Search results for "cellar"

showing 10 items of 230 documents

Micellar electrokinetic chromatography of polyamines and monoacetylpolyamines

2001

A selective procedure for qualitative and quantitative analysis of ten polyamines by micellar electrokinetic chromatography (MEKC) was developed. Benzoylated polyamines and acetylpolyamines in micellar phase of SDS (10 mM) were separated at 25 degrees C by 20 mM borate buffer pH 8.5, containing 8% ethanol, with an applied voltage of 25 kV (5 microA) and then detected at 198 nm. The experimental factors and operational parameters were optimized by performing analysis at different surfactant concentrations, pH, voltage and temperature with and without ethanol. The repeatibility of migration times and peak heights is a peculiarity of the method here described.

EthanolChromatographyOrganic ChemistryAnalytical chemistryReproducibility of ResultsGeneral MedicineHydrogen-Ion ConcentrationBiochemistryMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryPulmonary surfactantBORATE BUFFERPhase (matter)PolyaminesSample preparationDerivatizationQuantitative analysis (chemistry)Chromatography Micellar Electrokinetic CapillaryJournal of Chromatography A
researchProduct

An innovative method to produce green table olives based on "pied de cuve" technology

2015

The technology of “pied de cuve” (PdC) is applied in food process only to produce wines with an enriched community of pro-technological yeasts. PdC promotes the growth of the desirable microbial strains in a small volume of grape must acting as a starter inoculums for higher volumes. The aim of the present work was to investigate the use of partially fermented brines, a technology known as PdC, developed with lactic acid bacteria (LAB) on the microbiological, chemical and sensory characteristics of green fermented table olives during two consecutive campaigns. The experimental plan included two trials based on different PdCs: trial A, PdC obtained with Lactobacillus pentosus OM13; trial B, …

Food HandlingLactic acid bacteria; Lactobacillus pentosus; Nocellara del Belice table olive; Pied de cuve; Volatile organic compounds; Yeasts; Food Science; MicrobiologyColony Count MicrobialLactobacillus pentosusSensory analysisMicrobiologychemistry.chemical_compoundStarterOleaYeastsLactic acid bacteriaCluster AnalysisFood scienceAromaPrincipal Component AnalysisVolatile Organic Compoundsbiologybusiness.industrySmall volumeLactobacillus pentosufood and beverageshemic and immune systemsBiodiversitySettore AGR/15 - Scienze E Tecnologie AlimentariHydrogen-Ion ConcentrationVolatile organic compoundbiology.organism_classificationNocellara del Belice table oliveYeastBiotechnologyLactic acidSettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreeLactobacillusPhenotypechemistryTasteFermentationFood MicrobiologyFood TechnologyFermentationSaltsPied de cuvebusinessBacteriaFood ScienceSettore AGR/16 - Microbiologia Agraria
researchProduct

High-Performance PCR for Alleles Discrimination of Chromo-Helicase-DNA Binding Protein (CHD1) Gene in Bird Sexing

2023

Genetic analyses aiming at assessing the presence of specific sequences or alleles are often carried out by PCR. Sexing of most birds is nowadays based on PCR with “universal” primers and relies on the assessment of the presence of the sex-linked CHD1-Z and -W alleles. The entire workflow is relatively time-consuming, especially for batch analyses, whereas methods that allow carrying out the entire procedure in a short time are highly desirable. The only method for outdoor analyses reported so far relies on LAMP; however; it fails to work properly in Procellariiformes. Besides improving the LAMP test; we have developed a PCR-based DNA amplification procedure (named high-performance PCR); wh…

General Immunology and Microbiologyhigh-performance PCRloop-mediated isothermal amplification (LAMP)fast DNA extractionGeneral Agricultural and Biological SciencesGeneral Biochemistry Genetics and Molecular BiologyProcellariiformesrapid bird sexingBiology
researchProduct

Analysis of pharmaceutical preparations containing antihistamine drugs by micellar liquid chromatography

2005

Rapid chromatographic procedures for analytical quality control of pharmaceutical preparations containing antihistamine drugs, alone or together with other kind of compounds are proposed. The method uses C18 stationary phases and micellar mobile phases of cetyltrimethylammonium bromide (CTAB) with either 1-propanol or 1-butanol as organic modifier. The proposed procedures allow the determination of the antihistamines: brompheniramine, chlorcyclizine, chlorpheniramine, diphenhydramine, doxylamine, flunarizine, hydroxyzine, promethazine, terfenadine, tripelennamine and triprolidine, in addition to caffeine, dextromethorphan, guaifenesin, paracetamol and pyridoxine in different pharmaceutical …

GuaifenesinChlorpheniramineTime FactorsClinical BiochemistryPharmaceutical Science1-PropanolPiperazinesDosage formAnalytical Chemistry1-ButanolChlorcyclizineDrug DiscoverymedicineTriprolidineMicellesSpectroscopyDosage FormsChromatographyCetrimoniumChemistryReproducibility of ResultsBrompheniramineBrompheniraminePromethazinePharmaceutical PreparationsDoxylamineMicellar liquid chromatographyCetrimonium CompoundsHistamine H1 AntagonistsChromatography Liquidmedicine.drugJournal of Pharmaceutical and Biomedical Analysis
researchProduct

The solubilisation behaviour of some dichloroalkanes in aqueous solutions of PEO-PPO-PEO triblock copolymers: a dynamic light scattering, fluorescenc…

2006

The aggregation behaviour of PEO-PPO-PEO triblock copolymers in water and in water + chlorinated additive mixtures was studied by means of fluorescence spectroscopy, dynamic light scattering (DLS), and small-angle neutron scattering (SANS). The copolymers were chosen such as to investigate the effects of molecular architecture (L35 and 10R5) and molecular weight by keeping constant the hydrophilic/hydrophobic balance (F88 and F108). 1,2-Dichloroethane was used as a prototype of water basins contaminants. The hydrodynamic radius of the block copolymer aggregates (R(h,M)) and the intensity ratio of pyrene of the first and the third vibrational band (I(1)/I(3)) were determined as a function of…

Hydrodynamic radiusAnalytical chemistryGeneral Physics and AstronomyMICELLIZATIONNeutron scatteringPHASE-BEHAVIORFluorescence spectroscopyPolyethylene GlycolsDynamic light scattering:OSCILLATORY SHEAR MEASUREMENTSBLOCK-COPOLYMERAlkanesCopolymerOrganic chemistryMOLAR VOLUMESSURFACTANTSPhysical and Theoretical ChemistrySolubilityTEMPERATUREAqueous solutionChemistryWaterSmall-angle neutron scatteringSolutionsMICELLAR STRUCTURENeutron DiffractionRefractometrySpectrometry FluorescenceSolubilityWATER-OIL SYSTEMSPropylene GlycolsTHERMODYNAMIC PROPERTIESChlorinePhysical chemistry chemical physics : PCCP
researchProduct

Micellar liquid Chromatographic determination of diuretics by diazotization and coupling with the Bratton-Marshall reagent

1997

Abstract A Chromatographic procedure that uses micellar mobile phases of sodium dodecyl sulphate (SDS) and propanol at pH 3 is reported for the determination, in urine samples, of thiazide diuretics (althiazide, bendroflumethiazide, chlorothiazide, hydrochlorothiazide, hydroflumethiazide, and trichloromethiazide), and other diuretics having a sulphonamide substituent in the benzene ring. Precolumn derivatization with sodium nitrite and N -(1-naphthyl)ethylenediamine, to form the coloured azo dyes of the hydrolyzed diuretics, decreased the polarity of the compounds and, consequently, their retention in the micellar eluents, and permitted detection in the visible region, eliminating thus the …

HydroflumethiazideChromatographySodiumchemistry.chemical_elementBiochemistryAnalytical ChemistryMatrix (chemical analysis)HydrochlorothiazidechemistryMicellar liquid chromatographyReagentmedicineEnvironmental ChemistryBendroflumethiazideSpectroscopyThiazidemedicine.drugAnalytica Chimica Acta
researchProduct

In vitro evaluation of poloxamer in situ forming gels for bedaquiline fumarate salt and pharmacokinetics following intramuscular injection in rats

2019

Graphical abstract

In situPO Propylene oxideIV IntravenousP338 Poloxamer 338lcsh:RS1-441Pharmaceutical Sciencechemistry.chemical_compoundn Sample sizeSD Standard deviationIM Intramuscularchemistry.chemical_classificationC0 Analyte plasma concentration at time zeroDoE Design of experimentsUV UltravioletPharmacology. TherapyK2.EDTA Potassium ethylenediaminetetraacetic acidLC–MS/MS Liquid chromatography-tandem mass spectrometryH&E Hematoxylin and eosintmax Sampling time to reach the maximum observed analyte plasma concentrationIn situ forming gelsCMC Critical micellar concentrationCmax Maximum observed analyte plasma concentrationIntramuscular injectionDN Dose normalizedGPT Gel point temperaturePLGA Poly-(DL-lactic-co-glycolic acid)TFA Trifluoroacetic acidCAN AcetonitrileATP Adenosine 5′ triphosphateSalt (chemistry)Polyethylene glycolPoloxamerArticlelcsh:Pharmacy and materia medicaPharmacokineticsIn vivoUHPLC Ultra-high performance liquid chromatographyPharmacokineticsAUClast Area under the analyte concentration versus time curve from time zero to the time of the last measurable (non-below quantification level) concentrationEO Ethylene oxideNMP N-methyl-2-pyrrolidoneComputingMethodologies_COMPUTERGRAPHICSAUC∞ Area under the analyte concentration vs time curve from time zero to infinite timeP407 Poloxamer 407In vitro releasePoloxamerCMT Critical micellar temperatureGel erosionIn vitrot1/2 Apparent terminal elimination half-lifechemistryMDR-TB Multi-drug resistant tuberculosisAUC80h Area under the analyte concentration versus time curve from time zero to 80 htlast Sampling time until the last measurable (non-below quantification level) analyte plasma concentrationMRM Multiple reaction monitoringNuclear chemistrySustained releaseInternational Journal of Pharmaceutics: X
researchProduct

Determination of urea-derived pesticides in fruits and vegetables by solid-phase preconcentration and capillary electrophoresis

2001

A multiresidue analytical method based on solid-phase extraction (SPE) enrichment combined with capillary electrophoresis (CE), using micellar electrokinetic capillary chromatography (MEKC), was developed to determine ten substituted urea pesticides in orange and tomato samples. Several factors such as pH, composition and concentration of the buffer, concentration of surfactant, addition of organic solvent, and working voltage were optimized to obtain the best compound separation in the shortest time. Separation can be achieved in 7 min using a micellar aqueous pH 9 buffer composed of 4 mM borate and 35 mM sodium dodecyl sulfate. After an SPE procedure, which provided a 10-fold enrichment, …

InsecticidesClinical BiochemistryFood ContaminationBiochemistryMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisVegetablesUreamedia_common.cataloged_instanceSolid phase extractionPesticidesSodium dodecyl sulfateEuropean unionMicellesmedia_commonDetection limitChromatographyAqueous solutionHerbicidesMethanolElectrophoresis CapillarySodium Dodecyl SulfatechemistryFruitEnrichment factorELECTROPHORESIS
researchProduct

Effect of ionization and the nature of the mobile phase in quantitative structure-retention relationship studies.

2005

Abstract The octanol–water distribution constant, commonly called partition coefficient, Po/w, is a parameter often retained as a measure of the hydrophobicity of a molecule. log Po/w, for a given molecule, can be conveniently evaluated constructing correlation lines between standard retention factor logarithms (log k) in reversed-phase liquid chromatography (RPLC) and standard log Po/w values. Many compounds of pharmaceutical interest can be quite hydrophobic and have, simultaneously, basic nitrogen atoms or acidic sulfur containing groups in their structure. This renders them ionizable. The hydrophobicity of the molecular drug form (Po/w value) is completely different from its ionic form …

IonsChromatographyChemistryElutionOrganic ChemistryDistribution constantAnalytical chemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHydrophobic effectPartition coefficientStructure-Activity RelationshipMicellar liquid chromatographyLipophilicityChromatography LiquidJournal of chromatography. A
researchProduct

Effect of sodium dodecyl sulphate and Brij-35 on the analysis of sulphonamides in physiological samples using direct injection and acetonitrile gradi…

2016

Micellar liquid chromatography (MLC) is a reversed-phase (RP) mode, which often does not require gradient elution, since the peaks of mixtures of compounds within a large range of polarities appear more evenly distributed in the chromatograms of isocratic elution, giving rise to a “gradient effect”. However, the use of a gradient of organic solvent may still be convenient to shorten the total analysis time. This work compares the separation of 15 sulphonamides using conventional hydro-organic RPLC and MLC with the surfactants sodium dodecyl sulphate (SDS) and Brij-35, and both isocratic and gradient elution with acetonitrile. The observed behaviour is rationalized attending to the interacti…

Isocratic elutionChromatographyChemistryElutionGeneral Chemical EngineeringSodium010401 analytical chemistryGeneral EngineeringAnalytical chemistrychemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundStationary phaseMicellar liquid chromatographyPhase (matter)AlkylbenzenesAcetonitrileAnalytical Methods
researchProduct