Search results for "PreP"

showing 10 items of 1334 documents

Supercritical Fluid Extraction and Supercritical Fluid Chromatography of Vitamin E in Pharmaceutical Preparations

1999

ChromatographyVitamine eChemistryGeneral Chemical EngineeringVitamin Emedicine.medical_treatmentSupercritical fluid extractionDosage formlaw.inventionlawSupercritical fluid chromatographymedicineFlame ionization detectorSample preparationQuantitative analysis (chemistry)Journal of High Resolution Chromatography
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Peptides analysis in blood plasma using on-line system of supported liquid membrane and high-performance liquid chromatography

2005

The potential of using supported liquid membrane (SLM) technique, combined with reversed-phase high-performance liquid chromatography (RP-HPLC) has been investigated for the determination of peptides in human blood plasma. The peptides studied were (DL)Leu(DL)Phe, MetLeuPhe, GlyLeuTyr and ValGluProlleProTyr. The carrier (Aliquat 336) was incorporated in membrane phase in order to facilitate the transport of investigated peptides. After extraction, the analyte-enriched acceptor phase was directly injected into an HPLC system for analysis. With SLM, high selectivity and efficiency were achieved for extraction of peptides in aqueous solutions. Lower extraction efficiency was obtained in plasma…

Chromatographyaliquat 336Extraction (chemistry)Analytical chemistryUltrafiltrationReversed-phase chromatographyAliquat 336BiochemistryHigh-performance liquid chromatographyAnalytical ChemistryStandard curvechemistry.chemical_compoundMembranechemistrypeptidesEnvironmental ChemistrySample preparationsupported liquid membraneHPLCSpectroscopyblood plasmaAnalytica Chimica Acta
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A LC/MS/MS method for the simultaneous quantification of free and masked fumonisins in maize and maize-based products

2008

An LC-ESI-MS/MS method for the simultaneous detection of the main fumonisins and their hydrolysed derivatives is described, allowing for a simplified sample preparation without previous clean up. The method has a very low quantification limit (10 µg/kg for FB1, 12 µg/kg for FB2 and FB3, 70 µg/kg for HFB1, HFB2 and HFB3 in maize flour) and a very good recovery for all the analytes. The method has been applied to check several maize-based foods for the presence of free and bound forms of fumonisins, the latter being determined after alkaline hydrolysis as hydrolysed derivatives. Bound fumonisins were found to be present not only in thermally treated maize-based products but also in mild proc…

Chromatographybusiness.industryPublic Health Environmental and Occupational HealthToxicologyFood safetyMass spectrometryClean-upchemistry.chemical_compoundchemistryLc ms msSample preparationFood scienceMycotoxinbusinessFood ScienceWorld Mycotoxin Journal
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Comparison of spectrophotometric and HPLC methods for determining sialic acid in infant formulas

2011

Abstract Two methods for determining sialic acid in infant formulas – spectrophotometry and HPLC with fluorescence detection – have been optimised and validated, the first one allows to determine total sialic acid while the second allows to differentiate the two main forms of sialic acid (N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc)). A common sample preparation procedure (hydrolysis and purification) for both methods has been proposed. The linearity (from 6 to 150 μg of total sialic acid in the assay for spectrophotometry, and from 12.5 to 250 ng and 1 to 5 ng of Neu5Ac and Neu5Gc, respectively, for HPLC) is adequate. The detection and quantification limits (0.29…

Chromatographymedicine.diagnostic_testRelative standard deviationGeneral MedicineHigh-performance liquid chromatographyFluorescenceAnalytical ChemistrySialic acidHydrolysischemistry.chemical_compoundInfant formulachemistrySpectrophotometrymedicineSample preparationFood ScienceFood Chemistry
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Sensing Chiral Drugs by Using CdSe/ZnS Nanoparticles Capped withN-Acetyl-L-Cysteine Methyl Ester

2013

Chiral quantum dots (QDs), differing in their core or shell size and, consequently, in their optical properties, were synthesized by the treatment of commercially available amine-capped quantum dots with methyl ester N-acetyl-L-cysteine (CysP). Interestingly, their colloidal methanol solutions remain stable for several months. Their NMR and IR spectra were in accordance with CysP binding to the QD surface through two anchoring groups; its thiolate (strongly bound) and the carbonyl group of its ester (weaker bound) group, whereas their circular dichroism (CD) spectra showed a new broad redshifted band, suggesting that the attachment to the QD surface modified the conformational equilibrium t…

Circular dichroismNaproxenStereochemistryInfrared spectroscopyIbuprofenSulfidesCatalysischemistry.chemical_compoundNaproxenQuantum DotsCadmium CompoundsmedicineSelenium CompoundsConformational isomerismChemistryCircular DichroismArylOrganic ChemistryEstersStereoisomerismGeneral ChemistryFluorescenceAcetylcysteineCrystallographySpectrometry FluorescenceFlurbiprofenPharmaceutical PreparationsKetoprofenZinc CompoundsQuantum dotEnantiomermedicine.drugChemistry - A European Journal
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HPLC study on the ‘history’ dependence of gramicidin A conformation in phospholipid model membranes

1989

AbstractA novel HPLC methodology for the study of gramicidin A reconstituted in model membranes has been tested in comparison with circular dichroism data. It is shown that this chromatographic technique not only corroborates most of the recent spectroscopic results but allows one to explain them in terms of mass fractions of different actual conformational species of GA in the phospholipid assemblies. In particular, the dependence of the inserted peptide configuration on the organic solvent and other parameters involved in the ‘history’ of the sample preparation and handling has been analyzed by HPLC in two phospholipid model systems: small unilamellar vesicles and micelles. Moreover, a sl…

Circular dichroismProtein ConformationMolecular ConformationBiophysicsPhospholipidPeptideBiochemistryHigh-performance liquid chromatographyMicellechemistry.chemical_compoundStructural BiologyGramicidin A conformationGeneticsGramicidin ASample preparationMolecular BiologyChromatography High Pressure Liquidchemistry.chemical_classificationChromatographyChemistryCircular DichroismGramicidinMembranes ArtificialCell BiologyModels TheoreticalCDMembraneLiposomesPhospholipid vesiclePhosphatidylcholinesHPLCFEBS Letters
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Exploring the binding of Pt drugs to gold nanoparticles for controlled passive release of cisplatin.

2011

CisplatinChemistryPharmaceutical ScienceMetal NanoparticlesAntineoplastic AgentsHydrogen-Ion ConcentrationCombinatorial chemistryDrug StabilityColloidal goldDelayed-Action PreparationsmedicineHumansGoldCisplatinmedicine.drugJournal of controlled release : official journal of the Controlled Release Society
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Changes in Cerebral Amino Acid Transport During Development

1976

The transport of metabolites to and from the central nervous system is of considerable interest. To a greater extent than most other tissues, central nervous system tissue invitro takes up amino acids to well above their concentrations in the incubation medium. Presumably the transport systems responsible for this uptake and for efflux invitro are also those responsible for transport between brain cells in living animals2.

Citric acid cyclechemistry.chemical_classificationmedicine.anatomical_structureSlice preparationBiochemistryChemistryCentral nervous systemmedicineEffluxIncubationIn vitroFetal brainAmino acid
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Ciudadanía y enseñanza de la historia. Resultados de una intervención en la formación de maestros

2011

Producción Científica

Ciudadanía - Países de la Unión Europea5312.04 EducaciónUNESCO::HISTORIAUNESCO::PEDAGOGÍA::Preparación y empleo de profesoresDocentes - Formación:PEDAGOGÍA::Preparación y empleo de profesores [UNESCO]Educación civicaHistoria - Estudio y enseñanzadidáctica de la historia formación ciudadana ciudadanía europea formación del profesorado:HISTORIA [UNESCO]
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Strategies to In Vitro Assessment of Major Human CYP Enzyme Activities by Using Liquid Chromatography Tandem Mass Spectrometry

2008

At the early stage of drug discovery, thousands of new chemical entities (NCEs) may be screened before a single candidate can be identified for development. Determining the role of CYP enzymes in the metabolism of a compound and evaluating the effect of NCEs on human CYP activities are key issues in pharmaceutical development as they may explain inter-subject variability, drug-drug interactions, non-linear pharmacokinetics and toxic effects. Reliable methods for determining enzyme activities are needed to characterize an individual CYP enzyme and to obtain a tool for the evaluation of its role in drug metabolism in humans. Different liquid chromatography tandem mass spectrometry methodologi…

Clinical BiochemistryDrug Evaluation PreclinicalIn Vitro TechniquesTandem mass spectrometrySubstrate SpecificityCytochrome P-450 Enzyme SystemPharmacokineticsTandem Mass SpectrometryIn vivoLiquid chromatography–mass spectrometryCytochrome P-450 Enzyme InhibitorsHumansPharmacokineticsEnzyme inducerChromatography High Pressure LiquidCytochrome P-450 Enzyme InhibitorsPharmacologyChromatographybiologyDrug discoveryChemistryPharmaceutical PreparationsBiochemistryEnzyme InductionHepatocytesMicrosomes Liverbiology.proteinDrug metabolismCurrent Drug Metabolism
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