Search results for "Amphiphile"

showing 10 items of 270 documents

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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Reactive Self-Assembly and Specific Cellular Delivery of NCO-sP(EO-stat-PO)-Derived Nanogels

2018

This study presents the reactive self-assembly of isocyanate functional and amphiphilic six-arm, star-shaped polyether prepolymers in water into nanogels. Intrinsic molecular amphiphilicity, mainly driven by the isophorone moiety at the distal endings of the star-shaped molecules, allows for the preparation of spherical particles with an adjustable size of 100-200 nm by self-assembly and subsequent covalent cross-linking without the need for organic solvents or surfactants. Covalent attachment of a fluorescence dye and either the cell-penetrating TAT peptide or a random control peptide sequence shows that only TAT-labeled nanogels are internalized by HeLa cells. The nanogels thus specifical…

Polymers and Plasticsta221Bioengineering02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene GlycolsBiokemia solu- ja molekyylibiologia - Biochemistry cell and molecular biologyBiomaterialschemistry.chemical_compoundnanogelsDrug Delivery SystemsAmphiphileMaterials ChemistryHumansPolyethyleneimineMoleculeMoietynanopolymeeritreactive self-assemblyPeptide sequenceFluorescent DyesIsophoronegeelitta1182nanobiotekniikka021001 nanoscience & nanotechnologyIsocyanate0104 chemical scienceschemistryCovalent bondBiophysicsNanoparticlesSelf-assembly0210 nano-technologyHeLa CellsBiotechnology
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Hydrophilic/Hydrophobic Nanostripes in Lipopolymer Monolayers

2000

PolymersAir water interfaceChemistryElectronsAtomic and Molecular Physics and OpticsNanostructuresPolyethylene GlycolsChemical engineeringLiposomesAmphiphileMonolayerPhysical and Theoretical ChemistryHydrophilic hydrophobicHydrophobic and Hydrophilic InteractionsAmphiphilic copolymerChemPhysChem
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Interaction Between drug loaded Polyaspartamide-polylactide-polisorbate based micelles and cell membrane models: a calorimetric study

2011

Amphiphilic biodegradable copolymers, for their ability to self-assemble into micelle-like aggregates, with a suitable loading capacity, are of emerging interest for the delivery of water-insoluble drugs. α,β-Poly[(N-hydroxyethyl)-dl-aspartamide] (PHEA) is suitable to obtain amphiphilic graft copolymers. These copolymers can be obtained starting from PHEA-ethylenediamine (PHEA-EDA) which is functionalized with polysorbate 80 (PS₈₀, like targeting residues to the brain) and polylactide (PLA, like hydrophobic chains) in order to obtain polymeric micelles of PHEA-EDA-PS₈₀-PLA potentially useful to release drugs to the central nervous system. In this paper, the interaction and absorption of PHE…

PolymersPolyestersFlurbiprofenPolysorbatesPharmaceutical ScienceMicellechemistry.chemical_compoundDifferential scanning calorimetryDrug DiscoveryAmphiphilemedicineMicellesPolysorbateLiposomeCalorimetry Differential ScanningChemistryVesiclepolyaspartamide polysorbate micellesCell MembraneBiological membraneKineticsSpectrometry FluorescenceFlurbiprofenSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoLiposomesBiophysicsMolecular Medicinelipids (amino acids peptides and proteins)medicine.drug
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Coordinative Binding of Polymers to Metal-Organic Framework Nanoparticles for Control of Interactions at the Biointerface

2019

Metal-organic framework nanoparticles (MOF NPs) are of growing interest in diagnostic and therapeutic applications, and due to their hybrid nature, they display enhanced properties compared to more established nanomaterials. The effective application of MOF NPs, however, is often hampered by limited control of their surface chemistry and understanding of their interactions at the biointerface. Using a surface coating approach, we found that coordinative polymer binding to Zr- fum NPs is a convenient way for peripheral surface functionalization. Different polymers with biomedical relevance were assessed for the ability to bind to the MOF surface. Carboxylic acid and amine containing polymers…

PolymersSurface PropertiesGeneral Physics and AstronomyNanoparticleBiointerfaceNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesNanomaterialsAmphiphileHumansGeneral Materials ScienceMetal-Organic Frameworkschemistry.chemical_classificationChemistryfungiGeneral EngineeringProteinsBiological TransportPolymer021001 nanoscience & nanotechnology0104 chemical sciencesSurface coatingNanoparticlesSurface modificationMetal-organic frameworkZirconium0210 nano-technologyHeLa CellsProtein Binding
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Correct oligomerization is a prerequisite for insertion of the central molecular domain of staphylococcal α-toxin into the lipid bilayer

1995

Staphylococcal alpha-toxin is a primarily hydrophilic molecule that binds as a monomer to target membranes and then aggregates to form amphiphilic oligomers that represent water-filled transmembrane channels. Current evidence indicates that a region located in the center of the molecule inserts deeply into the bilayer. In the present study, we sought to determine whether membrane insertion was triggered by the oligomerization process, and whether insertion correlated with pore formation. Double mutants of alpha-toxin were prepared in which His-35 was replaced by Arg, and cysteine residues were introduced at positions 69, 130 and 186. Substitution of His-35 with Arg rendered the toxin molecu…

Pore formationBacterial ToxinsLipid BilayersMolecular ConformationBiophysics(Staphylococcus)Arginineα-ToxinBiochemistryHemolysin ProteinsMembrane Lipidschemistry.chemical_compound2-NaphthylamineAmphiphileOligomerizationCysteineLipid bilayerFluorescent DyesTransmembrane channelsPore-forming toxinBilayerCell BiologyMembraneMonomerchemistryBiochemistryMutationPore-forming toxinBiophysicsMembrane insertionCysteineBiochimica et Biophysica Acta (BBA) - Biomembranes
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Impact of Branching on the Solution Behavior and Serum Stability of Starlike Block Copolymers.

2019

The size control of nanomedicines for tumor diagnosis and therapy is of high importance, since it enables or disables deep and sufficient tumor penetration. Amphiphilic star-shaped block copolypept(o)ides offer substantial promise to precisely adjust the hydrophobic core and the hydrophilic corona, independent of each other, and therefore simultaneously control the size dimension in the interesting size range from 10 to 30 nm. To gain access to core-shell structures of such sizes, 3-arm and 6-arm PeptoStars, based on poly(gamma-tert-butyloxycarbonyl-L-glutamate)-b-polysarcosine (pGlu(OtBu)-b-pSar), were prepared via controlled living ring-opening polymerization (ROP) of the corresponding N-…

Protein Conformation alpha-HelicalMaterials sciencePolymers and PlasticsPolysarcosineSize-exclusion chromatographyBioengineering02 engineering and technology010402 general chemistryBranching (polymer chemistry)01 natural sciencesPolymerizationBiomaterialsPlasmaAmphiphileMaterials ChemistryCopolymerHumanschemistry.chemical_classificationMolecular massSarcosinePolymer021001 nanoscience & nanotechnology0104 chemical sciencesPolymerizationchemistryChemical engineeringNanoparticlesProtein Corona0210 nano-technologyPeptidesOligopeptidesBiomacromolecules
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Natural or synthetic nucleic acids encapsulated in a closed cavity of amphiphiles

2013

In this review some aspects of the interactions of organized structures of amphiphiles with natural or synthetic DNAs are briefly considered. In particular DNAs encapsulated in closed cavities of amphiphiles, specifically giant vesicles and water-in-oil droplets and reverse micelles, are dealt with. Two main applications of giant vesicles are reviewed in detail, namely their use as microreactors where reactions can be followed by optical microscopy on a single vesicle and in synthetic biology as protocell models or as potential semi-synthetic ‘‘living’’ cells. Water-in-oil droplets uses for rapid and relatively low-cost DNA amplification by PCR reaction are described as well as for in vitro…

ProtocellAqueous solutionChemistryGeneral Chemical EngineeringVesicleNanotechnologyGeneral ChemistrymicroreactorsMicellepolynucleotides in water-in-oil dropletsSynthetic biologyDNA model polynucleotides giant vesicles Reverse micellesPolynucleotideAmphiphileBiophysicsNucleic acidmicroreactors; polynucleotides in giant vesicles; polynucleotides in water-in-oil dropletspolynucleotides in giant vesiclesRSC Advances
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