Search results for "Medical laboratory"

showing 10 items of 161 documents

A Multiple Local Models Approach to Accuracy Improvement in Continuous Glucose Monitoring

2011

Continuous glucose monitoring (CGM) devices estimate plasma glucose (PG) from measurements in compartments alternative to blood. The accuracy of currently available CGM is yet unsatisfactory and may depend on the implemented calibration algorithms, which do not compensate adequately for the differences of glucose dynamics between the compartments. Here we propose and validate an innovative calibration algorithm for the improvement of CGM performance.CGM data from GlucoDay(®) (A. Menarini, Florence, Italy) and paired reference PG have been obtained from eight subjects without diabetes during eu-, hypo-, and hyperglycemic hyperinsulinemic clamps. A calibration algorithm based on a dynamic glo…

Blood Glucosemedicine.medical_specialtyCalibration (statistics)Endocrinology Diabetes and MetabolismMonitoring Ambulatory030209 endocrinology & metabolismBiosensing TechniquesAccuracy improvementSensitivity and Specificity01 natural sciencesGlobal model03 medical and health sciences0302 clinical medicineEndocrinologyInternal medicineBlood Glucose Self-MonitoringDiabetes MellitusmedicineHumansGlucose dynamicsPlasma glucoseContinuous glucose monitoringbusiness.industryBlood Glucose Self-Monitoring010401 analytical chemistryReproducibility of ResultsPattern recognition0104 chemical sciencesMedical Laboratory TechnologyEndocrinologyCalibration algorithmArtificial intelligencebusinessAlgorithmsDiabetes Technology & Therapeutics
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Flow Cytometric Analysis of Calcium Mobilization in Whole‐Blood Platelets

2003

Flow cytometry provides a convenient method to evaluate platelet activation by following the kinetics of intracellular free Ca2+, using sensitive fluorescent indicators that can be loaded into intact cells. Moreover, in the clinical setting, whole-blood techniques have obvious advantages to avoid artifactual platelet activation and allow the maintenance of near-physiological conditions. This unit describes a fast and sensitive flow cytometric procedure using the Ca2+-sensitive dye fluo-3 AM and the platelet-specific antibody CD41-PE to determine the kinetics of intracellular Ca2+ mobilization in whole-blood platelets with minimal manipulation of the samples. The technique may be applied to …

Blood PlateletsPlatelet Membrane Glycoprotein IIbHistologyStimulation030204 cardiovascular system & hematologyBiochemistryFlow cytometry03 medical and health sciences0302 clinical medicineThrombinMethodsmedicineAnimalsHumansPlateletCalcium SignalingPlatelet activationFluorescent Dyes030304 developmental biologyWhole blood0303 health sciencesAniline Compoundsmedicine.diagnostic_testChemistryAntibodies MonoclonalGeneral MedicineFlow CytometryIn vitro3. Good healthKineticsMedical Laboratory TechnologyXanthenesBiochemistryBiophysicsCalciumIntracellularmedicine.drugCurrent Protocols in Cytometry
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Determination of particle number and brightness using a laser scanning confocal microscope operating in the analog mode

2008

We describe a method to obtain the brightness and number of molecules at each pixel of an image stack obtained with a laser scanning microscope. The method is based on intensity fluctuations due to the diffusion of molecules in a pixel. For a detector operating in the analog mode, the variance must be proportional to the intensity. Once this constant has been calibrated, we use the ratio between the variance and the intensity to derive the particle brightness. Then, from the ratio of the intensity to the brightness we obtain the average number of particles in the pixel. We show that the method works with molecules in solution and that the results are comparable to those obtained with fluctu…

BrightnessHistologyMicroscopeLaser scanningGreen Fluorescent ProteinsCHO CellsTransfectionFluorescencelaw.inventionCricetulusOpticslawCricetinaeMicroscopyAnimalsParticle SizeInstrumentationMicroscopy ConfocalN&B confocal microscopyPixelbusiness.industryDynamic rangeChemistryDetectorPhoton countingMedical Laboratory TechnologyAnatomybusinessAlgorithms
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Measurement of T Cell Activation After 16‐hr In Vitro Stimulation with Concanavalin A

2010

A flow cytometry assay that can be used to directly determine the proportion of activated T lymphocytes in human whole blood samples after stimulation with concanavalin A is presented here. Human whole blood is incubated with fluorescently labeled antibodies (against CD3, CD4, CD8, and CD69), erythrocytes are then lysed, and the samples are analyzed using a flow cytometer. The assay presented is able to differentiate between CD4+ and CD8+ T lymphocytes. Thus, it is possible to quantify both lymphocyte populations in parallel, as well as the respective proportions of activated T lymphocytes, all from one sample. An additional advantage of this assay is that it was developed to assay whole bl…

CD4-Positive T-LymphocytesCell ExtractsErythrocytesTime FactorsHistologyLymphocyteCD3T cellCD8-Positive T-LymphocytesLymphocyte ActivationBiochemistryImmunophenotypingFlow cytometryConcanavalin AmedicineHumansCytotoxic T cellWhole bloodbiologymedicine.diagnostic_testAntibodies MonoclonalCD28General MedicineFlow CytometryMolecular biologyLymphocyte SubsetsMedical Laboratory Technologymedicine.anatomical_structureConcanavalin Abiology.proteinCurrent Protocols in Cytometry
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Can Hepatoma Cell Lines be Re-differentiated to be Used in Drug Metabolism Studies?

2013

Knowledge of metabolism, enzymes so far involved, and potential enzyme-inhibiting or enzyme-inducing properties of new compounds is a key issue in drug development. Primary cultured hepatocytes, cytochrome P450 (CYP)-engineered cells and hepatoma cell lines are currently being used for this purpose, but only primary cultures can produce a metabolic profile of a drug similar to that found in vivo and can respond to inducers. Because of their limited accessibility, alternatives to replace human hepatocytes are currently being explored, including the immortalisation of hepatocytes by using different strategies (i.e. SV40 T-large antigen, conditionally immortalised hepatocytes, transfection wi…

Carcinoma Hepatocellularbiologybusiness.industryTransgeneCellular differentiationLiver NeoplasmsCytochrome P450Cell DifferentiationGeneral MedicineTransfectionToxicologyGeneral Biochemistry Genetics and Molecular BiologyBiotechnologyCell biologyMedical Laboratory TechnologyCytochrome P-450 Enzyme SystemDrug developmentCell cultureCell Line Tumorbiology.proteinHumansbusinessTranscription factorDrug metabolismTranscription FactorsAlternatives to Laboratory Animals
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The selection of serum-independent PC12 cells for a more-reliable manganese cytotoxicity test.

2007

A major issue concerning the protocols of heavy metal cytotoxicity tests with PC12 cells was the hypothesis that serum in the culture medium might sequester the metal, thus altering the results obtained. However, serum withdrawal impairs the viability of PC12 cells themselves, thus impeding cytotoxicity testing in the absence of serum. In this study, we repeatedly selected undifferentiated, totally non-adherent PC12 cells in Petri dishes. Surprisingly, we discovered that these cells could survive and proliferate in serum-free medium. Moreover, features such as NGF-responsiveness, resazurin reduction potential, doubling rate, protein content, and basal caspase-3 enzyme activity, were equiva…

Cell SurvivalAdrenal Gland NeoplasmsPheochromocytomaToxicologyAnimal Testing AlternativesPC12 CellsGeneral Biochemistry Genetics and Molecular BiologyCulture Media Serum-Freelaw.inventionchemistry.chemical_compoundlawDoubling timeCytotoxic T cellAnimalsCytotoxicityManganesebiologyChemistryPetri dishResazurinGeneral MedicineEnzyme assayIn vitroRatsMedical Laboratory TechnologyBiochemistryToxicitybiology.proteinAlternatives to laboratory animals : ATLA
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Dimethylsulfoxide as carrier in enzyme cytochemistry.

1971

Addition of dimethylsulfoxide (DMSO) to the incubation medium of succinate dehydrogenase in a concentration of 10% enhances the staining reaction in the hyphae of the fungus Cercosporella herpotrichoides after an incubation period of 15 min. Controls without DMSO remain unstained. DMSO causes a rapid penetration of the components of the medium through the mucilage that covers the hyphae.

CercosporellaHistologyintegumentary systembiologyHyphaStaining and LabelingHistocytochemistryorganic chemicalsSuccinate dehydrogenasefungiCell BiologyStainingIncubation periodMedical Laboratory TechnologyBiochemistryMucilagebiology.proteinCytochemistryDimethyl SulfoxideMitosporic FungiMolecular BiologyIncubationHistochemie. Histochemistry. Histochimie
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Acute Toxicity Testing in Vitro and the Classification and Labelling of Chemicals

1996

Chemical compoundbusiness.industryGeneral MedicinePharmacologyToxicologyGeneral Biochemistry Genetics and Molecular BiologyToxicologyMedical Laboratory Technologychemistry.chemical_compoundInvestigation methodschemistryLabellingToxicityMedicineToxicokineticsbusinessAcute toxicity testingAlternatives to Laboratory Animals
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Kinetics and equilibrium in insulin radioimmunoassay.

2002

The kinetics of insulin reaction has been studied with its specific antibody immobilized on the inner wall of the reaction tube; the radioimmunoanalytical determination of such a substance is based on the reaction. Independent variables were labelled and unlabelled insulin concentrations, temperature, viscosity, and the medium's ionic strength. Biexponential kinetics was found to be dependent on the concentrations fitted to the models discussed in the paper. The effect of temperature shows activation parameters similar to the viscous flow energy of water, which suggests that the reaction is diffusion-controlled. The results of the viscosity analysis points at the clearly negative influence …

ChemistryInsulinmedicine.medical_treatmentClinical BiochemistryImmunologyKineticsAnalytical chemistryRadioimmunoassayTemperatureRadioimmunoassayDielectricBiochemistryMedical Laboratory Technologychemistry.chemical_compoundViscosityKineticsReaction rate constantIonic strengthGlycerolmedicineImmunology and AllergyHumansInsulinJournal of immunoassayimmunochemistry
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Partial least squares attenuated total reflectance IR spectroscopy versus chromatography: the greener method

2012

Method election is a complex task that must be done carefully in order to ensure the capability of analytical methodologies to provide appropriate data for problem solving. This is a real challenge in all fields, but especially with bioanalysis, which in many cases involves the need to do a large number of determinations in complex

ChromatographyBioanalysisChromatographyChemistryClinical BiochemistryInfrared spectroscopyGreen Chemistry TechnologyGeneral MedicineAnalytical ChemistryMedical Laboratory TechnologyAttenuated total reflectionSpectroscopy Fourier Transform InfraredPartial least squares regressionLeast-Squares AnalysisGeneral Pharmacology Toxicology and PharmaceuticsBioanalysis
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