Search results for "nap"

showing 10 items of 2226 documents

On the Derivatization of Drugs Using 1-Nitroso-2-naphthol, 4-aminoantipyrine and 2,6-Dihaloquinone Chlorimides

1992

Coupling of 1-nitroso-2-naphthol (1N2N), 4-aminoantipyrine (4-AAP), 2,6-dichloroquinone chlorimide (DCQC) and 2,6-dibromoquinone chlorimide (DBQC) with several bioactive substances, including adren...

ChromatographyBiochemistry (medical)Clinical BiochemistryEther1 nitroso 2 naphtholBiochemistryAnalytical Chemistrychemistry.chemical_compoundInvestigation methodschemistryElectrochemistryOrganic chemistryPhenolsDerivatizationSpectroscopyAnalytical Letters
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In Vitro and In Silico Studies of Two 1,4-Naphthoquinones and Their Topical Formulation in Bigels.

2021

Background: 1,4-Naphthoquinones (1,4-NQs) are secondary plant metabolites with numerous biological activities. 1,4-NQs display low water solubility and poor bioavailability. Bigels are a new technology with great potential, which are designated as drug delivery systems. Biphasic bigels consisting of solid and liquid components represent suitable formulations improving diffusion and bioavailability of NQs into the skin. Objective: We evaluated the in silico and in vitro activity of 5,8-dihydroxy-1,4-naphthoquinone (M1) and 2,3-dichloro-5,8-dihydroxy-1,4-naphthoquinone (M2) on elastase and assessed their cytotoxicity towards COLO38 melanoma cells. The 1,4-NQs were loaded into bigels for topi…

ChromatographyElastasePharmaceutical ScienceResazurinHydrogelsPermeationIn vitroBioavailabilitySolventMolecular Docking Simulationchemistry.chemical_compoundDrug Delivery SystemschemistryDrug deliveryCytotoxicityRheologyNaphthoquinonesCurrent drug delivery
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Extractive-spectrophotometric determination of furosemide with sodium 1,2-naphthoquinone-4-sulphonate in pharmaceutical formulations

1997

ABSTRACT An extractive-spectrophotometric study based on the reaction of furosemide with 1,2-naphthoquinone-4-sulphonate (NQS) is described. Optimal conditions are: NaH2PO4-Na2HPO4 pH 7.5, NQS 7.7×...

ChromatographySodiumBiochemistry (medical)Clinical BiochemistryNQSchemistry.chemical_element12-NaphthoquinoneBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryElectrochemistrymedicineEphedrineSpectroscopymedicine.drug
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Spectrophotometric Determination of Hydralazine with 2-Hydroxy-1-naphthaldehyde in Pharmaceuticals

1991

Abstract A new extraction-spectrophotometric method for the determination of hydralazine, based on its reaction with 2-hydroxy-1-naphthaldehyde at 25 °C, is described. The calibration curve was linear between 0.4 and 6 mg/mL of hydralazine. The molar absorbtivity of the product at 408 nm is 40 900 L · mol − 1 · cm − 1 . The method described was applied to the analysis of hydralazine in pharmaceutical preparations containing reserpine, hydrochlorothiazide, bendrofluorthiazine, propranolol, and other substances. The agreement with the U.S.P. XXI method was satisfactory for tablets and injections, but not for pellets.

ChromatographySpectrophotometry Infraredmedicine.diagnostic_testChemistryCalibration curveTemperaturePharmaceutical SciencePropranololHydrogen-Ion ConcentrationNaphthalenesReserpineHydralazineHydralazineDosage formHydrochlorothiazideSpectrophotometrySolventsmedicineIndicators and ReagentsSpectrophotometry Ultravioletmedicine.drugJournal of Pharmaceutical Sciences
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Quality control of commercial mustard by thin-layer chromatography

2005

Horseradish samples ( Cochlearis armoracia L. ) and mustard samples ( Sinapis alba L. ) were extracted with 70:30 ( v/v ) methanol-water in accordance with ISO method 91671. Samples of commercial mustard with and without horseradish were submitted to the same extraction procedure. Separation of the active compounds from these samples were performed on silica gel 60 plates with preconcentration zone and on silica gel F 254 high-performance thin-layer chromatography plates, with iso -propanol-25% ammonia, 90 + 10 ( v/v ), containing different volumes of distilled water (1, 2, 3, or 5 parts), as mobile phases. After development the compounds were visualized in UV light at λ = 254 nm or by expo…

ChromatographybiologySilica gelClinical BiochemistryExtraction (chemistry)SinapisIodine vaporbiology.organism_classificationBiochemistryThin-layer chromatographyAnalytical ChemistryAmmoniachemistry.chemical_compoundchemistryDistilled waterJournal of Planar Chromatography – Modern TLC
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Kinetic-Spectrophotometric Determination of Primary and Secondary Amines by Reaction with 1-2 Naphthoquinone-4-Sulphonate.

1994

Abstract A kinetic-spectrophotometric method for the determination of primary and secondary amines is described. It is based on the coloured reaction of these amines with sodium 1,2 Naphthoquinone 4-sulphonate (NQS) in the presence of a non-ionic surfactant. For each determination the optimum conditions were studied and found to be as follows: pH 10.5. Carbonate-bicarbonate buffer 0.1M, Triton X-100 0.1%, Temperature 45°C, and NQS 6.4 × 10−3 M and interval of time 45–180s at wavelength 490 nm. The parameters used for the quantitative determinations are the reaction rate and the increase in the absorbance of the kinetic curves. This procedure has been applied to the determination of ephedrin…

Chromatographymedicine.diagnostic_testBiochemistry (medical)Clinical BiochemistryNQSBiochemistryNaphthoquinoneAnalytical ChemistryReaction rateAbsorbancechemistry.chemical_compoundSulfonatechemistrySpectrophotometryElectrochemistrymedicineDerivatizationQuantitative analysis (chemistry)SpectroscopyAnalytical Letters
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EDTA excess Zn(II) back-titration in the presence of 4-(2-pyridylazo)-resorcinol indicator and naphthol green beta as inert dye for determining Cr(II…

2006

The colour changes of 4-(2-pyridylazo)-resorcinol and naphthol green beta as new screening metallochromic indicator in back-titration of EDTA excess with Zn(II) to determine Cr(III)/EDTA complex was investigated with the help of tristimulus colorimetry. Specific colour discrimination (SCD) and L*, a*, b* 1976 parameters were successfully applied to evaluate the quality of colour transition at the end-point in non-alkaline media and in the presence of Zn(II) and Ca(II) which resulted in non-interfering species at 1x10(-3) M and 2x10(-3) M, respectively. The above concentrations are comparable with those used for Cr(III). Validation of the fast and accurate reported method was performed by at…

ChromiumEnvironmental EngineeringHealth Toxicology and Mutagenesischemistry.chemical_elementIndustrial WasteZincResorcinolNaphtholsWaste Disposal FluidComplexometric titrationlaw.inventionWater PurificationChromiumchemistry.chemical_compoundlawEnvironmental ChemistryColorimetryColoring AgentsWaste Management and DisposalEdetic AcidModels StatisticalResorcinolsPollutionZincchemistryWastewaterModels ChemicalEnvironmental chemistryCalciumAtomic absorption spectroscopyWater Pollutants ChemicalNuclear chemistryWaste disposalJournal of hazardous materials
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Gas—liquid chromatographic analyses

1985

Abstract The gas chromatographic retention behaviour of methylethyl, 1-methylpropyl, 2-methylpropyl, 1,2-dimethylpropyl, 1-methylbutyl and 3-methylbutyl esters of benzoic and o-, m- and p-chlorobenzoic acids on low-polarity (SE-30) and polar (OV-351) capillary columns under several temperature-programmed and isothermal conditions is reported. The retention data and the Kovats retention indices for all 24 components are given and the separation of a complex mixture is discussed. The retention index increments have been used to examine the effects of chain branching and chlorine substitution. The results are compared with those for n-alkyl benzoates and monochlorobenzoates.

ChryseneCapillary actionNitro compoundchemistry.chemical_elementFluoreneBranching (polymer chemistry)BiochemistryIsothermal processAnalytical Chemistrychemistry.chemical_compoundCapillary columnChlorineOrganic chemistryMethyleneAlkylBenzoic acidNaphthalenechemistry.chemical_classificationDegree of unsaturationChromatographyElutionOrganic ChemistryGeneral MedicinePhenanthreneBenzoatesChromatographic separationHydrocarbonchemistryPolarKovats retention indexGas chromatographyGas liquid chromatographicJournal of Chromatography A
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Detection of Reactive Quinones in the Metabolism of Polycyclic Aromatic Hydrocarbons by the Formation of their Glutathione Conjugates

1996

Abstract The biotransformation of polycyclic aromatic hydrocarbons to quinones by rat liver microsomes was investigated. The employment of an electrochemical detector allowed the specific detection of quinones separated by reverse phase HPLC with higher sensitivity as compared to UV detection. Microsomal incubations of benzo[a]pyrene (BP) resulted in the formation of 1,6-, 3,6- and 6,12-quinones, of naphthalene in the detection of naphthalene-1,4-quinone, whereas ortho-quinones could only be detected in trace amounts. Additional protein binding studies showed that only 9–22% of synthetic ortho-quinones could be recovered from microsomal incubations. In order to scavenge possible reactive qu…

ChryseneChromatographyPolymers and PlasticsChemistryOrganic ChemistryGlutathioneQuinonechemistry.chemical_compoundBenzo(a)pyreneBiochemistryBiotransformationMaterials ChemistryMicrosomePyreneNaphthalenePolycyclic Aromatic Compounds
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Naphthalene production by microorganisms associated with termites: Evidence from a microcosm experiment

2009

Abstract There have been several reports published which suggest that it is possible that the polycyclic aromatic hydrocarbons (PAHs) naphthalene (NAPH), phenanthrene (PHEN) and perylene (PERY) in tropical environments have a biological source. This source might be related to the activity of termites or their associated microorganisms. We aimed to provide direct evidence for the biological production of NAPH, PHEN and PERY by conducting microcosm experiments in the State of Tocantins, Brazil, in which termite nests (with or without termites) were placed in an enclosed environment in which we controlled all PAH fluxes and monitored changes of PAH stocks. The experiments were carried out with…

ChrysenebiologyEcologyMicroorganismSoil ScienceBiodegradationPhenanthrenebiology.organism_classificationMicrobiologyAcenaphthylenechemistry.chemical_compoundchemistryNestEnvironmental chemistryNasutitermesMicrocosmSoil Biology and Biochemistry
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