Search results for "liquid chromatography"

showing 10 items of 942 documents

Derivatization of ephedrine with o-phthaldialdehyde for liquid chromatography after treatment with sodium hypochlorite.

2000

The usefulness of the reaction with NaClO followed by derivatization with o-phthaldialdehyde (OPA) and N-acetyl-L-cysteine (NAC) has been investigated for the chromatographic analysis of ephedrine. The influence of parameters affecting the two-stage reaction has been evaluated, including concentration of NaClO, time of reaction, temperature and pH. On the basis of these studies, conditions for the pre-column and (automated) post-column determination of ephedrine are presented. The described conditions have been applied to the measurement of ephedrine in the concentration intervals 0.2-20.0 microg/ml and 2.0-50.0 microg/ml for the pre-column and post-column methods, respectively. The possibi…

EphedrineChromatographySodium HypochloriteOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyFluorescence spectroscopyAnalytical ChemistryO-Phthalaldehydechemistry.chemical_compoundchemistrySodium hypochloritemedicineSample preparationEphedrineDerivatizationDerivative (chemistry)o-Phthalaldehydemedicine.drugChromatography LiquidJournal of chromatography. A
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Physico-chemical stability of eribulin mesylate containing concentrate and ready-to-administer solutions.

2013

Objectives The aim of this study was to determine the stability of commercially available eribulin mesylate containing injection solution as well as diluted ready-to-administer solutions stored under refrigeration or at room temperature. Methods Stability was studied by a novel developed stability-indicating reversed-phase high-performance liquid chromatography (RP-HPLC) assay with ultraviolet detection (detection wavelength 200 nm). Triplicate test solutions of eribulin mesylate containing injection concentrate (0.5 mg/mL) and with 0.9% sodium chloride solution diluted ready-to-administer preparations (0.205 mg/mL eribulin mesylate in polypropylene (PP) syringes, 0.020 mg/mL eribulin mesyl…

Eribulin MesylateChromatographybusiness.industryReproducibility of ResultsInjection solutionPharmacologyKetonesHigh-performance liquid chromatographyPharmaceutical SolutionsOncologyDrug StabilityMedicinePharmacology (medical)Chemical stabilitybusinessFuransChromatography High Pressure LiquidDrug PackagingJournal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
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Determination of N-acetyl-l-glutamine in urine by HPLC

1986

The determination of N-acetyl-l-glutamine (AC-GLN) in urine of rats after derivatization with xanthydrol by HPLC is described. The urine samples were collected from two groups of rats, one group fed normal nutrition, the other treated with AC-GLN. About 5 mM/l AC-GLN was detected in urine of untreated animals, whereas the excretion of the other group was in the range of 50 mM/l corresponding to about 50 wt.-% of the given AC-GLN.

Excretionchemistry.chemical_compoundChromatographyChemistryClinical BiochemistryN-acetyl-L-glutamineGeneral Materials ScienceGeneral MedicineUrineXanthydrolDerivatizationHigh-performance liquid chromatographyAnalytical ChemistryFresenius' Zeitschrift für analytische Chemie
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Studies of polyamines transport through liquid membranes with D2EHPA as a carrier.

2008

The transport of polyamines through the liquid membranes with di‐2‐ethylhexyl phosphoric acid (D2EHPA) was investigated. The study was performed in three main steps: liquid–liquid extraction (LLE), bulk liquid membrane (BLM) extraction, and supported liquid membrane (SLM) extraction. Equilibrium distribution experiments allowed determining the extraction constants and stoichiometric coefficients for each polyamine. It turned out that one amino group binds two molecules of carrier (one D2EHPA dimer) and the extractability of polyamine rises with the increase in number of function groups in the molecule. The BLM and SLM experiments showed that despite considerable differences in distribution …

Extraction (chemistry)Analytical chemistryFiltration and SeparationDi-(2-ethylhexyl)phosphoric acidMembranes ArtificialAcceptorHigh-performance liquid chromatographyextraction equilibriumAnalytical ChemistryChemical kineticschemistry.chemical_compoundKineticsliquid membranesMembranechemistryLiquid–liquid extractiondi-2-ethylhexyl phosphoric acidtransport mechanismPolyaminesPhosphoric acidChromatography High Pressure LiquidJournal of separation science
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Fenibuta piemaisījumu kvantitatīvas noteikšanas metodes optimizācija un validācija

2021

Kokina. P., zinātniskie vadītāji: Dr. ķīm. V. Bartkevičs (LU), Dr. ķīm. A. Bolotin (AS Olainfarm). Maģistra darbs, 147 lappuses, 184 attēli, 75 tabulas, 15 literatūras avoti, 16 pielikumi. Latviešu valodā. Maģistra darbā ir veikta divu piemaisījumu(4-amino-3-fenilbutānskābes etilestera hidrohlorīds un 4-fenil-2-pirrolidons) kvantitatīvas noteikšanas analīzes metodes optimizācija un validācija farmaceitiskā preperāta Noofen® aktīvajai farmaceitiskai vielai (AFV) fenibuts. Metodes optimizācija un validācija bija nepieciešama farmaceitiskā preparāta Noofen® kvalitātes kontroles vajadzībām. Fenibuta paraugi tika analizēti ar augsti efektīvo šķidruma hromatogrāfiju (AEŠH). Optimizācija tika vērs…

FENIBUTS PHENIBUTPIEMAISĪJUMU NOTEIKŠANAS OPTIMIZĀCIJA OPTIMIZATION OF IMPURITY DETERMINATION METHODAUGSTI EFEKTĪVĀ ŠĶIDRUMA HROMATOGRĀFIJA HIGH PERFORMANCE LIQUID CHROMATOGRAPHY4-FENIL-2-PIRROLIDONS 4-PHENYL-2- PYRROLIDONEĶīmija4-AMINO3-FENILBUTĀNSKĀBES ETILESTERA HIDROHLORĪDS 4-AMINO3-PHENYLBUTANOIC ACID ETHYL ESTER HYDROCHLORIDE
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Capillary Liquid Chromatography for the Determination of Terpenes in Botanical Dietary Supplements

2021

Dietary supplements of botanical origin are increasingly consumed due to their content of plant constituents with potential benefits on health and wellness. Among those constituents, terpenes are gaining attention because of their diverse biological activities (anti-inflammatory, antibacterial, geroprotective, and others). While most of the existing analytical methods have focused on establishing the terpenic fingerprint of some plants, typically by gas chromatography, methods capable of quantifying representative terpenes in herbal preparations and dietary supplements with combined high sensitivity and precision, simplicity, and high throughput are still necessary. In this study, we have e…

Farnesenenatural productsPharmaceutical ScienceOrange (colour)01 natural sciencesArticleTerpenedietary supplementschemistry.chemical_compoundPharmacy and materia medica0404 agricultural biotechnologyLinaloolDrug DiscoveryLimoneneChromatography010401 analytical chemistryR04 agricultural and veterinary sciencesplant materials040401 food sciencecapillary liquid chromatography0104 chemical sciencesRS1-441chemistryMyrceneGreen coffee extractMedicineMolecular MedicineGas chromatographyterpenesPharmaceuticals
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Preparative separation of phospholipids by flash-HPLC

1988

Flash (photography)ChromatographyChemistryClinical BiochemistryGeneral Materials ScienceGeneral MedicineHigh-performance liquid chromatographyAnalytical ChemistryFresenius' Zeitschrift für analytische Chemie
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Simultaneous determination of four 5-hydroxy polymethoxyflavones by reversed-phase high performance liquid chromatography with electrochemical detect…

2009

Accumulating evidence has suggested the potential health-promoting effects of 5-hydroxy polymethoxyflavones (5-OH-PMFs) naturally existing in citrus genus. However, research efforts are hampered by the lack of reliable and sensitive methods for their determination in plant materials and biological samples. Using reversed-phase high performance liquid chromatography (HPLC) equipped with electrochemical (EC) detection, we have developed a fast and highly sensitive method for quantification of four 5-OH-PMFs, namely 5-hydroxy-6,7,8,3',4'-pentamethoxyflavone, 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone, 5-hydroxy-6,7,4'-trimethoxyflavone, and 5-hydroxy-6,7,8,4'-tetramethoxyflavone. The method wa…

FlavonoidsDetection limitOrange juicechemistry.chemical_classificationCitrusAccuracy and precisionChromatographyOrganic ChemistryFlavonoidReproducibility of ResultsElectrochemical TechniquesGeneral MedicineReversed-phase chromatographyElectrochemical detectionHydrogen-Ion ConcentrationFlavonesSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryBeverageschemistryLinear ModelsChromatography High Pressure LiquidCitrus × sinensisJournal of Chromatography A
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Isolation and Characterization of Structurally Novel Antimutagenic Flavonoids from Spinach (Spinacia oleracea)

2001

Thirteen compounds, isolated from spinach (Spinacia oleracea), acted as antimutagens against the dietary carcinogen 2-amino-3-methylimidazo[4,5-f]quinoline in Salmonella typhimurium TA 98. The antimutagens were purified by preparative and micropreparative HPLC from a methanol/water (70:30, v/v) extract of dry spinach (commercial product) after removal of lipophilic compounds such as chlorophylls and carotenoids by solid-phase extraction (SPE). Pure active compounds were identified by instrumental analysis including FT-IR, (1)H and (13)C NMR, UV-vis spectroscopy, and mass spectrometry. All of these compounds were flavonoids and related compounds that could be attributed to five groups: (A, m…

FlavonoidsSalmonella typhimuriumchemistry.chemical_classificationSpinaciaChromatographybiologyQuinolineFlavonoidExtraction (chemistry)Antimutagenic AgentsGeneral Chemistrybiology.organism_classificationHigh-performance liquid chromatographyStructure-Activity Relationshipchemistry.chemical_compoundchemistryBiochemistrySpinacia oleraceaQuinolinesSpinachGeneral Agricultural and Biological SciencesCarotenoidAntimutagenChromatography High Pressure LiquidMutagensJournal of Agricultural and Food Chemistry
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Supercritical fluid extraction and HPLC determination of relevant polyphenolic compounds in grape skin.

2005

The polyphenols determined are: (+)-catechin, (-)-epicatechin, rutin, quercetin and trans-resveratrol. Suitable conditions of supercritical fluid extraction were established using ethanol as a modifier of the polarity solvent (supercritical carbon dioxide). Final extraction conditions were: 20% v/v ethanol, 60degreesC, 250 bars and flow rate 2 mL/min. Static step time and dynamic step time were established using a selected grape skin sample. The extract was collected in water; the more polar polyphenols ((+)-catechin and (-)-epicatechin) remain in solution but rutin, quercetin and trans-resveratrol precipitate in this medium, thereby the solution of the extracted polyphenols was filtered. (…

FlavonoidsSupercritical carbon dioxideChromatographyEthanolChemistryExtraction (chemistry)Supercritical fluid extractionPolyphenolsFiltration and SeparationChromatography Supercritical FluidHigh-performance liquid chromatographySupercritical fluidAnalytical ChemistryAcetic acidchemistry.chemical_compoundRutinPhenolsFruitVitisQuercetinChromatography High Pressure LiquidJournal of separation science
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