Search results for "Mphi"

showing 10 items of 626 documents

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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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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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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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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Aggregation behavior of amphiphilic p(HPMA)-co-p(LMA) copolymers studied by FCS and EPR spectroscopy.

2012

A combined study of fluorescence correlation spectroscopy and electron paramagnetic resonance spectroscopy gave a unique picture of p(HPMA)-co-p(LMA) copolymers in aqueous solutions, ranging from the size of micelles and aggregates to the composition of the interior of these self-assembled systems. P(HPMA)-co-p(LMA) copolymers have shown high potential as brain drug delivery systems, and a detailed study of their physicochemical properties can help to elucidate their mechanism of action. Applying two complementary techniques, we found that the self-assembly behavior as well as the strength of hydrophobic attraction of the amphiphilic copolymers can be tuned by the hydrophobic LMA content or…

Polymers and PlasticsPolymersBioengineeringFluorescence correlation spectroscopyMicelleModels Biologicallaw.inventionBiomaterialsSurface-Active AgentsDrug Delivery SystemslawPolymer chemistryAmphiphileMaterials ChemistrySide chainCopolymerElectron paramagnetic resonanceAlkylMicelleschemistry.chemical_classificationChemistryElectron Spin Resonance SpectroscopyDomperidoneHydrophobeSpectrometry FluorescenceLiposomesMethacrylatesHydrophobic 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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Secondary Structure-Driven Self-Assembly of Thiol-Reactive Polypept(o)ides

2021

Secondary structure formation differentiates polypeptides from most of the other synthetic polymers, and the transitions from random coils to rod-like α-helices or β-sheets represent an additional parameter to direct self-assembly and the morphology of nanostructures. We investigated the influence of distinct secondary structures on the self-assembly of reactive amphiphilic polypept(o)ides. The individual morphologies can be preserved by core cross-linking via chemoselective disulfide bond formation. A series of thiol-responsive copolymers of racemic polysarcosine-block-poly(S-ethylsulfonyl-dl-cysteine) (pSar-b-p(dl)Cys), enantiopure polysarcosine-block-poly(S-ethylsulfonyl-l-cysteine) (pSa…

Polymers and PlasticsPolymersChemistryBioengineeringAntiparallel (biochemistry)MicelleArticleProtein Structure SecondaryPolymerizationBiomaterialsCrystallographyEnantiopure drugPolymerizationAmphiphileMaterials ChemistryCopolymerSulfhydryl CompoundsSelf-assemblyProtein secondary structureMicellesBiomacromolecules
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HPMA copolymers as surfactants in the preparation of biocompatible nanoparticles for biomedical application.

2012

In this work we describe the application of amphiphilic N-(2-hydroxypropyl)methacrylamide (HPMA)-based copolymers as polymeric surfactants in miniemulsion techniques. HPMA-based copolymers with different ratios of HPMA (hydrophilic) to laurylmethacrylate (LMA; hydrophobic) units were synthesized by RAFT polymerization and postpolymerization modification. The amphiphilic polymers can act as detergents in both the miniemulsion polymerization of styrene and the miniemulsion process in combination with solvent evaporation, which was applied to polystyrene and polylactide. Under optimized conditions, monodisperse colloids can be prepared. The most promising results could be obtained by using the…

Polymers and PlasticsPolymersPolyestersDispersityBioengineeringBiocompatible MaterialsPolymerizationBiomaterialschemistry.chemical_compoundSurface-Active AgentsPolymer chemistryAmphiphileMaterials ChemistryCopolymerMethacrylamideHumansReversible addition−fragmentation chain-transfer polymerizationColloidsMicroscopy ConfocalChemistryMiniemulsionPolymerizationMethacrylatesNanoparticlesPolystyreneHydrophobic and Hydrophilic InteractionsHeLa CellsBiomacromolecules
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The comparative spreading behavior of enantiomeric and racemic tyrosine amphiphiles

1985

Several derivatives of tyrosine or its methyl ester have been synthesized in which the para hydroxyl group on the aromatic side chain has been converted to a long chain alkyl ether or urethane. The surface behavior of these compounds is discussed. Enantiomeric discrimination, the ability of a chiral molecule to distinguish between mirror-image stereoisomers, has been investigated for the urethane derivates by comparing the surface pressure-area isotherms of the enantiomer with that of the racemic compound. Enantiomeric discrimination was demonstrated for the methyl ester analog, but was not conclusively observed for the zwitterionic compounds. Possible structural requirements for enantiomer…

Polymers and PlasticsStereochemistryorganic chemicalschemistry.chemical_compoundColloid and Surface ChemistrychemistryPulmonary surfactantMonolayerAmphiphilepolycyclic compoundsMaterials ChemistrySide chainOrganic chemistryheterocyclic compoundsPhenolsPhysical and Theoretical ChemistryTyrosineEnantiomerEnantiomeric excessColloid & Polymer Science
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Orientation, recognition, and photoreaction of nucleolipids in model membranes

1990

Amphiphiles with nucleobases and nucleosides as headgroups have been synthesized. Their surface behavior was investigated in monolayers at the air/water interface. The double chain nucleolipids form stable monolayers with nearly identical surface pressure-area diagrams, whereas the spreading behavior of the mono chain amphiphiles is dominated by the various nucleobase-headgroups. When measuring the interactions between nucleolipid monolayers and nucleobases (monomeric and polymeric ones), specific base-base effects could be observed: the complementary nucleobases solubilized in the subphase expand the monolayer more than the non-complementary ones. Photodimerization reactions of thymine-amp…

Polymers and PlasticsStereochemistrytechnology industry and agricultureSynthetic membraneNucleobaseDouble chainCrystallographychemistry.chemical_compoundColloid and Surface ChemistryMonomerMembranechemistrySolubilizationMonolayerAmphiphileMaterials ChemistryPhysical and Theoretical ChemistryColloid & Polymer Science
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