Search results for "quantitative analysi"

showing 10 items of 307 documents

Determination of Caffeine in Analgesic Formulations Using the Apparent Content Curves Method

1994

Abstract The determination of caffeine by UV spectroscopy in pharmaceutical samples, containing different compounds which provide spectral interferences as aspirin, paracetamol, chlorfeniramine or propylphenazone, is carried out. The proposed procedure is based on the apparent content curves method in order to resolve binary, ternary and multicomponent mixtures. Results obtained are, in all cases, in agreement with contents found by a HPLC procedure used as reference method.

ChromatographyBiochemistry (medical)Clinical BiochemistryAnalgesicAnalytical chemistryBiochemistryHigh-performance liquid chromatographyDosage formAnalytical Chemistrychemistry.chemical_compoundUltraviolet visible spectroscopychemistryContent (measure theory)ElectrochemistryTernary operationCaffeineQuantitative analysis (chemistry)SpectroscopyAnalytical Letters
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Indirect determination of paracetamol in pharmaceutical formulations by inhibition of the system luminol–H2O2–Fe(CN)63− chemiluminescence

1999

After a large drug scanning, the system Luminol-H2O2-Fe(CN)6(3-) is proposed for first time for the indirect determination of paracetamol. The method is based on the oxidation of paracetamol by hexacyanoferrate (III) and the subsequent inhibitory effect on the reaction between luminol and hydrogen peroxide. The procedure resulted in a linear calibration graph over the range 2.5-12.5 microg ml(-1) of paracetamol with a sample throughput of 87 samples h(-1). The influence of foreign compounds was studied and, the method was applied to determination of the drug in three different pharmaceutical formulations.

ChromatographyCalibration curveClinical BiochemistryAnalgesicAnalytical chemistryPharmaceutical ScienceDosage formAnalytical ChemistryLuminollaw.inventionchemistry.chemical_compoundchemistrylawDrug DiscoveryFerricyanideHydrogen peroxideQuantitative analysis (chemistry)SpectroscopyChemiluminescenceJournal of Pharmaceutical and Biomedical Analysis
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Determination of the flavor enhancer maltol through a FIA — direct chemiluminescence procedure

2001

Abstract A new FIA — direct chemiluminescence method is proposed for the determination of maltol, based upon the oxidation of the food additive by KMnO 4 in sulfuric acid medium at 80°C enhanced by hexadecylpyridinium chloride (HD) and formic acid (HCOOH). The calibration graph is linear over the range 0.5–4.0 mg l −1 of maltol, with a R.S.D. ( n =50, 0.5 mg l −1 ) of 2.9%, LOD ( s / n =3) of 10 mg l −1 and sample throughput of 153 h −1 .

ChromatographyCalibration curveFormic acidStereochemistryMaltolSulfuric acidBiochemistryChlorideAnalytical Chemistrylaw.inventionchemistry.chemical_compoundchemistrylawmedicineEnvironmental ChemistryQuantitative analysis (chemistry)SpectroscopyFlavorChemiluminescencemedicine.drugAnalytica Chimica Acta
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Simple high-performance liquid chromatographic assay for polyamines and their monoacetyl derivatives.

1993

A rapid reversed-phase high-performance liquid chromatographic method, using pre-column derivatization with benzoyl chloride and ultraviolet detection at 254 nm, was developed for the simultaneous measurement of polyamines and their monoacetyl derivatives. Calibration curves were linear for concentrations from 1.25 to 25 nmol/ml. The method was employed to assay these compounds in chick embryo retina explants using organic solvent extraction and 1,7-diaminoheptane as an internal standard. This simple and sensitive method can be applied to routine determinations of these compounds in various biological samples.

ChromatographyCalibration curveOrganic solventExtraction (chemistry)Reproducibility of ResultsAcetylationGeneral ChemistryChick EmbryoDiaminesHigh-performance liquid chromatographyRetinachemistry.chemical_compoundBenzoyl chloridechemistryPolyaminesAnimalsSpectrophotometry UltravioletDerivatizationQuantitative analysis (chemistry)Chromatography High Pressure LiquidJournal of chromatography
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Validation of a high-performance chromatographic method for determination of cefotaxime in biological samples

1999

An analytical method for detecting and quantifying cefotaxime in plasma and several tissues is described. The method was developed and validated using plasma and tissues of rats. The samples were analyzed by reversed phase liquid chromatography (HPLC) with UV detection (254 nm). Calibration graphs showed a linear correlation (r > 0.999) over the concentration ranges of 0.5–200 μg/mL and 1.25–25 μg/g for plasma and tissues, respectively. The recovery of cefotaxime from plasma standards prepared at the concentrations of 25 μg/mL and 100 μg/mL was 98.5 ± 3.5% and 101.8 ± 2.2%, respectively. The recovery of cefotaxime from tissue standards of liver, fat and muscle, prepared at the concentration…

ChromatographyCefotaximePharmacokineticsChemistryCoefficient of variationBlood plasmamedicineReversed-phase chromatographyBiochemistryQuantitative analysis (chemistry)High-performance liquid chromatographyAntibacterial agentmedicine.drugFresenius' Journal of Analytical Chemistry
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Spectrofluorimetric determination of emetine by flow injection using barium peroxide and UV derivatization

1993

Abstract The flow-injection spectrofluorimetric determination of emetine was carried out by photoderivatization in the presence of barium peroxide, in a flow-injection assembly in which the PTFE tubing in the injection valve is helically coiled around the lamp. The sample solution merges with a barium peroxidephosphoric acid solution and then the resulting mixture is irradiated; pure distilled water is used as a carrier stream. The calibration graph is linear over the range 0.05–50 μ g ml −1 of emetine dihydrochloride. The influence of foreign compounds was studied and the method was applied to the determination of emetine in injection and human urine samples.

ChromatographyChemistryCalibration curveEmetine HydrochlorideFluorescence spectrometrychemistry.chemical_elementBariumBiochemistryAnalytical Chemistrychemistry.chemical_compoundDistilled waterBarium peroxideEnvironmental ChemistryDerivatizationQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Determination of phenoxy acid herbicides in drinking waters by HPLC and solid phase extraction

1998

Abstract An HPLC procedure for determining phenoxy acid herbicides in waters is described. A LichroSpher RP select B octadecyl-silane analytical column and spectrophotometric detection at 230 nm were used. Adequate retention was achieved with a mobile phase containing MeOH/phosphate buffer 10−2 M pH 2.5/PnOH (50/42/8, v/v). The herbicides were isolated from water samples by using a single solid phase extraction procedure with C18 solid-phase columns. An enrichment factor of 500 is achieved. The coefficients of variation of the method were generally lower than 2.7% at 0.4 μg L−1 herbicide concentration levels. Recoveries ranged between 93 and 118%. The results obtained indicate that the prop…

ChromatographyChemistryClinical BiochemistryPharmaceutical ScienceReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundDicambaSample preparationSolid phase extractionWater pollutionEnrichment factorQuantitative analysis (chemistry)
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Continuous flow-injection-atomic absorption spectrometric method for the determination of Ondansetron

1995

Abstract A flow-injection procedure for the indirect determination of the new drug Ondansetron is proposed. The method is based on the reaction of the drug in an oxidative solid-phase reactor included in the flow assembly. The reactor was made by lead dioxide physically entrapped by polymerization; the released lead(II) was monitored by atomic absorption spectrometry at 217.0 nm. The procedure gave a linear calibration graph up to 20 μg ml−1 of Ondansetron with a sample throughput of 338 samples h−1.

ChromatographyChemistryContinuous flowCalibration curveAnalytical chemistryLead dioxideBiochemistryDosage formAnalytical Chemistrylaw.inventionOndansetronchemistry.chemical_compoundPolymerizationlawmedicineEnvironmental ChemistryAtomic absorption spectroscopyQuantitative analysis (chemistry)Spectroscopymedicine.drugAnalytica Chimica Acta
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Determination of tetracyclines in multi-specie animal tissues by pressurized liquid extraction and liquid chromatography–tandem mass spectrometry

2009

Abstract A specific, sensitive and robust pressurized liquid extraction (PLE) and liquid chromatography tandem mass spectrometry (LC–MS/MS) method for determining tetracycline, chlortetracycline, oxytetracycline and doxycycline in bovine, swine, poultry and lamb muscle tissues is presented. PLE was performed using an ASE ® 200 from Dionex and water as extractant, followed by solid-phase extraction (SPE) using an Oasis HLB cartridge. The method was validated for beef, chicken, pork and lamb meat in compliance with the requirements set by Commission Decision, 2002/657/EC [Commission Decision 2002/657/EC (2002). Implementing Council Directive 96/23/EC concerning the performance of analytical m…

ChromatographyChemistryExtraction (chemistry)General MedicineOxytetracyclineMass spectrometryAnalytical ChemistryLiquid chromatography–mass spectrometrymedicinemedia_common.cataloged_instanceSample preparationSolid phase extractionEuropean unionQuantitative analysis (chemistry)Food Sciencemedicine.drugmedia_commonFood Chemistry
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Determination of busulfan in human plasma using high-performance liquid chromatography with pre-column derivatization and fluorescence detection.

1999

A rapid, sensitive and reproducible high-performance liquid chromatographic assay for busulfan in human plasma was developed. After extraction of plasma samples with acetonitrile and methylene chloride, busulfan and the internal standard [1,5-bis(methanesulfonyloxy)pentane] were derivatized with 8-mercaptoquinoline to yield fluorescent compounds which were detected with a fluorescence detector equipped with filters of 360 nm (excitation) and 425 nm (emission). Calibration graphs showed a linear correlation (r>0.9990) over the concentration range of 20-2000 ng/ml. The recovery of busulfan from plasma standards was 70+/-5%. The detection and quantification limits for busulfan in plasma sample…

ChromatographyChemistryExtraction (chemistry)Reproducibility of ResultsGeneral ChemistryReference StandardsHigh-performance liquid chromatographyFluorescenceSensitivity and SpecificityFluorescence spectroscopyPentanechemistry.chemical_compoundSpectrometry FluorescenceCalibrationmedicineHumansDerivatizationQuantitative analysis (chemistry)Antineoplastic Agents AlkylatingBusulfanBusulfanChromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical sciences and applications
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