Search results for "Spectroscopy"

showing 10 items of 10293 documents

Extractive Spectrophotometric Determination of Ondansetron by Ion-Pair Formation with Bromocresol Green

1996

Abstract An empirical spectrophotometric procedure for the determination of the antiemetic ondansetron is carried out. The method is based on the formation of a 1:1 ion pair with bromocresol green in the pH range over 3.2 – 4.4, extraction into chloroform layer and spectrophotometric measurement at 420.8 nm. The calibration graph is linear over the range 0.1 – 20 μg ml−1 ondansetron, with a relative standard deviation of 2.7%; the influence of foreign substances is also studied. The method is applied to ondansetron determination in human urine.

ChromatographyChloroformBromocresol greenmedicine.diagnostic_testCalibration curveBiochemistry (medical)Clinical BiochemistryExtraction (chemistry)Ion pairsBiochemistryAnalytical ChemistryOndansetronchemistry.chemical_compoundchemistrySpectrophotometryElectrochemistrymedicineQuantitative analysis (chemistry)Spectroscopymedicine.drugAnalytical Letters
researchProduct

Liquid chromatography-Fourier transform infrared spectrometric determination of cholesterol in animal greases

1997

Abstract Stearic acid, cholesterol and cholesteryl palmitate have been separated in less than 14 min by liquid chromatography on a column (3.9 mm i.d.×150 mm) of Nova-Pack C 18 (5 μm) using chloroform–acetonitrile (45 : 55) as mobile phase pumped at 0.5 ml min −1 ; Fourier transform infrared (FTIR) spectrometry was employed for both, general detection at 2868 or 2855 cm −1 and selective detection at 3285 cm −1 for stearic acid and 3526 cm −1 for cholesterol. In all cases a baseline established at 3900 cm −1 , 9-point smoothing and chromatographic peak height measurements were used. The method has been validated by application to the determination of cholesterol in animal greases and fish oi…

ChromatographyChloroformCholesterolMass spectrometryBiochemistryAnalytical Chemistrychemistry.chemical_compoundsymbols.namesakeFourier transformchemistrysymbolsEnvironmental Chemistrylipids (amino acids peptides and proteins)Petroleum etherStearic acidFourier transform infrared spectroscopySpectroscopySaponificationAnalytica Chimica Acta
researchProduct

Chromatographic analysis of phenethylamine-antihistamine combinations using C8, C18 or cyano columns and micellar sodium dodecyl sulfate-pentanol mix…

2001

The chromatographic behaviour of binary and ternary mixtures of several phenethylamines (phenylephrine, phenylpropanolamine, ephedrine, pseudoephedrine and methoxyphenamine) and antihistamines (pheniramine, carbinoxamine, doxylamine, chlorpheniramine, dexchlorpheniramine, dexbrompheniramine, diphenhydramine, tripolidine, azatadine and phenyltoloxamine), found in cough-cold pharmaceutical preparations, was studied using C8, C18 and cyano columns, micellar mobile phases of sodium dodecyl sulfate (SDS) and pentanol and UV detection. Using a C8 column and mobile phases of 0.05 mol l-1 SDS-6% v/v pentanol or 0.15 mol l-1 SDS-2% v/v pentanol at pH 7, more than 30 different phenethylamine-antihist…

ChromatographyChromatographyMethoxyphenaminePhenethylaminesPseudoephedrineAscorbic acidBiochemistrySensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundNasal DecongestantschemistryPhenyltoloxaminePhenethylaminesElectrochemistrymedicineHistamine H1 AntagonistsEnvironmental ChemistryCarbinoxaminePheniramineSodium dodecyl sulfateSpectroscopymedicine.drugThe Analyst
researchProduct

Synthesis and characterization of alumina R chemically modified withn-octyl for use as a stationary phase in TLC

2003

A stationary phase for thin-layer chromatography has been prepared by attaching 1-octene to alumina R. This stationary phase has been characterized by elemental analysis, measurement of specific surface area, IR spectroscopy, and by chromatographic testing.

ChromatographyClinical BiochemistryInfrared spectroscopyReversed-phase chromatographyBiochemistryThin-layer chromatographyAnalytical ChemistryCharacterization (materials science)chemistry.chemical_compoundColumn chromatographychemistryElemental analysisSpecific surface areaSemicarbazoneJournal of Planar Chromatography – Modern TLC
researchProduct

Estimation of the Compatibility Between Poly(Methylmethacrylate) and Poly(Styrene Co Vinyl Phenol) Blends from Dilute Solution Measurements

2006

Abstract The compatibility of poly(methyl methacrylate) (PMMA) with poly(styrene‐co‐vinyl phenol) (PS‐VPh) with two different contents of vinyl phenol, 5.8 and 7.2%, in dilute tetrahydrofuran solutions has been investigated by size exclusion chromatography and fluorescence spectroscopy at 25°C. The chromatographic technique permits the evaluation of the preferential solvation at different PMMA/PS‐VPh ratios. Changes in the fluorescence properties of PS‐VPh, caused by its association with PMMA, were used to obtain the fraction of copolymer bound to PMMA at diverse PMMA compositions. Both techniques agree quantitatively in every system, indicating that the association increases when the PMMA …

ChromatographyClinical BiochemistrySize-exclusion chromatographytechnology industry and agricultureFluorescence spectrometryPharmaceutical Sciencemacromolecular substancesequipment and suppliesBiochemistryFluorescence spectroscopyAnalytical ChemistryStyrenebody regionsGel permeation chromatographychemistry.chemical_compoundchemistryCopolymerPhenolMethyl methacrylateJournal of Liquid Chromatography & Related Technologies
researchProduct

Off-line dansylation of amines using C18 solid-phase packings: study of the fluorescence and chemiluminescence detection by post-column derivatizatio…

1999

Abstract Dansylation of amines (primaries and secondaries) using C18 solid-phase supports is described. The time of analysis and the handing sample have been markedly improved with respect to those required for solution dansylation. The dansylated amine derivates were injected onto the liquid chromatography system and fluorescence detected. The sensitivity and selectivity is better than the other dansylation procedures described in the literature and also better than other derivatization reagents such 1,2-napthoquinone 4-sulfonate (NQS) or 3,5-dinitrobenzoyl chloride (3,5-DNB). Dansyl compounds can also form chemiluminescent derivatives, therefore a post-column derivatization procedure with…

ChromatographyDansyl chlorideOxalic acidNQSBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistrypolycyclic compoundsEnvironmental ChemistryAmine gas treatingSolid phase extractionTCPODerivatizationSpectroscopyAnalytica Chimica Acta
researchProduct

New approaches based on modified Gaussian models for the prediction of chromatographic peaks

2012

Abstract The description of skewed chromatographic peaks has been discussed extensively and many functions have been proposed. Among these, the Polynomially Modified Gaussian (PMG) models interpret the deviations from ideality as a change in the standard deviation with time. This approach has shown a high accuracy in the fitting to tailing and fronting peaks. However, it has the drawback of the uncontrolled growth of the predicted signal outside the elution region, which departs from the experimental baseline. To solve this problem, the Parabolic-Lorentzian Modified Gaussian (PLMG) model was developed. This combines a parabola that describes the variance change in the peak region, and a Lor…

ChromatographyDegree (graph theory)Chemistrymedia_common.quotation_subjectGaussianParabolaCauchy distributionVariance (accounting)BiochemistrySignalAsymmetryStandard deviationAnalytical Chemistrysymbols.namesakesymbolsEnvironmental ChemistrySpectroscopymedia_commonAnalytica Chimica Acta
researchProduct

Comparison of two vibrational procedures for the direct determination of mancozeb in agrochemicals.

2007

The direct determination of mancozeb in agrochemicals has been made by diamond attenuated total reflectance (ATR) Fourier transform infrared spectroscopy in the middle range (DATR-MIR) and diffuse reflectance infrared Fourier transform spectroscopy in the near range (DR-NIR) methods using in both cases a previous identification of the samples using a dendrographic classification and an appropriate partial least squares (PLS) calibration established from a set of nine external standards and optimized for each type of sample. It was analyzed a heterogeneous population of 11 samples obtained from the Spanish market, containing different co-formulated products, such as fosetyl-Al, copper oxychl…

ChromatographyDiffuse reflectance infrared fourier transformChemistryAttenuated total reflectionDirect methodPartial least squares regressionCalibrationAnalytical chemistryInfrared spectroscopyFourier transform infrared spectroscopyFourier transform spectroscopyAnalytical ChemistryTalanta
researchProduct

Determination of diphenhydramine hydrochloride by flow injection with Bromophenol Blue and turbidimetric measurement

1990

The study of a number of diphenhydramine-dye systems was carried out in order to determine the most suitable precipitate for the turbidimetric determination of diphenhydramine using flow injection (FI). The reagent selected was Bromophenol Blue. The chemical and FI variables were optimised. The calibration graph was linear over the concentration range 50-230 p.p.m. of diphenhydramine hydrochloride. A number of interfering substances were also investigated.

ChromatographyDiphenhydramine hydrochlorideCalibration curveDiphenhydramineBromophenol blueBiochemistryAnalytical Chemistrychemistry.chemical_compoundDiphenhydraminechemistryNephelometry and TurbidimetryReagentElectrochemistrymedicineEnvironmental ChemistryIndicators and ReagentsBromphenol BlueSpectroscopymedicine.drugThe Analyst
researchProduct

Method development for the determination of 1,1-dimethylhydrazine by the high-performance liquid chromatography-mass spectrometry technique.

2018

Unsymmetrical dimethyl hydrazine is highly toxic, carcinogenic compound, widely used for organic synthesis and drug development. Therefore, due to its high reactivity, direct analysis is problematic. Current study proposes to use derivatization reaction to increase selectivity and sensitivity of high-performance liquid chromatography–mass spectrometry method. Different derivatization agents were tested and optimal reaction media was found. Derivatization was performed by using small amounts of reagents to lower the cost of analysis. The full validation of the method was performed and it can be used in a routine control in pharmaceutical analysis. Method sensitivity is 0.15 ppm, and lineari…

ChromatographyElectrospray ionization010401 analytical chemistryGeneral Medicine010402 general chemistryTandem mass spectrometryMass spectrometry01 natural sciencesHigh-performance liquid chromatographyAtomic and Molecular Physics and Optics0104 chemical scienceschemistry.chemical_compoundchemistryDimethylhydrazineReactivity (chemistry)Organic synthesisDerivatizationSpectroscopyEuropean journal of mass spectrometry (Chichester, England)
researchProduct