Search results for "Mace"

showing 10 items of 4713 documents

Estimation of the Compatibility Between Poly(Methylmethacrylate) and Poly(Styrene Co Vinyl Phenol) Blends from Dilute Solution Measurements

2006

Abstract The compatibility of poly(methyl methacrylate) (PMMA) with poly(styrene‐co‐vinyl phenol) (PS‐VPh) with two different contents of vinyl phenol, 5.8 and 7.2%, in dilute tetrahydrofuran solutions has been investigated by size exclusion chromatography and fluorescence spectroscopy at 25°C. The chromatographic technique permits the evaluation of the preferential solvation at different PMMA/PS‐VPh ratios. Changes in the fluorescence properties of PS‐VPh, caused by its association with PMMA, were used to obtain the fraction of copolymer bound to PMMA at diverse PMMA compositions. Both techniques agree quantitatively in every system, indicating that the association increases when the PMMA …

ChromatographyClinical BiochemistrySize-exclusion chromatographytechnology industry and agricultureFluorescence spectrometryPharmaceutical Sciencemacromolecular substancesequipment and suppliesBiochemistryFluorescence spectroscopyAnalytical ChemistryStyrenebody regionsGel permeation chromatographychemistry.chemical_compoundchemistryCopolymerPhenolMethyl methacrylateJournal of Liquid Chromatography & Related Technologies
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A theoretical plate model accounting for slow kinetics in chromatographic elution.

2011

The chromatographic elution has been studied from different perspectives. However, in spite of the simplicity and evident deficiencies of the plate model proposed by Martin and Synge, it has served as a basis for the characterization of columns up-to-date. This approach envisions the chromatographic column as an arbitrary number of theoretical plates, each of them consisting of identical repeating portions of mobile phase and stationary phase. Solutes partition between both phases, reaching the equilibrium. Mobile phase transference between the theoretical plates is assumed to be infinitesimally stepwise (or continuous), giving rise to the mixing of the solutions in adjacent plates. This yi…

ChromatographyComputer simulationElutionChemistryOrganic ChemistryKineticsGeneral MedicineModels TheoreticalKinetic energyBiochemistryAnalytical ChemistryVolumetric flow rateSolutionsKineticsPharmaceutical PreparationsMass transferPartition (number theory)Theoretical plateChromatography High Pressure LiquidJournal of chromatography. A
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Effects of polysorbate 80 on amiodarone intestinal absorption in the rat

1995

Abstract Amiodarone is a widely used anti-arrhythmic agent which shows physico-chemical properties that are highly suitable for diffusion across lipophilic absorbing membranes, however,.its low aqueous solubility could represent the rate-limiting step for absorption, making it erratic and variable. In a previous paper, the influence of an anionic surfactant (sodium lauryl sulphate) at variable supramicellar concentrations was studied. The absorption rate constants of amiodarone decreased as the surfactant concentration increased, and absorption was unusually fast at lower surfactant concentrations. The previously proposed equations for interpreting the relationships between the amiodarone a…

ChromatographyDiffusionPharmaceutical ScienceAmiodaronePolyvinyl alcoholIntestinal absorptionchemistry.chemical_compoundMembranePharmacokineticschemistryPulmonary surfactantmedicineAbsorption (chemistry)medicine.drugInternational Journal of Pharmaceutics
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Novel insights into excipient effects on the biopharmaceutics of APIs from different BCS classes: Lactose in solid oral dosage forms

2014

Excipients encompass a wide range of properties that are of importance for the resulting drug product. Regulatory guidelines on biowaivers for immediate release formulations require an in depth understanding of the biopharmaceutic effects of excipients in order to establish bioequivalence between two different products carrying the same API based on dissolution tests alone. This paper describes a new approach in evaluating biopharmaceutic excipient effects. Actually used quantities of a model excipient, lactose, formulated in combination with APIs from different BCS classes were evaluated. The results suggest that companies use different (relative) amounts depending on the characteristics o…

ChromatographyDrug CompoundingBiopharmaceuticsAdministration OralPharmaceutical ScienceExcipientLactoseBioequivalenceQuality by DesignDosage formBiopharmaceuticsExcipientschemistry.chemical_compoundchemistrymedicineHumansDrug productImmediate releaseLactosemedicine.drugEuropean Journal of Pharmaceutical Sciences
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In Vitro and In Silico Studies of Two 1,4-Naphthoquinones and Their Topical Formulation in Bigels.

2021

Background: 1,4-Naphthoquinones (1,4-NQs) are secondary plant metabolites with numerous biological activities. 1,4-NQs display low water solubility and poor bioavailability. Bigels are a new technology with great potential, which are designated as drug delivery systems. Biphasic bigels consisting of solid and liquid components represent suitable formulations improving diffusion and bioavailability of NQs into the skin. Objective: We evaluated the in silico and in vitro activity of 5,8-dihydroxy-1,4-naphthoquinone (M1) and 2,3-dichloro-5,8-dihydroxy-1,4-naphthoquinone (M2) on elastase and assessed their cytotoxicity towards COLO38 melanoma cells. The 1,4-NQs were loaded into bigels for topi…

ChromatographyElastasePharmaceutical ScienceResazurinHydrogelsPermeationIn vitroBioavailabilitySolventMolecular Docking Simulationchemistry.chemical_compoundDrug Delivery SystemschemistryDrug deliveryCytotoxicityRheologyNaphthoquinonesCurrent drug delivery
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EVALUATION OF THE ELUTION STRENGTH OF THE SURFACTANT AND ORGANIC SOLVENT IN HYBRID MICELLAR MOBILE PHASES

2001

The global ability of a mixed mobile phase (with two or more modifiers) to elute a solute is often measured without distinguishing between the elution strength of each modifier. An algorithm is proposed to evaluate the elution strength of the modifiers in hybrid micellar mobile phases containing a surfactant and an organic solvent. The algorithm is based on a mechanistic retention model that takes into account the competing equilibria of solutes among aqueous-organic phase, micelle, and stationary phase. The change in the elution strength of surfactant and organic solvent with respect to the concentration of both modifiers is also examined. The results are discussed according to the values …

ChromatographyElutionChemistrySodiumClinical BiochemistryPharmaceutical ScienceChemical modificationchemistry.chemical_elementAlcoholBiochemistryMicelleMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundPulmonary surfactantPhase (matter)Journal of Liquid Chromatography & Related Technologies
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BEHAVIOUR OF GRAPHITIZED CARBON BLACK IN THE EXTRACTION OF POLAR NON-IONIC NITROGEN-CONTAINING PESTICIDES. A CHECKING OF HYPOTHESES

2000

Graphitized Carbon Black (GCB) extractive cartridges are evaluated for on-line coupling with a C8 analytical column to determine eleven carbamates and one carboximide pesticide from spiked deionized water at the 1.2 μg/L level. Several experiments were carried out to ascertain whether GCB saturation, pesticide degradation on the surface, existence of by-pass channels, mobility among the bulk cartridge, or strong retention on the surface interfere with the determination of pesticides. Problems in on-line CGB elution are partially solved by modifying the acetonitrile/water gradient to contain a front of 100% acetonitrile for a few seconds. Eluting the same GCB cartridges off-line with dichlor…

ChromatographyElutionClinical BiochemistryPharmaceutical ScienceReversed-phase chromatographyCarbon blackBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryPesticide degradationSample preparationSolid phase extractionDichloromethaneJournal of Liquid Chromatography & Related Technologies
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Micellar liquid chromatography: suitable technique for screening analysis.

2002

The screening capability of micellar liquid chromatography (MLC) is discussed using the reported chromatographic data of several sets of compounds (amino acids, beta-blockers, diuretics, phenethylamines, phenols, polynuclear aromatic hydrocarbons, steroids and sulfonamides) and new results (sulfonamides and steroids). The chromatographic data are treated with an interpretive optimisation resolution procedure to obtain the best separation conditions. Usually, the pH and the concentration of surfactant (sodium dodecyl sulfate, SDS, or cetyltrimethylammonium bromide) for the optimal mobile phase were 2.5-3 and0.12 M, respectively. The nature and concentration of organic solvent depended on the…

ChromatographyElutionOrganic ChemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPropanolPartition coefficientchemistry.chemical_compoundColumn chromatographychemistryPharmaceutical PreparationsMicellar liquid chromatographySodium dodecyl sulfateChromatography LiquidJournal of chromatography. A
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Determination of sialic acid and gangliosides in biological samples and dairy products: A review

2009

Gangliosides are sphingolipids containing one or more moieties of sialic acid in their structure. Both gangliosides and sialic acid are bioactive compounds related to animal physiology. Due to their biological relevance, analytical methods adapted to each type of matrix have been developed over time. The present study reviews the main methods applied to the analysis of sialic acid and gangliosides in biological samples and dairy products.

ChromatographyGangliosideChromatographySpectrum AnalysisClinical BiochemistryPharmaceutical ScienceSphingolipidN-Acetylneuraminic AcidAnalytical ChemistrySialic acidcarbohydrates (lipids)chemistry.chemical_compoundGlycolipidBiochemistrychemistryMilk productsGangliosidesDrug DiscoveryAnimalsDairy ProductsQuantitative analysis (chemistry)SpectroscopyJournal of Pharmaceutical and Biomedical Analysis
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Continuous-flow spectrophotometric determination of sulfadiazine by diazotisation with in situ preparation of nitrite

1995

Abstract Nitrite is prepared in situ for the determination of sulfadiazine. The method is based on solid-phase reduction of copperized cadmium of nitrate; the nitrite reagent merges with the sample stream in hydrochloric acid medium and the resulting mixture is injected into the water carrier, pure distilled water, and then merges with the N-(1-naphthyl)ethylendiamine reagent and is measured spectrophotometrically at 542.0 nm. The calibration graph is linear over the range 0.5–50 μg ml−1 sulfadiazine, mid-range R.S.D. = 0.3% (n = 5) and sample throughput 72 h−1. The procedure is applied to sulfadiazine determination in a pharmaceutical formulation and to in vitro dissolution studies of two …

ChromatographyHydrochloric acidPharmaceutical formulationBiochemistryDosage formAnalytical Chemistrychemistry.chemical_compoundSulfadiazinechemistryDistilled waterReagentmedicineEnvironmental ChemistryNitriteSpectroscopymedicine.drugAntibacterial agentAnalytica Chimica Acta
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