Search results for "Meri"

showing 10 items of 7596 documents

In vitro fibrillogenesis of the amyloid beta 1-42 peptide: cholesterol potentiation and aspirin inhibition.

2002

Understanding the formation of extracellular amyloid neurofibrillar bundles/senile plaques and their role in the development of Alzheimer's disease is of considerable interest to neuroscientists and clinicians. Major components of the extracellular neurofibrillar bundles are polymerized amyloid beta (Abeta) peptides (1-40), (1-42) and (1-43), derived in vivo from the soluble amyloid precursor protein (sAPP) by proteolytic (beta- and gamma-secretase) cleavage. The Abeta(1-42) peptide is widely considered to be of greatest significance in relation to the pathogenesis of Alzheimer's disease. A well-defined ultrastructural characteristic within Alzheimer dense plaques is the presence of helical…

AmyloidAmyloid betaGeneral Physics and AstronomyPeptideFibrilStructural BiologyAlzheimer DiseaseAmyloid precursor proteinAnimalsHumansGeneral Materials ScienceSenile plaqueschemistry.chemical_classificationAmyloid beta-PeptidesbiologyAspirinChemistryP3 peptideFibrillogenesisCell BiologyRatsSphingomyelinsMicroscopy ElectronCholesterolBiochemistrybiology.proteinlipids (amino acids peptides and proteins)PeptidesDimerizationCopperMicron (Oxford, England : 1993)
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Cholesterol facilitates interactions between α‐synuclein oligomers and charge‐neutral membranes

2015

AbstractOligomeric species formed during α-synuclein fibrillation are suggested to be membrane-disrupting agents, and have been associated with cytotoxicity in Parkinson’s disease. The majority of studies, however, have revealed that the effect of α-synuclein oligomers is only noticeable on systems composed of anionic lipids, while the more physiologically relevant zwitterionic lipids remain intact. We present experimental evidence for significant morphological changes in zwitterionic membranes containing cholesterol, induced by α-synuclein oligomers. Depending on the lipid composition, model membranes are either unperturbed, disrupt, or undergo dramatic morphological changes and segregate …

AmyloidParkinson's diseaseFluorescent DyeBiophysicsPlasma protein bindingBiochemistryOligomerProtein Structure SecondaryMultiphoton microscopyMembrane phase separationCell membranechemistry.chemical_compoundGeneticStructural Biology2-NaphthylamineLaurdan fluorescenceGeneticsFluorescence microscopemedicineMolecular BiologyFluorescent DyesLaurateα-SynucleinMembranesChemistryMedicine (all)2-NaphthylamineCell MembraneMembraneCell BiologySettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)CholesterolMembranemedicine.anatomical_structureBiophysicBiochemistryStructural biologyOligomeralpha-SynucleinParkinson’s diseaseProtein MultimerizationLaurdanLauratesProtein BindingFEBS Letters
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Monitoring of the decorative ornaments of the roman villa del casale at Piazza Armerina (Enna)

2008

Analisi multispettrale analisi colorimetrica villa romana del casale di piazza Armerina dipinti murali
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Tuning the selectivity of molecularly imprinted polymer extraction of arylcyclohexylamines: From class-selective to specific

2020

Abstract A molecularly imprinted polymer (MIP) has been prepared in presence of 3-hydroxy phencyclidine (3-OH PCP) as template by bulk polymerization using N,N-dimethylformamide, as porogenic solvent, for the selective solid-phase extraction (SPE) of arylcyclohexylamines from oral fluids. Experimental variables of the extraction procedure have been studied in order to increase both, extraction recovery of 3-OH PCP, used as model analyte, and imprinting factor. By modifying the composition of the washing solvent, the selectivity of the MIP extraction procedure can be tuned, moving from an arylcyclohexylamine selective method to a 3-OH PCP specific method. The applicability of the synthesized…

AnalyteArylcyclohexylamineBulk polymerizationSurface PropertiesIon-mobility spectrometry02 engineering and technology01 natural sciencesBiochemistryPolymerizationAnalytical ChemistryMolecularly Imprinted PolymersIon Mobility SpectrometrymedicineEnvironmental ChemistryParticle SizeSpectroscopyDetection limitCyclohexylaminesChromatographyMolecular StructureChemistry010401 analytical chemistryMolecularly imprinted polymer021001 nanoscience & nanotechnology0104 chemical sciencesSolvent0210 nano-technologySelectivitymedicine.drugAnalytica Chimica Acta
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Amphetamine-type stimulants analysis in oral fluid based on molecularly imprinting extraction

2018

Abstract A methamphetamine-based molecularly imprinted polymer (MIP) has been prepared by bulk polymerization to recognize new psychoactive substances (NPS) of the amphetamine, cathinones and 2C families in oral fluid samples, being the first precedent of a synthetized MIP for the extraction and preconcentration 32 NPS including amphetamine type substances and synthetic cathinones from oral fluids. Pre-polymerization complex and resulting materials were appropriately characterized by infrared spectroscopy, scanning electron microscopy, and nitrogen adsorption-desorption isotherms. Appropriateness of the material for the specific recognition of the target analytes was also evaluated through …

AnalyteCathinoneIon-mobility spectrometryInfrared spectroscopy02 engineering and technologyChemical FractionationMass spectrometry01 natural sciencesBiochemistryPolymerizationAnalytical ChemistryMolecular ImprintingmedicineHumansEnvironmental ChemistrySolid phase extractionSpectroscopyDetection limitChromatographyChemistrySolid Phase Extraction010401 analytical chemistryMolecularly imprinted polymerGreen Chemistry Technology021001 nanoscience & nanotechnologyBody Fluids0104 chemical sciencesAmphetamineCentral Nervous System StimulantsAdsorption0210 nano-technologymedicine.drugAnalytica Chimica Acta
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Application of solid-phase microextraction combined with derivatization to the enantiomeric determination of amphetamines.

2005

Abstract The utility of combining chiral derivatization and solid-phase microextraction (SPME) for the enantiomeric analysis of primary amphetamines by liquid chromatography has been investigated. Different derivatization/extraction strategies have been evaluated and compared using the chiral reagent o -phthaldialdehyde (OPA)– N -acetyl- l -cysteine (NAC) and fibres with a Carbowax-templated resin coating. Amphetamine, norephedrine and 3,4-methylenedioxyamphetamine (MDA) were used as model compounds. On the basis of the results obtained, a new method is presented based on the derivatization of the analytes in solution followed by SPME of the OPA–NAC derivatives formed. The proposed conditio…

AnalyteClinical BiochemistryPhenylpropanolaminePharmaceutical ScienceSolid-phase microextractionAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryHumansDerivatizationSpectroscopyChromatography High Pressure LiquidAqueous solutionChromatographyExtraction (chemistry)AmphetaminesReproducibility of ResultsStereoisomerismSolutionsSpectrometry FluorescencechemistryReagentCentral Nervous System StimulantsIndicators and ReagentsEnantiomerQuantitative analysis (chemistry)Journal of pharmaceutical and biomedical analysis
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Rapid determination of pharmaceuticals in wastewater by direct infusion HRMS using target and suspect screening analysis

2021

Abstract A wide-scope screening of active pharmaceutical ingredients (APIs) and their transformation products (TPs) in wastewater can yield valuable insights and pinpoint emerging contaminants that have not been previously reported. Such information is relevant to investigate their occurrence and fate in various environmental compartments. In this study, we explored the applicability of direct infusion high resolution mass spectrometry (DI-HRMS) for comprehensive and rapid detection of APIs and their TPs in wastewater samples. The method was developed using a Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) system and incorporated both wide-scope suspect screening and…

AnalyteEnvironmental EngineeringChromatography010504 meteorology & atmospheric sciencesWastewater010501 environmental sciencesQuechers01 natural sciencesPollutionRapid detectionFourier transform ion cyclotron resonanceScreening analysisPharmaceutical PreparationsWastewaterNorth AmericaEnvironmental ChemistryEnvironmental scienceSewage treatmentWaste Management and DisposalEffluentWater Pollutants ChemicalChromatography Liquid0105 earth and related environmental sciencesScience of The Total Environment
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Quantitative colorimetric analysis of some inorganic salts using digital photography

2011

An analytical imaging approach to the quantitation of dissolved chemical species absorbed in the visible spectral region is reported. The approach uses digital images of a series of standard solutions of the target substance and their processing with appropriate software to assign a numeric value to each standard in terms of color intensity. Such a value is directly proportional to the analyte concentration and allows the construction of a calibration graph. The results thus obtained are compared with those provided by the classical spectrophotometricmethod used to run calibration curves for colored substances. The chemical imaging technique is relative simple and affordable; in fact, it ca…

AnalyteINGENIERIA DE LA CONSTRUCCIONbusiness.product_categoryChemistrybusiness.industryCalibration curveBiochemistry (medical)Clinical BiochemistryComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISIONAnalytical chemistryDigital photographyColorimetric-imaging analysisStandard solutionBiochemistryAnalytical ChemistryDigital imageVisible spectrophotometryElectrochemistryComputer visionArtificial intelligenceNumeric ValuebusinessColorimetric analysisSpectroscopyDigital camera
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Off-line coupling of multidimensional immunoaffinity chromatography and ion mobility spectrometry: A promising partnership.

2015

The extreme specificity of immunoaffinity chromatography (IAC) columns coupled to the high sensitivity of ion mobility spectrometry (IMS) measurements makes this combination really useful for rapid, selective, and sensitive determination of a high variety of analytes in different samples. The capabilities of the IAC-IMS coupling have been highlighted under three different scenarios: (i) multiclass residue analysis using a single IAC column, (ii) multiclass residue analysis using stacked IAC columns, and (iii) isomer analysis. In the first case, the determination of three strobilurin fungicides - azoxystrobin, picoxystrobin, and pyraclostrobin - in water and strawberry juice was considered, …

AnalyteIon-mobility spectrometryPyridinesAnalytical chemistryWineBiochemistryFragariaSensitivity and SpecificityChromatography AffinityAnalytical Chemistrychemistry.chemical_compoundWineResidue (complex analysis)ChromatographyElutionOrganic ChemistryWaterStereoisomerismGeneral MedicineStrobilurinsFungicides IndustrialFruit and Vegetable JuicesPyrimidineschemistryAcrylatesAzoxystrobinStrobilurinMethacrylatesPyrazolesPyrimethanilCarbamatesJournal of chromatography. A
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Analysis of basic drugs by liquid chromatography with environmentally friendly mobile phases in pharmaceutical formulations

2017

Abstract Basic drugs are positively charged in the usual working pH (2–8) in reversed-phase liquid chromatography. This gives rise to a strong association with the residual ionized silanols in conventional silica-based stationary phases, which is translated in poor peak shape and high consumption of organic solvent to get appropriate retention times. Micellar mobile phases containing surfactants give rise to modified stationary phases, where silanols are masked, improving the peak shape. However, mobile phases containing the anionic surfactant sodium dodecyl sulfate (SDS) require a small amount of organic solvent to conveniently decrease the retention of cationic analytes. An alternative is…

AnalyteMethod validation01 natural sciencesAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPulmonary surfactantlawmedicineSample preparationSodium dodecyl sulfateBrij-35β-Adrenoceptor antagonistsSodium dodecyl sulfateSpectroscopyFiltrationChromatography010405 organic chemistryChemistry010401 analytical chemistryCationic polymerizationEnvironmentally friendly0104 chemical sciencesOxprenololPharmaceutical formulationsmedicine.drug
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