Search results for "Macromolecular Substance"

showing 10 items of 882 documents

Size Tunable Core Crosslinked Micelles from HPMA-Based Amphiphilic Block Copolymers

2017

A variety of core crosslinkable hydroxypropylmethacrylamide-based block copolymers are synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization, which are composed of hydroxypropyl-methacrylate as hydrophilic block combined with a statistical hydrophobic block from laurylmethacrylate and the photo crosslinkable monomer. It is discovered that the self-assembled micellar aggregates from these systems vary strongly in size depending not only on the velocity of the polarity switch (nanoprecipitation or slow dialysis) but also on the solvent from which they were dialyzed. In this way micellar aggregates with an Rh varying between 15 and 80 nm can be prepared from the…

Polymers and PlasticsOrganic Chemistrytechnology industry and agricultureChain transfermacromolecular substances02 engineering and technologyRaft010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesMicelle0104 chemical scienceschemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryAmphiphileMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationPhysical and Theoretical Chemistry0210 nano-technologyMacromolecular Chemistry and Physics
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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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In situ forming hydrogels of hyaluronic acid and inulin derivatives for cartilage regeneration.

2014

An in situ forming hydrogel obtained by crosslinking of amino functionalized hyaluronic acid derivatives with divinylsulfone functionalized inulin (INU-DV) has been here designed and characterized. In particular two hyaluronic acid derivatives bearing respectively a pendant ethylenediamino (EDA) portion (HA-EDA) and both EDA and octadecyl pendant groups (HA-EDA-C18) were crosslinked through an azo-Michael reaction with INU-DV. Gelation time and consumption of DV portions have been evaluated on hydrogel obtained using HA-EDA and HA-EDA-C18 derivatives with a concentration of 3% w/v and a ratio 80/20 w/w respect to the crosslinker INU-DV. The presence of pendant C18 chains improves mechanical…

Polymers and PlasticsPolymersInulinmacromolecular substancesHydrolysischemistry.chemical_compoundChondrocytesTissue engineeringHyaluronidaseHyaluronic acidPolymer chemistryMaterials ChemistrymedicineAnimalsRegenerationHyaluronic Acidchemistry.chemical_classificationTissue EngineeringChemistryOrganic Chemistrytechnology industry and agricultureInulinHydrogelsPolymerhydrogels hyaluronic acid inulinCartilageCross-Linking ReagentsSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSelf-healing hydrogelsMichael reactionMicroscopy Electron ScanningCattlemedicine.drugCarbohydrate polymers
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Biodegradable pH-Sensitive Poly(ethylene glycol) Nanocarriers for Allergen Encapsulation and Controlled Release

2015

In the last decades, the number of allergic patients has increased dramatically. Allergen-specific immunotherapy (SIT) is the only available cause-oriented therapy so far. SIT reduces the allergic symptoms, but also exhibits some disadvantages; that is, it is a long-lasting procedure and severe side effects like anaphylactic shock can occur. In this work, we introduce a method to encapsulate allergens into nanoparticles to avoid severe side effects during SIT. Degradable nanocarriers combine the advantage of providing a physical barrier between the encapsulated cargo and the biological environment as well as responding to certain local stimuli (like pH) to release their cargo. This work int…

Polymers and PlasticsProton Magnetic Resonance SpectroscopyNanoparticleBioengineeringmacromolecular substancesmedicine.disease_causePolyethylene GlycolsBiomaterialschemistry.chemical_compoundAllergenPolymer chemistryPEG ratioMaterials ChemistrymedicineHumansNanotechnologyDrug CarriersAcetalAllergensHydrogen-Ion ConcentrationEndolysosomeControlled releaseCombinatorial chemistrychemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationChromatography GelNanocarriersEthylene glycolBiomacromolecules
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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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Peculiar behavior of degenerative chain transfer polymerization of a phosphonated methacrylate

2009

Living/controlled radical polymerization of dimethyl(methacryloyloxy)methyl phosphonate (MAPC) has been attempted using degenerative transfer to produce block copolymers. RAFT polymerization of this monomer is sensitive to very low level of oxygen and in any case limited to low monomer conversion. Reverse iodine transfer polymerization (RITP) leads to higher monomer conversion with a limited amount of living polymer (55% by H NMR), precluding an efficient synthesis of block copolymers. A PMMA-b-PMAPC diblock copolymer was therefore synthesized by iodine transfer polymerization (ITP) of MAPC from a PMMA-Imacro-chain transfer agent prepared by RITP. The diblock copolymer, purified by selectiv…

Polymers and PlasticsRadical polymerizationmacromolecular substances02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesLiving free-radical polymerizationChain-growth polymerizationPolymer chemistryMaterials ChemistryReversible addition−fragmentation chain-transfer polymerizationPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSChemistryOrganic Chemistrytechnology industry and agricultureChain transfer021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymersPolymerizationPrecipitation polymerizationLiving polymerization0210 nano-technology
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Tuning the life-time of supramolecular hydrogels using ROS-responsive telechelic peptide-polymer conjugates

2019

Abstract The synthesis of multi-stimuli responsive peptide-poly(ethylene glycol) ABA-type conjugates is reported. The β-sheet encoded intramolecular folding and intermolecular self-assembly into 1D nanorods is based on a phenylalanine(F)-methionine(M)-histidine(H) FMHMHF hexapeptide sequence, and the supramolecular nanorods are stabilised by a shielding corona of hydrophilic PEG polymers. Interstrand crosslinking leads to the formation of physical networks and hydrogels at physiological pH and at room temperature. The thioether functional groups integrate oxidation responsive properties in the supramolecular polymer assemblies. We show that the glucose fuelled and glucose oxidase catalysed …

Polymers and PlasticsSupramolecular chemistryGeneral Physics and Astronomymacromolecular substances02 engineering and technology010402 general chemistry01 natural sciencesRedoxchemistry.chemical_compoundThioetherMaterials ChemistryGlucose oxidasechemistry.chemical_classificationbiologyChemistryOrganic Chemistrytechnology industry and agriculturePolymer021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesSupramolecular polymersSelf-healing hydrogelsbiology.protein0210 nano-technologyEthylene glycolEuropean Polymer Journal
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Capitalizing on Protecting Groups to Influence Vinyl Catechol Monomer Reactivity and Monomer Gradient in Carbanionic Copolymerization

2017

everal vinyl catechol-based monomers with systematically varied acetal protecting groups suitable for carbanionic polymerization are introduced. All monomers are based on the 4-vinyl benzodioxole or 5-vinyl benzodioxole structure and differ in the nature of the protecting group for the catechol functionalities. Different symmetric ketones are used for the protection of the diol functionality. Polymers with average molecular weight from 2500 to 25 000 g mol−1 (Mw/Mn < 1.15) are obtained from homopolymerization of the protected monomers. All monomers are examined regarding the influence of the protecting group on the copolymerization behavior with styrene, using in situ 1H NMR kinetic studies…

Polymers and Plasticsorganic chemicalsOrganic ChemistryAcetaltechnology industry and agriculturemacromolecular substances02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesStyrenechemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerReactivity (chemistry)Physical and Theoretical Chemistry0210 nano-technologyProtecting groupMacromolecular Chemistry and Physics
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Sumatriptan Succinate Transdermal Delivery Systems for The Treatment of Migraine

2007

We have successfully obtained sumatriptan transdermal systems with different polymer compositions: methyl cellulose (MC), polyvinyl pyrrolidone (PVP) and a polyvinyl pyrrolidone (PVP)-polyvinyl alcohol (PVA) mixture. The systems contained 1,2-propylenglycol (MC) or sorbitol as a plasticizer (PVP and PVP-PVA), methacrylate copolymer as an adhesive agent, and an occlusive liner. Azone (5%, w/w) was incorporated into all the systems as a percutaneous enhancer. Transdermal systems are thin, transparent and non-adhesive when in a dry state. The permeation of sumatriptan succinate across pig ear skin was studied using the systems prepared. The formulation with MC polymer produced a statistically …

PolymersSwineChemistry PharmaceuticalDrug CompoundingMigraine DisordersSkin AbsorptionPharmaceutical Sciencemacromolecular substancesAbsorption (skin)MethylcellulosePharmacologyAdministration CutaneousPermeabilityDosage formchemistry.chemical_compoundPolymethacrylic AcidsPlasticizersSumatriptan SuccinatemedicineAnimalsSorbitolTechnology PharmaceuticalVasoconstrictor AgentsSkinTransdermalDrug Carriersintegumentary systemSumatriptanChemistrytechnology industry and agriculturePlasticizerPovidoneAzepinesIontophoresisPermeationPropylene GlycolSerotonin Receptor AgonistsKineticsSumatriptanPolyvinyl AlcoholMethyl celluloseDiffusion Chambers CultureTissue AdhesivesNuclear chemistrymedicine.drugJournal of Pharmaceutical Sciences
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THE LIGHT-HARVESTING SYSTEM OF THE UNICELLULAR ALGA Mantoniella squamata (PRASINOPHYCEAE): EVIDENCE FOR THE LACK OF A PHOTOSYSTEM I-SPECIFIC ANTENNA …

1993

The light-harvesting complexes (LHC) were isolated from the unicellular alga Mantoniella squamata (Prasinophyceae) by sucrose-density centrifugation. Beside the major LHC (II), a photosystem I complex was obtained that could be dissociated into a photosystem I core complex and an associated LHC I. In contrast to other chlorophyll b-containing antennae, both LHC II as well as LHC I were observed to be identical with respect to the following features: the molecular weights, the isoelectric points and the retention behavior on anion-exchange chromatography of the apoproteins, the pigment content and the absorption and fluorescence spectra

PrasinophyceaeFluorescence spectrometryfood and beveragesmacromolecular substancesGeneral MedicineBiologyPhotosystem Ibiology.organism_classificationBiochemistryPigmentchemistry.chemical_compoundIsoelectric pointchemistryAlgaevisual_artChlorophyllBotanypolycyclic compoundsvisual_art.visual_art_mediumBiophysicsPhysical and Theoretical ChemistryPhotosystemPhotochemistry and Photobiology
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