Search results for "Photometry"

showing 10 items of 797 documents

Flow injection-spectrophotometric determination of cresol compounds in water by reaction withp-aminophenol

1993

A spectrophotometric method has been developed for the simultaneous determination ofo-cresol andm-cresol in water by reaction withp-aminophenol (PAP). Three different methodologies have been assayed; (i) batch analysis, after reaction in an alkaline medium in the presence of dissolved molecular oxygen as oxidizing agent, (ii) a stopped-flow procedure, carried out in the presence of KIO4 and (iii) a flow injection method based on the same approach. The batch procedure requires 22 min for the full development of colour witho-cresol and 12 min form-cresol. In the stopped-flow mode, using KIO4 and a reaction time of 12 min, better sensitivity can be obtained for both compounds and limits of det…

Detection limitFlow injection analysisChromatographymedicine.diagnostic_testo-CresolCresolAnalytical ChemistryAbsorbancechemistry.chemical_compoundchemistrySpectrophotometryparasitic diseasesOxidizing agentmedicineDerivatizationmedicine.drugMicrochimica Acta
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A multicommuted flow system with solenoid micro-pumps for paraquat determination in natural waters.

2007

A flow system designed with solenoid micro-pumps is proposed for the determination of paraquat in natural waters. The procedure involves the reaction of paraquat with dehydroascorbic acid followed by spectrophotometric measurements. The proposed procedure minimizes the main drawbacks related to the standard chromatographic procedure and to flow analysis and manual methods with spectrophotometric detection based on the reaction with sodium dithionite, i.e. high solvent consumption and waste generation and low sampling rate for chromatography and high instability of the reagent in the spectrophotometric procedures. A home-made 10-cm optical-path flow cell was employed for improving sensitivit…

Detection limitFlow injection analysisParaquatChromatographyAutoanalysismedicine.diagnostic_testHerbicidesCoefficient of variationAnalytical chemistryWaterHydrogen-Ion ConcentrationDehydroascorbic AcidAnalytical ChemistrySolventSodium dithionitechemistry.chemical_compoundKineticschemistryParaquatSpectrophotometryReagentSpectrophotometryFlow Injection AnalysismedicineTechnology PharmaceuticalTalanta
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o-Dianisidine: a new reagent for selective spectrophotometric, flow injection determination of chlorine

2002

A flow injection analysis (FIA) procedure for the determination of free chlorine in industrial formulations and water samples is proposed. The manifold is provided with a gas-diffusion unit which permits the removal of interfering species and also the preconcentration of chlorine. The determination of chlorine is performed on the basis of the oxidation by o-dianisidine as a chromogenic reagent to a coloured product which can be monitored at 445 nm. The method (for a preconcentration step of 60 s) is linear over the range 0.04-1.00 mg l(-1) of chlorine, the limit of detection is 0.04 mg l(-1), the reproducibility of the procedure (as RSD of the slope) is 3.7% for a series of four independent…

Detection limitFlow injection analysisReproducibilityChromatographyChemistryChromogenicDianisidineAnalytical chemistrychemistry.chemical_elementO DianisidineBiochemistryAnalytical ChemistryChromogenic CompoundsSpectrophotometryReagentFlow Injection Analysispolycyclic compoundsElectrochemistryChlorineEnvironmental ChemistryChlorineSelectivityWater Pollutants ChemicalSpectroscopyThe Analyst
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Optimization of clean-up procedure for patulin determination in apple juice and apple purees by liquid chromatography

2009

Patulin (PAT) is a mycotoxin produced in fruits, mainly in apples, by several fungal species that can be carried into industrial apple juice by-products during factory processing. An analytical method for determination of PAT in apple juice and another one for determination of this compound in apple purees and apple compotes by liquid chromatography are proposed in the present paper. These methods have better precision and sensitivity than previously reported methods and focus mainly on extraction and clean-up. To accomplish analytical methods with higher accuracy, lower limits of detection and simpler procedures for application in quality control of the goods, different extraction and clea…

Detection limitMalusChromatographybiologyExtraction (chemistry)Food ContaminationHydrogen-Ion Concentrationbiology.organism_classificationAnalytical ChemistryBeveragesPatulinchemistry.chemical_compoundPatulinchemistryFruitMalusBy-productSpectrophotometry UltravioletSample preparationFood scienceFood qualityMycotoxinChromatography LiquidTalanta
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GFAAS determination of selenium in infant formulas using a microwave digestion method.

1994

A method for determining the selenium content of infant formulas is proposed. It includes wet digestion with nitric acid and hydrogen peroxide in medium pressure teflon bombs in a microwave oven and determination by graphite furnace atomic absorption spectrometry (GFAAS). The absence of interferences is checked. Values obtained for the limit of detection (19.4 ng/g), precision (RSD = 2.2%) and accuracy by analysis of a reference material show that the method is reliable.

Detection limitMicrowave ovenSpectrophotometry AtomicAnalytical chemistrychemistry.chemical_elementInfantHydrogen PeroxideNitric Acidlaw.inventionchemistry.chemical_compoundSeleniumchemistrylawNitric acidHumansSample preparationInfant FoodMagnesiumMicrowave digestionGraphite furnace atomic absorptionAtomic absorption spectroscopyMicrowavesSeleniumPalladiumFood ScienceDie Nahrung
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Automated determination of reboxetine by high-performance liquid chromatography with column-switching and ultraviolet detection.

2000

A fully automated method including column-switching and isocratic high-performance liquid chromatography (HPLC) was developed for quantitative analysis of the new antidepressant reboxetine, a noradrenaline reuptake inhibitor. After serum injection into the HPLC system and on-line sample clean-up on a silica C8 (10x4.0 mm I.D.) clean-up column with an eluent consisting of 2.5% acetonitrile in deionized water, the chromatographic separation was performed on an analytical column (Lichrospher CN; 250x4.6 mm I.D.) with an eluent of acetonitrile-aqueous potassium phosphate buffer (0.008 M, pH 6.4) (50:50). The UV detector was set at 273 or 226 nm. The limit of quantification was about 15 ng/ml at…

Detection limitQuality ControlChromatographymedicine.diagnostic_testAdrenergic Uptake InhibitorsReboxetineMorpholinesAnalytical chemistryGeneral ChemistryHigh-performance liquid chromatographychemistry.chemical_compoundAutomationReboxetineColumn chromatographychemistryPotassium phosphateTherapeutic drug monitoringSpectrophotometrymedicineHumansSpectrophotometry UltravioletQuantitative analysis (chemistry)Chromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical sciences and applications
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Quality control of pharmaceuticals containing clenbuterol by thermal lens spectrometry.

1996

An ultrasensitive absorptiometric procedure for the determination of clenbuterol in pharmaceutical preparations was developed. Clenbuterol was diazotized with nitrite and coupled with 1-(naphthyl)ethylenediamine, and the absorbance of the azo dye formed was measured by both spectrophotometry and ultrasensitive thermal lens spectrometry (TLS). The TLS limit of detection was 1.5 ppb, 14-fold lower than with a Hewlett-Packard diode array spectrophotometer. Thus, the TLS procedure can be advantageously applied to quality control of clenbuterol at the individual dose level and in small samples. Repeatability as relative standard deviation was 1.5% (50 ppb, n = 6).

Detection limitQuality ControlChromatographymedicine.diagnostic_testClinical BiochemistryPharmaceutical ScienceRepeatabilityAdrenergic beta-AgonistsMass spectrometryAnalytical ChemistryAbsorbancechemistry.chemical_compoundchemistryClenbuterolSpectrophotometryDrug DiscoverymedicineClenbuterolSpectrophotometry UltravioletDerivatizationQuantitative analysis (chemistry)Spectroscopymedicine.drugTabletsJournal of pharmaceutical and biomedical analysis
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Simultaneous determinations of zirconium, hafnium, yttrium and lanthanides in seawater according to a co-precipitation technique onto iron-hydroxide.

2013

Very low concentrations (pg mL(-1) or sub-pg mL(-1) level) along with the high salinity are the main problems in determining trace metal contents in seawater. This problem is mainly considered for investigations of naturally occurring YLOID (Y and Lanthanides) and Zr and Hf in order to provide precise and accurate results. The inductively coupled plasma mass spectrometry (ICP-MS), both in high and low resolution, offers many advantages including simultaneous analyses of all elements and their quantitative determination with detection limits of the order of pg mL(-1). However in the analysis of YLOID in seawater, a better determination needs an efficient combination of ICP-MS measurement wit…

Detection limitQuality ControlZirconiumSpectrophotometry AtomicAnalytical chemistrychemistry.chemical_elementFlocculationYttriumFerric CompoundsLanthanoid Series ElementsAnalytical ChemistryWorking rangeHafniumTrace ElementsCertified reference materialschemistryLimit of DetectionSeawaterSeawaterYttriumZirconiumInductively coupled plasma mass spectrometryHafniumTalanta
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Automated determination of amisulpride by liquid chromatography with column switching and spectrophotometric detection.

2003

A fully automated chromatographic method including on-line blood serum or plasma clean-up, isocratic high-performance liquid chromatography (HPLC) and spectrophotometric detection was developed for quantitative analysis of the new antipsychotic drug amisulpride. After injection of serum or plasma onto the HPLC system and clean-up on a pre-column (10x4.0 mm I.D.) filled with Silica CN 20 micrometer (pore size 10 nm) by an eluent consisting of 8% acetonitrile in deionized water, the chromatographic separation was performed on Lichrospher CN (5 micrometer; 250x4.6 mm I.D.) by an eluent consisting of 50% acetonitrile and 50% aqueous potassium phosphate buffer (0.008 M, pH 6.4). The UV detector …

Detection limitReproducibilityChromatographyClinical BiochemistryAnalytical chemistryCell BiologyGeneral MedicineReference StandardsBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyBlood serumchemistryPotassium phosphateSpectrophotometryHumansAmisulprideSulpirideAcetonitrileQuantitative analysis (chemistry)Chromatography High Pressure LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Thermal Lens Spectrometric Detection of Catecholamines after Oxidation to Aminochromes

1992

Abstract Experimental conditions for the spectrophotometric and thermal lens spectrometry (TLS) detection of catecholamines after oxidation to aminochromes with hexacyanoferrate (III) are optimized. At the low concentrations used in TLS, and in a 0.07 M citrate buffer, catecholamine oxidation can be performed at pH 7 and is immediate, whereas a lower pH value is required in spectrophotometry to avoid aminochrome polymerisation, the oxidation reactions being much slower. Similar TLS sensitivities are obtained for all catecholamines which facilitates HPLC evaluation. Sensitivity can be enhanced using a 50% ethanol-water medium. The linear dynamic range extends over two orders of magnitude, th…

Detection limitReproducibilityChromatographymedicine.diagnostic_testChemistryBiochemistry (medical)Clinical BiochemistryMass spectrometryBiochemistryRedoxHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionLens (optics)lawSpectrophotometryElectrochemistrymedicineUrine sampleSpectroscopyAnalytical Letters
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