Search results for "Polymersome"

showing 10 items of 15 documents

Active surfaces engineered by immobilizing protein-polymer nanoreactors for selectively detecting sugar alcohols.

2016

We introduce active surfaces generated by immobilizing protein-polymer nanoreactors on a solid support for sensitive sugar alcohols detection. First, such selective nanoreactors were engineered in solution by simultaneous encapsulation of specific enzymes in copolymer polymersomes, and insertion of membrane proteins for selective conduct of sugar alcohols. Despite the artificial surroundings, and the thickness of the copolymer membrane, functionality of reconstituted Escherichia coli glycerol facilitator (GlpF) was preserved, and allowed selective diffusion of sugar alcohols to the inner cavity of the polymersome, where encapsulated ribitol dehydrogenase (RDH) enzymes served as biosensing e…

Models MolecularMaterials scienceMembrane permeabilityPolymersSurface PropertiesBiophysicsBioengineering02 engineering and technologyNanoreactorBiosensing Techniques010402 general chemistryRibitolAquaporins01 natural sciencesPermeabilityBiomaterialschemistry.chemical_compoundSugar AlcoholsEscherichia coliOrganic chemistrySugar alcoholRibitolchemistry.chemical_classificationEscherichia coli Proteins021001 nanoscience & nanotechnology0104 chemical sciencesNanostructuresMembraneImmobilized ProteinschemistryMechanics of MaterialsPolymersomeCeramics and Composites0210 nano-technologyBiosensorSugar Alcohol DehydrogenasesSugar Alcohol DehydrogenasesBiomaterials
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Pentafluorophenyl Ester-based Polymersomes as Nanosized Drug-Delivery Vehicles

2015

In this work, activated ester chemistry is employed to synthesize biocompatible and readily functionalizable polymersomes. Via aminolysis of pentafluorophenyl methacrylate-based precursor polymers, an N-(2-hydroxypropyl) methacrylamide (HPMA)-analog hydrophilic block is obtained. The precursor polymers can be versatile functionalized by simple addition of suitable primary amines during aminolysis as demonstrated using a fluorescent dye. Vesicle formation is proven by cryoTEM and light scattering. High encapsulation efficiencies for hydrophilic cargo like siRNA are achieved using dual centrifugation and safe encapsulation is demonstrated by gel electrophoresis. In vitro studies reveal low cy…

PolymersomesMaterials sciencePolymers and Plastics02 engineering and technology010402 general chemistryMethacrylate01 natural scienceschemistry.chemical_compoundAminolysisHPMAPolymer chemistryMaterials ChemistryMethacrylamideReversible addition−fragmentation chain-transfer polymerizationRAFT polymerizationVesicleOrganic Chemistry021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistrydrug deliveryPolymersomeDrug deliveryactivated esters0210 nano-technologyDrug carrierMacromolecular Rapid Communications
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Block copolymers in giant unilamellar vesicles with proteins or with phospholipids

2013

Biocompatible, highly water-soluble, nonionic, amphiphilic block copolymers having different hydrophobic blocks and architectures, but similar molecular size and chemical nature of the hydrophilic blocks, were investigated to check for their ability to form hybrid giant unilamellar vesicles with proteins, and for their interactions with giant unilamellar phospholipid vesicles (GUV). PGM14-b-PPO34-b-PGM14 (PGM-PPO-PGM) consists of a poly(propylene oxide) middle block and outer poly(glycerol monomethacrylate) blocks. Ch-PEG32-b-lPG18 (Ch-PEG-lPG) and Ch-PEG30-b-hbPG17 (Ch-PEG-hbPG) have a linear poly(ethylene glycol) block, linked to a cholesterol end group and to a linear (lPG) or hyperbranc…

chemistry.chemical_compoundEnd-groupchemistryChemical engineeringVesicleAmphiphilePolymer chemistryPolymersomePhospholipidCopolymerPhysical and Theoretical ChemistryLipid bilayerEthylene glycolFaraday Discussions
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Mastering the Tools: Natural versus Artificial Vesicles in Nanomedicine

2020

Naturally occurring extracellular vesicles and artificially made vesicles represent important tools in nanomedicine for the efficient delivery of biomolecules and drugs. Since its first appearance in the literature 50 years ago, the research on vesicles is progressing at a fast pace, with the main goal of developing carriers able to protect cargoes from degradation, as well as to deliver them in a time- and space-controlled fashion. While natural occurring vesicles have the advantage of being fully compatible with their host, artificial vesicles can be easily synthetized and functionalized according to the target to reach. Research is striving to merge the advantages of natural and artifici…

liposomesolymersomesnanotherapeuticComputer scienceBiomedical EngineeringPharmaceutical SciencenanotherapeuticsNanotechnology02 engineering and technologyexosomes010402 general chemistry01 natural sciencesExtracellular vesiclesArtificial vesicleBiomaterialsexosomenanomaterialsSettore CHIM/02 - Chimica FisicaDrug CarriersVesicleBiological Transport021001 nanoscience & nanotechnologynanomedicineMicrovesicles0104 chemical sciencespolymersomesPolymersomeliposomeNanomedicinenanomaterialextracellular vesicleartificial vesicles0210 nano-technologyextracellular vesiclesMerge (version control)
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Nanovesicles as Drug Delivery Vehicles: Liposomes and Polymersomes

2015

LiposomeChemistryDrug deliveryPolymersomeNanotechnology
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Rational design of ABC triblock terpolymer solution nanostructures with controlled patch morphology

2016

Block copolymers self-assemble into a variety of nanostructures that are relevant for science and technology. While the assembly of diblock copolymers is largely understood, predicting the solution assembly of triblock terpolymers remains challenging due to complex interplay of block/block and block/solvent interactions. Here we provide guidelines for the self-assembly of linear ABC triblock terpolymers into a large variety of multicompartment nanostructures with C corona and A/B cores. The ratio of block lengths NC/NA thereby controls micelle geometry to spheres, cylinders, bilayer sheets and vesicles. The insoluble blocks then microphase separate to core A and surface patch B, where NB co…

Materials scienceNanostructureScienceta221ChemieGeneral Physics and AstronomyNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesMicelleGeneral Biochemistry Genetics and Molecular BiologyArticleCopolymer[CHIM]Chemical SciencesLamellar structureSoft matterMultidisciplinaryta114VesicleBilayerQGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineeringPolymersome0210 nano-technology
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Techniques To Control Polymersome Size

2015

Polymersomes as synthetic analogues of liposomes appear frequently in relevant literature as promising candidates for a wide range of different applications including drug delivery, theranostic multitools, and nanoreactors. In particular, as nanotransporters for nanomedical applications in vivo, requirements concerning the reproducible manufacturing and reliable size control are extremely high. This Perspective highlights the importance of size control especially in the context of nanomedicine and gives an overview of the theoretical background of amphiphilic self-assembly leading to different preparation methods, where their feasibility of controlling polymersomes’ size is discussed.

Inorganic ChemistryPreparation methodPolymers and PlasticsComputer scienceOrganic ChemistryPolymersomeDrug deliveryMaterials ChemistryNanomedicineContext (language use)NanotechnologyMacromolecules
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Viscoelasticity of pore-spanning polymer membranes derived from giant polymersomes

2010

We show how the viscoelastic properties of membranes formed from poly(butadiene)-block-poly(ethylene oxide) (PB130-b-PEO66) block copolymers can be locally accessed by atomic force microscopy. Polymer membranes are spread on microstructured porous silicon substrates from PB130-b-PEO66 vesicles by decreasing the osmotic pressure of the solution. Local viscoelastic properties of the pore-spanning polymer membranes were obtained from site-specific indentation experiments. Elastic moduli of these membranes were in the order of few MPa, while the elastic moduli of cross-linked membranes considerably increased to few GPa. Furthermore, the energy dissipation and velocity dependence of the hysteres…

Materials scienceSynthetic membrane02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesViscoelasticity0104 chemical sciencesHysteresisMembraneIndentationPolymersomeRelaxation (physics)Composite material0210 nano-technologyElastic modulusSoft Matter
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PeptoSomes for Vaccination: Combining Antigen and Adjuvant in Polypept(o)ide-Based Polymersomes.

2017

In this work, the first vaccine is reported based on a PeptoSome, which contains a model antigen (SIINFEKL) and adjuvant (CpG). PeptoSomes are polypept(o)ide-based polymersomes built of a block-copolymer with polysarcosine (PSar) as the hydrophilic block (X n = 111) and poly(benzyl-glutamic acid) (PGlu(OBn)) as the hydrophobic one (X n = 46). The polypept(o)ide is obtained with low dispersity index of 1.32 by controlled ring-opening polymerization. Vesicle formation by dual centrifugation technique allows for loading of vesicles up to 40 mol%. PeptoSomes are characterized by multiangle dynamic light scattering, static light scattering, and cryogenic transmission electron microscopy (cryoTEM…

Hydrodynamic radiusPolymers and Plasticsmedicine.medical_treatmentT-LymphocytesDispersityGene ExpressionBioengineeringchemical and pharmacologic phenomenaBone Marrow Cells02 engineering and technology010402 general chemistryLymphocyte Activation01 natural sciencesBiomaterialsPeptoidsDynamic light scatteringAntigenAdjuvants ImmunologicMaterials ChemistrymedicineHumansStatic light scatteringAntigensVaccinesChemistryVesicleVaccinationSarcosineDendritic Cells021001 nanoscience & nanotechnologyMolecular biologyCoculture Techniques0104 chemical sciencesOligodeoxyribonucleotidesPolymersomeB7-1 AntigenCytokinesB7-2 Antigen0210 nano-technologyPeptidesAdjuvantBiomarkersBiotechnologyMacromolecular bioscience
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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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