Search results for "Ionic strength"

showing 10 items of 198 documents

Solution properties of polyelectrolytes

1991

Abstract Chromatographic data for sodium polystyrene sulphonate were obtained on both silica- and polymer-based size-exclusion supports using mobile phases of various pH and ionic strength. Deviations of the elution volume were observed towards both lower and higher values relative to the reference calibration graph obtained with uncharged standards. An empirical correlation is proposed in order to account for all the secondary effects observed. The general applicability of this correlation was further tested for chromatographic data obtained for a series of peptides and proteins on a silica-based support under very different eluent conditions. Deviations from ideal elution behaviour such a…

chemistry.chemical_classificationChromatographyAqueous solutionCalibration curveChemistryElutionSodiumSize-exclusion chromatographyOrganic ChemistryInorganic chemistryAnalytical chemistrychemistry.chemical_elementGeneral MedicinePolymerBiochemistryPolyelectrolyteAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyIonic strengthSodium nitratePhase (matter)Ideal (ring theory)Sodium polystyrene sulphonateJournal of Chromatography A
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Chiral separation of ephedrines by liquid chromatography using β-cyclodextrins

2001

β-cyclodextrins (β-CDs) have been evaluated as chiral recognition agents for the enantioseparation of ephedrines by liquid chromatography (LC). The compounds tested were norephedrine, ephedrine, pseudoephedrine, N-methylephedrine and N-methylpseuoephedrine. Two possibilities have been investigated, the employment of a chiral stationary phase consisting of immobilized β-cyclodextrin, and the addition of the chiral selector to the mobile phase. In the latter approach the following chiral agents have been assayed, native β-cyclodextrin (β-CD), methyl-β-cyclodextrin (M-β-CD), carboxyethyl-β-cyclodextrin (CE-β-CD), carboxymethyl-β-cyclodextrin (CM-β-CD) and hydroxypropyl-β-cyclodextrin (HP-β-CD)…

chemistry.chemical_classificationChromatographyCyclodextrinBiochemistryAnalytical ChemistryNasal decongestantChiral column chromatographySolventchemistryIonic strengthmedicineEnvironmental ChemistryEphedrineEnantiomerChiral derivatizing agentSpectroscopymedicine.drugAnalytica Chimica Acta
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Isolation From Human Calcium Oxalate Renal Stones of Nephrocalcin, a Glycoprotein Inhibitor of Calcium Oxalate Crystal Growth. Evidence That Nephroca…

1987

We have determined that the organic matrix of calcium oxalate kidney stones contains a glycoprotein inhibitor ofcalcium oxalate crystal growth (nephrocalcin) that resembles nephrocalcin present in the urine of patients with calcium oxalate stones and differs from nephrocalcin from the urine of normal people. Pulverized calcium oxalate renal stones were extracted with 0.05M EDTA, pH 8.0; nephrocalcin eluted in five peaks using DEAE-cellulose column chromatography, and each peak was further resolved by Sephacryl S-200 column chromatography. Four ofthe fiveDEAE peaks corresponded to those usually found in nephrocalcin from urine; the fifth eluted at a lower ionic strength than any found in uri…

chemistry.chemical_classificationChromatographyUrologyCalcium oxalateUrinemedicine.diseaseOxalateAmino acidchemistry.chemical_compoundColumn chromatographychemistryBiochemistryIonic strengthCarboxyglutamic acidmedicineKidney stonesJournal of Urology
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Development of competitive enzyme-linked immunosorbent assays for boscalid determination in fruit juices

2012

Abstract Boscalid is a modern, broad-spectrum carboxamide pesticide highly efficient against most fungal diseases affecting valuable crops. In this study, a boscalid-mimicking derivative with a six-carbon spacer arm replacing the chlorine atom at the pyridine ring of the target molecule was synthesized and coupled to carrier proteins. Following rabbit immunization, antibodies against this agrochemical were obtained for the first time, and they were characterised in terms of affinity and specificity, tolerance to solvents, and robustness to changes in buffer pH and ionic strength, using two assay formats. Both of the optimised immunoassays showed limits of detection below 0.1 μg/L. Moreover,…

chemistry.chemical_classificationDetection limitChromatographymedicine.diagnostic_testPesticide residuemedicine.drug_classCarboxamideGeneral MedicinePesticideAnalytical ChemistryEnzymechemistryIonic strengthImmunoassaymedicineHaptenFood ScienceFood Chemistry
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Characterization of interaction between tricyclic structures containing pharmaceuticals, their models and humic substances.

2011

Their persistence and wide consumption identify pharmaceuticals as “emerging pollutants”. The complexation of pharmaceuticals containing adamantine ring structures and their model substances with humic acids (HA) of different origins was compared using fluorescence spectroscopy as a function of pH, humic acid concentration, ionic strength, and molecular mass of HA. Binding constants between the studied pharmaceuticals and humic acids were calculated. A combination of dynamic and static quenching processes as indicated by nonlinear Stern-Volmer plots and high Kd values were positively correlated with the concentration of carboxyl groups in the studied humic acids. For basic functional group-…

chemistry.chemical_classificationEnvironmental EngineeringQuenching (fluorescence)Molecular massMolecular Structurecomplex mixturesWaste Disposal FluidFluorescence spectroscopyCharacterization (materials science)Water PurificationHydrophobic effectchemistryPharmaceutical PreparationsIonic strengthOrganic chemistryHumic acidHumic SubstancesWater Pollutants ChemicalWater Science and TechnologyTricyclicWater science and technology : a journal of the International Association on Water Pollution Research
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Solution properties of polyelectrolytes. II. Comparison of the effects of both polyion and eluent salt concentrations on the calibrations in aqueous …

1987

The elution behaviour of charged water-soluble polymers (sodium polystyrene sulphonate) in both salt-free and NaCl-containing aqueous mobile phases has been investigated by size-exclusion chromatography. A comparative analysis has been established between the results as a function of polyion and salt concentrations, which demonstrates that the chromatographic behaviour is similar in both cases. The variation of the slopes of the different concentration-dependent calibration curves is discussed in terms of polyelectrolyte conformational changes. Finally, a semi-empirical model has been developed to predict the dependence of the elution volume in either polyion or salt concentration, and its …

chemistry.chemical_classificationGel permeation chromatographyAqueous solutionChromatographyColumn chromatographyChemistryElutionIonic strengthSize-exclusion chromatographyGeneral EngineeringGeneral Materials SciencePolymerPolyelectrolyteBritish Polymer Journal
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Interpenetrated 3D porous scaffolds of silk fibroin with an amino and octadecyl functionalized hyaluronic acid

2015

An ethylenediamine (EDA) and octadecylamine (-C18) hyaluronic acid (HA) derivative, named HA-EDA-C18, has been used for the production of interpenetrated composite biomaterials with silk fibroin. The peculiar ionic strength sensibility of this HA derivative allows the production of porous matrices without the need for chemical crosslinking. Scaffolds have been produced through a salt leaching procedure by exploiting the properties of silk fibroin and HA-EDA-C18 to physically crosslink when forced through a syringe loaded with NaCl. The porosity of the sponges, comprised between 70-80%, was dependent on the amount of each polymer and NaCl size distribution. Moreover, through FT-IR analysis, …

chemistry.chemical_classificationGeneral Chemical EngineeringfungiComposite numbertechnology industry and agricultureFibroinEthylenediamineGeneral ChemistryPolymerequipment and supplieschemistry.chemical_compoundchemistryHyaluronidaseIonic strengthEnzymatic hydrolysisHyaluronic acidPolymer chemistrymedicinesponges scaffolds fibroin hyaluronic acidmedicine.drugRSC Advances
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Competing salt effects on phase behavior of protein solutions: tailoring of protein interaction by the binding of multivalent ions and charge screeni…

2014

The phase behavior of protein solutions is affected by additives such as crowder molecules or salts. In particular, upon addition of multivalent counterions, a reentrant condensation can occur; i.e., protein solutions are stable for low and high multivalent ion concentrations but aggregating at intermediate salt concentrations. The addition of monovalent ions shifts the phase boundaries to higher multivalent ion concentrations. This effect is found to be reflected in the protein interactions, as accessed via small-angle X-ray scattering. Two simulation schemes (a Monte Carlo sampling of the counterion binding configurations using the detailed protein structure and an analytical coarse-grain…

chemistry.chemical_classificationIonsCondensationOsmolar ConcentrationSurfaces Coatings and FilmsIonProtein–protein interactionProtein structurechemistryX-Ray DiffractionIonic strengthComputational chemistryPhase (matter)Scattering Small AngleMaterials ChemistryMoleculeHumansSaltsPhysical and Theoretical ChemistryCounterionSerum AlbuminThe journal of physical chemistry. B
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Binding of water-soluble, globular proteins to anionic model membranes

2009

Abstract The role of electrostatics is studied in the adsorption of proteins to negatively charged (phosphatidylcholine/phosphatidylglycerol, PC/PG) and neutral (PC) small unilamellar vesicles (SUVs). For model proteins the interaction is monitored vs . pH at low ionic strength. The adsorption behaviour of lysozyme, myoglobin and albumin (isoelectronic point, p I 5–11) is investigated in SUVs, along with changes of the fluorescence emission spectra of the charged proteins, via their adsorption on SUVs. Significant adsorption of the proteins to negatively charged SUVs is found only at pH values, where the number of positive charge moieties exceeds the number of negative charge moieties on th…

chemistry.chemical_classificationPhosphatidylglycerolChemistryGlobular proteinOrganic ChemistryInorganic chemistryAnalytical chemistryEffective nuclear chargeAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundAdsorptionMyoglobinIonic strengthPhosphatidylcholineProtein–lipid interactionSpectroscopyJournal of Molecular Structure
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PolyAT chemical denaturation in w/o microemulsion

2004

CD and UV spectroscopies have been used to investigate the effects caused by the addition of either strong acid-or base-containing microemulsions on the behaviour of the synthetic polynucleotide polyAT entrapped in the aqueous core of a cationic quaternary water-in-oil microemulsion (μE). The titrations were performed in the presence of variable concentrations of NaCl, in the range 0.00 to 0.60 M. In both cases, the primary effect was the reversible transition from B-double helix to random coil of the guest polynucleotide. However, in the microemulsive medium, the number of moles of protons (RH) and hydroxide ions (ROH) per mole of titrable sites are independent of the salt concentration bu…

chemistry.chemical_classificationPolyATAqueous solutionBase (chemistry)denaturationInorganic chemistryCationic polymerizationGeneral Physics and Astronomychemistry.chemical_compoundchemistrySettore CHIM/03 - Chimica Generale E InorganicaPolynucleotideIonic strengthHydroxideMicroemulsionTitrationPhysical and Theoretical ChemistryPhys. Chem. Chem. Phys.
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