Search results for "Solution"

showing 10 items of 5638 documents

Trehalose-hydroxyethylcellulose microspheres containing vancomycin for topical drug delivery.

2001

Abstract A new formulation, in which vancomycin is entrapped into trehalose and hydroxyethylcellulose (Natrosol ® ) spherical matrices, is described. Microspheres were produced by the solvent evaporation method. The entrapped drug was fully recovered following microspheres dissolution. Differential scanning calorimetry analyses proved that Natrosol maintains trehalose in its amorphous form. The stabilizing effects of trehalose on vancomycin were evaluated even after long storage and heating of microspheres. Calorimetric data indicated no decomposition of the entrapped drug. In vitro drug release, already performed by using a general two-compartment linear time-invariant open model, suggests…

Active ingredientChromatographyChemistryStereochemistryPharmaceutical ScienceTrehaloseGeneral MedicineTrehaloseDosage formMicrospheresAnti-Bacterial Agentschemistry.chemical_compoundDifferential scanning calorimetryDrug Delivery SystemsSolubilityVancomycinLiberationDrug carrierCelluloseDissolutionBiotechnologyAntibacterial agentEuropean journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
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ChemInform Abstract: High-Resolution Solid-State NMR Spectroscopy of Steroids and Their Derivatives

2013

Abstract: Steroids are an important class of organic compounds containing a vast array of biologically and physiologically essential molecules. Due to their availability, relatively straightforward derivatizability, and endogeneity, they are widely used in pharmacological applications. The investigation of molecular and physicochemical properties of active pharmaceutical ingredients (APIs) in the solid state is important, because these properties are directly related to their pharmacological activity. Several methods are available for this purpose. Solid-state NMR spectroscopy offers a nondestructive and flexible technique, providing both structural and dynamic information. It can be applie…

Active ingredientSolid-state nuclear magnetic resonanceChemistrySolid-stateMoleculeHigh resolutionGeneral MedicineNuclear magnetic resonance spectroscopySpectroscopyCombinatorial chemistryAmorphous solidChemInform
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High-Resolution Solid-State NMR Spectroscopy of Steroids and Their Derivatives

2013

Abstract: Steroids are an important class of organic compounds containing a vast array of biologically and physiologically essential molecules. Due to their availability, relatively straightforward derivatizability, and endogeneity, they are widely used in pharmacological applications. The investigation of molecular and physicochemical properties of active pharmaceutical ingredients (APIs) in the solid state is important, because these properties are directly related to their pharmacological activity. Several methods are available for this purpose. Solid-state NMR spectroscopy offers a nondestructive and flexible technique, providing both structural and dynamic information. It can be applie…

Active ingredientSolid-state nuclear magnetic resonancePolymorphism (materials science)ChemistryMoleculeOrganic chemistryHigh resolutionNuclear magnetic resonance spectroscopySpectroscopyInstrumentationCombinatorial chemistrySpectroscopyAmorphous solidApplied Spectroscopy Reviews
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The sustainable synthesis of levetiracetam by an enzymatic dynamic kinetic resolution and an ex-cell anodic oxidation

2021

Levetiracetam is an active pharmaceutical ingredient widely used to treat epilepsy. We describe a new synthesis of levetiracetam by a dynamic kinetic resolution and a ruthenium-catalysed ex-cell anodic oxidation. For the enzymatic resolution, we tailored a high throughput screening method to identify Comamonas testosteroni nitrile hydratase variants with high (S)-selectivity and activity. Racemic nitrile was applied in a fed-batch reaction and was hydrated to (S)-(pyrrolidine-1-yl)butaneamide. For the subsequent oxidation to levetiracetam, we developed a ligand-free ruthenium-catalysed method at a low catalyst loading. The oxidant was electrochemically generated in 86% yield. This route pro…

Active ingredientbiologyNitrile010405 organic chemistry010402 general chemistrybiology.organism_classification01 natural sciencesPollutionCombinatorial chemistry0104 chemical sciencesKinetic resolutionCatalysischemistry.chemical_compoundchemistryNitrile hydrataseYield (chemistry)medicineEnvironmental ChemistryComamonas testosteroniLevetiracetammedicine.drugGreen Chemistry
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Improving active learning methods using spatial information

2011

Active learning process represents an interesting solution to the problem of training sample collection for the classification of remote sensing images. In this work, we propose a criterion based on the spatial information that can be used in combination with a spectral criterion in order to improve the selection of training samples. Experimental results obtained on a very high resolution image show the effectiveness of regularization in spatial domain and open challenging perspectives for terrain campaigns planning. © 2011 IEEE.

Active learningContextual image classificationComputer sciencebusiness.industryvery-high-resolution (VHR) imagesTerrainspatial informationsupport vector machines (SVMs)Machine learningcomputer.software_genreRegularization (mathematics)Support vector machineArtificial intelligencebusinessImage resolutioncomputerSpatial analysis
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Aqueous coefficient calculations for chemicals and drugs

1999

Aqueous functional group activity coefficients (AQUAFAC) is a group‐contribution method for estimating the aqueous coefficients. We have written a program for the calculation of these coefficients. The solubility S w of alkanes shows variation of 8 orders of magnitude. The comparison with experiment shows that AQUAFAC gives good S w estimations. For 4'‐substituted acetanilides, I‐, Br‐, nitro‐, Cl‐, F‐ and methoxy‐substituents decrease S w, while formyl‐ and amino‐substituents increase S w. For acetaminophen esters, S w decreases from the acetate to the decanoate. The S w of 29 barbiturates shows typical errors of 0.4 log S w units. For the cyclo‐alkane‐l’,5‐spirobarbituric acids, S w decre…

Activity coefficientAqueous solutionHealth Toxicology and MutagenesisAnalytical chemistryPollutionCyclopropanechemistry.chemical_compoundchemistryNitroEnvironmental ChemistryCyclooctaneOrganic chemistryOrders of magnitude (speed)SolubilityAcetanilideToxicological & Environmental Chemistry
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Polycarboxylic acids in sea water: acid–base properties, solubilities, activity coefficients, and complex formation constants at different salinities

2016

This paper reports the results of the investigations carried out in synthetic sea water at different salinities for different classes of polycarboxylic acids. The investigations can be summarized as follows: (a) Determination of the protonation constants in such multicomponent solution in a salinity range 15 ≤ S ≤ 45, at t = 25 °C, for the linear dicarboxylic acids HOOC-(CH2) n –COOH (0 ≤ n ≤ 8), and aromatic polycarboxylic acids (o-phthalic and 1,2,4-benzenetricarboxylic acids). For malonic, succinic, 1,2,3-benzenetricarboxylic, and 1,2,3,4-benzenetetracarboxylic acids, investigations were also carried out at t = 10 and 37 °C; (b) Determination of the total and intrinsic solubility (S T an…

Activity coefficientBase (chemistry)Inorganic chemistryChemistry (all).Salt (chemistry)ProtonationProtonation02 engineering and technologyCalorimetry010402 general chemistry01 natural sciencesMetal complexDeprotonationProtonation Solubility Synthetic sea water Salt effect Metal complex Calorimetry020401 chemical engineeringSalt effectSettore CHIM/01 - Chimica Analitica0204 chemical engineeringSolubilitychemistry.chemical_classificationAqueous solutionGeneral ChemistrySynthetic sea water0104 chemical sciencesSolubilitychemistrySpecific ion interaction theoryMonatshefte für Chemie - Chemical Monthly
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Activity coefficients and Donnan coion exclusion in charged membranes with weak-acid fixed charge groups

1998

Abstract We have studied theoretically the effects that the dissociation equilibrium of weak-acid fixed charge groups (e.g. carboxyl groups) exerts on the mean activity coefficients in charged membranes using a Donnan formalism. The model calculations indicate that unless carbon dioxide is excluded from the external aqueous solution, the pH of the membrane solution can be low enough to affect significantly the effective fixed charge concentration and the coion exclusion when the membrane fixed charge concentration is high compared with the external solution salt concentration. Although this problem was already pointed out in previous studies, the possibility that the pH and salt concentrati…

Activity coefficientChromatographyAqueous solutionChemistrySalt effectThermodynamicsFiltration and SeparationEquilibrium equationBiochemistryDissociation (chemistry)Formalism (philosophy of mathematics)MembraneFixed chargeGeneral Materials SciencePhysical and Theoretical ChemistryJournal of Membrane Science
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Modelling of the ternary system H3PO4/H2O/TBP

2002

Abstract A thermodynamic model is presented for the extraction of phosphoric acid from water by tri-n-butylphosphate (TBP), from aqueous solutions containing 0–6 mol/kg phosphoric acid. The activity coefficient of phosphoric acid was calculated from experimental data using Pitzer’s equation, and those of the components in the organic phase were calculated by Sergievskii–Danus’s relationship. The proposed model gives a satisfactory description of the distribution of phosphoric acid and water, in the considered concentration range, by taking into account the formation of the following species: TBP, TBP·H2O, H3PO4·TBP and (TBP)2·H3PO4·H2O.

Activity coefficientChromatographyAqueous solutionTernary numeral systemChemistryGeneral Chemical EngineeringInorganic chemistryExtraction (chemistry)General Physics and AstronomyThermodynamic modelchemistry.chemical_compoundPhase (matter)Physical and Theoretical ChemistryPhosphoric acidFluid Phase Equilibria
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Hydrolysis and chemical speciation of dioxouranium(VI) ion in aqueous media simulating the major ion composition of seawater

2004

Abstract The hydrolysis and chemical speciation of the dioxouranium(VI) ion at 25 °C was studied in a number of binary electrolytes (LiCl, NaCl, MgCl2, CaCl2, Na2SO4) and some mixtures (NaCl–Na2SO4, NaNO3–Na2SO4, CaCl2–MgCl2) as well as artificial seawater (SSWE) as a function of ionic strength. The results in LiCl, CaCl2 and MgCl2 solutions confirmed the formation of (UO2)2(OH)22+, (UO2)3(OH)42+, (UO2)3(OH)5+ and (UO2)3(OH)7− species (at I=0 mol l−1: log Tβ22=−5.76, log Tβ34=−11.82, log Tβ35=−15.89 and log Tβ37=−29.26). For NaNO3, NaCl and artificial seawater the hydrolysis constant for the formation of the UO2(OH)+ species was also determined (at I=0 mol l−1: log Tβ11=−5.19). The results …

Activity coefficientHydrolysis constantUranium speciationAqueous solutionChemistryHydrolysisInorganic chemistryPitzer parametersIonic bondingArtificial seawaterGeneral ChemistryDependence on ionic strengthOceanographyUranylIon pair formationIonDioxouranium(VI)chemistry.chemical_compoundIonic strengthEnvironmental ChemistryChemical speciationHydrolysis; Dioxouranium(VI); Chemical speciation; Seawater; Dependence on ionic strength; Dependence on ionic medium; Pitzer parameters; Ion pair formationSeawaterDependence on ionic mediumWater Science and Technology
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