Search results for "Analytical"

showing 10 items of 9586 documents

Liquid/Gas and Liquid/Liquid Phase Equilibria of the System Water/Bovine Serum Albumin

2013

The thermodynamic behavior of the system H2O/BSA was studied at 25 °C within the entire composition range: vapor pressure measurements via head space sampling gas chromatography demonstrate that the attainment of equilibria takes more than one week. A miscibility gap was detected via turbidity and the coexisting phases were analyzed. At 6 °C the two phase region extends from ca. 34 to 40 wt % BSA; it shrinks upon heating. The polymer rich phase is locally ordered, as can be seen under the optical microscope using crossed polarizers. The Flory-Huggins theory turns out to be inappropriate for the modeling of experimental results. A phenomenological expression is employed which uses three adju…

chemistry.chemical_classificationChromatography GasChemistrySpinodal decompositionVapor pressureLiquid gasAnalytical chemistryWaterSerum Albumin BovinePolymerPolarizerSurfaces Coatings and Filmslaw.inventionOptical microscopelawPhase (matter)Materials ChemistryAnimalsThermodynamicsCattleGas chromatographyPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Modelling retention and peak shape of small polar solutes analysed by nano-HPLC using methacrylate-based monolithic columns.

2019

Abstract The development of methacrylate-based monolithic columns was studied for the separation of pharmaceutical hydrophilic compounds in nano-liquid chromatography. The selected polymerisation mixture consisted of 7.5% hexyl methacrylate, 4.5% methacrylic acid and 18.0% ethylene dimethacrylate (w/w), in a binary porogenic solvent (35:35 w/w 1-propanol/1,4-butanediol). The polymer synthesised with this mixture has a good permeability, not excessive back-pressure, and reasonable retention times for polar and non-polar solutes. Monolithic columns (12 cm total capillary length, 100 μm i.d.), prepared with this mixture, were able to produce hydrogen bonding and electrostatic interactions, giv…

chemistry.chemical_classificationChromatography010401 analytical chemistry02 engineering and technologyPolymer021001 nanoscience & nanotechnologyMethacrylate01 natural sciencesBiochemistryHigh-performance liquid chromatography0104 chemical sciencesAnalytical ChemistrySolventchemistry.chemical_compoundchemistryMethacrylic acidEnvironmental ChemistryAlkylbenzenesParticle size0210 nano-technologySelectivitySpectroscopyAnalytica chimica acta
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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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Application of a weakly basic dimethylamino-modified silica ion exchanger to the separation of oligonucleotides

1979

Abstract LiChrosorb RP-8, RP-18 and Diol as well as a newly synthesized basic dimethylamino-modified silica ion-exchanger (DMA-silica) were applied for the separation of adenylic acid, cytidylic acid and uridylic acid oligoribonucleotides. On LiChrosorb RP-8 and RP-18, respectively, in aqueous buffered eluents (K 2 HPO 4 - H 3 PO 4 ), the retention of oligonucleotides was increased with decreasing number of nucleotide units in the solute, i.e., with increasing hydrophobic character. The elution behaviour of ologonucleotides on LiChrosorb Diol followed the same order but took place according to a size-exclusion mechanism. The retention of oligonucleotides on DMA-silica is assumed to be based…

chemistry.chemical_classificationChromatographyAqueous solutionIon exchangeElutionOrganic ChemistryDiolIonic bondingSalt (chemistry)General MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryOligoribonucleotidesNucleotideJournal of Chromatography A
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Interactions between non-volatile water-soluble molecules and aroma compounds in Camembert cheese

2002

Abstract Interactions between selected aroma compounds and non-volatile water-soluble molecules were studied using dynamic headspace-gas chromatography. A model water-soluble extract (MWSE), previously constructed in gustatory and physico-chemical accordance with the crude Camembert cheese WSE, allowed the contribution of non-volatiles to the headspace composition of volatile compounds to be assessed. The presence of the MWSE increased the headspace concentration of 2-heptanone, 1-octen-3-ol and 3-methylbutanol, showing that these three volatile compounds were released by MWSE. Omission tests performed on MWSE allowed for the impact of each MWSE component on aroma compounds release to be de…

chemistry.chemical_classificationChromatographyAqueous solutionbiologyChemistry010401 analytical chemistryOrganolepticPeptide04 agricultural and veterinary sciencesGeneral Medicine[SDV.IDA] Life Sciences [q-bio]/Food engineeringbiology.organism_classification040401 food science01 natural sciences0104 chemical sciencesAnalytical ChemistryAmino acid0404 agricultural biotechnology[SDV.IDA]Life Sciences [q-bio]/Food engineeringMoleculeComposition (visual arts)Gas chromatographyAromaComputingMilieux_MISCELLANEOUSFood Science
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RP-HPLC Determination of Tiger Nut and Orgeat Amino Acid Contents

2005

The amino acid profile of 11 samples of tiger nuts ( Cyperus esculentusL.) grown in the area of “L'Horta Nord” in Valencia (Spain) and one sample of African origin were determined, along with the amino acid contents of 10 samples of natural orgeat from Valencia. Protein was hydrolysed by hydrochloric acid at 110 °C for 23 h, and amino acids were derivatised with AQC and determined by RP-HPLC with fluorescence detection. The chromatographic conditions were optimised. The analytical parameters (detection and quantification limits, precision and accuracy) showed the method to be sufficiently sensitive and reproducible for determining amino acids resistant to acid hydrolysis in tiger nuts and o…

chemistry.chemical_classificationChromatographyArginine010405 organic chemistryGeneral Chemical Engineeringdigestive oral and skin physiologyfungi010401 analytical chemistryfood and beveragesBiology01 natural sciencesHigh-performance liquid chromatographyIndustrial and Manufacturing Engineering0104 chemical sciencesAmino acidHydrolysischemistryAcid hydrolysisTyrosineEssential amino acidHistidineFood ScienceFood Science and Technology International
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Study of binding media in works of art by gas chromatographic analysis of amino acids and fatty acids derivatized with ethyl chloroformate

1997

The aim of this work is to identify proteinaceous and oil binding media used in paintings from art collections in the Region of Valencia (Spain). This information is extremely useful for conservation and restoration work. The proposed procedure involves protein and glyceride hydrolysis from sub-milligram samples by treatment with hydrochloric acid, followed by neutralization, partition with chloroform and derivatization with ethyl chloroformate (ECF) of both the aqueous and the organic phases. The ECF derivatives of amino acids and azelaic, myristic, palmitic and stearic acids are separated by capillary gas chromatography. Amino acids are mainly found in the aqueous phase and long chain fat…

chemistry.chemical_classificationChromatographyAzelaic acidGlycerideOrganic ChemistryAqueous two-phase systemFatty acidGeneral MedicineBiochemistryAnalytical ChemistryAmino acidchemistry.chemical_compoundHydrolysischemistrymedicineOrganic chemistryEthyl chloroformateDerivatizationmedicine.drugJournal of Chromatography A
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Hydrophobicity of Ionizable Compounds. A Theoretical Study and Measurements of Diuretic Octanol−Water Partition Coefficients by Countercurrent Chroma…

1999

Countercurrent chromatography was used to determine the octanol−water partition coefficients (Po/w) of 23 diuretic drugs. The measured Po/w values ranged over 4 orders of magnitude from 0.05 to 550 (−1.3 < log Po/w < +2.7). All the compounds, except spironolactone, were ionizable. The Po/w values were strongly depending on the aqueous-phase pH. A theoretical model linking these values with the pH was derived for four cases:  (i) molecular acid−anionic base, (ii) cationic acid−molecular base, (iii) biprotic systems with two acidic or basic groups showing the same charge sign, and (iv) biprotic systems with ionizable groups showing different charges with special attention to the amino acid ca…

chemistry.chemical_classificationChromatographyBase (chemistry)Ammonium phosphateCarboxylic acidCationic polymerizationAnalytical chemistryAnalytical ChemistryPartition coefficientchemistry.chemical_compoundCountercurrent chromatographychemistryAmine gas treatingIonic compoundAnalytical Chemistry
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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
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Spectrophotometric Determination of Cystine with O-Phthalaldehyde in the Absence of Thiol

1988

Abstract A spectrophotometric method for the determination of cystine with o-phthalaldehyde (OPA) in the absence of thiol is described. When cystine is heated at 60[ddot]C for 30 min in a low excess of OPA (pH 9.5), a very stable derivative with 1:2 stoichiometry (cystine:OPA) and an absorption maximum at 335 nm (E = 4600) is formed. At pH < 1 the derivative is protonated (protonation constants: log K1 = 5.88 and log K2 = 3.70 at I = 0.1 and 20[ddot]C) and another absorption band at 440 nm (E = 3800) appears, which allows the determination of cystine in the presence of other amino acids.

chemistry.chemical_classificationChromatographyBiochemistry (medical)Clinical BiochemistryCystineProtonationBiochemistryAnalytical ChemistryAmino acidchemistry.chemical_compoundO-PhthalaldehydechemistryElectrochemistryThiolAbsorption (chemistry)SpectroscopyDerivative (chemistry)StoichiometryNuclear chemistryAnalytical Letters
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