Search results for "solution"

showing 10 items of 5638 documents

Hierarchical Mass Transfer Analysis of Drug Particle Dissolution, Highlighting the Hydrodynamics, pH, Particle Size, and Buffer Effects for the Disso…

2020

Dissolution is a crucial process for the oral delivery of drug products. Before being absorbed through epithelial cell membranes to reach the systemic circulation, drugs must first dissolve in the human gastrointestinal (GI) tract. In vivo and in vitro dissolutions are complex because of their dependency upon the drug physicochemical properties, drug product, and GI physiological properties. However, an understanding of this process is critical for the development of robust drug products. To enhance our understanding of in vivo and in vitro dissolutions, a hierarchical mass transfer (HMT) model was developed that considers the drug properties, GI fluid properties, and fluid hydrodynamics. T…

Chemistry PharmaceuticalDiffusionPharmaceutical Science02 engineering and technologyBuffers030226 pharmacology & pharmacyDiffusion03 medical and health sciences0302 clinical medicineMass transferDrug DiscoveryDissolution testingParticle SizeSolubilityDissolutionChemistryCheminformaticsHydrogen-Ion Concentration021001 nanoscience & nanotechnologyShear rateDrug LiberationKineticsModels ChemicalSolubilityChemical engineeringHydrodynamicsMolecular MedicineParticleParticle size0210 nano-technologyMolecular Pharmaceutics
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Impact of uncharged and charged stabilizers on in vitro drug performances of clarithromycin nanocrystals

2018

The purpose of this study was to evaluate the effect of charge on the in vitro drug performances of clarithromycin nanocrystals. To prepare different charges of nanocrystals, media milling was employed with the use of different stabilizing systems. The uncharged nanocrystals were prepared from poloxamer 407. The negatively and positively charged nanocrystals were stabilized using a combination of poloxamer 407 with sodium lauryl sulfate (SLS) and cetyltrimethylammonium bromide (CTAB), respectively. After production, the particle size of the negatively and positively charged nanocrystals was smaller than that of the uncharged one. The similar particle size of variously charged clarithromycin…

Chemistry PharmaceuticalDrug CompoundingPharmaceutical SciencePoloxamer02 engineering and technology030226 pharmacology & pharmacyCell LineExcipients03 medical and health scienceschemistry.chemical_compound0302 clinical medicineBromideClarithromycinMonolayermedicineHumansSurface chargeParticle SizeSolubilityDissolutionCetrimoniumChemistrySodium Dodecyl SulfateBiological TransportGeneral Medicine021001 nanoscience & nanotechnologyAnti-Bacterial AgentsDrug LiberationSolubilityChemical engineeringNanocrystalPoloxamer 407NanoparticlesParticle sizeCaco-2 Cells0210 nano-technologyBiotechnologymedicine.drugEuropean Journal of Pharmaceutics and Biopharmaceutics
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Formulation strategy towards minimizing viscosity mediated negative food effect on disintegration and dissolution of immediate release tablets.

2017

Food induced viscosity can delay disintegration and subsequent release of API from solid dosage form which may lead to severe reduction in the bioavailability of BCS type III compounds. Formulations of such tablets need to be optimized in view of this postprandial viscosity factor. In this study, three super disintegrants, croscarmellose sodium (CCS), cross-linked polyvinylpolypyrrolidone (CPD), and sodium starch glycolate (SSG) were assessed for their efficiency under simulated fed state. Tablets containing these disintegrants were compressed at 10 and 30 KN, while taking lactose as a soluble filler. In addition to other compendial tests, disintegration force of these formulations was meas…

Chemistry PharmaceuticalPharmaceutical ScienceLactose02 engineering and technology030226 pharmacology & pharmacyDosage formExcipients03 medical and health sciencesViscosity0302 clinical medicineDrug DiscoverySodium Starch GlycolateImmediate releaseDissolutionPharmacologyFOOD EFFECTChemistryViscosityOrganic Chemistryfood and beveragesPovidoneStarch021001 nanoscience & nanotechnologyBioavailabilityChemical engineeringSolubilityFoodCarboxymethylcellulose Sodium0210 nano-technologyFederal stateTabletsDrug development and industrial pharmacy
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Red and far-red sun-induced chlorophyll fluorescence as a measure of plant photosynthesis

2015

Remote estimation of Sun-induced chlorophyll fluorescence emitted by terrestrial vegetation can provide an unparalleled opportunity to track spatiotemporal variations of photosynthetic efficiency. Here we provide the first direct experimental evidence that the two peaks of the chlorophyll fluorescence spectrum can be accurately mapped from high-resolution radiance spectra and that the signal is linked to variations in actual photosynthetic efficiency. Red and far red fluorescence measured using a novel airborne imaging spectrometer over a grass carpet treated with an herbicide known to inhibit photosynthesis was significantly higher than the corresponding signal from an equivalent untreated…

Chemistry1900 General Earth and Planetary SciencesImaging spectrometerfood and beveragesFar-redPhotosynthetic efficiencyPhotosynthesisFluorescenceGEO/10 - GEOFISICA DELLA TERRA SOLIDA10122 Institute of GeographyGeophysicsRadianceddc:550General Earth and Planetary Sciences910 Geography & travel1908 GeophysicsControlled experimentfluorescence airborne sensor high resolution photosynthesisChlorophyll fluorescenceRemote sensing
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Metal film growth on regular and defective MgO(001) surface: A comparative ab initio simulation and thermodynamic study

2006

Abstract In order to understand the difference in metallic film growth modes on perfect and defective oxide substrates, we have combined ab initio B3LYP periodic calculations on the slab models of the corresponding Me/MgO(0 0 1) interfaces (Me = Ag, Cu) with thermodynamic theory of solid solutions. For a defectless magnesia surface, we confirm the experimentally observed submonolayer growth of 3D metallic islands (Ag possesses a higher trend than Cu). Formation of Fs centers (neutral O vacancies) on the substrate markedly enhances metal atom adsorption as compared to physisorption over regular sites on a defect-free substrate. For the first time, we predict that the presence of these surfac…

ChemistryAb initioOxideSurfaces and InterfacesSubstrate (electronics)Condensed Matter PhysicsSurfaces Coatings and FilmsMetalchemistry.chemical_compoundAdsorptionPhysisorptionComputational chemistryAb initio quantum chemistry methodsvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical chemistrySolid solutionSurface Science
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BacSr1−cTiO3 perovskite solid solutions: Thermodynamics from ab initio electronic structure calculations

2005

We suggest theoretical prediction for Ba"cSr"1"-"cTiO"3 perovskite solid solutions (BST) combining ab initio DFT/B3PW calculations and alloy thermodynamics. This approach is based on calculations of a series of ordered super-structures in Ba-Sr simple cubic sublattice immersed in the rest TiO"3 matrix. Although these structures are unstable with respect to the decomposition, the results of total energy calculations allow us to extract the necessary energy parameters and to calculate the phase diagram for the solid solutions (alloys). A novel approach applied to the BST system enables to predict that at T>400 K Ba and Sr atom distribution is random. But below this temperature at small c Ba a…

ChemistryAb initioThermodynamicsElectronic structureCubic crystal systemCondensed Matter PhysicsAtomic and Molecular Physics and OpticsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNanoclustersCondensed Matter::Materials ScienceAb initio quantum chemistry methodsElectrical and Electronic EngineeringPhase diagramPerovskite (structure)Solid solutionMicroelectronic Engineering
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Periodic behaviour in heterogeneous chemical reactions

1992

Abstract The authors present an analytical and numerical analysis for a solid-gas oxidation process represented by a set of coupled reaction rates equations. The equations describe the time evolution of four elementary process that govern the overall heterogeneous kinetics. The description formation of a new oxide unit considers: (1) an internal interface (oxide-metal) reaction by which an activated complex is formed; (2) the dissolution of the complex produce a chemical element σ; (3) the diffusion of σ through the oxide layer; and (4) an external interface (oxide-gas) reaction. The results reported here delinate the parameter region where chemical oscillations are present.

ChemistryActivated complexNumerical analysisKineticsTime evolutionOxideThermodynamicsGeneral ChemistryCondensed Matter PhysicsChemical reactionchemistry.chemical_compoundPhysical chemistryGeneral Materials ScienceDiffusion (business)DissolutionSolid State Ionics
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Evidences for the Formation of Chromium in the Unusual Oxidation State Cr(IV)

1999

Abstract Magnetic measurements on Tl x Cr 5 Se 8 (0≤ x ≤1) reveal that stoichiometric TlCr 5 Se 8 is a three-dimensional antiferromagnet with a Neel temperature T N of about 55 K. In contrast, samples with a reduced Tl content show highly unusual magnetic properties that are without precedent in the literature of magnetically coupled systems: upon lowering the temperature from 300 K the susceptibility reaches a maximum at about 125 K and then steeply drops to a value comparable to that obtained at room temperature. The height of this maximum increases first with decreasing Tl abundance reaching its largest value at a composition Tl 0.2 Cr 5 Se 8 and then decreases again for samples with x 3…

ChemistryAnalytical chemistrychemistry.chemical_elementCrystal structureCondensed Matter PhysicsMagnetic susceptibilityElectronic Optical and Magnetic Materialslaw.inventionInorganic ChemistryChromiumNuclear magnetic resonanceFerromagnetismlawMaterials ChemistryCeramics and CompositesAntiferromagnetismPhysical and Theoretical ChemistryElectron paramagnetic resonanceNéel temperatureSolid solutionJournal of Solid State Chemistry
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Motional Resistance Evaluation of the Quartz Crystal Microbalance to Study the Formation of a Passive Layer in the Interfacial Region of a Copper|Dil…

2015

A hyphenated technique based on vis–NIR spectroscopy and electrochemical quartz crystal microbalance with motional resistance monitoring was employed to investigate the dissolution of copper in acid media. Changes in motional resistance, current, mass, and absorbance during copper dissolution allow the evolution of the interfacial region of copper|diluted sulfuric solution to be understood. In particular, motional resistance is presented in this work as a useful tool to observe the evolution of the passive layer at the interface. During the forced copper electrodissolution in sulfuric solution, SO4(2–) favors the formation of soluble [Cu(H2O)6]2+. On the contrary, OH– involves the formation…

ChemistryAnalytical chemistrychemistry.chemical_elementSurfaces and InterfacesQuartz crystal microbalanceCondensed Matter PhysicsElectrochemistryCopperAbsorbanceElectrodeElectrochemistryGeneral Materials ScienceErosion corrosion of copper water tubesSpectroscopyDissolutionSpectroscopyLangmuir
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Synthesis and Isolation of Enantiomerically Enriched Cyclopenta[b]benzofurans Based on Products from Anodic Oxidation of 2,4-Dimethylphenol

2015

The anodic treatment of 2,4-dimethylphenol offers a powerful and direct method for the construction of a dehydrotetramer with four contiguous stereocentres on a multigram scale. The installation of propellanes on this scaffold using enantiomerically pure carbonyl compounds leads to a mixture of diastereomers. This mixture is easily separable using standard chromatography and gives rise to optically pure cyclopenta[b]benzofurans which are important scaffolds in a variety of natural products. The synthesis is easy to perform and allows a reliable access to chiral compounds with very high enantiomeric excess. It was possible to determine the absolute configuration of these compounds by compari…

ChemistryAnodic oxidationOrganic ChemistryVibrational circular dichroismAbsolute configurationDiastereomerOrganic chemistryPhysical and Theoretical ChemistryEnantiomerEnantiomeric excessElectrochemistryChiral resolutionEuropean Journal of Organic Chemistry
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