Search results for "Fen"

showing 10 items of 3710 documents

Off-line solid-phase microextraction and capillary electrophoresis mass spectrometry to determine acidic pesticides in fruits.

2003

A method based on solid-phase microextraction (SPME) and capillary electrophoresis/mass spectrometry (CE/ MS) is described for determining simultaneously five acidic pesticides (o-phenylphenol, ioxynil, haloxyfop, acifluorfen, picloram) in fruits. The CE device is coupled to an electrospray interface by a commercial sheath-flow adapter. Emphasis is placed on fulfillment of the speed and sensitivity requirements. The best separation is achieved using 32 mM ammonium formate/acid formic buffer at pH 3.1, with a working voltage of 25 kV. The MS detection of the five pesticides was performed in negative ionization mode. Full-scan spectra with base peaks corresponding to [M-H]- were obtained exce…

Detection limitChromatographyChemistryPlant ExtractsAnalytical chemistryElectrophoresis CapillaryFood ContaminationAcifluorfenMass spectrometrySolid-phase microextractionCapillary electrophoresis–mass spectrometryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisFruitAmmonium formateSample preparationPesticidesAnalytical chemistry
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Matrix effects on solid-phase microextraction of organophosphorus pesticides from water

1997

Abstract This study develops a method for solid-phase microextraction (SPME) of eight organophosphorus pesticides, diazinon, fenthion, fenitrothion (sumithion), methyl-parathion, parathion, methyl-trithion, ethion and triazophos, from water. Determination is carried out by gas chromatography with nitrogen-phosphorus detection. To perform the SPME, poly(dimethylsiloxane) and polyacrylate fibers were initially compared on the basis of their absorption capacities for the selected pesticides, and polyacrylate was selected to accomplish the rest of assays. The main factors affecting the SPME process such as memory effect, stirring rate, extraction temperature and absorption-time profile were stu…

Detection limitDiazinonChromatographyFenthionOrganic ChemistryGeneral MedicineEthionSolid-phase microextractionBiochemistryAnalytical Chemistrychemistry.chemical_compoundWastewaterchemistryTap waterSolid phase extractionJournal of Chromatography A
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Morphological abnormalities induced by Fenoxycarb on the pupa ofPhanerotoma (Phanerotoma) ocularisKohl (Hym., Braconidae)

1993

Fenoxycarb at concentrations of 0.001 μg/ml, 0.005 μg/ml, 0.01 μg/ml, 0.05μg/ml and 0.1 μg/ml had an adverse effect on the pupa of Phanerotoma (Phanerotoma) ocularis. When topically applied, it induced morphological abnormalities. The percentage of anomalous obtained depended of developmental pupal stage and was higher when was applied in the first moment of development (80 %-90 %) than in the final of development (50%-60%). These anomalous was inviables. Zusammenfassung Morphologische Abnormitaten bei Puppen von Phanerotoma (Phanerotoma) ocularis Kohl (Hym., Braconidae) nach Einwirkung von Fenoxycarb Fenoxycarb, in Konzentrationen von 0.001 μg/ml, 0.0005 μg/ml, 0.01 μg/ml, 0.05 |μg/ml und …

Developmental stagebiologyAnatomybiology.organism_classificationPupachemistry.chemical_compoundAnimal sciencechemistryInsect SciencePhanerotomaFenoxycarbChemical controlNymphAgronomy and Crop ScienceBraconidaeNon target organismJournal of Applied Entomology
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Applications and Limitations of Dendrimers in Biomedicine

2020

Biomedicine represents one of the main study areas for dendrimers, which have proven to be valuable both in diagnostics and therapy, due to their capacity for improving solubility, absorption, bioavailability and targeted distribution. Molecular cytotoxicity constitutes a limiting characteristic, especially for cationic and higher-generation dendrimers. Antineoplastic research of dendrimers has been widely developed, and several types of poly(amidoamine) and poly(propylene imine) dendrimer complexes with doxorubicin, paclitaxel, imatinib, sunitinib, cisplatin, melphalan and methotrexate have shown an improvement in comparison with the drug molecule alone. The anti-inflammatory therapy focus…

Diagnostic ImagingDrugtargeted releasemedia_common.quotation_subjectAnti-Inflammatory AgentsBiomedical TechnologyPharmaceutical ScienceDiflunisalContext (language use)02 engineering and technologyReview010402 general chemistryPiroxicam01 natural sciencesimagining diagnosticsAnalytical Chemistrydendrimerslcsh:QD241-441lcsh:Organic chemistryDendrimerToxicity TestsDrug DiscoverymedicineAnimalsHumansDistribution (pharmacology)DoxorubicinPhysical and Theoretical Chemistrymedia_commonCell DeathChemistryOrganic Chemistry021001 nanoscience & nanotechnologyIbuprofenCombinatorial chemistry0104 chemical sciencesdrug therapyChemistry (miscellaneous)Molecular Medicinecytotoxicity0210 nano-technologymedicine.drugMolecules
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Brief an Garlieb H. Merkel

1798

Ms. 930a, Nr. 12, Bl. 31r-34v Johannes Daniel Falk. Brief an Garlieb H. Merkel, Weimar, den 3. December 179[8?] Autora rokraksts / Autograph, vācu val. / Deutsch [8] lpp. / S. Attēlu numuri / Bildnummern: 930a-012-1, 930a-012-2-3, 930a-012-4-5, 930a-012-6-7, 930a-012-8 Im vorliegenden Brief vermischen sich private und berufliche Angelegenheiten sowie Klatsch miteinander. Nachdem Falk seine lange Antwortzeit zunächst damit begründet, dass er Merkels aktuelle Adresse nicht kenne, bringt er Neuigkeiten von der Krankheit einer nicht näher benannten Kammerrätin und nimmt an deren Leiden rege Anteil. Direkt im Anschluss präsentiert Falk den Stand seiner Verhandlungen mit Verlegern. Auch wenn Falk…

DichtungProvinzRichter Johann Paul Friedrich (auch Jean Paul 1763-1825)Herzogin von Sachsen-Weimar-Eisenach Luise (1757-1830)LiteraturMerķelis Garlībs Helvigs (1769-1850)J[…]sche BuchhandlungBöttiger Karl August (1760-1835)Schröter Corona Elisabeth Wilhelmine (1751-1802)Weimarer HofSchnupfenmateriePrahmer WilhelmRomantikSchmarotzerErziehungWieland Christoph Martin (1733-1813)Königliche Kommissionbrīvība un patiesībaFreiheit und WahrheitFalk Caroline (1778-1841)liekēdisklīnika BerlīnēestētikaMerkel Garlieb Helvig (1769-1850)ÄsthetikSander Johann Daniel (1759-1825):HUMANITIES and RELIGION [Research Subject Categories]Apgaismības laikmetsgrāmatu tirdzniecībaŠillers Frīdrihs (1759-1805)provinceSchiller F. "Wallenstein"Herder Johann Gottfried (1744-1803)Schiller Friedrich (1759-1805)literatūradzejaaudzināšanaCharité [Klinikum in Berlin]Falk Johann(es) Daniel (1768-1826)Sander’sche BuchhandlungiesnasLesings Gotholds Efraims (1729-1781)karaliskā komisijaBiester Johann Erich (1749-1816)romantikaAufklärungVeimāras galmsHerders Johans Gotfrīds (1744-1803)Cotta von Cottendorf Johann Friedrich (1764-1832)
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Diclofenac sodium and cyclosporin A inhibit human lens epithelial cell proliferation in culture.

1997

• Purpose: To investigate the effect of diclofenac sodium salt and cyclosporin A (CsA) on human lens epithelial cell (HLEC) growth in culture. • Methods: Cultures of HLEC were obtained from anterior capsules from extracapsular cataract surgery. Third-passage cells were seeded in 96-well plates in 0.1 ml culture medium. Cytotoxicity was estimated by the tetrazolium test in confluent monolayers after 24 h exposure to a wide range of concentrations of diclofenac and CsA. The effect of subcytotoxic concentrations of diclofenac and CsA on HLEC proliferation in subconfluent cultures was evaluated after 24 and 72 h of exposure. To investigate the relationship between PGEZ synthesis and the inhibit…

DiclofenacCell SurvivalBiologyPharmacologyDinoprostoneEpitheliumCellular and Molecular NeuroscienceDiclofenacIn vivoCyclosporin aChlorocebus aethiopsLens CrystallinemedicineAnimalsHumansCyclooxygenase InhibitorsCytotoxicityVero CellsCells CulturedAgedRadioimmunoassayEpithelial CellsDiclofenac SodiumMiddle AgedSensory Systemsstomatognathic diseasesOphthalmologyBiochemistryCell cultureCyclosporineLens epithelial cell proliferationCell DivisionImmunosuppressive Agentsmedicine.drugGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie
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Hepatic metabolism of diclofenac: role of human CYP in the minor oxidative pathways.

1999

The aim of this study was to re-examine the human hepatic metabolism of diclofenac, with special focus on the generation of minor hydroxylated metabolites implicated in the idiosyncratic hepatotoxicity of the drug. Different experimental approaches were used: human hepatocytes, human microsomes, and engineered cells expressing single human CYP (cytochromes P450). Human hepatocytes formed 3'-hydroxy-, 4'-hydroxy-, 5-hydroxy- 4',5-dihydroxy-, and N,5-dihydroxydiclofenac, as well as several lactams. Formation of 4'- and 5-hydroxydiclofenac by human liver microsomes followed a Michaelis-Menten kinetics (Km 9 +/- 1 microM; Vmax 432 +/- 15 pmol/min/mg and Km 43 +/- 5 microM; and Vmax 15.4 +/- 0.6…

DiclofenacMetaboliteIn Vitro TechniquesBiochemistryCell LineHydroxylationCytochrome P-450 CYP2C8chemistry.chemical_compoundTolbutamideCytochrome P-450 Enzyme SystemmedicineHumansBiotransformationCytochrome P-450 CYP2C9PharmacologybiologyAnti-Inflammatory Agents Non-SteroidalCytochrome P450Metabolismmedicine.anatomical_structureBiochemistrychemistrySteroid 16-alpha-HydroxylaseHepatocyteSteroid HydroxylasesMicrosomebiology.proteinMicrosomes LiverAryl Hydrocarbon HydroxylasesOxidation-ReductionDrug metabolismmedicine.drug
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The pyrrole moiety as a template for COX-1/COX-2 inhibitors

2000

Aroyl- and thiophene-substituted pyrrole derivatives have been synthesized as a new class of COX-1/COX-2 inhibitors. The inhibition of COX-1 was evaluated in a biological system using bovine PMNLs as the enzyme source, whereas LPS-stimulated human monocytes served as the enzyme source for inducible COX-2. The determination of the concentration of arachidonic acid metabolites was performed by HPLC for COX-1 and RIA for COX-2. Variation of the substitution pattern led to a series of active compounds which showed inhibition for COX-1 and COX-2. Structural requirements for the development of COX-1/COX-2 inhibitors are discussed.

DiclofenacNeutrophilsStereochemistryIndomethacinThiophenesHigh-performance liquid chromatographyMonocytesPyrrole derivativeschemistry.chemical_compoundDrug DiscoveryAnimalsHumansStructure–activity relationshipMoietyCyclooxygenase InhibitorsPyrrolesSulfonesPyrrolePharmacologychemistry.chemical_classificationArachidonic AcidCyclooxygenase 2 InhibitorsMolecular StructureAnti-Inflammatory Agents Non-SteroidalOrganic ChemistryMembrane ProteinsGeneral MedicineIsoenzymesEnzymechemistryMembrane proteinBiochemistryCyclooxygenase 2Prostaglandin-Endoperoxide SynthasesCyclooxygenase 1Leukocytes MononuclearCattleArachidonic acidEuropean Journal of Medicinal Chemistry
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Hydroxypropylmethylcellulose films for the ophthalmic delivery of diclofenac sodium

2012

Abstract Objectives The aim of this study was to prepare diclofenac/hydroxypropylmethylcellulose (HPMC) and diclofenac-loaded nanoparticles/HPMC films as potential systems for ocular delivery. Methods Two different concentration of the polymer were used: 1.5 and 2.0% w/v. Chitosan–hyaluronic acid nanoparticles were prepared by the ionotropic gelation technique. Nanoparticles were characterized by transmission electron microscopy, dynamic light scattering, drug encapsulation efficiency and rheological studies. In-vitro drug studies and corneal penetration release studies were carried out. Drug release mechanism was finally evaluated by fitting the Ritger and Peppas equation to data. In addit…

DiclofenacPolymersPharmaceutical ScienceNanoparticleAdministration OphthalmicMethylcellulosePharmacologyPermeabilityDosage formDrug Delivery SystemsHypromellose DerivativesDiclofenacDynamic light scatteringmedicineHyaluronic AcidDosage FormsPharmacologychemistry.chemical_classificationChitosanChemistryAnti-Inflammatory Agents Non-SteroidalDiclofenac SodiumPolymerPermeationHypromellose DerivativesNanoparticlesmedicine.drugNuclear chemistryJournal of Pharmacy and Pharmacology
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Inhibition of skin inflammation in mice by diclofenac in vesicular carriers: Liposomes, ethosomes and PEVs

2013

Diclofenac-loaded phospholipid vesicles, namely conventional liposomes, ethosomes and PEVs (penetration enhancer-containing vesicles) were developed and their efficacy in TPA (phorbol ester) induced skin inflammation was examined. Vesicles were made from a cheap and unpurified mixture of phospholipids and diclofenac sodium; Transcutol P and propylene glycol were added to obtain PEVs, and ethanol to produce ethosomes. The structure and lamellar organization of the vesicle bilayer were investigated by transmission electron microscopy and small and wide angle X-ray scattering, as well as the main physico-chemical features. The formulations, along with a diclofenac solution and commercial Volta…

DiclofenacSurface PropertiesDrug CompoundingSkin AbsorptionLipid BilayersPharmaceutical ScienceIn Vitro TechniquesDermatitis ContactMiceDiclofenacMicroscopy Electron TransmissionX-Ray DiffractionmedicineAnimalsSkinDrug CarriersLiposomeChromatographyEthanolChemistryBilayerVesicleAnti-Inflammatory Agents Non-SteroidalDiclofenac SodiumPenetration (firestop)PermeationPropylene GlycolLiposomesBiophysicsNanoparticlesNanocarriersmedicine.drugInternational Journal of Pharmaceutics
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