Search results for "Surfactant"

showing 10 items of 397 documents

Synthesis and characterization of taylor-made organo-clays for biotechnological applications

2014

Settore GEO/06 - Mineralogiaclay montmorillonite surfactant organo-claySettore CHIM/02 - Chimica Fisica
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TERAPIA CON SURFACTANTE PER VIA AEROSOLICA NELL’INALAZIONE DA BOROTALCO

2009

Settore MED/38 - Pediatria Generale E SpecialisticaSurfactante borotalco
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The influence of Span®20 on stratum corneum lipids in Langmuir monolayers: comparison with Azone®

2000

Recently we have proved that Span 20 has the same enhancer effect as Azone on in vitro percutaneous penetration of lipophilic compounds (logP(oct) from 1.34 to 2.33). The purpose of this work is to study the interactions of Span 20 with stratum corneum lipids monolayers and to compare them with Azone. The surface pressure-area characteristics of Span 20 in mixed monolayers with different model lipids (ceramides, cholesterol, free fatty acids and two mixtures of ceramides+cholesterol, and ceramides+cholesterol+free fatty acids) in similar proportions to that which exists in human stratum corneum lipids were recorded as compression isotherms at 25 degrees C. Azone was also investigated on mon…

Skin AbsorptionPharmaceutical ScienceExcipientCeramidesMole fractionDosage formchemistry.chemical_compoundPulmonary surfactantMonolayermedicineStratum corneumAnimalsHumansHexosesChromatographyintegumentary systemChemistryCholesterolAzepinesLipidsCholesterolmedicine.anatomical_structureCattlelipids (amino acids peptides and proteins)EpidermisAzonemedicine.drugInternational Journal of Pharmaceutics
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Determination of Pyrrole Derivatives and Hydroxyproline with 4-(Dimethylamino)benzaldehyde in a Micellar Medium

1994

Abstract The spectrophotometric determination of pyrrole derivatives and hydroxyproline with 4-(dimethylamino)benzaldehyde (Ehrlich's reagent) in a sodium dodecyl sulphate micellar medium is studied. Pyrrole and pyrrole-2-carboxylic acid were used as model compounds for the optimization of the procedure. In the micellar medium with 0.2 M HCl at 90° C, pyrrole reacts in 15 min, whereas a HCl concentration larger than 5 M is required in the absence of the surfactant. The sensitivity increases from 1.3 to 5.6-fold with respect to the use of a non-micellar medium, for some pyrrole derivatives. The procedure is applied to the determination of hydroxyproline in meat samples.

SodiumBiochemistry (medical)Clinical Biochemistrychemistry.chemical_elementBiochemistryPyrrole derivativesAnalytical ChemistryBenzaldehydechemistry.chemical_compoundHydroxyprolinechemistryPulmonary surfactantReagentElectrochemistryOrganic chemistrySpectroscopyPyrroleAnalytical Letters
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LC of high to moderately polar basic drugs in urine with water and detergent, and direct injection

2016

Background: Micellar LC was first proposed as a ‘green’ mode using mobile phases of water and surfactant. However, in most procedures a small amount of organic solvent is required to decrease the retention to convenient values. Results & methodology: Mixed micellar mobile phases prepared with both cationic (sodium dodecyl sulphate) and nonionic surfactant (Brij-35) modulate the retention of high to moderately polar basic drugs to practical times, eliminating the need of organic solvent. While the mobile phase is continuously recycled through the system, the stationary phase performance is maintained after repetitive injection of the samples. Discussion & conclusion: Through an exte…

SodiumClinical Biochemistrychemistry.chemical_elementUrine010402 general chemistry01 natural sciencesPolyethylene GlycolsAnalytical ChemistrySurface-Active AgentsPulmonary surfactantLimit of DetectionPhase (matter)HumansGeneral Pharmacology Toxicology and PharmaceuticsMicellesChromatographyChemistryOrganic solvent010401 analytical chemistryCationic polymerizationSodium Dodecyl SulfateWaterGeneral Medicine0104 chemical sciencesMedical Laboratory TechnologyPharmaceutical PreparationsStationary phaseFlow Injection AnalysisPolarChromatography LiquidBioanalysis
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Halloysite nanotubes as nanoreactors for heterogeneous micellar catalysis

2021

Abstract Hypothesis Electrostatic attractions between the anionic head group of sodium alkylsulphates and the positively charged inner surface of halloysite nanotubes (HNTs) drive to the formation of tubular inorganic micelles, which might be employed as nanoreactors for the confinement of non polar compounds in aqueous media. On this basis, sodium alkylsulphates/halloysite hybrids could be efficient nanocatalysts for organic reactions occurring in water. Experiments Sodium decylsulphate (NaDeS) and sodium dodecylsulphate (NaDS) were selected for the functionalization of the halloysite cavity. The composition, the structure and the surface charge properties of the hybrid nanotubes were dete…

SodiumMicellar catalysischemistry.chemical_elementNanoreactorengineering.materialHalloysiteMicelleCatalysisBiomaterialsMicroviscosityColloid and Surface ChemistryPulmonary surfactantNanotechnologyMicellesNanotubesChemistryHalloysite nanotubesSodium alkylsulphatesNanomaterial-based catalystSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsInorganic micellesChemical engineeringengineeringSurface modificationClay
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Structure, stability, and fragmentation of sodium bis(2-ethylhexyl)sulfosuccinate negatively charged aggregates in vacuo by MD simulations.

2014

Negatively charged supramolecular aggregates formed in vacuo by n bis(2-ethylhexyl)sulfosuccinate (AOT(-)) anions and n + n(c) sodium counterions (i.e., [AOT(n) Na(n+nc)](nc)) have been investigated by molecular dynamics (MD) simulations for n = 1 to 20 and n(c) = -1 to -5. By comparing the maximum excess charge values of negatively and positively charged AOTNa aggregates, it is found that the charge storage capability is higher for the latter systems, the difference decreasing as the aggregation number increases. Statistical analysis of physical properties like gyration radii and moment of inertia tensors of aggregates provides detailed information on their structural properties. Even for …

SodiumSupramolecular chemistryMolecular Conformationchemistry.chemical_elementFragmentation patternsMolecular Dynamics SimulationAOTNa Self-assembling Charged reverse micelles Molecular dynamics simulation (MD) Supramolecular aggregates in vacuo Fragmentation patternsMicelleMolecular dynamicsSurface-Active AgentsPulmonary surfactantStructural BiologyAotNa; self-assembling; charged revrse micelle; Molecular Dynamics simulations; Supramolecular aggregates in vacuo; Fragmentation patternsSpectroscopyAlkylMicellesSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationIonsDioctyl Sulfosuccinic AcidAggregation numberAotNacharged revrse micelleself-assemblingSupramolecular aggregates in vacuoCrystallographychemistryThermodynamicsMolecular Dynamics simulationsCounterionJournal of the American Society for Mass Spectrometry
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Solubilisation of Chlorinated oils in triblock copolymers-surfactant mixed aggregates

2006

Solubilisation copolymer surfactantSettore CHIM/02 - Chimica Fisica
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Reversed-phase liquid chromatography with mixed micellar mobile phases of Brij-35 and sodium dodecyl sulphate: a method for the analysis of basic com…

2015

Micellar liquid chromatography (MLC) is a reversed-phase liquid chromatographic (RPLC) mode, which uses a surfactant as a modifier, with significant changes in retention and selectivity with regard to the classical RPLC mode that employs mixtures of water and organic solvent. The anionic sodium dodecyl sulphate (SDS) is the most usual surfactant in MLC, but it also requires the addition of an organic solvent to decrease the retention times and increase the efficiency. In particular, positively charged basic compounds are strongly retained by the stationary phase modified by adsorption of SDS monomers and require the addition of a strong solvent, such as propanol or pentanol. The non-ionic s…

SolventPropanolchemistry.chemical_compoundAdsorptionChromatographyPulmonary surfactantChemistryMicellar liquid chromatographyChemical polarityEnvironmental ChemistryReversed-phase chromatographySelectivityPollutionGreen Chemistry
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Surfactant self-assembly in the gas phase: Bis(2-ethylhexyl)sulfosuccinate- alkaline metal ion aggregates

2008

Molecular dynamics (MD) simulations were conducted for systems in vacuo consisting of n AOT anions (bis(2-ethylhexyl)sulfosuccinate ions) and n 1 or n Na+ ions up to n = 20. For n = 15, positively charged systems with Li+, K+, and Cs+ cations were also considered. All systems were observed to form reverse micelle-like aggregates whose centre is occupied by cations and polar heads in a very compact solid-like way, while globally the aggregate has the form of an elongated and rather flat ellipsoid. Various types of statistical analyses were carried out on the systems to enlighten structural and dynamical properties including gyration radius, atomic pair correlation functions, atomic B-factor …

Spectrometry Mass Electrospray IonizationREVERSE MICELLESElectrospray ionizationInorganic chemistrySupramolecular chemistrySalt (chemistry)LithiumMass SpectrometryIonSurface-Active AgentsPulmonary surfactantMaterials ChemistryWATERPhysical and Theoretical ChemistryAlkylchemistry.chemical_classificationChemistrySodiumSuccinatesAlkali metalSurfaces Coatings and FilmsSolutionsNANOCRYSTALSMetalsMESOSTRUCTURED FLUIDSGasesSelf-assembly
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