Search results for "ionic"

showing 10 items of 2016 documents

First trimester biochemical screening for Down's syndrome in singleton pregnancies conceived by assisted reproduction

2005

BACKGROUND: Serum biochemical markers [free betahCG (fbetahCG); pregnancy-associated plasma protein-A (PAPP-A)] used in first trimester Down's syndrome screening have not been fully investigated in pregnancies achieved by assisted reproduction techniques. We present data on pregnancies conceived by all types of assisted reproduction techniques, including pregnancies following ovum donation (OD) and a large sample by ICSI. METHODS: First trimester Down's syndrome screening was performed in 1054 normal singleton pregnancies: natural conception (n = 498), ovulation induction (OS, n = 97), IVF (n = 47), ICSI (n = 222) and OD (n = 190). RESULTS: No differences in maternal levels of fbetahCG and …

Down syndromemedicine.medical_specialtyReproductive Techniques AssistedPregnancy-associated plasma protein Amedicine.medical_treatmentPrenatal diagnosisBiologyPreimplantation genetic diagnosisEmbryo cryopreservationPregnancyPrenatal DiagnosismedicineHumansChorionic Gonadotropin beta Subunit HumanFalse Positive ReactionsGynecologyPregnancyurogenital systemObstetricsRehabilitationReproducibility of ResultsObstetrics and GynecologyGestational agemedicine.diseasePregnancy Trimester FirstReproductive MedicineFemaleOvulation inductionDown SyndromeBiomarkersHuman Reproduction
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Cationic Supramolecular Vesicular Aggregates for Pulmonary Tissue Selective Delivery in Anticancer Therapy

2016

The biopharmaceutical properties of supramolecular vesicular aggregates (SVAs) were characterized with regard to their physicochemical features and compared with cationic liposomes (CLs). Neutral and cationic SVAs were synthesized using two different copolymers of poly(aspartyl hydrazide) by thin-layer evaporation and extrusion techniques. Both copolymers were self-assembled in pre-formulated liposomes and formed neutral and cationic SVAs. Gemcitabine hydrochloride (GEM) was used as an anticancer drug and loaded by a pH gradient remote loading procedure, which significantly increased drug loading inside the SVAs. The resulting average size of the SVAs was 100 nm. The anticancer activity of …

DrugBiodistributionMacromolecular Substancesmedia_common.quotation_subjectSupramolecular chemistryAntineoplastic Agents02 engineering and technology010402 general chemistryHydrazideDeoxycytidine01 natural sciencesBiochemistryGemcitabine Hydrochloridesupramolecular chemistryStructure-Activity Relationshipchemistry.chemical_compoundDrug Delivery SystemsCationsDrug DiscoveryTumor Cells CulturedAnimalsHumansTissue DistributionCationic liposomeRats WistarGeneral Pharmacology Toxicology and Pharmaceuticsvesicular aggregatesCell Proliferationmedia_commonPharmacologyLiposomeDose-Response Relationship DrugMolecular StructurenanoparticleOrganic ChemistryCationic polymerization021001 nanoscience & nanotechnologyGemcitabineRats0104 chemical scienceschemistryBiochemistryantitumor agentliposomeMolecular MedicineDrug Screening Assays Antitumor0210 nano-technologyChemMedChem
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Montmorillonite nanodevices for the colon metronidazole delivery.

2013

The adsorption profiles of the antibiotic metronidazole (MNE) into the K10-montmorillonite (MMT-K10) clay and the subsequent release have been investigated as a function of pH and MNE/MMT-K10 ratio, in order to evaluate the potential of the MNE/MMT-K10 hybrids as controlled drug delivery system. The adsorption mechanism has been first elucidated by performing complementary equilibrium and kinetic studies and through the X-ray diffractometry (XRD) characterization of the obtained composite materials. The gathered results allowed us to propose a mechanism consisting of a multi-step pathway involving the neutral and the cationic form of the drug, which interact with different sites of the clay…

DrugColonmedia_common.quotation_subjectPharmaceutical ScienceDrug release kineticschemistry.chemical_compoundAdsorptionDrug Delivery SystemsMetronidazolemedicineOrganic chemistrymedia_commonSettore CHIM/02 - Chimica FisicaK10-montmorillonite metronidazole adsorption drug deliverySettore GEO/06 - MineralogiaCationic polymerizationAnti-Bacterial AgentsNanostructuresMetronidazoleMontmorillonitechemistryChemical engineeringSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliveryBentoniteOral retinoidmedicine.drugInternational journal of pharmaceutics
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Fluoride complexation of rutherfordium (Rf, element 104)

2000

The fluoride complexation of the group-4 elements Zr, Hf and Rf, and of the pseudo-homolog Th, has been investigated in mixed HNO3/HF solutions by studying Kd values on both cation exchange resins (CIX) and anion exchange resins (AIX) using the automated rapid chemistry apparatus ARCA. On the CIX, the four elements are strongly retained as cations below 10-3M HF. For Zr and Hf, the decrease of the Kd values due to the formation of fluoride complexes occurs between 10-3M HF and 10-2M HF. For Rf and Th, this decrease is observed at one order of magnitude higher HF concentrations. On the AIX, for Zr and Hf, a rise of the Kd values due to the formation of anionic fluoride complexes is observed …

Dubniumchemistry.chemical_compoundchemistryRutherfordiumInorganic chemistrychemistry.chemical_elementIonic bondingPhysical and Theoretical ChemistryFluorideIonRadiochimica Acta
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Micellization properties of cardanol as a renewable co-surfactant

2015

With the aim to improve the features of surfactant solutions in terms of sustainability and renewability we propose the use of hydrogenated natural and sustainable plant-derived cardanol as an additive to com- mercial surfactants. In the present study we demonstrated that its addition, in amounts as high as 10%, to commercial surfactants of different charge does not significantly affect surfactant properties. Conversely, the presence of hydrogenated cardanol can strongly affect spectrophotometric determination of CMC if preferential interactions with the dyes used take place. This latter evidence may be profitably exploited in surfactant manufacturing by considering that the concurrent pres…

Dynamic Laser Light Scattering.Sustainable surfactantIONIC SURFACTANTSTETRADECYLDIMETHYLAMINE OXIDEBiochemistryCardanolSurface-Active AgentsPhenolsPulmonary surfactantMoleculeOrganic chemistryFLUORESCENCEPhysical and Theoretical ChemistryMicellesCardanolCetrimoniumChemistrybusiness.industry-PotentialOrganic ChemistryWaterHYDROGENATED CARDANOLOrange OTTensiometryRenewable energyAGGREGATION NUMBERPREMICELLAR AGGREGATIONCetrimonium CompoundsSpectrophotometric determination of CMCGEMINI SURFACTANTSbusinessBEHAVIOROrganic & Biomolecular Chemistry
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Photophysical Properties of Charged Cyclometalated Ir(III) Complexes: A Joint Theoretical and Experimental Study

2011

The photophysical properties of a series of charged biscyclometalated [Ir(ppy)(2)(N boolean AND N)](1+) complexes, where ppyH is 2-phenylpyridine and N boolean AND N is 2,2'-bipyridine (bpy), 6-phenyl-2,2'-bipyridine (pbpy), and 6,6'-dipheny1-2,2'-bipyridine (dpbpy) for complexes 1, 2, and 3, respectively, have been investigated in detail. The photoluminescence performance in solution decreases from 1 to 3 upon attachment of phenyl groups to the ancillary ligand. The absorption spectra recorded over time suggest that complex 3 is less stable compared to complexes 1 and 2 likely due to a nucleophilic-assisted ancillary ligand-exchange reaction. To clarify this behavior, the temperature depen…

ELECTROLUMINESCENT DEVICESPhotoluminescenceAbsorption spectroscopyEMITTING ELECTROCHEMICAL-CELLSLigandChemistryCATIONIC IRIDIUM COMPLEXESAnalytical chemistryLARGE MOLECULESTURN-ON TIMESTRANSITION-METAL-COMPLEXESInorganic ChemistryCONCENTRATION GRADIENTSReaction rate constantTEMPERATURE-DEPENDENCEQUANTUM YIELDSPhysical chemistryPhysical and Theoretical ChemistryENERGY-GAP LAWInorganic Chemistry
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STUDIO GEOMORFOLOGICO DEL MARGINE IONICO DELLA CALABRIA: EVOLUZIONE MORFO-SEDIMENTARIA RECENTE ED INDIVIDUAZIONE DEGLI ELEMENTI DI PERICOLOSITA' GEOL…

2012

ELEMENTI DI PERICOLOSITA' GEOLOGICA.Settore GEO/02 - Geologia Stratigrafica E SedimentologicaSTUDIO GEOMORFOLOGICO DEL MARGINE IONICO DELLA CALABRIAEVOLUZIONE MORFO-SEDIMENTARIA
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Interaction of ionic compounds with multilamellar liposomes. An electrokinetic model

1998

Abstract We have proposed a theoretical model of interaction of ionic compounds (ionic adsorbate or ionic drugs), with multilamellar-liposomes, by means of their electrokinetic property variation with the ionic compound concentration. In this work, we show the complete development of the model proposed. Its theoretical results have been analysed to study the influence on the zeta-potential value of the following: number of membranes, size, shear-plane situation, critical concentration of formation (ccf), and the ionic compound concentration which annuls the zeta-potential value of the multilamellar-liposomes formed.

Electrokinetic phenomenaLiposomechemistry.chemical_compoundWork (thermodynamics)Colloid and Surface ChemistryMembraneChemical engineeringChemistryIonic strengthZeta potentialAnalytical chemistryIonic bondingIonic compoundColloids and Surfaces A: Physicochemical and Engineering Aspects
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Electrochemical study of copper chloride complexes in the RTIL 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide

2013

The electrochemistry of copper(I) and copper(II) chloride complexes in the RTIL 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide, BMPTf2N, has been studied with constant current electrolysis and cyclic staircase voltammetry at temperatures between 21.0 and 96.0 °C and in different concentrations of chloride. The chloride concentration was controlled by addition of 1-butyl-1-methylpyrrolidinium chloride, BMPCl. An important finding is the evidence of a three-coordinated complex, Cu(I)Cl32− which has not been found in organic chloroaluminates without a significant increase in temperature. Two Cu(I) species were found at molar ratios of [Cl−]/[Cu] < 4. The kinetic parameters for…

ElectrolysisGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementElectrochemistryChlorideCopperlaw.inventionchemistry.chemical_compoundElectron transferchemistrylawIonic liquidElectrochemistrymedicineCopper chlorideImideta116medicine.drugElectrochimica Acta
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Hidden Structural Features of Multicompartment Micelles Revealed by Cryogenic Transmission Electron Tomography

2014

The demand for ever more complex nanostructures in materials and soft matter nanoscience also requires sophisticated characterization tools for reliable visualization and interpretation of internal morphological features. Here, we address both aspects and present synthetic concepts for the compartmentalization of nanoparticle peripheries as well as their in situ tomographic characterization. We first form negatively charged spherical multicompartment micelles from ampholytic triblock terpolymers in aqueous media, followed by interpolyelectrolyte complex (IPEC) formation of the anionic corona with bis-hydrophilic cationic/neutral diblock copolymers. At a 1:1 stoichiometric ratio of anionic a…

Electron Microscope TomographyMaterials sciencePolymersProton Magnetic Resonance Spectroscopyta221electron tomographyGeneral Physics and AstronomyIonic bondingNanoparticleNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesMicelleCopolymerGeneral Materials ScienceSoft matterMicellesta218ta214ta114interpolyelectrolyte complexesGeneral EngineeringCationic polymerization021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineeringChromatography GelCryo-electron tomographySelf-assembly0210 nano-technologyACS Nano
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