Search results for " micelles"

showing 10 items of 84 documents

Tamoxifen-loaded polymeric micelles: preparation, physico-chemical characterization and in vitro evaluation studies.

2004

Several samples of polymeric micelles, formed by amphiphilic derivatives of PHEA, obtained by grafting into polymeric backbone of PEGs and/or hexadecylamine groups (PHEA-PEG-C(16) and PHEA-C(16)) and containing different amount of Tamoxifen, were prepared. All Tamoxifen-loaded polymeric micelles showed to increase drug water solubility. TEM studies provided evidence of the formation of supramolecular core/shell architectures containing drug, in the nanoscopic range and with spherical shape. Samples with different amount of encapsulated Tamoxifen were subjected to in vitro cytotoxic studies in order to evaluate the effect of Tamoxifen micellization on cell growth inhibition. All samples of T…

Polymers and PlasticsAntineoplastic Agents HormonalPolymersSupramolecular chemistryBioengineeringMicellePolyethylene GlycolsBiomaterialsPlasmaDrug Delivery SystemsTamoxifen polymeric micelles polyaspartammideAmphiphileMaterials ChemistryOrganic chemistryHumansMicellesAqueous solutionMolecular StructureChemistryHydrogen-Ion ConcentrationTamoxifenMembraneSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliveryLiberationDrug carrierPeptidesBiotechnologyNuclear chemistryMacromolecular bioscience
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in vitro biological evaluation of folate-functionalized block copolymer micelles for selective anti-cancer drug delivery.

2008

The main objective of this study was to evaluate the ability of folic acid-functionalized diblock copolymer micelles to improve the delivery and uptake of two poorly water-soluble anti-tumor drugs, tamoxifen and paclitaxel, to cancer cells through folate receptor targeting. The diblock copolymer used in this study comprised a hydrophilic poly[2-(methacryloyloxy)ethyl phosphorylcholine] (MPC) block, carrying at the chain end the folate targeting moiety, and a pH-sensitive hydrophobic poly[2-(diisopropylamino)ethyl methacrylate] (DPA) block (FA-MPC-DPA). The drug-loading capacities of tamoxifen- and paclitaxel-loaded micelles were determined by high performance liquid chromatography and the m…

Polymers and PlasticsPaclitaxelPhosphorylcholineBioengineeringMicelleBiomaterialsDrug Delivery SystemsFolic AcidPolymethacrylic AcidsPolymer chemistryBLOCK COPOLYMERS MICELLES DRUG DELIVERYMaterials ChemistryHumansCytotoxicityMicellesPhosphorylcholineChemistryAntineoplastic Agents PhytogenicEnd-groupTamoxifenSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoFolate receptorCancer cellBiophysicsCaco-2 CellsDrug carrierK562 CellsFolate targetingBiotechnologyMacromolecular bioscience
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Physicochemical investigation of cobalt?iron cyanide nanoparticles synthesized by a novel solid?solid reaction in confined space

2004

Cobalt–iron cyanide (Cox[Fe(CN)6]) nanoparticles have been synthesized by a novel solid–solid reaction in the confined space of dry sodium bis(2-ethylhexyl)sulfosuccinate (AOT) reversed micelles dispersed in n-heptane. The reaction has been carried out by mixing two dry AOT/n-heptane solutions containing CoCl2 and K4Fe(CN)6 or K3Fe(CN)6 nanoparticles in the micellar core, respectively. By UV-Vis spectroscopy it was ascertained that, after the mixing process, the formation of stable nanoparticles is fast and complete. Microcalorimetric measurements of the thermal effect due to the Cox[Fe(CN)6] nanoparticle formation allowed the determination of the stoichiometric ratio (x) and of the molar e…

Polymers and PlasticsSmall-angle X-ray scatteringCyanidechemistry.chemical_elementNanoparticleMicellechemistry.chemical_compoundColloid and Surface ChemistryAdsorptionCobalt–iron cyanide complexes Nanoparticles Solid–solid reaction Confinement effect AOT reversed micelleschemistryX-ray photoelectron spectroscopyMaterials ChemistryPhysical chemistryOrganic chemistryPhysical and Theoretical ChemistryCobaltStoichiometrySettore CHIM/02 - Chimica FisicaColloid and Polymer Science
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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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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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GALACTOSE-FUNCTIONALISED POLYMERIC MICELLES AS HEPATOCYTE-TARGETED CARRIERS

2012

RIBAVIRIN TRIPALMITATELIVER TARGETINGPOLYMERIC MICELLES
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Kinetic evidence for the solubilization of pyridine-2-azo-p-dimethylaniline in alkanediyl-α,ω-bis(dimethylcetylammonium nitrate) surfactants. Role of…

2004

The incorporation of the bidentate ligand pyridine-2-azo-p-dimethylaniline (PADA) into micellar aggregates of the dimeric cationic surfactants propanediyl-, hexanediyl- and dodecanediyl-alpha,omega-bis(dimethylcetylammonium nitrate) (16-3-16,2NO(3)(-), 16-6-16,2NO(3)(-) and 16-12-16,2NO(3)(-), respectively) has been studied at 25 degreesC by examining the kinetics of the complexation reaction of the Ni(II) ion with this ligand. For comparison, cetyltrimethylammonium nitrate ( CTAN), which can be considered as the "monomeric'' surfactant of 16-3-16,2NO(3)(-), has also been used. The kinetic data have shown that, for 16-3-16,2NO(3)(-) and CTAN, at a surfactant concentration below the critical…

Reaction mechanismInorganic chemistryMicelleCATIONIC GEMINI SURFACTANTSCatalysisHydrophobic effectReaction rate constantPulmonary surfactantDIMERIC SURFACTANTSPolymer chemistryMaterials ChemistryWATERELECTRON TRANSFERANGLE NEUTRON SCATTERINGInterfaces (materials) Optical waveguides metal ionsAqueous solutionAGGREGATION PROPERTIESChemistryAQUEOUS SOLUTIONCationic polymerizationGeneral ChemistryANIONIC MICELLESSUBSTITUTED FERROCENESCritical micelle concentrationBROMIDE SURFACTANTSANGLE NEUTRON SCATTERING; CATIONIC GEMINI SURFACTANTS; AQUEOUS SOLUTION; BROMIDE SURFACTANTS; DIMERIC SURFACTANTS; SUBSTITUTED FERROCENES; AGGREGATION PROPERTIES; ELECTRON TRANSFER; ANIONIC MICELLES; WATERNew J. Chem.
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Cholesterol-Inulin Conjugates for Efficient SN38 Nuclear Delivery: Nanomedicines for Precision Cancer Therapy

2022

An amphiphilic inulin-thiocholesterol conjugate (INU-Cys-TC) was strategically designed as a biodegradable core-shell nanocarrier of 7-ethyl-10-hydroxy-camptothecin (SN38) to enhance its solubility and stability in aqueous media, thus exploiting its brilliant anticancer effect. INU-Cys-TC was designed to have the hydrophilic inulin backbone (external shell) partially functionalized with hydrophobic thiocholesterol moieties (internal core) through a biodegradable disulfide bond due to cysteamine bridges. Thiocholesterol moieties impair redox-sensitive self-assembling abilities, yielding to nano-sized micelles in aqueous media capable of efficiently encapsulating a high amount of SN38 (DL = 8…

SN38Cancer ResearchinulinOncologytriple negative breast cancerdrug deliverycolorectal cancerpolymeric micellesinulin; SN38; drug delivery; polymeric micelles; colorectal cancer; triple negative breast cancerCancers; Volume 14; Issue 19; Pages: 4857
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Inulin derivatives obtained via enhanced microwave synthesis as potential drug delivery system.

2013

Settore CHIM/09 - Farmaceutico Tecnologico ApplicativoInulin enanched microwave synthesisDoxorubicin micelles
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NOVEL AMPHIPHILIC COPOLYMERS BASED ON POLYASPARTAMIDE GRAFT WITH SQUALENE RESIDUES TO OBTAIN MICELLES AS COLLOIDAL DRUG CARRIERS.

2009

Settore CHIM/09 - Farmaceutico Tecnologico ApplicativoPHEA SQUALENE MICELLES DRUG CARRIERS.
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