Search results for "drug delivery."

showing 10 items of 692 documents

Biocompatible polymers coated Solid Lipid Microparticles (SLM) for pulmonary delivery

2015

FLUTICASONE PROPIONATEdrug deliverypolymers microparticles lungLIPID NANOPARTICLESLUNG
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Highly Homogeneous Biotinylated Carbon Nanodots: Red-Emitting Nanoheaters as Theranostic Agents toward Precision Cancer Medicine

2019

Very recent red-emissive carbon nanodots (CDs) have shown potential as near-infrared converting tools to produce local heat useful in cancer theranostics. Besides, CDs seem very appealing for clinical applications combining hyperthermia, imaging, and drug delivery in a single platform capable of selectively targeting cancer cells. However, CDs still suffer from dramatic dot-to-dot variability issues such that a rational design of their structural, optical, and chemical characteristics for medical applications has been impossible so far. Herein, we report for the first time a simple and highly controllable layer-by-layer synthesis of biotin-decorated CDs with monodisperse size distribution, …

Fluorescence-lifetime imaging microscopyphotothermal therapyMaterials scienceCell SurvivalAntineoplastic AgentsNanotechnology02 engineering and technology010402 general chemistrytargeted cancer therapy01 natural sciencesDrug Delivery Systemsbiotincarbon nanodotCell Line TumorCarbon nanodotsHumansGeneral Materials SciencePrecision MedicineRational designimagingPhotothermal therapy021001 nanoscience & nanotechnologyCarbonNanostructures0104 chemical sciencesbiotin; carbon nanodots; imaging; photothermal therapy; targeted cancer therapy.Settore CHIM/09 - Farmaceutico Tecnologico ApplicativoBiotinylationDrug deliveryCancer cellMCF-7 CellsSurface modification0210 nano-technologyACS Applied Materials & Interfaces
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Photoluminescent decoration of iron oxide magnetic nanoparticles for dual-imaging applications

2018

A selective functionalization of dopamine amino group with the photoluminescent 7-nitroben-zofurazan was achieved through a one-pot protection-functionalization-deprotection sequence. The resulting fluorescent catecholic ligand was used as a capping agent for iron oxide nanoparticles thus obtaining photoluminescent magnetic nanoparticles (PL-MNPs). The PL-MNPs were then embedded into PLGA-b-PEG polymeric nanocarriers which quenched the emission of the capping agent. Full recovery of fluorescence was observed after disassembling the polymeric layer of the nanoparticle, thus supporting the use of PL-MNPs as a multifunctional system for targeted drug delivery.

Fluorescent nanoparticleMaterials scienceAtomic and Molecular Physics and OpticDopamineMagnetic nanoparticleIron oxideNanoparticleNanotechnologyBioengineering02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundGeneral Materials ScienceChemistry (all)technology industry and agricultureSettore CHIM/06 - Chimica OrganicaGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsFluorescenceAtomic and Molecular Physics and Optics0104 chemical scienceschemistryTargeted drug deliveryDual-imagingModeling and SimulationDrug deliveryDrug deliverySurface modificationMagnetic nanoparticlesMaterials Science (all)0210 nano-technologyIron oxide nanoparticles
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Development of injectable and durable kefiran hydro-alcoholic gels.

2020

Injectable, in-situ forming kefiran gels have been developed for potential applications as implantable drug delivery devices or scaffolds for tissue regeneration. Concentrated solutions (4, 5 and 6%w) of kefiran, extracted from kefir grains, have been assessed in term of viscosity and injectability through G26 syringe needles, and for their ability to undergo gelation upon mixing with different alcohols. Propylene glycol (PG) has been selected as gelling agent because it ensures homogenous gelation in relatively short times (from few minutes up to 6 h). The investigation of the rheological behavior of kefiran/PG gels varying polymer concentration and temperature (25 degrees C and 37 degrees…

GelationXYLOGLUCANCell Survival02 engineering and technologyBiochemistryPolyvinyl alcoholSCAFFOLDSCULTURE03 medical and health scienceschemistry.chemical_compoundViscosityDrug Delivery SystemsRheologyStructural BiologyPolysaccharidesmedicineHumansKefiran gelsMolecular BiologyKINETICS030304 developmental biologyCell Proliferationchemistry.chemical_classification0303 health sciencesIn-situ forming gelsIn-situ forming gelKefiranHydrogelsGeneral MedicineBuffer solutionPolymer021001 nanoscience & nanotechnologyPropylene GlycolChemical engineeringchemistryAlcoholsDrug deliverySettore CHIM/07 - Fondamenti Chimici Delle TecnologieSwellingmedicine.symptom0210 nano-technologyRheologyInternational journal of biological macromolecules
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Disparity between Inter-Patient Molecular Heterogeneity and Repertoires of Target Drugs Used for Different Types of Cancer in Clinical Oncology

2020

Inter-patient molecular heterogeneity is the major declared driver of an expanding variety of anticancer drugs and personalizing their prescriptions. Here, we compared interpatient molecular heterogeneities of tumors and repertoires of drugs or their molecular targets currently in use in clinical oncology. We estimated molecular heterogeneity using genomic (whole exome sequencing) and transcriptomic (RNA sequencing) data for 4890 tumors taken from The Cancer Genome Atlas database. For thirteen major cancer types, we compared heterogeneities at the levels of mutations and gene expression with the repertoires of targeted therapeutics and their molecular targets accepted by the current guideli…

Gene mutationMedical OncologychemotherapyGenomeTranscriptomelcsh:ChemistryDrug Delivery SystemsProstateNeoplasmstumor heterogeneityMedicineCluster AnalysisMolecular Targeted TherapyPathology MolecularPrecision Medicinelcsh:QH301-705.5targeted therapeuticscancer drugsSpectroscopyExome sequencingGeneral MedicineGenomicspersonalized medicineComputer Science ApplicationsDrug repositioningmedicine.anatomical_structureAntineoplastic AgentsComputational biologyCatalysisArticleInorganic Chemistrymolecular diagnosticsGenetic HeterogeneityDrug TherapyExome SequencingHumansPhysical and Theoretical ChemistryMolecular Biologygenomeclinical oncologybusiness.industryOrganic ChemistryMolecular diagnosticsmutationslcsh:Biology (General)lcsh:QD1-999MutationPersonalized medicinebusinesstranscriptomeInternational Journal of Molecular Sciences
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Natural payload delivery of the doxorubicin anticancer drug from boron nitride oxide nanosheets

2019

International audience; We studied the behavior of doxorubicin (DOX; an anticancer drug) molecules loaded on a boron nitride oxide nanosheet (BNO-NS) using the density functional theory (DFT), time-dependent density functional theory (TDDFT), and molecular dynamic (MD) simulation methods. We found that DOX molecules in pi-pi or covalent interaction with BNO-NS preserve their optical properties in water. Moreover, the BNO-NS vector allowed stabilizing the DOX molecules on a cellular membrane contrary to isolated DOX that randomly moved in the solvent box without any interaction with the cell membrane. From these results, we conclude that hydrophilic BNO-NS represents a good candidate for DOX…

General Physics and Astronomy02 engineering and technologyMolecular dynamics010402 general chemistry01 natural sciences[SPI.MAT]Engineering Sciences [physics]/MaterialsCell membranechemistry.chemical_compoundmedicinepolycyclic compoundsTime-dependent density functional theoryMolecule[CHIM]Chemical SciencesDoxorubicin[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicsBoron nitride oxide nanosheetsNanosheet[SPI.ACOU]Engineering Sciences [physics]/Acoustics [physics.class-ph]Therapeutic agentsChemistrytechnology industry and agricultureSurfaces and InterfacesGeneral ChemistryTime-dependent density functional theory021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsSolventmedicine.anatomical_structureBoron nitrideDrug deliveryBiophysics0210 nano-technologymedicine.drug
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Inhalable polymer-glycerosomes as safe and effective carriers for rifampicin delivery to the lungs

2016

Rifampicin loaded glycerosomes, vesicles composed of phospholipids, glycerol and water, were combined with trimethyl chitosan chloride (TMC) to prepare TMC-glycerosomes or, alternatively, with sodium hyaluronate (HY) to obtain HY-glycerosomes. These new hybrid nanovesicles were tested as carriers for pulmonary delivery of rifampicin. Glycerosomes without polymers were also prepared and characterized. All vesicles were similar: they were spherical, multilamellar and able to incorporate good amount of rifampicin (EE%∼55%). The addition of the polymers to the formulations allowed an increase of mean diameter. All the glycerosomes, in particular HY-glycerosomes, were able to deliver the drug to…

GlycerolMaleDrugStaphylococcus aureusCell SurvivalPolymersmedia_common.quotation_subjectSodium hyaluronateMicrobial Sensitivity Tests02 engineering and technologyPharmacology030226 pharmacology & pharmacy03 medical and health scienceschemistry.chemical_compoundDrug Delivery Systems0302 clinical medicineColloid and Surface ChemistryMicroscopy Electron TransmissionIn vivoAdministration InhalationGlycerolmedicineAnimalsHumansTissue DistributionRats WistarPhysical and Theoretical ChemistryAntibiotics AntitubercularLungmedia_commonDrug CarriersLiposomeVesicleSurfaces and InterfacesGeneral Medicine021001 nanoscience & nanotechnologychemistryA549 CellsLiposomesNanoparticlesRifampin0210 nano-technologyDrug carrierRifampicinBiotechnologymedicine.drugColloids and Surfaces B: Biointerfaces
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Phosphonylation Controls the Protein Corona of Multifunctional Polyglycerol-Modified Nanocarriers.

2018

Nanocarriers are a platform for modern drug delivery. In contact with blood, proteins adsorb to nanocarriers, altering their behavior in vivo. To reduce unspecific protein adsorption and unspecific cellular uptake, nanocarriers are modified with hydrophilic polymers like poly(ethylene glycol) (PEG). However, with PEG the attachment of further functional structures such as targeting units is limited. A method to introduce multifunctionality via polyglycerol (PG) while maintaining the hydrophilicity of PEG is introduced. Different amounts of negatively charged phosphonate groups (up to 29 mol%) are attached to the multifunctional PGs (Mn 2-4 kg mol-1 , Ð < 1.36) by post-modification. PGs are …

GlycerolPolymers and PlasticsPolymersBioengineeringProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene GlycolsBiomaterialschemistry.chemical_compoundPEG ratioMaterials ChemistryHumansDrug Carriers021001 nanoscience & nanotechnologyPhosphonate0104 chemical sciencesMiniemulsionchemistryDrug deliveryBiophysicsNanoparticlesProtein CoronaAdsorptionNanocarriers0210 nano-technologyEthylene glycolBiotechnologyProtein adsorptionMacromolecular bioscience
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Orthogonal Click Conjugation to the Liposomal Surface Reveals the Stability of the Lipid Anchorage as Crucial for Targeting

2016

Synthetic access to multiple surface decorations are a bottleneck in the development of liposomes for receptor mediated targeting. This opens a complex multiparameter space, exploration of which is severely limited in terms of sample numbers and turnaround times. Here, we unlock this technological barrier by a combination of a milligram-scale liposome formulation using dual centrifugation and orthogonal click chemistry on the liposomal surface. Application of these techniques to conceptually new amphiphilic compounds, which feature norbornene and alkyne groups at the apex of sterically stabilizing, hyperbranched polyglycerol moieties, revealed a particular influence of the membrane anchor o…

GlycerolPolymersStereochemistryAlkyne02 engineering and technology010402 general chemistry01 natural sciencesCatalysisFolic AcidAmphiphileHumanschemistry.chemical_classificationLiposomeOrganic ChemistryGeneral ChemistryReceptor-mediated endocytosis021001 nanoscience & nanotechnologyLipids0104 chemical sciencesCholesterolMembraneFolic acidchemistryLiposomesDrug deliveryClick chemistryBiophysicsClick Chemistry0210 nano-technologyChemistry - A European Journal
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New biodegradable hydrogels based on a photocrosslinkable modified polyaspartamide: synthesis and characterization

1999

Abstract α,β-Poly( N -2-hydroxyethyl)- dl -aspartamide (PHEA), a synthetic water-soluble biocompatible polymer, was derivatized with glycidyl methacrylate (GMA), in order to introduce in its structure chemical residues having double bonds and ester groups. The obtained copolymer (PHG) contained 29 mol% of GMA residues. PHG aqueous solutions at various concentrations ranging from 30 to 70 mg/ml were exposed to a source of UV rays at λ 254 nm in the presence or in the absence of N , N ′-methylenebisacrylamide (BIS); the formation of compact gel phases was observed beginning from 50 mg/ml. The obtained networks were characterized by FT-IR spectrophotometry and swelling measurements which evide…

Glycidyl methacrylateMagnetic Resonance SpectroscopyDouble bondPolymersUltraviolet RaysBiophysicsBiochemistryEsterasechemistry.chemical_compoundDrug Delivery SystemsEnzymatic hydrolysisSpectrophotometrySpectroscopy Fourier Transform InfraredPolymer chemistrymedicineCopolymerMolecular Biologychemistry.chemical_classificationAcrylamidesAqueous solutionmedicine.diagnostic_testChemistryWaterHydrogelsHydrogen-Ion ConcentrationBiodegradation EnvironmentalSelf-healing hydrogelsEpoxy CompoundsMethacrylatesPeptidesBiochimica et Biophysica Acta (BBA) - General Subjects
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