Search results for "MICELLES"

showing 10 items of 233 documents

Micelles, Rods, Liposomes, and Other Supramolecular Surfactant Aggregates: Computational Approaches

2017

Surfactants are an interesting class of compounds characterized by the segregation of polar and apolar domains in the same molecule. This peculiarity makes possible a whole series of microscopic and macroscopic effects. Among their features, their ability to segregate particles (fluids or entire domains) and to reduce the surface/interfacial tension is the utmost important. The interest in the chemistry of surfactants never weakened; instead, waves of increasing interest have occurred every time a new field of application of these molecules has been discovered. All these special characteristics depend largely on the ability of surfactants to self-assemble and constitute supramolecular struc…

Molecular dynamicSupramolecular chemistryIonic bondingNanotechnologyHealth Informatics010402 general chemistry01 natural sciencesMicelleGeneral Biochemistry Genetics and Molecular BiologySurface tensionSurface-Active AgentsMolecular dynamicsPulmonary surfactantSurfactantSide chainMoleculeComputer SimulationRodMicellesBiochemistry Genetics and Molecular Biology (all)Mass spectrometryChemistry010401 analytical chemistryWaterComputer Science Applications1707 Computer Vision and Pattern Recognition0104 chemical sciencesComputer Science ApplicationsLiposomeChemical physicsLiposomesGasesMicelle
researchProduct

Nanoparticulate Systems for Drug Delivery and Targeting to the Central Nervous System

2010

Brain delivery is one of the major challenges for the neuropharmaceutical industry since an alarming increase in brain disease incidence is going on. Despite major advances in neuroscience, many potential therapeutic agents are denied access to the central nervous system (CNS) because of the existence of a physiological low permeable barrier, the blood-brain barrier (BBB). To obtain an improvement of drug CNS performance, sophisticated approaches such as nanoparticulate systems are rapidly developing. Many recent data demonstrate that drugs could be transported successfully into the brain using colloidal systems after i.v. injection by several mechanisms such as endocytosis or P-glycoprotei…

Movement disorders/Parkinson’s diseaseDrug CarriersPolymersSurface PropertiesReviewsBrainAlzheimer's diseaseMultiple sclerosisDrug Delivery SystemsMovement disorders/Parkinson's diseaseSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoLiposomesNeuropsychopharmacology.AnimalsHumansNanoparticlesMultiple sclerosiParticle SizeNeuropsychopharmacologyAlzheimer’s diseaseMicellesCentral Nervous System Agents
researchProduct

Galactosylated polymeric carriers for liver targeting of sorafenib

2014

In this paper, we describe the preparation of liver-targeted polymeric micelles potentially able to carry sorafenib to hepatocytes for treatment of hepatocarcinoma (HCC), exploiting the presence of carbohydrate receptors, ASGPR. These micelles were prepared starting from a galactosylated polylactide-polyaminoacid conjugate. This latter was obtained by chemical reaction of α,β-poly(N-2-hydroxyethyl) (2-aminoethylcarbamate)-d,l-aspartamide (PHEA-EDA) with polylactic acid (PLA), and subsequent reaction with lactose, leading to PHEA-EDA-PLA-GAL copolymer. Liver-targeted sorafenib-loaded micelles were obtained in aqueous media at low PHEA-EDA-PLA-GAL copolymer concentration value with nanometer …

NiacinamideSorafenibBiodistributionPolyestersBiological AvailabilityPharmaceutical ScienceAntineoplastic AgentsPharmacologyKidneyMicellechemistry.chemical_compoundPolylactic acidHepatic cell-targeted carriersmedicineZeta potentialAnimalsLungneoplasmsMicellesDrug CarriersActive targetingPhenylurea CompoundsHepatic cell-targeted carrierGalactoseActive targeting; Galactosylation; Hepatic cell-targeted carriers; Polymeric micellesSorafenibEthylenediaminesdigestive system diseasesMice Inbred C57BLLiverBiochemistrychemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoGalactosylationDrug deliveryPolymeric micellesFemalePeptidesDrug carrierSpleenmedicine.drugConjugateInternational Journal of Pharmaceutics
researchProduct

Photocleavable core cross-linked polymeric micelles of polypept(o)ides and ruthenium(II) complexes

2021

Core cross-linking of polymeric micelles has been demonstrated to contribute to enhanced stability that can improve the therapeutic efficacy. Photochemistry has the potential to provide spatial resolution and on-demand drug release. In this study, light-sensitive polypyridyl-ruthenium(II) complexes were combined with polypept(o)ides for photocleavable core cross-linked polymeric micelles. Block copolymers of polysarcosine-block-poly(glutamic acid) were synthesized by ring-opening N-carboxyanhydride polymerization and modified with aromatic nitrile-groups on the glutamic acid side chain. The modified copolymers self-assembled into micelles and were cross-linked by cis-diaquabis(2,2'-bipyridi…

NitrileCell SurvivalPolymersBiomedical Engineeringchemistry.chemical_elementMicelleChorioallantoic MembraneGel permeation chromatographychemistry.chemical_compoundMicroscopy Electron TransmissionCell Line TumorPolymer chemistrySide chainCopolymerAnimalsHumansGeneral Materials ScienceMicellesPhotolysisCryoelectron MicroscopyGeneral ChemistryGeneral MedicineRutheniumchemistryPolymerizationRuthenium CompoundsPeptidesChickensLinker
researchProduct

About entangled networks of worm-like micelles: a rejected hypothesis

1996

We report new results from small-angle neutron scattering on d(1 2)-cyclohexane/lecithin/water micellar solutions performed as a function of the water content (w(o)), temperature (T) and dispersed phase volume fraction (phi). The data from dilute samples are interpretable in terms of the existence of giant cylindrical reverse micelles and are well fit with a core-shell model (that provides the micelle structure and dimensions) with values of 28 and 45 Angstrom for the inner core and the outer shell radii, almost independent on temperature and concentration. Such a result could appear consistent with the current idea that worm-like micelles are living polymers. On the contrary, the appearanc…

ORGANOGELSPolymers and PlasticsSANSChemistryInner coreForm factor (quantum field theory)Concentration effectThermodynamicsMineralogyliving polymersNeutron scatteringgelsSmall-angle neutron scatteringMicelleLIGHT-SCATTERINGCondensed Matter::Soft Condensed MatterColloid and Surface ChemistryMICROEMULSIONSMicellar solutionsMaterials Chemistryreverse micellesPhysical and Theoretical ChemistryStructure factorLECITHIN REVERSE MICELLESColloid and Polymer Science
researchProduct

Micellar versus hydro-organic mobile phases for retention-hydrophobicity relationship studies with ionizable diuretics and an anionic surfactant

2004

Abstract Logarithm of retention factors (log  k ) of a group of 14 ionizable diuretics were correlated with the molecular (log  P o/w ) and apparent (log  P app ) octanol–water partition coefficients. The compounds were chromatographed using aqueous–organic (reversed-phase liquid chromatography, RPLC) and micellar–organic mobile phases (micellar liquid chromatography, MLC) with the anionic surfactant sodium dodecyl sulfate (SDS), in the pH range 3–7, and a conventional octadecylsilane column. Acetonitrile was used as the organic modifier in both modes. The quality of the correlations obtained for log  P app at varying ionization degree confirms that this correction is required in the aqueou…

OctanolsChromatographyStatic ElectricityOrganic ChemistryAnalytical chemistryWaterGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPartition coefficientHydrophobic effectSurface-Active Agentschemistry.chemical_compoundchemistryPulmonary surfactantMicellar liquid chromatographySpectrophotometry UltravioletSodium dodecyl sulfateDiureticsAcetonitrileChromatography High Pressure LiquidMicellesJournal of Chromatography A
researchProduct

STRATEGIE DI DIREZIONAMENTO ALL’EPATOCARCINOMA DI FARMACI ANTITUMORALI MEDIANTE SISTEMI NANOPARTICELLARI E DI VISUALIZZAZIONE IN CELLULE TUMORALI DEL…

Lo scopo di questo lavoro di tesi è stato quello di realizzare nuovi sistemi nanoparticellari per il direzionamento di farmaci o di agenti per l’imaging, potenzialmente utilizzabili per la terapia e/o per la diagnosi dell’epatocarcinoma (HCC), in particolare per quelle forme caratterizzate dall’overespressione del recettore di membrana degli epatociti ASGP-R o del recettore mitocondriale TSPO. In particolare, nel capitolo 2 sono state descritte la sintesi, la caratterizzazione chimico fisica, la capacità di internalizzazione cellulare e l’efficacia antitumorale di un nuovo sistema nanoparticellare, costituito da un dendrimero a struttura poli-amido-aminica (PAMAM) di quarta generazione, opp…

PAMAM dendrimerLactobionic acidQD nanoparticleTSPO receptorSPIONimagingSorafenibASGPR receptor; TSPO receptor; HEPATOCELLULAR CARCINOMA; Lactobionic acid; Sorafenib; PAMAM dendrimer; QD nanoparticles; Micelles pegilated; SPION; magnetic targeting;imaging;magnetic targetingASGPR receptorMicelles pegilatedSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoHEPATOCELLULAR CARCINOMA
researchProduct

Spectroscopic characterization of red perylimide/surfactant nanocomposites

2011

Novel photoluminescent materials formed by some selected surfactants, metal derivatives of bis(2-ethylhexyl) sulfosuccinate (M(AOT)n; M = Na+, Co2+, Er3+ and Yb3+), bis(2-ethylhexyl) amine (BEEA), bis(2-ethylhexy1) phosphoric acid (HDEHP) and a 1:1 BEEA/HDEHP mixture, doped with the red perylimide (ROT-300) have been prepared, and their optical properties have been tested by absorption spectroscopy and steady state and timeresolved fluorescence. Experimental results show spectral shifts of the typical ROT-300 absorption and fluorescence bands with respect to that in apolar solvent medium. Data analysis leads consistently to attribute this feature mainly to the freezing of the diffusive move…

PERYLENEROT ASEMaterials sciencePhotoluminescenceDye laserMICELLESAbsorption spectroscopyDYEMechanical EngineeringAnalytical chemistryDNAFluorescenceMicelleMechanics of MaterialsLiquid crystalGeneral Materials ScienceLASERAbsorption (chemistry)LuminescenceSettore CHIM/02 - Chimica Fisica
researchProduct

SMOOTHLY SHIFTING FLUORESCENT WINDOW: TUNABLE “OFF-ON-OFF” MICELLAR BIOSENSORS FOR pH

2009

POLYMERIC MICELLES fluorescent biosensorpH-windowSettore CHIM/09 - Farmaceutico Tecnologico Applicativoself-assembling
researchProduct

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
researchProduct