Search results for "api"

showing 10 items of 8586 documents

Method and apparatus using selected superparamagnetic labels for rapid quantification of immunochromatographic tests

2009

Mika PA Laitinen1, Jari Salmela2, Leona Gilbert1, Risto Kaivola1, Topi Tikkala2, Christian Oker-Blom1, Jukka Pekola3, Matti Vuento11Department of Biological and Environmental Science; 2Department of Physics, University of Jyväskylä, Jyväskylä, Finland; 3Low Temperature Laboratory, Helsinki University of Technology, Helsinki, FinlandAbstract: A rapid method and instrumentation for quantification of immunochromatographic tests (ICT) are described. The principle and performance of the method was demonstrated by measuring the levels of human chorionic gonadotropin (hCG) present in urine. The test format was a sandwich assay using two distinct monoclonal antib…

Detection limitAnalyteendocrine systemChromatographyChemistryCapillary actionmedicine.drug_classBiomedical EngineeringBioengineeringBioinformaticsMonoclonal antibodyLinear rangemedicineUrine sampleBiosensorhormones hormone substitutes and hormone antagonistsSuperparamagnetismOriginal ResearchNanotechnology Science and ApplicationsNanotechnology, Science and Applications
researchProduct

Immunochromatographic Assay for Quantitation of Milk Progesterone.

1996

We describe a rapid immunochromatographic method for the quantitation of progesterone in bovine milk. The method is based on a 'competitive' assay format using the monoclonal antibody to progesterone and a progesterone-protein conjugate labelled with colloidal gold particles. The monoclonal antibody to progesterone is immobilized as a narrow detection zone on a porous membrane. The sample is mixed with colloidal gold particles coated with progesterone-protein conjugate, and the mixture is allowed to migrate past the detection zone. Migration is facilitated by capillary forces. The amount of labelled progesterone-protein conjugate bound to the detection zone, as detected by photometric scann…

Detection limitBovine milkChromatographymedicine.drug_classCapillary actionChemistryGeneral Chemical EngineeringAntibodies MonoclonalCross ReactionsMonoclonal antibodySensitivity and SpecificityChromatography AffinityMilkColloidal goldPorous membranemedicineAnimalsCattleChromatography Thin LayerProgesteroneConjugateActa Chemica Scandinavica
researchProduct

Capillary electrophoresis for the determination of pesticide residues

2003

Capillary electrophoresis (CE) is becoming an advantageous tool for determining pesticide residues in environmental matrices because of its simplicity and high separation efficiency. However, inadequate limits of detection (LODs) and a lack of selective detectors limit the technique. The present review gives an overview of current developments in off-column and on-column approaches to trace enrichment in analysing real samples, and summarises the determination of pesticides residues by conventional CE as well as by the emerging techniques, such as CE-mass spectrometry (MS). The usefulness of these approaches in environmental applications is documented.

Detection limitCapillary electrophoresisChromatographyPesticide residueChemistryPesticideMass spectrometrySpectroscopyAnalytical ChemistryTrAC Trends in Analytical Chemistry
researchProduct

Separation of plutonium and neptunium species by capillary electrophoresis-inductively coupled plasma-mass spectrometry and application to natural gr…

2003

Capillary electrophoresis (CE) was coupled to ICPMS in order to combine the good performance of this separation technique with the high sensitivity of the ICPMS for the analysis of plutonium and neptunium oxidation states. The combination of a fused-silica capillary with a MicroMist AR 30-I-FM02 nebulizer and a Cinnabar small-volume cyclonic spray chamber yielded the best separation results. With this setup, it was possible to separate a model element mixture containing neptunium (NpO2(+)), uranium (UO2(2+)), lanthanum (La3+), and thorium (Th4+) in 1 M acetic acid. The same conditions were also suitable for the separation of various oxidation states of plutonium and neptunium in different a…

Detection limitCapillary electrophoresischemistryNeptuniumAnalytical chemistryThoriumchemistry.chemical_elementUraniumMass spectrometryInductively coupled plasma mass spectrometryAnalytical ChemistryPlutoniumAnalytical chemistry
researchProduct

Fishing for a drug: solid-phase microextraction for the assay of clozapine in human plasma

1999

Solid-phase microextraction (SPME) was investigated as a sample preparation method for assaying the neuroleptic drug clozapine in human plasma. A mixture of human plasma, water, loxapine (as internal standard) and aqueous NaOH was extracted with a 100-micron polydimethylsiloxane (PDMS) fiber (Supelco). Desorption of the fiber was performed in the injection port of a gas chromatograph at 260 degrees C (HP 5890; 30 m x 0.53 mm I.D., 1 micron film capillary; nitrogen-phosphorous selective detection). Fibers were used repeatedly in up to about 75 analyses. The recovery was found to be 3% for clozapine from plasma after 30 min of extraction. However, in spite of the low recovery, the analyte was…

Detection limitChromatography GasChromatographymedicine.diagnostic_testChemistryReproducibility of ResultsLoxapineGeneral ChemistryReference StandardsSolid-phase microextractionSensitivity and SpecificityHigh-performance liquid chromatographyMatrix (chemical analysis)Therapeutic drug monitoringmedicineHumansSample preparationSolid phase extractionGas chromatographyClozapineJournal of Chromatography B: Biomedical Sciences and Applications
researchProduct

Determination of thyreostatics in animal feed by micellar electrokinetic chromatography

1999

The determination of the thyreostatics 2-thiouracil, its derivatives (4-methyl-2-thiouracil, 4-propyl-2-thiouracil and 4-phenyl-2-thiouracil) and methimazole in manufactured dried animal feed by micellar electrokinetic chromatography (MEKC) is described. A 99 +/- 5% extraction yield at the 20 micrograms g-1 level (n = 8) was achieved by shaking the milled fodder with methanol-1 M NaOH (80 + 20). Aliquots of the supernatant were injected in a 75 microns x 33.5 cm uncoated silica capillary using pressure; separation was performed at 23 degrees C with 15 kV (positive polarity) in a background electrolyte (BGE) containing 40 mM sodium dihydrogenphosphate, 50 mM sodium dodecyl sulfate and 15 mM …

Detection limitChromatographyAnimal feedSodiumExtraction (chemistry)chemistry.chemical_elementAnimal FeedBiochemistryThiouracilMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundAntithyroid AgentschemistryFodderElectrochemistryAnimalsEnvironmental ChemistrySodium dodecyl sulfateQuantitative analysis (chemistry)SpectroscopyChromatography Micellar Electrokinetic CapillaryThe Analyst
researchProduct

On-line removal of mass interferences in palladium determination by ICP-MS using modified capillaries coupled to micro-flow nebulizers

2001

This paper describes a novel approach developed for on-line removal of interferences within modified capillaries coupled to micro-flow nebulizers, for palladium determination by inductively coupled plasma mass spectrometry (ICP-MS). A strong cation exchanger [2-(4-chlorosulfophenyl)ethyltrichlorosilane)] was covalently bound to the silica capillary that was coupled to a microconcentric nebulizer (MCN) or to a direct injection nebulizer (DIN). The modified surface of the capillary was able to selectively retain copper and yttrium from aqueous samples at pH 7.5 during the sample introduction step, while Pd was not retained and 105Pd could be determined in the absence of interferent elements. …

Detection limitChromatographyAqueous solutionIon exchangeCapillary actionAnalytical chemistrychemistry.chemical_elementYttriumAnalytical ChemistryNebulizerchemistryInductively coupled plasma mass spectrometrySpectroscopyPalladiumJ. Anal. At. Spectrom.
researchProduct

Automatic in-tube SPME and fast liquid chromatography: A cost-effective method for the estimation of dibuthyl and di-2-ethylhexyl phthalates in envir…

2007

A 80-cm length commercially available capillary coated with 95% polydimethylsiloxane and 5% polydiphenylsiloxane (TBR-5) was employed to carry out on-line extraction and preconcentration of dibuthyl phthalate (DBP) and di-2-ethylhexyl phthalate (DEHP) in the chromatographic system. The coated capillary was placed between the sample injection loop and the injection needle of an autosampler. Variables affecting the automatic in-tube solid-phase microextraction (SPME) were optimized. A Genesis C(18) (5 cm x 4.6 mm i.d., 4 microm particle size) was employed as analytical column. The achieved limits of detection by use of diode array detection were 1 and 2.5 microg L(-1), respectively. The propo…

Detection limitChromatographyCapillary actionCost-Benefit AnalysisCoefficient of variationExtraction (chemistry)PhthalateAnalytical chemistryReproducibility of ResultsSolid-phase microextractionSensitivity and SpecificityBiochemistryDibutyl PhthalateAnalytical Chemistrychemistry.chemical_compoundchemistryDiethylhexyl PhthalateEnvironmental ChemistrySample preparationParticle sizeWater Pollutants ChemicalSpectroscopyAnalytica Chimica Acta
researchProduct

Analysis of post-harvest fungicides by micellar electrokinetic chromatography.

2001

A method based on solid-phase extraction (SPE) and micellar electrokinetic chromatography (MEKC) was developed for the simultaneous determination of carbendazim, imazalil, methylthiophanate, O-phenylphenol, prochloraz, procimidone, thiabendazole and triadimefon residues in grape, lettuce, orange and tomato. Selectivity and resolution were studied changing the pH and the concentration of the buffer, the type and concentration of surfactant and the methanol content in the mobile phase. A buffer consisting of 4 mM borate with 75 mM sodium cholate (pH 9.2) gave the best results. The recoveries of the fungicides in spiked fruit and vegetable samples ranged from 30 to 105%, and the limits of dete…

Detection limitChromatographyCarbendazimOrganic ChemistryReproducibility of ResultsSodium Dodecyl SulfateGeneral MedicineBuffersSodium CholateBiochemistryMicellar electrokinetic chromatographyAnalytical ChemistryFungicides IndustrialFungicidechemistry.chemical_compoundSurface-Active AgentsTriadimefonchemistryFruitSample preparationSolid phase extractionSodium CholateChromatography Micellar Electrokinetic CapillaryJournal of chromatography. A
researchProduct

Chiral separation of bupivacaine enantiomers by capillary electrophoresis partial-filling technique with human serum albumin as chiral selector

2004

Abstract Capillary electrophoresis (CE) is a powerful technique for enantiomer separations due to its intrinsic high separation efficiencies, speed of analysis, low reagent consumption and small sample requirements. However, some chiral selectors present strong background UV absorption providing high detection limits. The present paper deals with the application of the partial-filling technique to the separation of bupivacaine enantiomers by capillary electrophoresis using human serum albumin (HSA) as chiral selector. In this procedure the cationic surfactant cetyltrimethylammonium bromide (CTAB) was used as a dinamic capillary coating in order to reduce the electro-osmotic flow and detect …

Detection limitChromatographyChemistryCapillary actionOrganic ChemistryAnalytical chemistryElectrophoresis CapillaryStereoisomerismGeneral MedicineElectrolyteHuman serum albuminBupivacaineBiochemistryAnalytical ChemistryCapillary electrophoresisPharmaceutical PreparationsReagentmedicineAnesthetics LocalEnantiomerEnantiomeric excessmedicine.drugJournal of Chromatography A
researchProduct