Search results for " pharmacy."

showing 10 items of 356 documents

Surface Functionality and Water Adsorption Studies of α-Aluminium (III) Oxide Nanoparticles by near Infrared Spectroscopy

2019

The adsorption of water on aluminium (III) oxide nanoparticle surface was studied by near infrared (NIR) spectroscopy. The comparison of NIR spectra at 40% and 60% humidity were reported in this work and were analyzed using second derivative techniques. The second derivative spectra were used to understand the chemistry of adsorption of water molecules. Small amounts of samples were dried under vacuum at 230 °C before the analysis. The analysis of the spectra confirms the presence of three different hydroxyl groups on aluminium (III) oxide surface. The spectra acquired during the adsorption of water molecules show the characteristic peaks in the range of 5400-5100 cm-1 corresponding to the …

Materials scienceMechanical EngineeringNear-infrared spectroscopyOxidechemistry.chemical_elementNanoparticle010501 environmental sciences030226 pharmacology & pharmacy01 natural sciences03 medical and health scienceschemistry.chemical_compound0302 clinical medicineAdsorptionchemistryChemical engineeringMechanics of MaterialsAluminiumGeneral Materials Science0105 earth and related environmental sciencesSecond derivativeKey Engineering Materials
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Study of Morphology of Reactive Dissolution Interface Using Fractal Geometry

1996

J. Pharm. Sci. ISI Document Delivery No.: VF662 Times Cited: 7 Cited Reference Count: 15 Tromelin, A Gnanou, JC Andres, C Pourcelot, Y Chaillot, B; International audience; The determination of reactive fractal dimension was carried out using two forms of the Noyes-Whitney equation, -dQ/dt = K(Q/Q(0))(DR/3) and -d Q/dt = K' R(DR-3) using the Richardson plot on the basis of previous data obtained by dissolution of an orthoboric acid powder. The correlation of the results provided by the two ways of calculation allows proposal of the hypothesis that dissolution begins on a specific population of reactive sites and probably promotes the formation of microporous volumes or cracks.

Materials scienceMorphology (linguistics)Pharmaceutical ScienceThermodynamics02 engineering and technology030226 pharmacology & pharmacyFractal dimension03 medical and health sciences0302 clinical medicineFractalfractaldimension[CHIM.ANAL]Chemical Sciences/Analytical chemistrysurface morphologysurfaceParticle SizeSolubilitydissolution rateDissolutionMicroporous material021001 nanoscience & nanotechnology[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[SDV.SP.PG]Life Sciences [q-bio]/Pharmaceutical sciences/Galenic pharmacologySolubilityMicroscopy Electron ScanningParticle size0210 nano-technologySpecific populationJournal of Pharmaceutical Sciences
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Influence of the parameters molecular structure and granularity on the compactibility of a powder

1995

Drug Dev. Ind. Pharm. ISI Document Delivery No.: RP128 Times Cited: 3 Cited Reference Count: 14 Andres, c ndiaye, a thomas, c tromelin, a chaillot, b pourcelot, y; International audience; The aim of this study was to determine whether it is possible to obtain better characterization of materials in order to find out if these one are suitable in Quality Assurance for direct tableting. We tried to show that a methodological approach combining chemical, physical and technological aspects could control the direct compression process. We chose orthoboric acid as a study model for the direct compression. From a chemical point of view, our findings show only one crystalline molecular structure (RX…

Materials sciencePharmaceutical Sciencemolecular structure02 engineering and technologypowdergranularity030226 pharmacology & pharmacy03 medical and health sciencesTableting0302 clinical medicineRheology[CHIM.ANAL]Chemical Sciences/Analytical chemistryDrug DiscoveryMoleculePharmacologyOrganic Chemistry021001 nanoscience & nanotechnologyCompression (physics)Characterization (materials science)[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallography[SDV.SP.PG]Life Sciences [q-bio]/Pharmaceutical sciences/Galenic pharmacologyGas pycnometerHomogeneouscompactibilityGranularity0210 nano-technologyBiological system
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Development and In Vitro Evaluation of Lyotropic Liquid Crystals for the Controlled Release of Dexamethasone.

2017

Made available in DSpace on 2018-12-11T17:33:26Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-08-02 Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) In this study, amphiphilic polymers were investigated as biomaterials that can control dexamethasone (DXM) release. Such materials present interfacial properties in the presence of water and an oily phase that can result in lyotropic liquid crystalline systems (LLCS). In addition, they can form colloidal nanostructures similar to those in living organisms, such as bilayers and hexagonal and cubic phases, which can be exploited to solubilize lipophilic drugs to sustain their release and enhance bioavailability. It was…

Materials sciencePolymers and PlasticsAmphiphilic polymersdexamethasone02 engineering and technology030226 pharmacology & pharmacyArticleDexamethasonelcsh:QD241-44103 medical and health scienceschemistry.chemical_compound0302 clinical medicinelcsh:Organic chemistryLyotropicControlled releaseNanostructured systemsLamellar structurelyotropic liquid crystalsIsopropyl myristatedrug releasechemistry.chemical_classificationPolarized light microscopyChromatographySmall-angle X-ray scatteringfungiDrug releaseGeneral ChemistryPolymerkinetic modelKinetic modelamphiphilic polymers; lyotropic liquid crystals; controlled release; drug release; kinetic model; dexamethasone; nanostructured systems021001 nanoscience & nanotechnologyControlled releaseLyotropic liquid crystalschemistryChemical engineeringnanostructured systemsLyotropic liquid crystal0210 nano-technologycontrolled releaseamphiphilic polymersPolymers
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Artificial neural network based particle size prediction of polymeric nanoparticles.

2017

Particle size of nanoparticles and the respective polydispersity are key factors influencing their biopharmaceutical behavior in a large variety of therapeutic applications. Predicting these attributes would skip many preliminary studies usually required to optimize formulations. The aim was to build a mathematical model capable of predicting the particle size of polymeric nanoparticles produced by a pharmaceutical polymer of choice. Polymer properties controlling the particle size were identified as molecular weight, hydrophobicity and surface activity, and were quantified by measuring polymer viscosity, contact angle and interfacial tension, respectively. A model was built using artificia…

Materials sciencePolymersChemistry PharmaceuticalDispersityPharmaceutical ScienceNanoparticleNanotechnology02 engineering and technology030226 pharmacology & pharmacyPolyethylene GlycolsSurface tensionContact angle03 medical and health sciencesViscosity0302 clinical medicineParticle Sizechemistry.chemical_classificationDrug CarriersGeneral MedicinePolymer021001 nanoscience & nanotechnologychemistryChemical engineeringParticleNanoparticlesParticle sizeNeural Networks Computer0210 nano-technologyBiotechnologyEuropean journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
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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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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
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A Novel Disintegration Tester for Solid Dosage Forms Enabling Adjustable Hydrodynamics.

2016

A modified in vitro disintegration test device was designed that enables the investigation of the influence of hydrodynamic conditions on disintegration of solid oral dosage forms. The device represents an improved derivative of the compendial PhEur/USP disintegration test device. By the application of a computerized numerical control, a variety of physiologically relevant moving velocities and profiles can be applied. With the help of computational fluid dynamics, the hydrodynamic and mechanical forces present in the probe chamber were characterized for a variety of device moving speeds. Furthermore, a proof of concept study aimed at the investigation of the influence of hydrodynamic condi…

Materials scienceTime FactorsPharmaceutical ScienceAdministration Oral02 engineering and technologyComputational fluid dynamics030226 pharmacology & pharmacyDosage form03 medical and health sciences0302 clinical medicineShear stressTechnology PharmaceuticalComputer SimulationImmediate releasebusiness.industryMechanicsModels Theoretical021001 nanoscience & nanotechnologyBody FluidsFasted stateHydrodynamics0210 nano-technologybusinessShear StrengthSoftwareTabletsJournal of pharmaceutical sciences
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Engineering of Nanofibrous Amorphous and Crystalline Solid Dispersions for Oral Drug Delivery

2018

Poor aqueous solubility (<0.1 mg/mL) affects a significant number of drugs currently on the market or under development. Several formulation strategies including salt formation, particle size reduction, and solid dispersion approaches have been employed with varied success. In this review, we focus primarily on the emerging trends in the generation of amorphous and micro/nano-crystalline solid dispersions using electrospinning to improve the dissolution rate and in turn the bioavailability of poorly water-soluble drugs. Electrospinning is a simple but versatile process that utilizes electrostatic forces to generate polymeric fibers and has been used for over 100 years to generate synthet…

Materials scienceamorphousoral drug deliveryPharmaceutical Sciencelcsh:RS1-44102 engineering and technologyReview030226 pharmacology & pharmacylcsh:Pharmacy and materia medica03 medical and health sciences0302 clinical medicineamorphoucrystallineaqueous solubility enhancementDissolutionelectrospinningsolid dispersion021001 nanoscience & nanotechnologyElectrospinningAmorphous solidSynthetic fiberChemical engineeringPARTICLE SIZE REDUCTION0210 nano-technologyDispersion (chemistry)Oral retinoidSalt formation
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LC-MS/MS characterisation and determination of dansyl chloride derivatised glyphosate, aminomethylphosphonic acid (AMPA), and glufosinate in foods of…

2021

Abstract Glyphosate and other polar and acidic pesticides have been particularly studied due to the concerns over widespread and intensive use. The chemical properties of these compounds necessitate use of customised methods, such as derivatisation or ion exchange chromatography. These approaches present a compatibility problem with ESI-MS due to presence of salts and non-volatile compounds. For that reason, a simple procedure has been developed for the extraction, pre-column derivatisation with dansyl chloride (5-(dimethylamino)naphthalene-1-sulfonyl chloride), and mass spectrometric detection of glyphosate, AMPA, and glufosinate after the separation on a C18 stationary phase. The dansyl d…

MeatClinical BiochemistryIon chromatographyOrganophosphonatesIon suppression in liquid chromatography–mass spectrometry030226 pharmacology & pharmacy01 natural sciencesBiochemistryAnalytical ChemistryMatrix (chemical analysis)03 medical and health scienceschemistry.chemical_compound0302 clinical medicineTandem Mass SpectrometryAnimalsAminomethylphosphonic acidDerivatizationDansyl CompoundsChromatographyAminobutyrates010401 analytical chemistryDansyl chlorideExtraction (chemistry)Pesticide ResiduesCell BiologyGeneral MedicineHoney0104 chemical scienceschemistryReagentCattleCucumis sativusFood AnalysisChromatography LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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