Search results for "whole blood"

showing 10 items of 112 documents

Platelet Reactivity in Hemophilia a. Flow Cytometry Study to Detect the Hemorragic Phenotype

2016

Abstract INTRODUCTION Hemophilia A (HA) is a rare inherited genetic disorder linked to the X chromosome, characterized by joint bleeding in patients with severe disease with <1% of factor VIII (FVIII)(White et al. Thromb Haemost 2001). However, there are cases of severe HA with less bleeding than usual and it has been postulated that there must be other contributors to the hemorrhagic phenotype, including a platelet dysfunction (Van Bladel et al. Haematologica 2011). In this study we analyzed platelet reactivity in a cohort of 16 male patients with severe HA in prophylactic treatment by flow cytometry. The control group was 15 healthy male subjects. METHODS A longitudinal prospective obs…

Agonistmedicine.medical_specialtyVenipuncturemedicine.diagnostic_testmedicine.drug_classbusiness.industryImmunologyCell BiologyHematologyBiochemistryGastroenterologyFlow cytometryBasal (phylogenetics)Internal medicineStatistical significanceImmunologymedicinePlateletPlatelet activationbusinessWhole bloodBlood
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Materials and methods of signal enhancement for spectroscopic whole blood analysis: Novel research overview

2017

Abstract The early diagnosis of diseases is crucial for reducing morbidity and mortality and also for improving the quality of treatment process. Among various biological samples used to follow up the concentrations of disease markers, whole blood sensing can efficiently decrease analysis time by means of introducing methods with no pretreatment. In addition, the direct detection of markers in whole blood facilitates testing procedure and minimize the possibility of the loss of analytes in the process. Therefore, the assay of unprocessed whole blood is becoming increasingly important in clinical diagnostics and biomedical research. Incorporation of new advanced materials plays a major role …

AnalyteComputer science010401 analytical chemistryTreatment processNanotechnology02 engineering and technologyAdvanced materials021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistrySignal enhancementOptical sensingDisease markers0210 nano-technologySpectroscopyBiomedical engineeringPoint of careWhole bloodTrAC Trends in Analytical Chemistry
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Transmembrane electrochemistry of erythrocytes: Direct electrochemical test for detecting hemolysis in whole blood

2016

A rapid method for detecting hemolysis in whole blood based on a direct electrochemical assay either in venous blood and finger blood, respectively at glassy carbon and screen-printed graphite electrodes is described. The presence of hemolysis is detected from characteristic voltammetric signatures associated to Fe-heme units in healthy and hemolyzed erythrocytes. The voltammetric response of blood was also investigated using scanning electrochemical microscopy (SECM) and scanning tunneling microscopy (STM) and involved transmembrane electrochemistry of erythrocytes superimposed to molecular electrochemistry of heme-containing proteins and heme fragments in the plasma. Voltammetric testing …

Analytical chemistry02 engineering and technologyGlassy carbon010402 general chemistryElectrochemistry01 natural sciencesScanning electrochemical microscopyBlood plasmaMaterials ChemistrymedicineElectrochemistryElectrical and Electronic EngineeringInstrumentationWhole bloodHemolysis indexDetection limitChromatographyChemistryMetals and AlloysVenous blood021001 nanoscience & nanotechnologyCondensed Matter Physicsmedicine.diseaseHemolysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsVenous bloodFinger blood0210 nano-technology
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Optimization of selenium determination in human milk and whole blood by flow injection hydride atomic absorption spectrometry.

1998

abstract A flow injection hydride atomic absorption spectrometry (FI-HAAS) method was developed for determining selenium in human milk and whole blood after microwave digestion of the sample. The sample (2 mL human milk or 0.25 mL blood) was introduced into the microwave vessel with 1.5 mL HN03 and 0.25 mL H202 and 300 W (4 min) and 600 W (4 min) were applied. The digestion was completed by heating to 140 C (2-3 h). Se (VI) was reduced to Se (IV) with hydrochloric acid. The instrumental conditions for FI-HAAS (concentrations of reducing agent and carrier acid, flow rate of argon carrier gas, and sample volume injected) were optimized. The detection limit of the proposed method was 0.23 ng/m…

Analytical chemistrychemistry.chemical_elementHydrochloric acidAnalytical Chemistrylaw.inventionchemistry.chemical_compoundSeleniumlawPregnancyEnvironmental ChemistryHumansMicrowave digestionWhole bloodPharmacologyDetection limitFlow injection analysisChromatographyMilk HumanSpectrophotometry AtomicchemistryFlow Injection AnalysisFemaleIndicators and ReagentsAtomic absorption spectroscopyAgronomy and Crop ScienceQuantitative analysis (chemistry)SeleniumFood ScienceJournal of AOAC International
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Evaluation of a new pooling strategy based on leukocyte count for rapid quantification of allele frequencies.

2007

Abstract Background: Allele frequencies of single-nucleotide polymorphisms (SNPs) can be quantified from DNA pools. The conventional preparation of DNA pools requires DNA isolation and quantification for each blood sample. We hypothesized that pooling of whole blood samples according to their leukocyte count, which determines DNA content, would be as reliable as the conventional pooling method but much less tedious to perform. Methods: We collected 100 whole blood samples and measured the leukocyte count. Samples were frozen until further use. After thawing, pools were generated by combining aliquots containing an equal number of leukocytes. In parallel, DNA was extracted from another aliqu…

AutoanalysisBiochemistry (medical)Clinical BiochemistryPoolingSingle-nucleotide polymorphismDNABiologyMolecular biologyDNA extractionPolymorphism Single NucleotideLeukocyte CountGene FrequencyGenotypeLeukocytesPyrosequencingHumansAlleleAllele frequencyWhole bloodClinical chemistry
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Unraveling the In Vivo Protein Corona

2021

Understanding the behavior of nanoparticles upon contact with a physiological environment is of urgent need in order to improve their properties for a successful therapeutic application. Most commonly, the interaction of nanoparticles with plasma proteins are studied under in vitro conditions. However, this has been shown to not reflect the complex situation after in vivo administration. Therefore, here we focused on the investigation of magnetic nanoparticles with blood proteins under in vivo conditions. Importantly, we observed a radically different proteome in vivo in comparison to the in vitro situation underlining the significance of in vivo protein corona studies. Next to this, we fou…

BiodistributionProtein CoronaCell Communication02 engineering and technology010402 general chemistry01 natural sciencesArticleMiceprotein coronaIn vivoAnimalsTissue DistributionMagnetite Nanoparticleslcsh:QH301-705.5biodistributionplasmaWhole bloodChemistrynanoparticleGeneral Medicine021001 nanoscience & nanotechnologyBlood proteinsIn vitro0104 chemical sciencesMice Inbred C57BLin vivoRAW 264.7 Cellslcsh:Biology (General)ProteomeBiophysics0210 nano-technologyserumEx vivoCells
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Leukocyte–platelet aggregates—a phenotypic characterization of different stages of peripheral arterial disease

2016

The formation of monocyte-platelet aggregates and neutrophil-platelet aggregates (MPA and NPA, respectively) is influenced by inflammation, but also might contribute to an exacerbation of inflammatory responses in atherosclerotic plaque. The purpose of this study was to analyze MPA and NPA proportions in regard to different stages of peripheral arterial disease (PAD). Forty-five patients with intermittent claudication (IC) (3 groups: Rutherford (R)-1, R-2, and R-3; each n = 15), 20 patients with critical limb ischemia (CLI) (Rutherford 5 (40%) and 6 (60%)), and 20 healthy controls were studied. Analyses of monocyte (Mon) subpopulations (CD14++CD16- (classical) Mon1, CD14++CD16+ (intermediat…

Blood PlateletsMale0301 basic medicinemedicine.medical_specialtyNeutrophilsLipopolysaccharide ReceptorsInflammationComorbidity030204 cardiovascular system & hematologyFibrinogenMonocytesProinflammatory cytokinePeripheral Arterial Disease03 medical and health sciences0302 clinical medicineRisk FactorsInternal medicineLeukocytesmedicineHumansPlateletReceptors ImmunologicAgedCell AggregationWhole bloodAged 80 and overbusiness.industryMonocyteReceptors IgGHematologyGeneral MedicineCritical limb ischemiaMiddle AgedFlow CytometryIntermittent claudicationBlood Cell CountPhenotype030104 developmental biologyEndocrinologymedicine.anatomical_structureImmunologyFemalemedicine.symptombusinessCell Adhesion MoleculesBiomarkersmedicine.drugPlatelets
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Synthesis and Evaluation of a Novel Series of Pyrrolizine Derivatives as Dual Cyclooxygenase-1 and 5-Lipoxygenase Inhibitors

1997

The aim of our study was to investigate structure activity relationship following the replacement of the 6-phenyl substituent at the 6,7-diaryl-2,3-dihydropyrrolizine template by various heteroaromatic residues. In this context we developed a new, efficient, and highly sensitive test method for the screening of dual cyclooxygenase-1 (COX-1) and 5-lipoxygenase (5-LOX) inhibitors. We used human platelets as a source of COX-1 and human PMNLs as a source of 5-LOX. Both cell types were isolated from the same volume of blood. PGE2 and LTB4 respectively were determined by highly selective and sensitive ELISA kits, using monoclonal antibodies. For a single determination at most 0.5 mL whole blood i…

Blood PlateletsMaleNeutrophilsmedicine.drug_classPharmaceutical ScienceContext (language use)Monoclonal antibodyChemical synthesisDrug DiscoverymedicineHumansStructure–activity relationshipCyclooxygenase InhibitorsPyrrolesLipoxygenase InhibitorsWhole bloodArachidonate 5-LipoxygenasebiologyChemistryMembrane ProteinsIn vitroIsoenzymesBiochemistryProstaglandin-Endoperoxide SynthasesEnzyme inhibitorArachidonate 5-lipoxygenaseCyclooxygenase 1biology.proteinFemaleArchiv der Pharmazie
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Analysis and comparison of autologous platelet-rich plasma preparation systems used in the treatment of enthesopathies: A preliminary study

2021

Background Autologous platelet-rich plasma (PRP) injection is an alternative but widely accepted method for the treatment of degenerative changes in tendon attachments known as enthesopathies. The PRP is considered a safe source for high concentrations of the growth factors involved in the healing process. Despite initial promising outcomes, many recent studies report conflicting results for this treatment. This may be due to differences in the concentrations of platelets and growth factors in PRPs obtained using different methods. Objectives The aim of this study was to compare PRP preparation systems in terms of morphotic components and selected growth factors to find the most appropriate…

Blood PlateletsMaleVascular Endothelial Growth Factor APlatelet-derived growth factormedicine.medical_treatmentPopulationMedicine (miscellaneous)EnthesopathyGeneral Biochemistry Genetics and Molecular Biologyplatelet-derived growth factorTransforming Growth Factor beta1AndrologyLeukocyte Countchemistry.chemical_compoundEpidermal growth factorgrowth factorsInternal MedicinemedicineHumansPharmacology (medical)PlateleteducationGenetics (clinical)Whole bloodeducation.field_of_studyEpidermal Growth FactorPlatelet-Rich Plasmabusiness.industryGrowth factorVascular endothelial growth factorchemistryPlatelet-rich plasmaReviews and References (medical)businessAdvances in Clinical and Experimental Medicine
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Preparation and Application of an Innovative Thrombocyte/Leukocyte-Enriched Plasma to Promote Tissue Repair in Chelonians

2015

Platelet concentrates are widely used in mammalian regenerative medicine to improve tissue healing. Chelonians (Testudines) would benefit from the application of thrombocyte preparations to regenerate damaged tissues, since traumatic injuries are leading causes of morbidity and mortality for both wild-living and domesticated animals. The aim of this study was to establish a protocol that optimized the recovery of the thrombocytes from blood samples and to show the efficacy of thrombocyte-enriched plasma in chelonians. Peripheral blood samples were obtained from Testudo spp. (n = 12) and Trachemys scripta elegans (n = 10). Blood cells were fractionated by sodium diatrizoate-sodium polysucros…

Blood PlateletsPathologymedicine.medical_specialtySodiumchemistry.chemical_elementlcsh:MedicineCentrifugationCalciumBiologyRegenerative MedicineAndrologyPlasmaBlood plasmamedicineLeukocytesAnimalsCentrifugationPlateletlcsh:ScienceWhole bloodCryopreservationMultidisciplinarylcsh:RTissue repairTurtleschemistryPlatelet-rich plasmalcsh:QResearch ArticlePLoS ONE
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