Search results for "calibration"

showing 10 items of 890 documents

Cavity ring down spectrometry for disease diagnostics using exhaled air

2017

In this paper we report the current stage of the development of a cavity ring-down spectrometer (CRDS) system using exhaled human breath analysis for the diagnostics of different diseases like diabetes and later lung cancer. The portable CRDS system is made in ultraviolet spectral region using Nd:Yag laser 266 nm pulsed light. Calibration of the CRDS system was performed using generated samples by KinTek automated permeation tube system and self-prepared mixtures with known concentration of benzene and acetone in air. First experiments showed that the limits of detection for benzene and acetone are several tens of ppb.

Detection limitMaterials scienceSpectrometerAnalytical chemistrymedicine.disease_causeMass spectrometryLaserlaw.inventionchemistry.chemical_compoundBreath gas analysischemistrylawmedicineCalibrationBenzeneUltravioletBiophotonics—Riga 2017
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The 4th international comparison on EPR dosimetry with tooth enamel

2011

This paper presents the results of the 4th International Comparison of in vitro electron paramagnetic resonance dosimetry with tooth enamel, where the performance parameters of tooth enamel dosimetry methods were compared among sixteen laboratories from all over the world. The participating laboratories were asked to determine a calibration curve with a set of tooth enamel powder samples provided by the organizers. Nine molar teeth extracted following medical indication from German donors and collected between 1997 and 2007 were prepared and irradiated at the Helmholtz Zentrum Munchen. Five out of six samples were irradiated at 0.1, 0.2, 0.5, 1.0 and 1.5 Gy air kerma; and one unirradiated s…

Detection limitMolarRadiationChemistryCalibration curvebusiness.industryTooth enamelKermamedicine.anatomical_structurestomatognathic systemCalibrationmedicineEpr dosimetryDosimetryNuclear medicinebusinessInstrumentationRadiation Measurements
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Determination of total mercury in nuts at ultratrace level

2014

Abstract Total mercury, at μg kg−1 level, was determined in different types of nuts (cashew nut, Brazil nuts, almond, pistachio, peanut, walnut) using a direct mercury analyser after previous sample defatting and by cold vapour atomic fluorescence spectrometry. There is not enough sensitivity in the second approach to determine Hg in previously digested samples due to the strong matrix effect. Mercury levels in 25 edible nut samples from Brazil and Spain were found in the range from 0.6 to 2.7 μg kg−1 by using the pyrolysis of sample after the extraction of the nut fat. The accuracy of the proposed method was confirmed by analysing certified reference materials of Coal Fly Ash-NIST SRM 1633…

Detection limitNutfood and beverageschemistry.chemical_elementMercuryRice flourBiochemistryDefattingfood.foodAnalytical ChemistryMercury (element)Spectrometry FluorescenceCertified reference materialsfoodchemistryLimit of DetectionCalibrationNutsEnvironmental ChemistryFood scienceSpectroscopyFood contaminantBrazil nutAnalytica Chimica Acta
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Photo-induced chemiluminescence-based determination of diphenamid by using a multicommuted flow system

2007

This manuscript deals with the application of molecular connectivity calculations to predict the photo-induced chemiluminescent behaviour of the family of herbicides grouped as amides. Several compounds of this group were theoretically studied by means of a general discriminant equation formerly obtained, being 18 of them (plus eight from the chloroacetanilide sub-group) predicted with a high probability as photo-induced chemiluminescent. Empirical confirmation of the chemiluminometric behaviour was performed with some few commercially available amide herbicides. On the basis of these results, a new multicommutation-photo-chemiluminescent method is proposed for the determination of the diph…

Detection limitReproducibilityChromatographyChemistryAnalytical chemistryRepeatabilityAnalytical Chemistrylaw.inventionchemistry.chemical_compoundSodium hydroxidelawAmideCalibrationPhotodegradationChemiluminescenceTalanta
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Optimization of transmission near infrared spectrometry procedures for quality control of pesticide formulations

2006

The use of different response functions to be optimized in the frame of the use of near infrared spectrometry for quality control of active principles in agrochemical formulations has been evaluated. Both, simple functions, based on parameters like sensitivity, repeatability, accuracy, signal to noise ratio, limit of detection or sample throughput, and a complex function, considering all the aforementioned aspects, were employed in the development of a new method for Iprodione determination in agrochemicals. Optimization strategies were based on the previous screening of the most important instrumental factors like number of cumulated scans, nominal resolution, mirror velocity and zero fill…

Detection limitResolution (mass spectrometry)ChemistryRepeatabilityFactorial experimentBiochemistryAnalytical ChemistrySignal-to-noise ratioStatisticsCalibrationEnvironmental ChemistrySensitivity (control systems)Biological systemThroughput (business)SpectroscopyAnalytica Chimica Acta
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PLS-NIR determination of total sugar, glucose, fructose and sucrose in aqueous solutions of fruit juices

1997

Abstract An analytical procedure has been developed for the direct determination of sugars in fruit juice samples. The method is based on the partial least-squares (PLS) treatment of first derivative near infrared (NIR) spectroscopic data obtained between 1200 and 2450 nm, using 1 mm pathlength cell and a multicomponent calibration set, including seven binary mixtures and 10 ternary mixtures of glucose, fructose and sucrose. The limit of detection values found are of the order of 0.2 g/100 ml for total sugar and 0.2, 0.4 and 0.5 g/100 ml for glucose, fructose and sucrose, respectively. Relative standard deviation values obtained vary from 0.4% to 2.3% for six independent measurements of ind…

Detection limitSucroseChromatographyAqueous solutionNear-infrared spectroscopyCalibration setFructoseBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryEnvironmental ChemistryFruit juiceSugarSpectroscopyAnalytica Chimica Acta
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Multicommutation as an environmentally friendly analytical tool in the hydride generation atomic fluorescence determination of tellurium in milk.

2003

The aim of this study is to show the advantages of the emerging multicommutation methodology based on the use of solenoid valves for Te determination in milk by hydride generation atomic fluorescence spectrometry (HG-AFS). The delivery of a series of alternating sequential insertions of small volumes of samples and reagents gives rise to new hydrodynamic processes and exciting analytical potentials by controlling the time of flow through the on/off-switched solenoid valves. This drastically reduces the reagent consumption by a factor of 4 and the generation of effluents (590 mL h(-1) instead of 750 mL h(-1) generated by the continuous-mode measurement) and also provides an improvement in th…

Detection limitTime FactorsHydrideSpectrophotometry AtomicAnalytical chemistrychemistry.chemical_elementSolenoidBiochemistryAtomic fluorescence spectrometryEnvironmentally friendlyAnalytical ChemistrySonicationMilkchemistryReagentCalibrationCalibrationAnimalsRegression AnalysisTelluriumTelluriumMicrowavesHydrogenAnalytical and bioanalytical chemistry
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Methylmercury and inorganic mercury determination in fish by cold vapour generation atomic absorption spectrometry

2000

Abstract Given that organic mercury is more dangerous than the inorganic form and that it is converted into methylmercury by biological methylation, we have studied and optimized a simple method for measuring both organic and inorganic mercury contents in fish, using a spectroscopic vapour generation technique, with a sequential reduction of the digested sample with stannous chloride and sodium tetrahydroborate. Prior to applying the method the sample was subjected to alkaline wet digestion. Due to the matrix interferences calibration curves with matrix addition were needed for mercury determinations. The analytical parameters of the method were: linearity from 10 to 200 ng of Hg in the red…

Detection limitchemistry.chemical_classificationChromatographyChemistryCalibration curveSodiumchemistry.chemical_elementGeneral MedicineChlorideAnalytical ChemistryMercury (element)law.inventionchemistry.chemical_compoundlawEnvironmental chemistrymedicineAtomic absorption spectroscopyInorganic compoundMethylmercuryFood Sciencemedicine.drugFood Chemistry
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Flow injection biamperometric determination of chloramine-T in environmental, pharmaceutical and veterinary samples

2000

Abstract A flow injection assembly for the determination of chloramine-T is proposed. The sample (213 μl) is inserted into the carrier, de-ionized water flowing at 4.1 ml min−1. This carrier merges with a mixture of potassium iodide and sulphuric acid, and the resulting solution flows to the flow cell through a reactor 66 cm long. The chloramine-T oxidises the iodide to tri-iodide. The resulting iodide/iodine ratio is biamperometrically tested. The calibration graph is linear up to 65 μg ml−1 chloramine-T; the limit of detection is 0.5 μg ml−1; the relative standard deviation (r.s.d) of the calibration slope is 2.8% for a series of eight independent calibrations. The r.s.d. of a series of 7…

Detection limitchemistry.chemical_classificationVeterinary medicineCalibration curveIodideAnalytical chemistrychemistry.chemical_elementIodineBiochemistryAnalytical Chemistrychemistry.chemical_compoundWastewaterchemistryChloramine-TCalibrationEnvironmental ChemistryQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Determination of sertraline in rat plasma by HPLC and fluorescence detection and its application toin vivopharmacokinetic studies

2012

A simple, rapid, and sensitive HPLC method based on 9H-fluoren-9-ylmethyl chloroformate derivatization for the quantification of sertraline in rat plasma has been developed, requiring a plasma sample of only 0.1 mL, which was deproteinized and derivatized for 5 min in two single steps. The obtained derivative was stable at room temperature and was determined by HPLC using a fluorescence detector. The analytical column was a C(18) column and the mobile phase was acetonitrile and water (80:20, v/v). Calibration curves were linear in the range of 10-500 ng/mL. The limit of detection was approximately 3 ng/mL, and the lower limit of quantification was established at 10 ng/mL. The bias of the me…

Detection limitchemistry.chemical_compoundChromatographyPharmacokineticsChemistryCalibration curveFiltration and SeparationDerivativeChloroformateDerivatizationHigh-performance liquid chromatographyFluorescence spectroscopyAnalytical ChemistryJournal of Separation Science
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