Search results for "CARRIERS"

showing 10 items of 391 documents

Evaluation of the interaction and drug release from alpha,beta-polyaspartamide derivatives to a biomembrane model

2005

This article reports on a comparative study on the ability of various polymers, containing hydrophilic and/or hydrophobic groups, to interact with a biomembrane model using the differential scanning calorimetry (DSC) technique. Multilamellar vesicles of mixed dimyristoylphosphatidylcholine (DMPC) and dimyristoylphosphatidic acid (DMPA) were chosen as a model of cell membranes. The investigated samples were a water soluble polymer, the alpha,beta-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA) and its derivatives partially functionalized with polyethylene glycol (PEG2000) to obtain PHEA-PEG2000, with hexadecylamine (C16) to obtain PHEA-C16, and with both compounds to obtain PHEA-PEG2000-C16. Th…

Materials sciencePolymersPharmaceutical SciencePolyethylene glycolGlycerophospholipidsMicellePolyethylene Glycolschemistry.chemical_compoundDifferential scanning calorimetryOrganic chemistryAminesMicelleschemistry.chemical_classificationDrug CarriersAniline CompoundsCalorimetry Differential ScanningPOLYASTARTAMIDE DRUG RELEASE BIOMEMBRANE MODELVesicleAnti-Inflammatory Agents Non-Steroidaltechnology industry and agricultureTemperatureBiological membraneMembranes ArtificialGeneral MedicinePolymerCombinatorial chemistryHydrocarbonsMembranechemistrySolubilityKetoprofenDrug deliverylipids (amino acids peptides and proteins)DimyristoylphosphatidylcholinePeptides
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HPMA-based block copolymers promote differential drug delivery kinetics for hydrophobic and amphiphilic molecules.

2015

Abstract We describe a method how polymeric nanoparticles stabilized with (2-hydroxypropyl)methacrylamide (HPMA)-based block copolymers are used as drug delivery systems for a fast release of hydrophobic and a controlled release of an amphiphilic molecule. The versatile method of the miniemulsion solvent-evaporation technique was used to prepare polystyrene (PS) as well as poly-d/l-lactide (PDLLA) nanoparticles. Covalently bound or physically adsorbed fluorescent dyes labeled the particles’ core and their block copolymer corona. Confocal laser scanning microscopy (CLSM) in combination with flow cytometry measurements were applied to demonstrate the burst release of a fluorescent hydrophobic…

Materials sciencePolymersPolyestersBiomedical EngineeringNanoparticleFluorescent Antibody TechniqueNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryBiomaterialschemistry.chemical_compoundSurface-Active AgentsDrug Delivery SystemsAmphiphileCopolymerMethacrylamideHumansMolecular BiologyDrug CarriersGeneral MedicineLipid Droplets021001 nanoscience & nanotechnologyControlled release0104 chemical sciencesMiniemulsionDrug LiberationKineticschemistryDrug deliveryBiophysicsMethacrylatesNanoparticlesPolystyrenesNanocarriers0210 nano-technologyHydrophobic and Hydrophilic InteractionsBiotechnologyHeLa CellsActa biomaterialia
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Process parameters of microsphere preparation based on propylene carbonate emulsion-precursors.

2020

This study aimed for a detailed understanding of the impact of different process parameters involved during celecoxib-loaded microsphere preparation based on propylene carbonate emulsion-precursors.Microspheres were prepared by a modified emulsification-solvent extraction method. Performed investigations included polymer solubility and viscosity, microsphere size, morphology and stability, propylene carbonate content as well as celecoxib solid state, content and release.Rough-walled round microspheres with sizes between 21 µm and 122 µm and an internal sponge-like structure filled with residual propylene carbonate (content between 1.9 ± 0.1% and 6.7 ± 0.5% w/w) were obtained. Encapsulation …

Materials sciencePolymersSurface PropertiesChemistry PharmaceuticalDrug CompoundingPharmaceutical ScienceBioengineering02 engineering and technologyPolypropylenes030226 pharmacology & pharmacyMicrosphere03 medical and health scienceschemistry.chemical_compound0302 clinical medicineColloid and Surface ChemistryLactic AcidPhysical and Theoretical ChemistryParticle SizeDrug CarriersCalorimetry Differential ScanningViscosityOrganic Chemistry021001 nanoscience & nanotechnologyMicrospheresPLGADrug LiberationchemistryChemical engineeringSolubilityCelecoxibScientific methodPropylene carbonateEmulsionMicroscopy Electron ScanningSolventsEmulsions0210 nano-technologyPolyglycolic AcidJournal of microencapsulation
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High-resolution investigation of nanoparticle interaction with a model pulmonary surfactant monolayer.

2012

The pulmonary surfactant film spanning the inner alveolar surface prevents alveolar collapse during the end-exhalation and reduces the work of breathing. Nanoparticles (NPs) present in the atmosphere or nanocarriers targeted through the pulmonary route for medical purposes challenge this biological barrier. During interaction with or passage of NPs through the alveolar surfactant, the biophysical functioning of the film may be altered. However, experimental evidence showing detailed biophysical interaction of NPs with the pulmonary surfactant film are scant. In this study, we have investigated the impact of a hydrophobic polyorganosiloxane (AmOrSil20) NPs on the integrity as well as on the …

Materials scienceSiloxanesPolymersSurface PropertiesGeneral Physics and AstronomyHigh resolutionNanoparticleNanotechnologyMicroscopy Atomic Forcelaw.inventionPulmonary surfactantlawMonolayerGeneral Materials ScienceStructural organizationtechnology industry and agricultureGeneral EngineeringPulmonary Surfactantsrespiratory systemKineticsPhase imagingBiophysicsNanoparticlesElectron microscopeNanocarriersHydrophobic and Hydrophilic InteractionsACS nano
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Hybrid supramolecular gels of Fmoc-F/halloysite nanotubes: Systems for sustained release of camptothecin

2017

Supramolecular gel hybrids obtained by self-assembly of Fmoc-L-phenylalanine (Fmoc-F) in the presence of functionalized halloysite nanotubes (f-HNT) were obtained in biocompatible solvents and employed as carriers for the delivery of camptothecin (CPT) molecules. The synthesis of the new f-HNT material as well as its characterization are described. The properties of the hybrid hydrogels and organogels were analyzed by several techniques. The presence of small amounts of f-HNT allows good dispersion of the tubes and the subsequent formation of homogeneous gels. The experimental results show that f-HNT functions only as an additive in the hybrid gels and does not demonstrate gelator behavior.…

Materials scienceSupramolecular chemistryBiomedical EngineeringNanotechnology02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteChemistry (all); Biomedical Engineering; Materials Science (all)HeLamedicineMoleculeGeneral Materials Sciencehalloysite supramolecular gel campthotecin drug delivery rheological propertiesSettore CHIM/02 - Chimica FisicabiologyChemistry (all)Settore CHIM/06 - Chimica OrganicaGeneral ChemistryGeneral Medicine021001 nanoscience & nanotechnologybiology.organism_classification0104 chemical sciencesSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiChemical engineeringSelf-healing hydrogelsengineeringMaterials Science (all)Nanocarriers0210 nano-technologyDrug carrierCamptothecinmedicine.drug
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Cancer phototherapy in living cells by multiphoton release of doxorubicin from gold nanospheres

2020

Doxorubicin is a widely used but toxic cancer chemotherapeutic agent. In order to localize its therapeutic action and minimize side effects, it was covalently conjugated to peptide-encapsulated gold nanospheres by click-chemistry and then photo-released in a controlled fashion by a multiphoton process. Selective treatment of a chosen region in a 2D layer of U2Os cancer cells is shown by driving photorelease with 561 nm irradiation at mu W power. These results show promising directions for the development of practical applications based on nanocarriers that can ensure drug delivery with high spatial and temporal control.

Materials scienceTherapeutic actionBiomedical EngineeringCancerNanotechnologyGeneral ChemistryGeneral MedicineConjugated systemGold nanospheresmedicine.diseaseDrug deliveryCancer cellmedicineGeneral Materials ScienceDoxorubicinNanocarriersmedicine.drug
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Relaxation of photogenerated carriers in P3HT:PCBM organic blends.

2009

Relaxing in the sunlight. Long time-transient decays of photogenerated carriers in P3HT:PCBM blends for organic solar cells are interpreted in terms of the relaxation of hole carriers in a broad density of states. The after-pulse time-resolved microwave conductivity (TRMC) decays observed in P3HT:PCBM blends display a dependence on time close to t−β, independent of excitation intensity, in the 10 ns–1 μs range. This is explained in terms of the relaxation of carriers in a Gaussian density of states (DOS). The model is based on a demarcation level that moves with time by thermal release and retrapping of initially trapped carriers. The model shows that when the disorder is large the after-pu…

Materials scienceTime FactorsGeneral Chemical EngineeringThiophenesMolecular physicschemistry.chemical_compoundNuclear magnetic resonanceThermalSolar EnergyEnvironmental ChemistryGeneral Materials ScienceMicrowavesRange (particle radiation)photochemistryRelaxation (NMR)General EnergychemistryChlorobenzenesolar cellstransportCharge carrierPolymer blendFullerenesDispersion (chemistry)Excitationpolymer blendscharge carriersChemSusChem
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Nanovectorization of TRAIL with single wall carbon nanotubes enhances tumor cell killing

2015

International audience; Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL or Apo2L) is a member of the tumor necrosis factor (TNF) superfamily. This type II transmembrane protein is able to bound specifically to cancer cell receptors (i.e., TRAIL-R1 (or DR4) and TRAIL-R2 (or DR5)) and to induce apoptosis without being toxic for healthy cells. Because membrane-bound TRAIL induces stronger receptor aggregation and apoptosis than soluble TRAIL, we proposed here to vectorize TRAIL using single-walled carbon nanotubes (SWCNTs) to mimic membrane TRAIL. Owing to their exceptional and revolutional properties, carbon nanotubes, especially SWCNTs, are used in a wide range of physical or,…

Materials science[SDV.BIO]Life Sciences [q-bio]/BiotechnologyStereochemistryCarbon nanotubesBioengineeringTRAIL02 engineering and technologyTNF-Related Apoptosis-Inducing Ligand03 medical and health sciencesMicroscopy Electron TransmissionCell Line TumorNeoplasms[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyHumans[CHIM]Chemical SciencesGeneral Materials Science[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyReceptor[ SDV.BBM ] Life Sciences [q-bio]/Biochemistry Molecular BiologyComputingMilieux_MISCELLANEOUS030304 developmental biologyReceptor Aggregation0303 health sciencesNanotubes CarbonMechanical Engineeringnanovector[ SDV.BIO ] Life Sciences [q-bio]/BiotechnologyGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsnanomedicineTransmembrane protein[SDV.BIO] Life Sciences [q-bio]/BiotechnologyReceptors TNF-Related Apoptosis-Inducing LigandCell cultureApoptosisCancer cellCancer researchcancer therapydeath receptorTumor necrosis factor alphaNanocarriers0210 nano-technology
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Physical characterization of alginate-Pluronic F127 gel for endoluminal NABDs delivery

2014

Here we focus the attention on the physical characteristics of a highly biocompatible hydrogel made up of crosslinked alginate and Pluronic F127 (PF127). This is a composite polymeric blend we propose for artery endoluminal delivery of an emerging class of molecules named nucleic acid based drugs (NABDs). The physical characterization of our composite gel, i.e. mesh size distribution and PF127-alginate mutual organization after crosslinking, can significantly determine the NABDs release kinetics. Thus, to explore these aspects, different technical approaches, i.e. rheology, low/high field NMR and TEM, were used. While rheology provided information at the macroscopic and nano-level, the othe…

Materials sciencegel pavingAlginatesKineticsComposite numberNanotechnologyPoloxamerMicellerestenosisRheologyalginateArterial wallMicellesDrug Carriersgel paving; rheology; NMR; alginate; Pluronic; restenosisGeneral ChemistryPluronicPoloxamerCondensed Matter PhysicsNMRCharacterization (materials science)Chemical engineeringSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSolute diffusionrheologyNABDs release kinetics PF127 alginate gel paved stent artery endoluminal deliveryGels
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Short-course treatment of visceral leishmaniasis with liposomal amphotericin B (AmBisome).

1996

We evaluated liposomal amphotericin B (AmBisome; Vestar, San Dimas, CA) administered to 88 immunocompetent patients (56 children) with visceral leishmaniasis (VL) caused by Leishmania infantum. Thirteen patients received 4 mg/kg on days 1-5 and 10 (total dose, 24 mg/kg), and all were cured; 42 received 3 mg/kg on days 1-5 and 10 (18 mg/kg), and 41 were cured; 32 received 3 mg/kg on days 1-4 and 10 (15 mg/kg), and 29 were cured (amastigotes were not cleared from 1 child, and 2 relapsed). One adult was cured with a total dose of 12mg/kg. The four children who were not cured received 3 mg/kg for 10 days; none had further relapses. There were no significant adverse events. For VL due to L. infa…

Microbiology (medical)AdultMalemedicine.medical_specialtyAntifungal AgentsAdolescentmedicine.medical_treatmentGastroenterologyDrug Administration ScheduleleishmanisisInternal medicineAmphotericin BAmphotericin BMedicinevisceral leishmaniasisAnimalsHumansLeishmania infantumAdverse effectChildChemotherapyDrug Carriersbiologybusiness.industryInfantLeishmaniasisMiddle Agedmedicine.diseasebiology.organism_classificationSurgeryInfectious DiseasesVisceral leishmaniasisTreatment OutcomeTotal doseChild PreschoolLiposomesLeishmaniasis VisceralLiposomal amphotericinFemaleLeishmania infantumbusinessmedicine.drugClinical infectious diseases : an official publication of the Infectious Diseases Society of America
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