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showing 10 items of 2099 documents

Determination of muscimol and ibotenic acid in mushrooms of Amanitaceae by capillary electrophoresis

2014

In this study, the CZE method for rapid quantitative and qualitative determination of ibotenic acid and muscimol in Amanita mushrooms naturally grown in Poland was developed. The investigations included the species of A. muscaria, A. pantherina, and A. citrina, collected in southern region of Poland. The studied hallucinogenic compounds were effectively extracted with a mixture of methanol and 1 mM sodium phosphate buffer at pH 3 (1:1 v/v) using ultrasound-assisted procedure. The obtained extracts were separated and determined by CZE utilizing a 25 mM sodium phosphate running buffer adjusted to pH 3 with 5% content of acetonitrile v/v. The calibration curves for both analytes were linear in…

AmanitaamanitaceaeSodiumAmanitaClinical Biochemistrycapillary electrophoresischemistry.chemical_elementBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisLimit of DetectionAmanitaceaeChromatographybiologyChemistryElectrophoresis CapillaryReproducibility of Resultsbiology.organism_classificationPhosphateibotenic acidmuscimolMuscimolLinear ModelshallucinogensMethanolIbotenic acidElectrophoresis
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Synthesis of Peroxyapatite by Hydrothermal Processing

2014

Peroxide ions in apatite provides an additional resource for imparting an antibacterial capability in apatite. A hydrothermal process has been developed for including peroxide ions into the apatite lattice. Three oxygen generation compounds, hydrogen peroxide, ammonium persulphate and paracetic acid were investigated for peroxyapatite generation. Hydrogen peroxide provides the highest peroxide containing apatite. Both the oxygen generation and the apatite lattice formation represented the two critical factors for producing peroxyapatite. Unlike with high temperature processing, the cooling rate did not influence the retained peroxide content. This new process provides a building block for i…

Ammonium persulphateMechanical EngineeringInorganic chemistrychemistry.chemical_elementhydrogen peroxidePeroxideOxygenApatiteHydrothermal circulationIonantibacterialchemistry.chemical_compoundCooling ratechemistryhydrothermal processingMechanics of Materialsvisual_artvisual_art.visual_art_mediumGeneral Materials ScienceHydrogen peroxideperoxyapatiteKey Engineering Materials
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Amycolatopsis balhimycina gene expression under inorganic phosphate limitation

2009

Amycolatopsis balhimycina gene expression inorganic phosphate limitation
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Requirement for the Proton-Pumping NADH Dehydrogenase I of Escherichia Coli in Respiration of NADH to Fumarate and Its Bioenergetic Implications

1997

In Escherichia coli the expression of the nuo genes encoding the proton pumping NADH dehydrogenase I is stimulated by the presence of fumarate during anaerobic respiration. The regulatory sites required for the induction by fumarate, nitrate and O2 are located at positions around –309, –277, and downstream of –231 bp, respectively, relative to the transcriptional-start site. The fumarate regulator has to be different from the O2 and nitrate regulators ArcA and NarL. For growth by fumarate respiration, the presence of NADH dehydrogenase I was essential, in contrast to aerobic or nitrate respiration which used preferentially NADH dehydrogenase II. The electron transport from NADH to fumarate …

Anaerobic respirationAcetatesmedicine.disease_causeBiochemistryElectron TransportFumaratesEscherichia colimedicineDimethyl SulfoxideNADH NADPH OxidoreductasesAnaerobiosisEscherichia colichemistry.chemical_classificationElectron Transport Complex IEthanolbiologyNADH dehydrogenaseGene Expression Regulation BacterialProton PumpsElectron acceptorFumarate reductaseNADElectron transport chainGlycerol-3-phosphate dehydrogenaseBiochemistrychemistryElectron Transport Complex Ibiology.proteinEnergy MetabolismEuropean Journal of Biochemistry
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Micellar liquid chromatography determination of rivaroxaban in plasma and urine. Validation and theoretical aspects.

2019

A Micellar Chromatographic method to determine rivaroxaban in plasma and urine has been developed. The samples were dissolved in the mobile phase (SDS 0.05 M – 1-propanol 12.5%, phosphate buffered at pH 7) and 20 μL directly injected, avoiding the extraction and purification steps. Using a C18 column and running under isocratic mode at 1 mL/min, analyte was eluted without interference from the matrix in <6.0 min. The detection absorbance wavelength was set to 250 nm. The procedure was validated by Food and Drug Administration guidelines in terms of: system suitability, calibration range (0.05–5 mg/L), linearity, sensitivity, robustness, carry-over effect, specificity, accuracy (−11.1 to 4.2…

AnalyteClinical Biochemistrypartition equilibriumUrine030226 pharmacology & pharmacy01 natural sciencesBiochemistryAnalytical Chemistrymicellar chromatographyMatrix (chemical analysis)03 medical and health scienceschemistry.chemical_compound0302 clinical medicineRivaroxabanLimit of Detectiondirect injectionHumansMicellesvalidationChromatographyElutionanticoagulant010401 analytical chemistryExtraction (chemistry)biological fluidReproducibility of ResultsCell BiologyGeneral MedicinePhosphate0104 chemical scienceschemistryMicellar liquid chromatographyPartition equilibriumLinear ModelsChromatography LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Supramolecular Chemical Sensors Based on Pyrene Monomer-Excimer Dual Luminescence

2010

The past ten years have seen a spectacular development of chemical sensors based on the monomer-excimer dual luminescence of aromatic systems, such as pyrene. Either in the form of integrated or multicomponent molecular devices these chemosensors have been attracting a high interest above all because of their unique ratiometric properties. This review will focus on the latter systems, which can be classified into two classes: Firstly, the assembly of receptor-effector conjugates is triggerred by the analyte of interest. As a result, the sensor shows monomer to excimer fluorescence switching upon substrate binding. Secondly, the supramolecular assembly that constitutes the sensor is perturbe…

AnalytePyrenesOrganic ChemistryImidazolesOligonucleotidesSupramolecular chemistryNanotechnologyGeneral ChemistryExcimerBiochemistryFluorescenceSupramolecular assemblyDiphosphateschemistry.chemical_compoundMonomerchemistryPotassiumPyreneLuminescenceFluorescent Dyesgamma-CyclodextrinsChemistry - An Asian Journal
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Effect of sodium to barium substitution on the space charge implementation in thermally poled glasses for nonlinear optical applications

2009

Thermally poled niobium borophosphate glasses in the system 0.55(0.95-y) NaPO{sub 3}+y/2 Ba(PO{sub 3}){sub 2}+0.05Na{sub 2}B{sub 4}O{sub 7})+0.45Nb{sub 2}O{sub 5} were investigated for second order optical nonlinear (SON) properties. Bulk glasses were studied by Raman spectroscopy, thermal analysis, optical and dielectric measurements. The sodium to barium substitution does not lead to significant changes in optical properties, crystallization of glasses and coordination environment of polarizable niobium atoms. However, the ionic conductivity decreases drastically with the increase of barium concentration. Secondary ion mass spectroscopy has been used to determine the element distribution …

Analytical chemistryNiobiumchemistry.chemical_element02 engineering and technologyDielectric01 natural sciencesSpace chargeInorganic Chemistrysymbols.namesakeIonic conductivity0103 physical sciencesMaterials ChemistryPhysical and Theoretical Chemistry010302 applied physicsThermal polingSecond-harmonic generationNonlinear opticsBarium[CHIM.MATE]Chemical Sciences/Material chemistrySecond harmonic generation021001 nanoscience & nanotechnologyCondensed Matter PhysicsSpace chargeElectronic Optical and Magnetic MaterialschemistryBorophosphate glasses[ CHIM.MATE ] Chemical Sciences/Material chemistryContent (measure theory)Ceramics and Compositessymbols0210 nano-technologyRaman spectroscopy
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The lipoprotein receptor LRP1 modulates sphingosine-1-phosphate signaling and is essential for vascular development

2014

Low density lipoprotein receptor-related protein 1 (LRP1) is indispensable for embryonic development. Comparing different genetically engineered mouse models, we found that expression of Lrp1 is essential in the embryo proper. Loss of LRP1 leads to lethal vascular defects with lack of proper investment with mural cells of both large and small vessels. We further demonstrate that LRP1 modulates Gi-dependent sphingosine-1-phosphate (S1P) signaling and integrates S1P and PDGF-BB signaling pathways, which are both crucial for mural cell recruitment, via its intracellular domain. Loss of LRP1 leads to a lack of S1P-dependent inhibition of RAC1 and loss of constraint of PDGF-BB-induced cell migra…

AngiogenesisBlotting WesternBecaplerminEmbryonic DevelopmentNeovascularization PhysiologicRAC1BiologyReal-Time Polymerase Chain ReactionMural cellchemistry.chemical_compoundMiceCell MovementSphingosineHuman Umbilical Vein Endothelial CellsAnimalsHumansSphingosine-1-phosphateMolecular BiologyResearch ArticlesIn Situ HybridizationSphingosineTumor Suppressor ProteinsCell migrationCell BiologyProto-Oncogene Proteins c-sisLRP1ImmunohistochemistryCell biologyMicroscopy ElectronchemistryReceptors LDLLow-density lipoproteinSignal transductionLysophospholipidsGenetic EngineeringLow Density Lipoprotein Receptor-Related Protein-1Developmental BiologySignal Transduction
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Simultaneous endo and exo  Complex Formation of Pyridine[4]arene Dimers with Neutral and Anionic Guests

2017

The formation of complexes between hexafluorophosphate (PF6- ) and tetraisobutyloctahydroxypyridine[4]arene has been thoroughly studied in the gas phase (ESI-QTOF-MS, IM-MS, DFT calculations), in the solid state (X-ray crystallography), and in chloroform solution (1 H, 19 F, and DOSY NMR spectroscopy). In all states of matter, simultaneous endo complexation of solvent molecules and exo complexation of a PF6- anion within a pyridine[4]arene dimer was observed. While similar ternary complexes are often observed in the solid state, this is a unique example of such behavior in the gas phase.

Anion bindingStereochemistryhexafluorophosphateDimeraromatic hydrocarbonsIon mobility mass spectrometrycoordination complex010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundHexafluorophosphatePyridineMoleculePyridine[4]arenesAnion bindingta116Chloroformta114Resorcinarenes010405 organic chemistryGeneral ChemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesSolventCrystallographychemistryMolecular recognitionAngewandte Chemie International Edition
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Characterization of poly(4-vinylpyridine 1-oxide) by free-solution capillary electrophoresis and micellar electrokinetic chromatography

2008

The migration characteristics of poly(4-vinylpyridine 1-oxide) (PVP-NO) in phosphate buffers of acidic pH (20 mM H 3 PO 4 or NaH 2 PO 4 ) have been studied using both free-solution capillary electrophoresis (FSCE) and MEKC. To inhibit adsorption, 250 mM o-phosphoethanolamine (2-aminoethyl dihydrogen phosphate) was used. In FSCE, PVP-NO showed a narrow peak and a broader band, both having anionic behavior. These peak and band were attributed to the free and aggregated or micellized PVP-NO forms, respectively. According to surface tension measurements, the CMC of SDS in the BGE was 1.8 and 0.48 mM in the absence and in the presence of 1000 μpg/mL PVP-NO, respectively, and the association of t…

AnionsDetergentsClinical BiochemistryOxidemacromolecular substancesBuffersBiochemistryMicelleMicellar electrokinetic chromatographyAnalytical ChemistrySurface tensionchemistry.chemical_compoundCapillary electrophoresisAdsorptionSurface TensionMicellesLaunderingchemistry.chemical_classificationChromatographyChromatographytechnology industry and agricultureElectrophoresis CapillaryWaterPolymerPhosphateOrganophosphatesSolutionschemistryPolyvinylpyridine N-OxideELECTROPHORESIS
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