Search results for "Hydrogen-ion concentration"

showing 10 items of 769 documents

Evaluation of solid-phase extraction and stir-bar sorptive extraction for the determination of fungicide residues at low-microg kg(-1) levels in grap…

2004

Abstract A liquid chromatography–mass spectrometry method has been developed for determining bitertanol, carboxin, flutriafol, pyrimethanil, tebuconazole and triadimefon. The evaluation of both atmospheric pressure interfaces (API), atmospheric pressure chemical ionization (APCI) and electrospray (ESI) using positive and negative ionization modes, clearly shows that the studied pesticides are more sensitive using APCI in positive mode. Two procedures based on solid-phase extraction (SPE) and stir-bar sorptive extraction (SBSE) have been assessed for extracting these compounds in grape. The recoveries obtained by SPE in samples spiked at the limit of quantification (LOQ) level ranged from 60…

Detection limitSpectrometry Mass Electrospray IonizationChromatographyChemistryOrganic ChemistryExtraction (chemistry)Pesticide ResiduesReproducibility of ResultsAtmospheric-pressure chemical ionizationGeneral MedicineHydrogen-Ion ConcentrationMass spectrometryBiochemistryHigh-performance liquid chromatographyGas Chromatography-Mass SpectrometryAnalytical ChemistryFungicides Industrialchemistry.chemical_compoundLiquid chromatography–mass spectrometryPyrimethanilVitisSolid phase extractionAdsorptionMicrowavesChromatography High Pressure LiquidJournal of chromatography. A
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Separation of plasma membrane proteins of cultured human fibroblasts by affinity chromatography on bonded microparticulate silicas.

1984

Abstract Adsorbents for high-performance affinity chromatography were prepared by bonding proteins and reactive Procion triazine dyes to 3-isothiocyanatopropyl- and 3-aminopropylsilicas. The materials prepared were used successfully in the separation of hydrophobic plasma membrane proteins of cultured human fibroblasts. The data obtained show that the reaction of 3-isothiocyanatopropyltriethoxysilane (ITCPS) with the surface hydroxyl groups of silica yields a new and convenient route to preparing an “activated carrier” that is capable of coupling with potential affinity ligands containing amino functional groups. The reaction and bonding procedures of 3-isothiocyanatopropyltriethoxysilane a…

DetergentsSilica GelLigandsBiochemistryChromatography AffinityAnalytical ChemistryCatalysischemistry.chemical_compoundAdsorptionAffinity chromatographyIsothiocyanatesHumansColoring AgentsCells CulturedTriazineChromatographyAqueous solutionOrganic baseLigandOrganic ChemistryCell MembraneMembrane ProteinsGeneral MedicineFibroblastsHydrogen-Ion ConcentrationSilanesSilicon DioxideSolventMolecular WeightchemistryElectrophoresis Polyacrylamide GelJournal of chromatography
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The importance of a highly active and DeltapH-regulated diatoxanthin epoxidase for the regulation of the PS II antenna function in diadinoxanthin cyc…

2005

The present study focuses on the regulation of diatoxanthin (Dtx) epoxidation in the diadinoxanthin (Ddx) cycle containing algae Phaeodactylum tricornutum, Thalassiosira pseudonana, Cyclotella meneghiniana and Prymnesium parvum and its significance for the control of the photosystem II (PS II) antenna function. Our data show that Dtx epoxidase can exhibit extremely high activities when algal cells are transferred from high light (HL) to low light (LL). Under HL conditions, Dtx epoxidation is strongly inhibited by the light-driven proton gradient. Uncoupling of the cells during HL illumination restores the high epoxidation rates observed during LL. In Ddx cycle containing algae, non-photoche…

DiatomsPhotosystem IIbiologyLightPhysiologyZeaxanthin epoxidaseAlgal ProteinsDiadinoxanthinDiatoxanthinEukaryotaPhotosystem II Protein ComplexPlant ScienceHydrogen-Ion ConcentrationXanthophyllsPhotochemistrychemistry.chemical_compoundchemistryPhotoprotectionbiology.proteinElectrochemical gradientChlorella vulgarisOxidoreductasesAgronomy and Crop ScienceChlorophyll fluorescenceViolaxanthinJournal of plant physiology
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Evaluation of the pH effect of formulations on the skin permeability of drugs by biopartitioning micellar chromatography☆

2004

Dermal absorption of chemicals is an area of increasing interest for the pharmaceutical and cosmetic industries, as well as in dermal exposure and risk assessment processes. Biopartitioning micellar chromatography (BMC) is a mode of reversed phase micellar chromatography that has proved to be useful in the description and prediction of several pharmacological properties of xenobiotics including oral drug absorption, ocular and skin drug permeability. The present paper deals with the application of biopartitionig micellar chromatography to evaluate the pH effect on the skin permeability of twelve non-steroidal anti-inflammatory drugs and lidocaine. For this purpose the BMC retention of the w…

Dosage FormsKetoprofenChromatographyChemistrySkin AbsorptionAnti-Inflammatory Agents Non-SteroidalOrganic ChemistryLidocaineReversed-phase chromatographyAbsorption (skin)General MedicineHydrogen-Ion ConcentrationIbuprofenBiochemistryPermeabilityDosage formAnalytical Chemistrychemistry.chemical_compoundMicellar liquid chromatographyPermeability (electromagnetism)medicineSpectrophotometry UltravioletSalicylic acidChromatography Liquidmedicine.drugJournal of Chromatography A
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Coupling of the antiviral agent zidovudine to polyaspartamide and in vitro drug release studies.

1998

A macromolecular prodrug of the known antiretroviral agent zidovudine and alpha, beta-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA) was synthesized. A succinic spacer was present between the polymer and the drug, and 1,1'-carbonyldiimidazole was used as the coupling agent. In vitro drug release studies at pH 1.1, 5.5 and 7.4 indicated that limited amounts of intact drug were released from the conjugate. At pH 1.1 and 7.4 succinylzidovudine was released, and this was hydrolysed to give free zidovudine. In the presence of alpha-chymotrypsin, zidovudine was released preferentially in comparison with the succinyl derivative. The amounts of released zidovudine and succinylzidovudine were greater …

DrugActive ingredientDrug CarriersChemistryAnti-HIV Agentsmedia_common.quotation_subjectHydrolysisPharmaceutical ScienceProdrugPharmacologyHydrogen-Ion ConcentrationIn Vitro TechniquesIn vitroZidovudinemedicineLiberationChymotrypsinHumansProdrugsDrug carrierPeptidesZidovudinemedia_commonmedicine.drugConjugateJournal of controlled release : official journal of the Controlled Release Society
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Solid lipid nanoparticles containing tamoxifen characterization and in vitro antitumoral activity.

2005

Solid lipid nanoparticles (SLNs) containing tamoxifen, a nons- teroidal antiestrogen used in breast cancer therapy, were prepared by microemulsion and precipitation techniques. Tamoxifen loaded SLNs seem to have dimensional properties useful for parenteral administration, and in vitro plasmatic drug release studies demon- strated that these systems are able to give a prolonged release of the drug in the intact form. Preliminary study of antiproliferative ac- tivity in vitro, carried out on MCF-7 cell line (human breast cancer cells), demonstrated that SLNs, containing tamoxifen showed an antitumoral activity comparable to free drug. The results of char- acterization studies and of in vitro …

DrugOctanolsMaterials scienceTime FactorsAntineoplastic Agents Hormonalmedia_common.quotation_subjectPharmaceutical SciencePharmacologyColloidal Drug Delivery Systems Solid Lipid Nanoparticles (SLNs) TamoxifenBreast cancerDrug StabilityCell Line TumorSolid lipid nanoparticlemedicineHumansParticle Sizeskin and connective tissue diseasesmedia_commonCell ProliferationDrug CarriersWaterGeneral MedicineHydrogen-Ion Concentrationmedicine.diseaseAntiestrogenLipidsIn vitroNanostructuresbody regionsTamoxifenSolubilityDelayed-Action PreparationsCancer cellDrug carrierTamoxifenmedicine.drugDrug delivery
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The Biopharmaceutics Classification System: Subclasses for in vivo predictive dissolution (IPD) methodology and IVIVC

2013

The Biopharmaceutics Classification System (BCS) has found widespread utility in drug discovery, product development and drug product regulatory sciences. The classification scheme captures the two most significant factors influencing oral drug absorption; solubility and intestinal permeability and it has proven to be a very useful and a widely accepted starting point for drug product development and drug product regulation. The mechanistic base of the BCS approach has, no doubt, contributed to its wide spread acceptance and utility. Nevertheless, underneath the simplicity of BCS are many detailed complexities, both in vitro and in vivo which must be evaluated and investigated for any given…

Drugmedia_common.quotation_subjectAdministration OralPharmaceutical ScienceComputational biologyPharmacologyModels BiologicalPermeabilityArticleIntestinal absorptionQuality by DesignDosage formBiopharmaceuticsIVIVCIn vivoTerminology as TopicAnimalsHumansTechnology PharmaceuticalComputer SimulationPharmacokineticsIntestinal Mucosamedia_commonChemistryBiopharmaceuticsReproducibility of ResultsHydrogen-Ion ConcentrationBiopharmaceutics Classification SystemIntestinal AbsorptionPharmaceutical PreparationsSolubilityEuropean Journal of Pharmaceutical Sciences
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Mechanism of the Citrate Transporters in Carbohydrate and Citrate Cometabolism in Lactococcus and Leuconostoc Species

1998

ABSTRACT Citrate metabolism in the lactic acid bacterium Leuconostoc mesenteroides generates an electrochemical proton gradient across the membrane by a secondary mechanism (C. Marty-Teysset, C. Posthuma, J. S. Lolkema, P. Schmitt, C. Divies, and W. N. Konings, J. Bacteriol. 178:2178–2185, 1996). Reports on the energetics of citrate metabolism in the related organism Lactococcus lactis are contradictory, and this study was performed to clarify this issue. Cloning of the membrane potential-generating citrate transporter (CitP) of Leuconostoc mesenteroides revealed an amino acid sequence that is almost identical to the known sequence of the CitP of Lactococcus lactis . The cloned gene was exp…

EXPRESSIONLactococcusMolecular Sequence DataApplied Microbiology and BiotechnologyCitric AcidMicrobiologyACID BACTERIAchemistry.chemical_compoundBacterial ProteinsNUCLEOTIDE-SEQUENCELactococcusLeuconostocAmino Acid SequenceCloning MolecularElectrochemical gradientchemistry.chemical_classificationEcologybiologySymportersLACTATE EFFLUXLactococcus lactisfood and beveragesMETABOLIC ENERGYMembrane transportHydrogen-Ion Concentrationbiology.organism_classificationENERGY GENERATIONLACTIS BIOVAR DIACETYLACTISAmino acidchemistryBiochemistryLeuconostoc mesenteroidesESCHERICHIA-COLIFood MicrobiologyCarbohydrate MetabolismbacteriaKLEBSIELLA-PNEUMONIAECitric acidCarrier ProteinsLeuconostocFood ScienceBiotechnologyMEMBRANE-VESICLESApplied Environmental Microbiology
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Coxsackievirus A9 Infects Cells via Nonacidic Multivesicular Bodies

2014

ABSTRACT Coxsackievirus A9 (CVA9) is a member of the human enterovirus B species in the Enterovirus genus of the family Picornaviridae . According to earlier studies, CVA9 binds to αVβ3 and αVβ6 integrins on the cell surface and utilizes β2-microglobulin, dynamin, and Arf6 for internalization. However, the structures utilized by the virus for internalization and uncoating are less well understood. We show here, based on electron microscopy, that CVA9 is found in multivesicular structures 2 h postinfection (p.i.). A neutral red labeling assay revealed that uncoating occurs mainly around 2 h p.i., while double-stranded RNA is found in the cytoplasm after 3 h p.i. The biogenesis of multivesicu…

EchovirusEndosomemedia_common.quotation_subjectImmunologyCoxsackievirusmedicine.disease_causeMicrobiologyVirusCell Linechemistry.chemical_compoundVirologymedicineHumansInternalizationmedia_commonDynaminbiologyPhospholipase CMultivesicular BodiesBafilomycinEpithelial CellsHydrogen-Ion ConcentrationVirus Internalizationbiology.organism_classificationVirologyEnterovirus B HumanVirus-Cell InteractionsCell biologyMicroscopy ElectronchemistryInsect ScienceJournal of Virology
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Stability of PEI–DNA and DOTAP–DNA complexes: effect of alkaline pH, heparin and serum

2001

Abstract DNA complexes formed with nonviral vectors such as polyethylenimine (PEI) or 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) are widely used in gene therapy. These complexes prevent the interaction of DNA with the fluorescent probes usually employed to quantify DNA. We thus studied the procedures for DNA quantification from DNA complexes as well as their stability in the presence of DNase or mouse, rat and human sera. Release of the DNA from its complexes was accomplished by increasing the pH of the medium (from 7.3 to 13.4) or by adding heparin. The stability against degradation was tested in vitro, by incubating the complexes at 37°C in the presence of DNase I and sera from the …

Electrophoresis Agar GelPolyethylenimineHeparinChemistryPharmaceutical ScienceDNAHeparinHydrogen-Ion ConcentrationBlood proteinsMolecular biologyIn vitroFatty Acids MonounsaturatedQuaternary Ammonium CompoundsMicroscopy Electronchemistry.chemical_compoundElectrophoresisDrug StabilityBiochemistryNaked DNAmedicineDeoxyribonuclease IPolyethyleneimineDrug carrierDNAmedicine.drugJournal of Controlled Release
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