Search results for "Concentration."

showing 10 items of 1849 documents

Polymer−Surfactant Interactions. A Quantitative Approach to the Enthalpy of Transfer of Poly(Ethylene Glycol)s from Water to the Aqueous Sodium Perfl…

2000

The enthalpy of transfer (ΔHt) of nonionic polymers at a fixed concentration from water to aqueous substrate solutions as a function of the substrate concentration (fSmS) was determined. The substrates studied are sodium perfluorobutanoate to sodium perfluorooctanoate, and the polymers are poly(ethyleneglycol)s with molecular weights of 400 and 35 000. For the PEG 400-sodium perfluoroheptanoate−water systems, measurements were also performed at some polymer compositions. As a general feature, the enthalpy of transfer steeply changes with fSmS, reaching a maximum beyond which it decreases, tending to level off. A qualitative analysis of the enthalpy data assigned the steep increase of ΔHt to…

chemistry.chemical_classificationAqueous solutionSodiumEnthalpychemistry.chemical_elementSubstrate (chemistry)PolymerSurfaces Coatings and FilmschemistryChemical engineeringPulmonary surfactantCritical micelle concentrationPEG ratioPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
researchProduct

Effect of chelatants on gellan gel rheological properties and setting temperature for immobilization of living bifidobacteria.

1993

The effect of various concentrations of sequestrants (sodium citrate, sodium metaphosphate, and EDTA) was studied on gellan gel (1.5-2.5% (w/v)) setting temperature and rheological properties. Addition of EDTA between 0 and 0.8% (w/v) led to a progressive decrease of setting temperature. Citrate and metaphosphate decreased this parameter when added up to 0.4 or 0.6%, depending on gellan gum concentration, eventually resulting in the absence of gel formation at room temperature for the 1.5% gellan solution containing 0.4% citrate. This effect was accompanied by a significant decrease of gel strength and stiffness and might be attributed to the binding of the divalent cations required for cha…

chemistry.chemical_classificationBifidobacterium longumChromatographybiologyMetaphosphatePolysaccharides BacterialTemperatureConcentration effectHydrogen-Ion ConcentrationPolysaccharidebiology.organism_classificationGellan gumLactic acidCulture Mediachemistry.chemical_compoundchemistryCell MovementSodium citrateFermentationBifidobacteriumRheologyGelsBiotechnologyChelating AgentsBiotechnology progress
researchProduct

Long-term biodistribution study of HPMA- ran -LMA copolymers in vivo by means of 131 I-labeling

2018

Abstract Background For the evaluation of macromolecular drug delivery systems suitable pre-clinical monitoring of potential nanocarrier systems is needed. In this regard, both short-term as well as long-term in vivo tracking is crucial to understand structure-property relationships of polymer carrier systems and their resulting pharmacokinetic profile. Based on former studies revealing favorable in vivo characteristics for 18 F–labeled random (ran) copolymers consisting of N-(2-hydroxypropyl)methacrylamide (HPMA) and lauryl methacrylate (LMA) – including prolonged plasma half-life as well as enhanced tumor accumulation – the presented work focuses on their long-term investigation in the li…

chemistry.chemical_classificationCancer ResearchBiodistribution02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryIn vivoCritical micelle concentrationBiophysicsMolecular MedicineDistribution (pharmacology)MethacrylamideRadiology Nuclear Medicine and imagingNanocarriers0210 nano-technologyEx vivoNuclear Medicine and Biology
researchProduct

Life-time studies with capillary electrochromatography columns operated under different conditions.

2000

A test system has been established to permit the monitoring of the life-time performance of several reversed- phase capillary electrochromatography (CEC) columns. The retention factors, k(cec), peak symmetry coefficients, lambda(sym), and column efficiencies, N, of three neutral n-alkylbenzene analytes, namely ethyl-, n-butyl- and n-pentylbenzenes, were determined for Hypersil 3 microm n-octylsilica and n-octadecylsilica packed into CEC capillary columns of 100 microm I.D., with a packed length of 250 mm, and a total length of 335 mm. The performances of these CEC capillary columns were examined for a variety of eluents with pH values ranging between pH 2.0 - 8.0, similar to those employed …

chemistry.chemical_classificationCapillary electrochromatographyChromatographyCapillary actionOrganic ChemistryAnalytical chemistryGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationBiochemistryAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyHydrocarbonchemistryElectrochromatographyAlkylbenzenesTheoretical plateChromatography Micellar Electrokinetic CapillaryJournal of chromatography. A
researchProduct

Stabilization of immobilized cell systems using a modified metal surface, fructose polymer levan and a high cell concentration

1998

chemistry.chemical_classificationCellFructoseCell concentrationPolymerMetalchemistry.chemical_compoundmedicine.anatomical_structurechemistryChemical engineeringvisual_artvisual_art.visual_art_mediummedicineOrganic chemistry
researchProduct

Antidiabetic Behavior of Biguanides

1983

The existence of active electron pairs on some nitrogen atoms in phenformin hydrochloride is inferred from the presence of a hydrogen catalytic polarographic wave. This finding emphasizes the ability of biguanides to form hydrogen bridges with other molecular species such as amino acids and proteins, as well as to form coordination complexes with zinc and other metallic cations by means of these electron pairs. The antidiabetic action of phenformin and other related biguanides can be explained in terms of competition between these molecules and insulin to coordinate cationic oligoelements together with their ability to form hydrogen bonds between the biguanide moiety and insulin itself.

chemistry.chemical_classificationChemical PhenomenaChemistry PhysicalHydrogen bondChemistryBiguanidemedicine.drug_classInorganic chemistryBiguanidesCationic polymerizationPharmaceutical ScienceHydrogen-Ion ConcentrationPhenforminCombinatorial chemistryAmino acidchemistry.chemical_compoundPhenforminmedicineHypoglycemic AgentsInsulinMoleculeMoietyPhenformin HydrochloridePolarographyJournal of Pharmaceutical Sciences
researchProduct

Estimating the contribution of organic acids to northern hemispheric continental organic aerosol

2015

Using chemical ionization mass spectrometry to detect particle-phase acids (acid-CIMS) and aerosol mass spectrometry (AMS) measurements from Colorado, USA, and two studies in Hyytiala, Finland, we quantify the fraction of organic aerosol (OA) mass that is composed of molecules with acid functional groups (facid). Molecules containing one or more carboxylic acid functionality contributed approximately 29% (45-51%) of the OA mass in Colorado (Finland). Organic acid mass concentration correlates well with AMS m/z 44 (primarily CO2+), a commonly used marker for highly oxidized aerosol. Using the average empirical relationship between AMS m/z 44 and organic acids in these three studies, together…

chemistry.chemical_classificationChemical ionization010504 meteorology & atmospheric sciencesCarboxylic acid010501 environmental sciences01 natural sciencesAerosolGeophysicschemistry13. Climate actionEnvironmental chemistryGeneral Earth and Planetary SciencesAerosol mass spectrometryMass concentration (chemistry)0105 earth and related environmental sciencesOrganic acidGeophysical Research Letters
researchProduct

The role of pH on instability and aggregation of sickle hemoglobin solutions

2004

Understanding the physical basis of protein aggregation covers strong physical and biomedical interests. Sickle hemoglobin (HbS) is a point-mutant form of normal human adult hemoglobin (HbA). It is responsible for the first identified "molecular disease," as its propensity to aggregation is responsible for sickle cell disease. At moderately higher than physiological pH value, this propensity is inhibited: The rate of aggregate nucleation becomes exceedingly small and solubility after polymerization increases. These order-of-magnitude effects on polymer nucleation rates and concurrent relatively modest changes of solubility after polymerization are here shown to be related to both pH-induced…

chemistry.chemical_classificationChemistryHemoglobin SickleKineticsTemperatureNucleationPolymerHydrogen-Ion ConcentrationProtein aggregationBiochemistryKineticsSolubilityPolymerizationStructural BiologyPercolationBiophysicsHumansPhysical chemistryHemoglobinSolubilityHydrophobic and Hydrophilic InteractionsMolecular BiologyProteins: Structure, Function, and Bioinformatics
researchProduct

Hydrophobic and cation exchange mechanisms in the retention of basic compounds in a polymeric column.

2004

A cation exchange retention mechanism concomitant with the well-known hydrophobic partition mechanism in a polymeric column has been observed and investigated. This exchange process is attributed to ionization of some acidic sites present in the polymer column at basic mobile phase pH values. Several drugs of different basicity have been chromatographed on a polymeric PLRP-S column with methanol-water and acetonitrile-water mobile phases. The cation exchange between the protonated basic drug and the buffer cations (Na+, K+ and BuNH4+) is observed at the pH range where the protonated drug and the ionized sites of the column coexist. This process produces a shift of the retention versus pH pl…

chemistry.chemical_classificationChromatographyBase (chemistry)ChemistryPolymersOrganic ChemistryProtonationGeneral MedicinePolymerHydrogen-Ion ConcentrationBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHydrophobic effectIonizationPhase (matter)Cation Exchange ResinsColumn (data store)Journal of chromatography. A
researchProduct

1988

An apparatus for turbidimetric measurements of demixing temperatures under shear flow is presented, and the results of experiments with trans-decahydronaphthalene/polystyrene (TD/PS) solutions, investigating molecular weights ranging from 100 kg/mol to 1770 kg/mol, are compared with viscometric data. It is found that the sign and magnitude of shear effects depend on molecular weight (Mw), polymer concentration (c2), and shear rate (). For the first time, it was possible to study a solution which exhibits shear dissolution at low shear rates but shear demixing at high shear rates.

chemistry.chemical_classificationChromatographyChemistryConcentration effectThermodynamicsPolymerPure shearShear ratechemistry.chemical_compoundShear (geology)Polymer chemistryShear stressPolystyreneShear flowDie Makromolekulare Chemie
researchProduct