Search results for "Liberation"

showing 10 items of 198 documents

Chitosan-coated mesoporous MIL-100(Fe) nanoparticles as improved bio-compatible oral nanocarriers

2017

Nanometric biocompatible Metal-Organic Frameworks (nanoMOFs) are promising candidates for drug delivery. Up to now, most studies have targeted the intravenous route, related to pain and severe complications; whereas nanoMOFs for oral administration, a commonly used non-invasive and simpler route, remains however unexplored. We propose here the biofriendly preparation of a suitable oral nanocarrier based on the benchmarked biocompatible mesoporous iron(III) trimesate nanoparticles coated with the bioadhesive polysaccharide chitosan (CS). This method does not hamper the textural/structural properties and the sorption/release abilities of the nanoMOFs upon surface engineering. The interaction …

Materials scienceBiocompatibilityBioadhesiveQuímica organometàl·licaNanoparticleAdministration OralNanotechnology02 engineering and technologySurface engineering010402 general chemistry01 natural sciencesFerric CompoundsArticleChitosanchemistry.chemical_compoundHumansChitosanMultidisciplinaryNanotecnologia021001 nanoscience & nanotechnology3. Good health0104 chemical sciencesDrug LiberationKineticsLysergic Acid DiethylamideEnterocyteschemistryDrug deliveryNanoparticlesNanocarriersCaco-2 Cells0210 nano-technologyMesoporous material
researchProduct

Folic acid-functionalized graphene oxide nanosheets via plasma etching as a platform to combine NIR anticancer phototherapy and targeted drug deliver…

2020

PEGylated graphene oxide (GO) has shown potential as NIR converting agent to produce local heat useful in breast cancer therapy, since its suitable photothermal conversion, high stability in physiological fluids, biocompatibility and huge specific surface. GO is an appealing nanomaterial for potential clinical applications combining drug delivery and photothermal therapy in a single nano-device capable of specifically targeting breast cancer cells. However, native GO sheets have large dimensions (0.5-5 mu m) such that tumor accumulation after a systemic administration is usually precluded. Herein, we report a step-by-step synthesis of folic acid-functionalized PEGylated GO, henceforth named…

Materials scienceBiocompatibilityPlasma GasesCell SurvivalInfrared RaysBioengineeringNanotechnologyAntineoplastic Agents02 engineering and technology010402 general chemistrySettore CHIM/04 - Chimica Industriale01 natural sciencesNANOMEDICINECell LinePolyethylene GlycolsBiomaterialsBreast cancerBreast cancerFolic AcidCell MovementmedicineNANOPARTICLESABLATIONHumansDoxorubicinCANCER-CELLSAGENTSGraphene oxideDrug Carrierstechnology industry and agriculturePhotothermal therapyPhototherapy021001 nanoscience & nanotechnologymedicine.disease0104 chemical sciencesNanostructuresDrug LiberationTargeted drug deliverySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoMechanics of MaterialsDoxorubicinCancer cellDrug deliveryDoxorubicin HydrochlorideGraphiteSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologySYSTEMmedicine.drugMaterials scienceengineering. C, Materials for biological applications
researchProduct

Spray-Drying, Solvent-Casting and Freeze-Drying Techniques: a Comparative Study on their Suitability for the Enhancement of Drug Dissolution Rates.

2019

Purpose Solid dispersions (SDs) represent the most common formulation technique used to increase the dissolution rate of a drug. In this work, the three most common methods used to prepare SDs, namely spray-drying, solvent-casting and freezedrying, have been compared in order to investigate their effect on increasing drug dissolution rate. Methods Three formulation strategies were used to prepare a polymer mixture of polyvinyl-alcohol (PVA) and maltodextrin (MDX) as SDs loaded with the following three model drugs, all of which possess a poor solubility: Olanzapine, Dexamethasone, and Triamcinolone acetonide. The SDs obtained were analysed and compared in terms of drug particle size, drug-lo…

Materials scienceDrug Compoundingdissolution rate . freeze-drying . solid dispersion . solvent-casting method . spray-dryingPharmaceutical Science02 engineering and technology030226 pharmacology & pharmacyTriamcinolone AcetonideDexamethasoneExcipients03 medical and health sciencesFreeze-dryingchemistry.chemical_compound0302 clinical medicinePolysaccharidesPharmacology (medical)Dissolution testingSolubilityDesiccationDissolutionPharmacologyOrganic Chemistry021001 nanoscience & nanotechnologyMaltodextrinSolventDrug LiberationFreeze DryingChemical engineeringchemistryPharmaceutical PreparationsSolubilityOlanzapineSpray dryingPolyvinyl AlcoholSolventsMolecular MedicineParticle size0210 nano-technologyBiotechnologyPharmaceutical research
researchProduct

Mechanical, degradation and drug-release behavior of nano-grained Fe-Ag composites for biomedical applications.

2018

Abstract An original fabrication route of high-strength bulk Fe-5Ag and Fe-10Ag nanocomposites with enhanced degradation rate is reported. Near fully dense materials with fine nanostructures and uniform distribution of Ag nanoparticles were obtained employing high energy attrition milling of Fe-Ag2O powder blends followed by cold sintering – high pressure consolidation at ambient temperature that allowed the retention of the nanoscale structure. Annealing in hydrogen flow at 550 °C resulted in enhanced ductility without coarsening the nanostructure. The strength in compression of Fe5Ag and Fe10Ag nanocomposites was several-fold higher than the values reported for similar composites with mic…

Materials scienceNanostructureHot TemperatureSilverAnnealing (metallurgy)Cell SurvivalIronBiomedical EngineeringSinteringMetal Nanoparticles02 engineering and technology010402 general chemistry01 natural sciencesCorrosionBiomaterialsFlexural strengthVancomycinNano-ElectrochemistryHumansComposite materialMechanical PhenomenaDrug CarriersNanocompositeOsteoblasts021001 nanoscience & nanotechnologyGrain size0104 chemical sciencesCorrosionDrug LiberationMechanics of Materials0210 nano-technologyJournal of the mechanical behavior of biomedical materials
researchProduct

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
researchProduct

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
researchProduct

Influence of Polyvinyl Alcohol (PVA) on PVA-Poly-N-hydroxyethyl-aspartamide (PVA-PHEA) Microcrystalline Solid Dispersion Films

2020

AbstractThis study was conducted to formulate buccal films consisting of polyvinyl alcohol (PVA) and poly-N-hydroxyethyl-aspartamide (PHEA), to improve the dissolution of the drug through the oral mucosa. Ibuprofen sodium salt was used as a model drug, and the buccal film was expected to enhance its dissolution rate. Two different concentrations of PVA (5% w/v and 7.5% w/v) were used. Solvent casting was used to prepare films, where a solution consisting of drug and polymer was cast and allowed to dry. Attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM) were used to investigate the pr…

Materials sciencePolymersbuccal filmPharmaceutical ScienceIbuprofen02 engineering and technologyAquatic Science030226 pharmacology & pharmacyPolyvinyl alcohol03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDifferential scanning calorimetrySpectroscopy Fourier Transform InfraredDrug Discoveryibuprofen sodiumcrystallineSolubilityFourier transform infrared spectroscopyDissolutionPolyhydroxyethyl MethacrylateEcology Evolution Behavior and SystematicsAspartic AcidCalorimetry Differential ScanningEcologyGeneral MedicinePHEA021001 nanoscience & nanotechnologyAmidesSolventDrug LiberationMicrocrystallineSolubilitychemistryPolyvinyl AlcoholAttenuated total reflectionPVAMicroscopy Electron ScanningCrystallization0210 nano-technologyAgronomy and Crop ScienceResearch ArticleNuclear chemistry
researchProduct

COLLECTIVE DELIBERATION: A CONTEMPORARY CONTRIBUTION OF BRAZILIAN BIOETHICS TO THE SUS' (UNIFIELD HEALTH SERVICE) PRACTICES

2017

Resumo Este ensaio teve por objetivo analisar a necessidade de nova excelência profissional pautada na deliberação coletiva, debatendo a ética aplicada às questões de saúde nas experiências de Brasil e Espanha. O funcionamento prático dos comitês de bioética na Espanha avança na constituição do método deliberativo como participação coletiva na decisão profissional, discutindo a importância da democracia deliberativa para a construção de nova civilidade ética. No Brasil, após as primeiras décadas de construção do Sistema Único de Saúde, amplia-se o leque de participação dos profissionais, primeiramente nos conselhos de saúde e, com a resolução CNS n. 196/96, também nos comitês de ética em pe…

Medicine (General)030504 nursingexcelência profissionalprofessional excellenceexcelencia profesionaldeliberaçãoEducation (General)solidariedade críticadeliberacióndeliberation03 medical and health sciences0302 clinical medicinecritical solidarityR5-920democracia deliberativasolidaridad crítica030212 general & internal medicineL7-991bioética0305 other medical sciencebioethicsdeliberative democracy
researchProduct

Controlled Release of Metformin Hydrochloride from Core-Shell Nanofibers with Fish Sarcoplasmic Protein

2019

Ficai, Anton/0000-0002-1777-0525; Karademir, Betul/0000-0003-1762-0284 WOS:000503463400074 PubMed ID: 31658758 Background and Objectives: A coaxial electrospinning technique was used to produce core/shell nanofibers of a polylactic acid (PLA) as a shell and a polyvinyl alcohol (PVA) containing metformin hydrochloride (MH) as a core. Materials and Methods: Fish sarcoplasmic protein (FSP) was extracted from fresh bonito and incorporated into nanofiber at various concentrations to investigate the influence on properties of the coaxial nanofibers. The morphology, chemical structure and thermal properties of the nanofibers were studied. Results: The results show that uniform and bead-free struct…

Medicine (General)POLYMERIC NANOFIBERSChemical structurewound healingIn Vitro Techniquescoaxial electrospinningPolyvinyl alcoholArticleDELIVERYCrystallinitychemistry.chemical_compoundcoaxial electrospinning; fish sarcoplasmic protein; nanofibers; wound healingR5-920Differential scanning calorimetryPolylactic acidnanofibersSpectroscopy Fourier Transform InfraredMedicineAnimalsbusiness.industryTunaGeneral MedicineControlled releaseMetforminfish sarcoplasmic proteinDrug LiberationSarcoplasmic ReticulumchemistryChemical engineeringNanofiberDelayed-Action PreparationsPolyvinyl AlcoholELECTROSPUN NANOFIBERSCoaxialbusinessFIBERSMATRICES
researchProduct

Mechanistic analysis and experimental verification of bicarbonate-controlled enteric coat dissolution: Potential in vivo implications

2019

Enteric coatings have shown in vivo dissolution rates that are poorly predicted by traditional in vitro tests, with the in vivo dissolution being considerably slower than in vitro. To provide a more mechanistic understanding of this, the dependence of the release properties of various enteric-coated (EC) products on bulk pH and bicarbonate molarity was investigated. It was found that, at presumably in vivo-relevant values, the bicarbonate molarity is a more significant determinant of the dissolution profile than the bulk pH. The findings also indicate that this steep relationship between the dissolution of enteric coatings and bicarbonate molarity limits those coatings' performance in vivo.…

Molar concentrationChemistry PharmaceuticalBicarbonateInorganic chemistryKineticsPharmaceutical ScienceCapsules02 engineering and technologyBuffers030226 pharmacology & pharmacyExcipientsDiffusion layer03 medical and health scienceschemistry.chemical_compoundHypromellose Derivatives0302 clinical medicineIntestine SmallmedicineHumansIntestinal MucosaMesalamineDissolutionAcetaminophenCarbonic acidGeneral MedicineHydrogen-Ion Concentration021001 nanoscience & nanotechnologyEnteric coatingBicarbonatesDrug LiberationModels ChemicalSolubilitychemistryCarbon dioxide0210 nano-technologyBiotechnologymedicine.drugEuropean Journal of Pharmaceutics and Biopharmaceutics
researchProduct