Search results for "Amphiphile"

showing 10 items of 270 documents

Solid lipid nanoparticles from amphiphilic calixpyrroles

2016

Abstract Hypothesis Macrocyclic amphiphiles form interesting self-assembling structures, including solid lipid nanoparticles, which have potential applications in drug encapsulation. Aryl-extended calixpyrroles, which act as anion binding hosts, are expected to form solid lipid nanoparticles, even though the alkyl chains have unusual perpendicular geometry with respect to the hydrophilic head group. The preparation conditions and the alkyl chain length should affect the size and stability of the particles. Experiments Solid lipid nanoparticles of two aryl-extended calixpyrroles with resorcinol walls and either meso-dodecyl or meso-methyl alkyl chains were compared. Ethanolic solutions of th…

Nanoparticleamphiphilesolid lipid nanoparticle02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialszeta potentialColloid and Surface ChemistryDynamic light scatteringSolid lipid nanoparticleZeta potentialnanoparticle tracking analysisOrganic chemistrySurface chargeAnion bindingcalixpyrroleta116Alkylchemistry.chemical_classificationdynamic light scattering021001 nanoscience & nanotechnology540104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryChemical engineeringParticle size0210 nano-technologymacrocycle
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From Single Molecules to Nanostructured Functional Materials: Formation of a Magnetic Foam Catalyzed by Pd@FexO Heterodimers

2017

Multicomponent nanostructures containing purely organic or inorganic as well as hybrid organic–inorganic components connected through a solid interface are, unlike conventional spherical particles, able to combine different or even incompatible properties within a single entity. They are multifunctional and resemble molecular amphiphiles, like surfactants or block copolymers, which makes them attractive for the self-assembly of complex structures, drug delivery, bioimaging, or catalysis. We have synthesized Pd@FexO heterodimer nanoparticles (NPs) to fabricate a macroporous, hydrophobic, magnetically active, three-dimensional (3D), and template-free hybrid foam capable of repeatedly separati…

NanostructureMaterials scienceHydrosilylationNucleationNanoparticleNanochemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesNanomaterial-based catalyst0104 chemical scienceschemistry.chemical_compoundChemical engineeringchemistryAmphiphileGeneral Materials Science0210 nano-technologyHybrid materialACS Applied Nano Materials
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Secondary-Structure-Driven Self-Assembly of Reactive Polypept(o)ides: Controlling Size, Shape, and Function of Core Cross-Linked Nanostructures.

2017

Achieving precise control over the morphology and function of polymeric nanostructures during self-assembly remains a challenge in materials as well as biomedical science, especially when independent control over particle properties is desired. Herein, we report on nanostructures derived from amphiphilic block copolypept(o)ides by secondary-structure-directed self-assembly, presenting a strategy to adjust core polarity and function separately from particle preparation in a bioreversible manner. The peptide-inherent process of secondary-structure formation allows for the synthesis of spherical and worm-like core-cross-linked architectures from the same block copolymer, introducing a simple y…

NanostructureMaterials sciencePolarity (physics)Nanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMicelleCatalysis0104 chemical sciencesAmphiphileCopolymerParticleSelf-assembly0210 nano-technologyBlock (data storage)Angewandte Chemie (International ed. in English)
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Nanoassemblies Based on Supramolecular Complexes of Nonionic Amphiphilic Cyclodextrin and Sorafenib as Effective Weapons to Kill Human HCC Cells

2015

Sorafenib (Sor), an effective chemiotherapeutic drug utilized against hepatocellular carcinoma (HOC), robustly interacts with nonionic amphiphilic cyclodextrin (aCD, SC6OH), forming, in aqueous solution, supramolecular complexes that behave as building blocks of highly water-dispersible colloidal nanoassemblies. SC6OH/Sor complex has been characterized by complementary spectroscopic techniques, such as UV-vis, steady-state fluorescence and anisotropy, resonance light scattering and H-1 NMR. The spectroscopic evidences and experiments carried out in the presence of an adamantane derivative, which competes with drug for CD cavity, agree with the entrapment of Sor in aCD, pointing out the role…

NiacinamideErythrocytesPolymers and PlasticsCell SurvivalAdamantaneDrug CompoundingSupramolecular chemistryBioengineeringNanotechnologyAdamantaneAntineoplastic AgentsBinding CompetitiveHemolysisAmphiphilic Cyclodextrins; Nanoparticles; Sorafenib; HCC cellsHCC cellsBiomaterialschemistry.chemical_compoundSurface-Active AgentsIn vivoCell Line TumorAmphiphileMaterials ChemistryHumanschemistry.chemical_classificationCyclodextrinsAqueous solutionCyclodextrinPhenylurea CompoundsSorafenibFluorescenceCombinatorial chemistrydigestive system diseasesNanostructuresBINDING INTERACTION THERAPY PHARMACOKINETICS BIOAVAILABILITY NANOPARTICLESDrug LiberationKineticsnanoassembliecyclodextrinchemistryDelayed-Action PreparationsProton NMRHepatocytes
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1993

Nonlinear opticalChemistryAmphiphilePolymer chemistryMonolayerNonlinear opticsRing-opening metathesis polymerisationReactivity (chemistry)ChromophoreRing-opening polymerizationDie Makromolekulare Chemie, Rapid Communications
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Optically Active Hyperbranched Polyglycerol as Scaffold for Covalent and Noncovalent Immobilization of Platinum(II) NCN-Pincer Complexes. Catalytic A…

2004

New optically active hyperbranched polymers have been used as microenvironments as well as scaffolds for noncovalent and covalent immobilization of pincer platinum(II) complexes, respectively. The catalytic activity/selectivity of the incorporated platinum(II) complexes in these polymeric chiral supports was investigated. Chiral amphiphilic hyperbranched polyglycerols with core−shell “nanocapsules” structure, namely (−)-P(G40C160.5) (1) and (+)-P(G73C160.5) (2), have been prepared in two straightforward steps by ring-opening multibranching polymerization (ROMBP) of either (−)- or (+)-glycidol, resulting in (−)-PG40 (Mn = 3000, Mw/Mn = 1.3) or (+)-PG73 (Mn = 5500, Mw/Mn = 1.6), respectively.…

Organic Chemistrychemistry.chemical_elementCatalysisPincer movementInorganic Chemistrychemistry.chemical_compoundSulfonatechemistryPolymerizationCovalent bondAmphiphilePolymer chemistryPhysical and Theoretical ChemistrySelectivityPlatinumOrganometallics
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P(HPMA)-block-P(LA) copolymers in paclitaxel formulations: Polylactide stereochemistry controls micellization, cellular uptake kinetics, intracellula…

2012

In order to explore the influence of polymer microstructure and stereochemistry in biological settings, the synthesis, micellization, cellular fate and the use in paclitaxel formulations of poly(N-(2-hydroxypropyl)-methacrylamide)-block-poly(L-lactide) (P(HPMA)-block-P(LLA)) and poly(N-(2-hydroxypropyl)-methacrylamide)-block-poly(DL-lactide) block copolymers (P(HPMA)-block-P(DLLA)) were studied. To this end, P(HPMA)-block-P(lactide) block copolymers and their fluorescently labeled analogues were synthesized. The polymers exhibited molecular weights M-n around 20,000 g/mol with dispersities (D=M-w/M-n) below 1.3. In addition, the solution conformation of this new type of partially degradable…

PaclitaxelStereochemistryCell SurvivalPolyestersTacticityMolecular ConformationPharmaceutical ScienceMicellechemistry.chemical_compoundTacticityAmphiphilePolymer chemistryPolylactide block copolymersCopolymerHumansReversible addition−fragmentation chain-transfer polymerizationMicelleschemistry.chemical_classificationLactideRAFT polymerizationPoly(N-(2-hydroxypropyl)-methacrylamideBiological TransportPolymerStructure activity relationshipAntineoplastic Agents PhytogenicKineticschemistryDrug deliveryHPMA block copolymersMethacrylatesHeLa Cells
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Methods of protein surface PEGylation under structure preservation for the emulsion-based formation of stable nanoparticles

2016

Proteins show remarkable versatility as multifunctional materials for therapeutic applications. They can be easily modified with the toolkit of bioorganic chemistry and are particularly attractive because of their degradability and biocompatibility. Herein, we evaluate different methods for the attachment of multiple PEG chains on the surface of the enzyme lysozyme. For this, we activated standard 2 kDa mPEG chains with four different electrophilic groups and tested their ability to react with different amino acids on the surface of our model protein. The aim was to find an effective and at the same time mild modification method that preserves the native structure and activity of the enzyme…

PharmacologyBiocompatibilityChemistryOrganic ChemistryPharmaceutical ScienceNanoparticle02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesDrug DiscoveryEmulsionPEG ratioAmphiphilePEGylationMolecular MedicineBioorganic chemistryOrganic chemistrySolubility0210 nano-technologyMedChemComm
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Development of polymer-based nanoparticles for Zileuton delivery to the lung : PMeOx and PMeOzi surface chemistry reduces interactions with mucins

2021

In this paper, two amphiphilic graft copolymers were synthesized by grafting polylactic acid (PLA) as hydrophobic chain and poly(2-methyl-2-oxazoline) (PMeOx) or poly(2-methyl-2-oxazine) (PMeOzi) as hydrophilic chain, respectively, to a backbone of α,β-poly(N-2-hydroxyethyl)-D,L-aspartamide (PHEA). These original graft copolymers were used to prepare nanoparticles delivering Zileuton in inhalation therapy. Among various tested methods, direct nanoprecipitation proved to be the best technique to prepare nanoparticles with the smallest dimensions, the narrowest dimensional distribution and a spherical shape. To overcome the size limitations for administration by inhalation, the nano-into-micr…

Poly(2-oxazoline)sPolymers116 Chemical sciencesPharmaceutical ScienceMedicine (miscellaneous)Nanoparticle02 engineering and technology01 natural scienceschemistry.chemical_compoundDrug Delivery SystemsNanoparticlePolylactic acidCopolymerPolyaminesHydroxyureaGeneral Materials SciencePoly(2-oxazine)sDRUG-DELIVERYCells Culturedchemistry.chemical_classificationDrug CarriersCHALLENGESAIRWAY MUCUSPolymer021001 nanoscience & nanotechnologyGraftingDIFFUSIONPolyaspartamidePULMONARY DELIVERYDrug deliveryMolecular Medicine0210 nano-technologyHydrophobic and Hydrophilic Interactionsmedicine.drugLung inflammationPolyestersBiomedical EngineeringINHIBITIONBioengineeringBronchi010402 general chemistryPolylactic acidZileutonAmphiphileAdministration InhalationmedicineHumansPoly(2-oxazoline)RELEASEMucinsBronchial DiseasesEpithelial CellsZileuton0104 chemical scienceschemistryChemical engineeringSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoNanoparticlesASTHMAPoly(2-oxazine)
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Mucoadhesive PEGylated inulin-based self-assembling nanoparticles: In vitro and ex vivo transcorneal permeation enhancement of corticosteroids

2019

Abstract As transcorneal drug delivery is still a challenge, the scope of the present study was to prepare useful nanosystems able to enhance transcorneal permeation/penetration of drugs. Moreover, this work aims to evaluate the effectiveness of inulin-based nanosystems in the specific field of ocular drug delivery and the effect of PEG chains to promote mucoadhesion, stability and transcorneal penetration/permeation enhancer effect of self-assembling nanoparticles in vitro (transwell systems and HCE) and ex vivo (Franz cells and bovine cornea). In particular, inulin was chosen as the starting natural polysaccharide polymer to design a novel amphiphilic derivative named INU-EDA-RA-PEG capab…

Polyethylene glycolInulin Self-assembling nanoparticles Transcorneal delivery Retinoic acid Polyethylene glycolTranscorneal deliveryInulinInulinSelf-assembling nanoparticlesPharmaceutical ScienceNanoparticle02 engineering and technologyPenetration (firestop)Permeation021001 nanoscience & nanotechnology030226 pharmacology & pharmacy03 medical and health scienceschemistry.chemical_compound0302 clinical medicinechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliveryAmphiphilePEG ratioRetinoic acidMucoadhesionBiophysics0210 nano-technologyJournal of Drug Delivery Science and Technology
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