Search results for "Copolymer"

showing 10 items of 1003 documents

Chiral/Achiral Copolymers of Biphenylylacetylenes Bearing Various Substituents: Chiral Amplification through Copolymerization, Followed by Enhancemen…

2020

A series of dynamic helical homo- and copolymers of chiral and/or achiral biphenylylacetylenes (PBPAs) bearing achiral methoxymethoxy or acetyloxy groups at the 2,2′-positions along with a chiral o...

Bearing (mechanical)Materials sciencePolymers and PlasticsOrganic Chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesHelicityInversion (discrete mathematics)0104 chemical scienceslaw.inventionInorganic ChemistryCrystallographylawMaterials ChemistryCopolymer0210 nano-technologyMacromoleculeMacromolecules
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Calculation of phase diagrams not requiring the derivatives of the Gibbs energy demonstrated for a mixture of two homopolymers with the corresponding…

1995

A method is presented which allows the calculation of phase diagrams (spinodal, binodal and tie lines) on the basis of the Gibbs energy of mixing ΔG. No derivatives of ΔG with respect to the composition variables are required. This method is particularly useful in cases where the composition dependence of ΔG is very complex and no analytical representation of the derivatives can be given. The method is applied to a ternary mixture of two homopolymers with a copolymer consisting of the same monomers. The sequence distribution of the copolymer is kept constant between random and purely alternating, and phase diagrams are calculated for different chemical compositions of the copolymer. The com…

BinodalQuantitative Biology::BiomoleculesSpinodalPolymers and PlasticsChemistryOrganic ChemistryThermodynamicsCondensed Matter PhysicsCritical point (mathematics)Gibbs free energyCondensed Matter::Soft Condensed MatterInorganic Chemistrysymbols.namesakeMaterials ChemistrysymbolsCopolymerTernary operationMixing (physics)Phase diagramMacromolecular Theory and Simulations
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Compatibility between polystyrene copolymers and polymers in solution via hydrogen bonding

2006

Abstract It has been applied the concept of improving miscibility, by introducing and optimizing the extent of intermolecular hydrogen-bonding interactions between two polymers. We select a commodity polymer such as polystyrene, to study the compatibility in chloroform with poly(vinyl pyridine) and poly(vinyl pyrrolidone), both considered as proton acceptors. In order to enhance polymer–polymer miscibility, polystyrene is slightly modified by copolymerization with methacrylic acid, in the first case, and with vinyl-phenol comonomer, in the second one. In this way, two series of polystyrene-based copolymers are synthesized and characterized bearing ca. 8% (w/w) of –OH groups. The miscibility…

Binodalchemistry.chemical_classificationMaterials sciencePolymers and PlasticsComonomerOrganic ChemistryGeneral Physics and AstronomyPolymerMiscibilitychemistry.chemical_compoundchemistryMethacrylic acidPolymer chemistryMaterials ChemistryCopolymerPolystyreneIonomerEuropean Polymer Journal
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PEG-benzofulvene copolymer hydrogels for antibody delivery.

2010

A new amphiphilic copolymer have been synthesized starting from the hydrosoluble polyaspartylhydrazide (PAHy) polymer, by grafting both hydrophilic PEG(2000) chains and hydrophobic palmitic acid (C(16)) moieties on polymer backbone, and the structure of obtained PAHy-PEG(2000)-C(16) copolymer have been characterized by 2D (1)H/(13)C NMR experiments. PAHy-PEG(2000)-C(16) copolymer showed the ability of self-assembling in aqueous media giving a core-shell structure and resulted potentially useful for encapsulating and dissolving hydrophobic drug. The formation of micellar core-shell structure has been investigated by 2D (1)H NMR NOESY experiments. The presence of cross-peaks for protons of C(…

BiocompatibilityCell SurvivalPolymersSurface PropertiesPEG-benzofulvene immunoglobulin delivery hydrogelsimmunoglobulinsPharmaceutical SciencePolyethylene Glycolschemistry.chemical_compoundDrug Delivery SystemsCell Line TumorPolymer chemistryPEG ratioCopolymerHumansantibody deliverybenzofulvene copolymerschemistry.chemical_classificationChemistrytechnology industry and agricultureHydrogelsantibody delivery; benzofulvene copolymers; hydrogels; immunoglobulinsPolymerMacromonomerIndenesSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoImmunoglobulin GDrug deliverySelf-healing hydrogelsbenzofulvene copolymerhydrogelDrug Screening Assays AntitumorRheologyEthylene glycolInternational journal of pharmaceutics
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Polyhydroxyethylaspartamide-spermine copolymers: Efficient vectors for gene delivery

2008

Abstract Aim of this paper was that to prepare biocompatible, polyaspartamide based copolymers containing spermine or spermine/hydrophobic side chains able to condense nucleic acids and to transfect mammalian cells. Copolymers were prepared starting from α,β-poly-(N-2-hydroxyethyl)- d , l -aspartamide (PHEA) and exploiting the reactive hydroxyl groups in the polymeric side chains by subsequent activation reactions to obtain PHEA-Spermine (PHEA-Spm) and PHEA-Spermine-Butyramide (PHEA-Spm-C4). Molecular, physico-chemical and biological characterization of copolymers and interpolyelectrolyte complexes with plasmid DNA was performed. Experimental results evidenced that these copolymers are able…

Biocompatibilitygene delivery polyaspartamideCell SurvivalStereochemistryPharmaceutical ScienceSpermineGene deliveryBiologyTransfectionpolycationDNA Adductschemistry.chemical_compoundCell Line TumorCopolymerHumansLuciferasesCells CulturedErythrocyte MembraneGenetic transferinterpolyelectrolyte complexesGene Transfer TechniquesDNATransfectionCombinatorial chemistrychemistryNucleic acidSperminePeptidesDNAJournal of Controlled Release
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New gellan gum-graft-poly(D,L-lactide-co-glycolide) copolymers as promising bioinks: Synthesis and characterization

2020

This research focused on the aim of tackling the urgent demand of printable biomaterials, hence we synthetized and characterized three gellan gum-graft-poly(d,l-lactide-co-glycolide) copolymers (GGm-PLGA a, b and c) which differed in the graft substitution degree. We investigated the effect of the polyester chain grafted onto hydrophilic backbone of gellan gum in terms of physicochemical properties and the ability of the system to print 3D cell laden constructs. In particular, we evaluated thermo-rheological, ionotropic crosslinking, shear thinning, swelling and stability properties of these copolymers and their derived biomaterials and findings related to the degree of functionalization. M…

Biocompatible Materials02 engineering and technologyBiochemistry03 medical and health scienceschemistry.chemical_compoundMicePolylactic Acid-Polyglycolic Acid CopolymerGraft copolymersStructural BiologyMaterials TestingmedicineCopolymerAnimalsMolecular Biology030304 developmental biologyMechanical Phenomena0303 health sciencesShear thinningTissue EngineeringChemistryPolysaccharides BacterialBioprintingGeneral Medicine3T3 Cells021001 nanoscience & nanotechnologyGellan gumPolyesterChemical engineeringSurface modificationPoly d l lactideInkPoly (DL-lactide-co-glycolide) (PLGA)Swellingmedicine.symptom0210 nano-technologyRheologyGellan gum (GG)
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Characterization and biodistribution of Au nanoparticles loaded in PLGA nanocarriers using an original encapsulation process

2021

Due to their imaging and radiosensitizing properties, ultrasmall gadolinium chelate-coated gold nanoparticles (AuNP) represent a promising approach in the diagnosis and the treatment of tumors. However, their poor pharmacokinetic profile, especially their rapid renal clearance prevents from an efficient exploitation of their potential for medical applications. The present study focuses on a strategy which resides in the encapsulation of AuNP in large polymeric NP to avoid the glomerular filtration and then to prolong the vascular residence time. An original encapsulation procedure using the polyethyleneimine (PEI) was set up to electrostatically entrap AuNP in biodegradable poly(lactic-co-g…

BiodistributionGadoliniumMetal NanoparticlesNanoparticlechemistry.chemical_elementmacromolecular substances02 engineering and technologyPolyethylene glycol01 natural sciencesPolyethylene Glycolschemistry.chemical_compoundColloid and Surface ChemistryPolylactic Acid-Polyglycolic Acid Copolymer0103 physical sciencesAnimalsTissue DistributionParticle SizePhysical and Theoretical ChemistryDrug Carriers010304 chemical physicstechnology industry and agricultureSurfaces and InterfacesGeneral Medicine021001 nanoscience & nanotechnologyRatsEncapsulation (networking)PLGAchemistryColloidal goldBiophysicsNanoparticlesGoldNanocarriers0210 nano-technologyBiotechnologyColloids and Surfaces B: Biointerfaces
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Modifying the body distribution of HPMA-based copolymers by molecular weight and aggregate formation.

2011

There is a recognized need to create well-defined polymer probes for in vivo and clinical positron emission tomography (PET) imaging to guide the development of new generation polymer therapeutics. Using the RAFT polymerization technique in combination with the reactive ester approach, here we have synthesized well-defined and narrowly distributed N-(2-hydroxypropyl)methacrylamide homopolymers (pHPMA) (P1* and P2*) and random HPMA copolymers consisting of hydrophilic HPMA and hydrophobic lauryl methacrylate comonomers (P3* and P4*). The polymers had molecular weights below (P1* and P3*) and above the renal threshold (P2* and P4*). Whereas the homopolymers dissolve in isotonic solution as in…

BiodistributionPolymers and PlasticsPolymersBioengineeringFluorescence correlation spectroscopyBiomaterialschemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerMethacrylamideMoleculeAnimalsReversible addition−fragmentation chain-transfer polymerizationTissue Distributionchemistry.chemical_classificationMolecular StructureStereoisomerismPolymerRatsMolecular WeightchemistryCritical micelle concentrationPositron-Emission TomographyMethacrylatesRadiopharmaceuticalsBiomacromolecules
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Poloxamer/sodium cholate co-formulation for micellar encapsulation of Doxorubicin with high efficiency for intracellular delivery: an in-vitro bioava…

2020

Abstract Hypothesis Doxorubicin hydrochloride (DX) is widely used as a chemotherapeutic agent, though its severe side-effects limit its clinical use. A way to overcome these limitations is to increase DX latency through encapsulation in suitable carriers. However, DX has a high solubility in water, hindering encapsulation. The formulation of DX with sodium cholate (NaC) will reduce aqueous solubility through charge neutralization and hydrophobic interactions thus facilitating DX encapsulation into poloxamer (F127) micelles, increasing drug latency. Experiments DX/NaC/PEO-PPO-PEO triblock copolymer (F127) formulations with high DX content (DX-PMs) have been prepared and characterized by scat…

Biological AvailabilityPoloxamerbile salts; confocal microscopy; Doxorubicin hydrochloride; drug-delivery; PEO-PPO-PEO block copolymers; pluronics; tumour cell lines02 engineering and technologyconfocal microscopypluronics010402 general chemistry01 natural sciencesMicellePolyethylene GlycolsBiomaterialsHydrophobic effectColloid and Surface ChemistryPEO-PPO-PEO block copolymersbile saltsSolubilitySodium CholateMicellesChemistryDoxorubicin hydrochloridePoloxamerSodium Cholate021001 nanoscience & nanotechnologydrug-delivery0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDoxorubicinDrug deliveryBiophysicsDoxorubicin Hydrochloridetumour cell lines0210 nano-technologyIntracellular
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Synthesis of AB and ABA block copolymers as compatibilizers in nylon 6/polycarbonate blends

1996

Nylon 6 (Ny6) and Bisphenol A polycarbonate (PC) are immiscible and form biphasic blends. To improve the compatibility of Ny6 and PC several ABA and AB Ny6/PC block copolymers were synthesized, and their compatibilizing behavior on the blends were tested. Block copolymers were prepared by reacting monoamino- or diamino-terminated Ny6 homopolymers with high molecular weight PC at 130°C in anhydrous DMSO. The reaction of diamino- and monoamino-terminated Ny6 with polycarbonate produces block copolymers of the type PC-Ny6-PC (ABA) and PC-Ny6 (AB), respectively, plus a certain amount of unconverted PC degradated to lower molecular weights. To separate the block copolymer from the unconverted PC…

Bisphenol APolymers and PlasticsOrganic ChemistryChemical modificationCompatibilizationchemistry.chemical_compoundNylon 6chemistryvisual_artPolymer chemistryPolyamideMaterials ChemistryCopolymervisual_art.visual_art_mediumPolycarbonateTetrahydrofuranNuclear chemistryJournal of Polymer Science Part A: Polymer Chemistry
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