Search results for "Elution"

showing 10 items of 337 documents

Column-switching techniques for screening of diuretics and probenecid in urine samples

1994

A method based on high-performance liquid chromatography using column-switching is described for the screening of diuretics and probenecid in urine samples. The system uses a 20- x 2.1-mm i.d. precolumn, packed with a Hypersil ODS-C18, 30-microns stationary phase, for the on-line sample cleanup and enrichment. Untreated urine samples are directly injected, and the precolumn is flushed for 1 min with water to eliminate polar matrix components. The retained analytes are then back-flushed by means of a six-port switching valve onto a Hypersil ODS-C18 analytical column (5 microns, 250- x 4-mm i.d.), where they are separated using an acetonitrile/phosphate buffer (pH = 3) gradient elution. Under…

Doping in SportsAnalyteChromatographyProbenecidChemistrymedicine.medical_treatmentUrineAnalytical ChemistryProbenecidchemistry.chemical_compoundmedicineHumansGradient elutionColumn switchingDiureticDiureticsAcetonitrileQuantitative analysis (chemistry)Chromatography High Pressure Liquidmedicine.drugAnalytical Chemistry
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Loading, release and stability of epirubicin-loaded drug-eluting beads.

2015

Purpose The aim of this study was to determine the loading efficiency, physico-chemical stability and release of epirubicin-loaded DC Bead™ (Biocompatibles UK Ltd, a BTG International group company) (bead size 70–150 µm (=DC Bead M1™) and 100–300 µm) after loading with epirubicin solution (2 mg/ml) or reconstituted powder formulation (25 mg/ml) and controlled storage. Methods DC Bead™ were loaded with 76 mg epirubicin solution (Epimedac™, Medac GmbH) or 75 mg epirubicin powder formulation (Farmorubicin™, Pharmacia Pfizer GmbH) per 2 ml of beads. Drug loading efficiency and stability were determined by measuring the epirubicin concentration in the excess solution after predetermined interval…

Drug CompoundingDrug StorageBead030218 nuclear medicine & medical imaging03 medical and health sciences0302 clinical medicineDrug StabilitymedicinePharmacology (medical)Particle SizeChromatography High Pressure LiquidEpirubicinDrug CarriersChromatographyAntibiotics AntineoplasticDrug eluting beadsElutionbusiness.industrySyringesMicrospheresOncology030220 oncology & carcinogenesisvisual_artDrug releasevisual_art.visual_art_mediumPowdersbusinessEpirubicinmedicine.drugJournal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
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Rapid DNA elution procedure from agarose gels.

1996

Electrophoresis Agar GelChromatographyElutionBiophysicsCentrifugationCell BiologyDNABiochemistryMolecular Weightchemistry.chemical_compoundchemistryRapid dnaAgaroseMolecular BiologyAnalytical biochemistry
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A method for eluting DNA in a wide range of molecular weights from agarose gels

1991

We have developed a simple and rapid method for recovering DNAs of a wide range of molecular weights from agarose gels. A DNA-containing gel slice is placed on a Parafilm sheet in the center of a circular (positive) electrode and covered with a drop of buffer, while a linear (negative) electrode is placed on the top of the gel and driven about 1 mm into the gel itself. When a continuous current is applied, the DNA migrates into the buffer toward the circular electrode. We have obtained almost total recovery of DNAs up to 10 kb in size. Our method may also be used, under appropriate conditions, for higher molecular weight DNAs. The yield and all the biological assays performed on the DNAs ob…

Electrophoresis Agar GelGel electrophoresisChromatographyParafilmMolecular massElutionChemistryBiophysicsNucleic Acid HybridizationDNACell BiologyBiochemistryBuffer (optical fiber)Molecular Weightchemistry.chemical_compoundYield (chemistry)ElectrodeAgaroseMolecular BiologyAnalytical Biochemistry
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A novel approach for analysis of oligonucleotide-cisplatin interactions by continuous elution gel electrophoresis coupled to isotope dilution inducti…

2008

In this work we present a novel approach for in vitro studies of cisplatin interactions with 8-mer oligonucleotides. The approach is based on the recently developed coupling of continuous elution gel electrophoresis (GE) to an inductively coupled plasma-sector field mass spectrometer (ICP-SFMS) with the aim of monitoring the interaction process between this cytostatic drug and the nucleotides. In contrast to existing methods, the electrophoretic separation conditions used here allow both the determination of the reaction kinetics in more detail as well as the observation of dominant intermediates. Two different nucleotides sequences have been investigated for comparison purposes, one contai…

ElectrophoresisChromatographyProtein mass spectrometryElutionChemistryClinical BiochemistryAnalytical chemistryOligonucleotidesAntineoplastic AgentsMass spectrometryBiochemistryCapillary electrophoresis–mass spectrometrySample preparation in mass spectrometryAnalytical ChemistrySurface-enhanced laser desorption/ionizationMatrix-assisted laser desorption/ionizationKineticsSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationCisplatinInductively coupled plasma mass spectrometryElectrophoresis
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Multiresidue analysis of organic pollutants by in-tube solid phase microextraction coupled to ultra-high performance liquid chromatography-electrospr…

2013

In this work, in-tube solid phase microextraction (IT-SPME) coupling with ultra-high-pressure liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) multiresidue analytical method has been proposed for the first time for on-line enrichment of 9 analytes included in Water Frame Directive 2000/60/EC (WFD). The device was equipped with a GC TRB-5 capillary column, used as pre-concentration loop, and two conventional six-port injection valves. Water sample and desorption solvent volumes were tested. The optimum conditions were 4mL of processed sample followed by elution with 40μL of methanol. The analytes were detected with a mass spectrometer after being ionized positively using an elect…

ElectrosprayChromatographyChemistryElutionElectrospray ionizationOrganic ChemistryAnalytical chemistryPesticide ResiduesGeneral MedicineMass spectrometryTandem mass spectrometrySolid-phase microextractionBiochemistryAnalytical ChemistryLiquid chromatography–mass spectrometryTandem Mass SpectrometryDesorptionChromatography High Pressure LiquidSolid Phase MicroextractionWater Pollutants ChemicalJournal of chromatography. A
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Preconcentration and speciation of chromium in waters using solid-phase extraction and atomic absorption spectrometry

2000

Abstract A method for the preconcentration and speciation of chromium was developed. After formation of an anionic compound with ethylenediaminetetraacetic acid (CrY − ), Cr (VI) and Cr (III) are retained on a strong anionic phase (SAX) and controlled elution with 0.5 M NaCl permits their speciation. The retention and elution conditions were optimised, and interferences due to the presence of other ions such as Mg(II), Mn(II), Sn(II), Fe(III), Ba(II), Al(III), Ca(II), chloride, iodine, bromide, fluoride, sulphate, phosphate, bicarbonate and nitrate were studied. The detection limits were 0.4 μg l −1 and 1.1 μg l −1 for Cr(III) and Cr(VI), respectively, and reproducibility was 9%. The result…

ElutionAnalytical chemistrychemistry.chemical_elementEthylenediaminetetraacetic acidChlorideAnalytical Chemistrylaw.inventionchemistry.chemical_compoundChromiumchemistryBromidelawmedicineSolid phase extractionAtomic absorption spectroscopyFluorideNuclear chemistrymedicine.drugTalanta
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Enantiomerization of an inherently chiral resorcarene derivative: determination of the interconversion barrier by computer simulation of the dynamic …

2001

Abstract The inherently chiral tetrabenzoxazine resorcarene derivative 1 shows characteristic plateau-formation during enantioselective HPLC separation on the chiral stationary phase Chiralpak AD. By computer assisted peak form analysis of the elution profiles, obtained from temperature dependent dynamic HPLC (DHPLC) experiments, with ChromWin, the enantiomerization barrier Δ G # (298 K)=92±2 kJ mol −1 and the activation parameters Δ H # =53.0±1.8 kJ mol −1 and Δ S # =−131±14 J (K mol) −1 were determined.

ElutionOrganic ChemistryAnalytical chemistryForm analysisChiralpak ADResorcinareneChiral stationary phaseHigh-performance liquid chromatographyCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryPhysical and Theoretical ChemistryEnantioselective hplcDerivative (chemistry)Tetrahedron: Asymmetry
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Modelling of the elution behaviour in hybrid micellar eluents with different organic modifiers

1999

Abstract The elution behaviour in reversed-phase liquid chromatography (RPLC), with mobile phases containing micelles, can be described according to a distribution pattern among three phases: bulk water, micellar pseudophase and stationary phase. Several mechanistic equations based on this pattern, previously used to predict the retention in hybrid mobile phases of sodium dodecyl sulphate and propanol, were checked with several organic modifiers and a group of solutes of diverse polarity. The modifiers were the alcohols 1-propanol, 1-butanol and 1-pentanol, and other organic solvents widely used in conventional RPLC such as acetonitrile and tetrahydrofuran. New models were also proposed to …

ElutionSodiumAnalytical chemistrychemistry.chemical_elementAlcoholReversed-phase chromatographyBiochemistryMicelleAnalytical ChemistryPropanolchemistry.chemical_compoundchemistryEnvironmental ChemistryAcetonitrileSpectroscopyTetrahydrofuranAnalytica Chimica Acta
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Preparation and antioxidant activity of Radix Astragali residues extracts rich in calycosin and formononetin

2011

Abstract Radix Astragali is considered an excellent source of Traditional Chinese Medicine and a kind of famous restorative food. To make full usage of Radix Astragali, calycosin and formononetin were enriched through various macroporous resins from its residues, HPD500 resin, compared with other resins, offered the best effectiveness for the enrichment and separation of compounds. 35 °C was selected for its highest adoption capacity during static adsorption process, which can be obtained from adsorption isotherms. And then dynamic adsorption and desorption tests were carried out to optimize the operating parameters. After one run treatment with HPD500 resin, the contents of calycosin and f…

Environmental EngineeringAntioxidantChromatographyEthanolElutionmedicine.medical_treatmentBiomedical EngineeringBioengineeringchemistry.chemical_compoundAdsorptionCalycosinchemistryDesorptionmedicineFormononetinBiotechnologyBiochemical Engineering Journal
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