Search results for "Phenylpropanolamine"

showing 10 items of 10 documents

Capillary electrophoretic and extraction conditions for the analysis of Catha edulis FORKS active principles

2013

A capillary electrophoretic method, which allowed the detection and separation of the active principles of Catha edulis, i.e. cathinone, cathine and phenylpropanolamine, was developed. A suitable internal standard (nicotinamide), which permitted the quantification of the analytes reducing the variability of the migration times due to EOF changes, was identified. The analytical method was validated, assessing linearity, sensitivity and repeatability, showing optimal features for the analysis of the vegetable material. Moreover extraction conditions were investigated to achieve the exhaustion of the plant material in the fastest and most efficient way to meet the requirements of the Court.

AnalyteChromatographyMolecular StructureCathinonePlant ExtractsChemistryCapillary actionPhenylpropanolamineExtraction (chemistry)Vegetable materialElectrophoresis CapillaryReproducibility of ResultsCathaRepeatabilityPathology and Forensic MedicineElectrophoresisAlkaloidsSettore MED/43 - Medicina LegaleCathinone Cathine PhenylpropanolaminemedicineLawCathinemedicine.drug
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Application of solid-phase microextraction combined with derivatization to the enantiomeric determination of amphetamines.

2005

Abstract The utility of combining chiral derivatization and solid-phase microextraction (SPME) for the enantiomeric analysis of primary amphetamines by liquid chromatography has been investigated. Different derivatization/extraction strategies have been evaluated and compared using the chiral reagent o -phthaldialdehyde (OPA)– N -acetyl- l -cysteine (NAC) and fibres with a Carbowax-templated resin coating. Amphetamine, norephedrine and 3,4-methylenedioxyamphetamine (MDA) were used as model compounds. On the basis of the results obtained, a new method is presented based on the derivatization of the analytes in solution followed by SPME of the OPA–NAC derivatives formed. The proposed conditio…

AnalyteClinical BiochemistryPhenylpropanolaminePharmaceutical ScienceSolid-phase microextractionAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryHumansDerivatizationSpectroscopyChromatography High Pressure LiquidAqueous solutionChromatographyExtraction (chemistry)AmphetaminesReproducibility of ResultsStereoisomerismSolutionsSpectrometry FluorescencechemistryReagentCentral Nervous System StimulantsIndicators and ReagentsEnantiomerQuantitative analysis (chemistry)Journal of pharmaceutical and biomedical analysis
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Comparison of the performance of butanol and pentanol as modifiers in the micellar chromatographic determination of some phenethylamines

2000

Abstract A procedure was developed for the determination of several phenethylamines (amphetamine, arterenol, ephedrine, phenylephrine, phenylpropanolamine, mephentermine, methoxyphenamine, pseudoephedrine and tyramine), using micellar mobile phases of sodium dodecyl sulfate (SDS), a C18 column and UV detection. The drugs were eluted at short retention times with conventional acetonitrile–water or methanol–water mobile phases. In contrast, in the micellar system, they were strongly retained due to association with the surfactant adsorbed on the stationary phase, and needed the addition of butanol or pentanol to be eluted from the column. These modifiers allowed a simple way of controlling th…

ButanolsPhenethylaminesSensitivity and SpecificityBiochemistryMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundPentanolsPhenethylaminesmedicineEphedrineChromatography High Pressure LiquidMicellesChromatographyMethoxyphenamineElutionButanolOrganic ChemistryReproducibility of ResultsGeneral MedicinePseudoephedrinePharmaceutical PreparationschemistryIndicators and ReagentsSpectrophotometry UltravioletPhenylpropanolaminemedicine.drugJournal of Chromatography A
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Use of the Apparent Content Curves for the spectrophotometric identification of substances: identification of amphetamines

1994

The possibility of identification of substances which have similar spectral behaviour by means of Apparent Content Curves has been studied. This study is carried out with absorption, excitation and emission spectra of several amphetamines of widespread pharmaceutical use. Results obtained show that amphetamine, phenylpropanolamine, pseudoephedrine, phenylephrine, epinephrine, dopamine and methoxyamphetamine can be identified with a probability of >95%.

Chromatographymedicine.diagnostic_testChemistryAnalytical chemistryAbsorption (skin)PseudoephedrineBiochemistryAnalyse qualitativeAnalytical ChemistrySpectrophotometrymedicineStatistical analysisAmphetaminePhenylephrinePhenylpropanolaminemedicine.drugFresenius' Journal of Analytical Chemistry
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Detection of banned drugs in sport by micellar liquid chromatography

1992

Abstract A rapid method for the determination of banned drugs in sport (including stimulants, anabolic steroids and diuretics) based on micellar liquid chromatography is proposed. The mobile phase is an aqueous solution of a surfactant (sodium dodecyl sulphate in this instance) and the stationary phase is octadecylsilica. The retention parameters of the drugs were established and the effect of a mobile phase organic modifier on the chromatographic behaviour of the compounds was studied. Improvements in efficiency were achieved by control of the temperature of the mobile phase. This method allows the direct injection of urine samples for the determination of drugs excreted free in urine: ami…

Detection limitAmiphenazoleChromatographyMethoxyphenamineChemistryMetandienoneClostebolBiochemistryAnalytical Chemistrychemistry.chemical_compoundMicellar liquid chromatographymedicineEnvironmental ChemistryEphedrineSpectroscopyPhenylpropanolaminemedicine.drugAnalytica Chimica Acta
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Enantiomeric separation of amphetamine and related compounds by liquid chromatography using precolumn derivatization witho-phthaldialdehyde

2002

The utility of the derivatization reagento-phthaldialdehyde (OPA) in combination with the chiral thiol N-acetyl-L-cysteine (NAC) for the enantioselective analysis of primary amphetamines and structurally related substances has been investigated. The diastereomers obtained have been chromatographed on an achiral, reversed phase C18 column (125 mm×4 mm i.d., 5 μm), and detected fluorimetrically. The influence of parameters affecting the chromatographic separation as well as the derivatization reaction has been optimized, using amphetamine, norephedrine, norepinephrine and 3,4-methylenedioxyamphetamine (MDA) as model compounds. On the basis of the results obtained, possible conditions for the …

Detection limitChromatographyOrganic ChemistryClinical BiochemistryEnantioselective synthesisDiastereomerReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistrymedicineEnantiomerDerivatizationPhenylpropanolaminemedicine.drugChromatographia
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Stabilization of a nutraceutical omega-3 fatty acid by encapsulation in ultrathin electrosprayed zein prolamine.

2010

Docosahexaenoic acid (DHA) is a long chain polyunsaturated fatty acid of the omega-3 series (omega-3), which exerts strong positive influences on human health. The target of this study was the stabilization by encapsulation of this bioactive ingredient in zein ultrathin capsules produced by electrospraying. The zein ultrathin DHA encapsulation was observed by ATR-FTIR spectroscopy to be more efficient against degradation under both ambient conditions and in a confined space (so-called headspace experiment). In the latter case, that more closely simulates a sealed food packaging situation, the bioactive DHA was considerably more stable. By fitting the degradation data to a specific auto-deco…

Hot TemperatureDocosahexaenoic AcidsZeinPhenylpropanolamineGas Chromatography-Mass SpectrometryIngredientNutraceuticalNanocapsulesFatty Acids Omega-3Spectroscopy Fourier Transform InfraredOmega 3 fatty acidchemistry.chemical_classificationAldehydesVolatile Organic CompoundsChromatographyfood and beveragesFatty acidHumidityElectrochemical TechniquesFood packagingKineticschemistryModels ChemicalDocosahexaenoic acidPlant proteinTasteDietary SupplementsFood TechnologyOxidation-ReductionFood SciencePolyunsaturated fatty acidHalf-LifeJournal of food science
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A Comparison of the Efficacy and Tolerability of Solifenacin Succinate and Extended Release Tolterodine at Treating Overactive Bladder Syndrome: Resu…

2005

Abstract Objective: To compare two new generation antimuscarinics at their recommended doses for treatment of overactive bladder syndrome (OAB). Methods: A prospective, double blind, double-dummy, two-arm, parallel-group, 12-week study was conducted to compare the efficacy and safety of solifenacin 5 or 10mg and tolterodine extended release (ER) 4mg once daily in OAB patients. After 4 weeks of treatment patients had the option to request a dose increase but were dummied throughout as approved product labelling only allowed an increase for those on solifenacin. Results: Solifenacin, with a flexible dosing regimen, showed greater efficacy to tolterodine in decreasing urgency episodes, inconti…

MaleSolifenacin SuccinateQuinuclidinesmedicine.medical_specialtyUrinary urgencyTolterodine TartrateUrologyPhenylpropanolamineUrologyMuscarinic AntagonistsTolterodine TartrateCresolsDouble-Blind MethodTetrahydroisoquinolinesmedicineHumansProspective StudiesBenzhydryl CompoundsAnalysis of VarianceSolifenacinbusiness.industrySolifenacin SuccinateMiddle Agedmedicine.diseaseRegimenTreatment OutcomeUrinary IncontinenceTolerabilityOveractive bladderFemaleTolterodinemedicine.symptombusinessmedicine.drugEuropean Urology
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Determination of active ingredients in cough-cold preparations by micellar liquid chromatography.

2000

The chromatographic behaviour of some active ingredients in cough-cold pharmaceutical preparations, the antihistamine chlorpheniramine (or the dextro enantiomer dexchlorpheniramine), and the phenethylamines phenylephrine, phenylpropanolamine and pseudoephedrine, has been studied using a C(18) column, micellar mobile phases of sodium dodecyl sulphate (SDS) and pentanol, and with UV detection. All possible combinations of chlorpheniramine/phenethylamine were resolved and determined using a mobile phase of 0.15 M SDS-6% (v/v) pentanol at pH 7, with analysis time below 7 min. Repeatabilities and within laboratory precisions were evaluated at four different drug concentrations in the range 0.5-2…

Nasal decongestantChromatographyMicellar liquid chromatographyDexchlorpheniramineElutionChemistrymedicineAscorbic acidPseudoephedrinePhenylpropanolamineDosage formAnalytical Chemistrymedicine.drugTalanta
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New strategies for medical management of overactive bladder in children.

2011

Purpose of review The medical treatment of children with non-neurogenic overactive bladder syndrome (OAB) is still limited to a small number of drugs approved for use in childhood according to the national regulations of each country. Recent findings Over the last few years, there were several studies on the use of antimuscarinics other than oxybutynin in children, as well as some on the use of extended release oxybutynin and tolterodine and transdermal oxybutynin. It was shown that the combination of two different anticholinergics might be a well tolerated and successful option in children with OAB refractory to monotherapy, as well as administration of a receptor-selective antimuscarinic …

medicine.medical_specialtyQuinuclidinesBotulinum ToxinsCombination therapyTolterodine TartrateNortropanesUrologyPhenylpropanolamineUrologyUrinationMuscarinic AntagonistsBenzilatesCresolsTetrahydroisoquinolinesmedicineHumansBenzhydryl CompoundsOxybutyninIntensive care medicineChildSolifenacinbusiness.industryUrinary Bladder OveractiveStandard treatmentSolifenacin Succinatemedicine.diseaseBotulinum toxinReceptors MuscarinicOveractive bladderMandelic AcidsPropiverineTolterodinebusinessmedicine.drugCurrent opinion in urology
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