymerization, the acid-labile hexahydro-pyrimidine rings can be conveniently cleaved i…

Polymers and PlasticsDispersityEpoxide02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene GlycolsPolymerizationchemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerAminesMolecular StructureOrganic ChemistryAcetal021001 nanoscience & nanotechnology0104 chemical sciencesMolecular WeightMonomerchemistryPolymerizationAminalEpoxy Compounds0210 nano-technologyEthylene glycolMacromolecular rapid communications
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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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Ionic Hydrogel Based on Chitosan Cross-Linked with 6-Phosphogluconic Trisodium Salt as a Drug Delivery System.

2018

[EN] In this work, 6-phosphogluconic trisodium salt (6-PG(-)Na(+)) is introduced as a new aqueous and nontoxic cross-linking agent to obtain ionic hydrogels. Here, it is shown the formation of hydrogels based on chitosan cross-linked with 6-PG(-)Na(+). This formulation is obtained by ionic interaction of cationic groups of polymer with anionic groups of the cross linker. These hydrogels are nontoxic, do not cause dermal irritation, are easy to extend, and have an adequate adhesion force to be applied as polymeric film over the skin. This AWN formulation exhibits a first order release kinetic and can be applied as drug vehicle for topical administration or as wound dressing for wound healing…

Polymers and PlasticsPolymersAdministration TopicalIonic bondingSalt (chemistry)Bioengineering02 engineering and technology010402 general chemistry01 natural sciencesGluconatesHydrogel Polyethylene Glycol DimethacrylateBiomaterialsChitosanchemistry.chemical_compoundQUIMICA ORGANICADrug Delivery SystemsMaterials ChemistryHumanschemistry.chemical_classificationChitosanWound HealingAqueous solutionWound Closure TechniquesSodiumCationic polymerization021001 nanoscience & nanotechnology0104 chemical sciencesDrug vehicleKineticsCross-Linking ReagentsChemical engineeringchemistrySelf-healing hydrogelsDrug delivery0210 nano-technologyBiomacromolecules
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Click modification of multifunctional liposomes bearing hyperbranched polyether chains.

2014

Aiming at controlled modification of liposomal surface structures, we describe a postpreparational approach for surface derivatization of a new type of multifunctional, sterically stabilized liposomes. Application of dual centrifugation (DC) resulted in high encapsulation efficiencies above 50% at very small batch sizes with a total volume of 150 μL, which were conductive to fast and efficient optimization of variegated surface modification reactions. Cholesterol-polymer amphiphiles, including complex hyperbranched polyether structures bearing 1-4 terminal alkynes, were used in DC formulations to provide steric stabilization. The alkyne moieties were explored as anchors for the conjugation …

Polymers and PlasticsPolymersAlkyneBioengineeringCell LinePolyethylene GlycolsBiomaterialsPolymer chemistryAmphiphileMaterials ChemistryFluorescence Resonance Energy TransferMoleculeAnimalschemistry.chemical_classificationLiposomeMicroscopy ConfocalBrainEndothelial CellsSmall moleculeCombinatorial chemistryRatsFörster resonance energy transferchemistryDoxorubicinAlkynesLiposomesClick chemistrySurface modificationClick ChemistryBiomacromolecules
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Functionalization of Liposomes with Hydrophilic Polymers Results in Macrophage Uptake Independent of the Protein Corona

2019

Liposomes are established drug carriers that are employed to transport and deliver hydrophilic drugs in the body. To minimize unspecific cellular uptake, nanocarriers are commonly modified with poly(ethylene glycol) (PEG), which is known to minimize unspecific protein adsorption. However, to date, it has not been studied whether this is an intrinsic and specific property of PEG or if it can be transferred to hyperbranched polyglycerol (hbPG) as well. Additionally, it remains unclear if the reduction of unspecific cell uptake is independent of the “basic” carrier at which a surface functionalization with polymers is usually applied. Therefore, we studied the protein corona of differently fun…

Polymers and PlasticsPolymersBioengineeringProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesArticlePolyethylene GlycolsBiomaterialsMiceHydrophilic polymersMaterials ChemistryAnimalsHumansMacrophageDrug CarriersLiposomeChemistryMacrophagesBiological Transport021001 nanoscience & nanotechnology0104 chemical sciencesRAW 264.7 CellsLiposomesBiophysicsNanoparticlesSurface modificationProtein CoronaNanocarriers0210 nano-technologyDrug carrierHydrophobic and Hydrophilic InteractionsBiomacromolecules
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Universal Concept for the Implementation of a Single Cleavable Unit at Tunable Position in Functional Poly(ethylene glycol)s

2013

Poly(ethylene glycol) (PEG) with acid-sensitive moieties gained attention particularly for various biomedical applications, such as the covalent attachment of PEG (PEGylation) to protein therapeutics, the synthesis of stealth liposomes, and polymeric carriers for low-molecular-weight drugs. Cleavable PEGs are favored over their inert analogues because of superior pharmacodynamic and/or pharmacokinetic properties of their formulations. However, synthetic routes to acetal-containing PEGs published up to date either require enormous efforts or result in ill-defined materials with a lack of control over the molecular weight. Herein, we describe a novel methodology to implement a single acetalde…

Polymers and PlasticsPolymersChemistry PharmaceuticalBioengineeringAcetaldehydemacromolecular substancesPolyethylene GlycolsBiomaterialschemistry.chemical_compoundPEG ratioPolymer chemistryAmphiphileMaterials ChemistryMoietyEthylene oxideChemistryAcetaltechnology industry and agricultureProteinsSerum Albumin BovineCholesterolAnionic addition polymerizationAlcoholsPEGylationEpoxy CompoundsEthylene glycolBiomacromolecules
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Multifunctional Fe(III)-Binding Polyethers from Hydroxamic Acid-Based Epoxide Monomers.

2019

Multiple hydroxamic acids are introduced at poly(ethylene glycol) (PEG) via copolymerization of ethylene oxide with a novel epoxide monomer containing a 1,4,2-dioxazole-protected hydroxamic acid (HAAGE). AB- and ABA-type di- and triblock copolymers as well as statistical copolymers of HAAGE and ethylene oxide are prepared in a molecular weight range between 2600 and 12 000 g mol-1 with low dispersities (Ð < 1.2). Cleavage of the acetal protecting group after the polymerization is achieved by mild acidic treatment, releasing multiple free hydroxamic acids tethered to the polyether backbone. The chelation properties of different polymer architectures (statistical versus diblock and ABA triblo…

Polymers and PlasticsPolymersEpoxide02 engineering and technology010402 general chemistryHydroxamic Acids01 natural sciencesFerric CompoundsPolyethylene GlycolsPolymerizationchemistry.chemical_compoundCoordination ComplexesPolymer chemistryMaterials ChemistryCopolymerchemistry.chemical_classificationHydroxamic acidEthylene oxideOrganic ChemistryPolymer021001 nanoscience & nanotechnology0104 chemical sciencesMonomerPolymerizationchemistryEpoxy Compounds0210 nano-technologyEthylene glycolMacromolecular rapid communications
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