Search results for "High Performance Liquid Chromatography"

showing 10 items of 20 documents

Effect of Sunlight Exposure on Anthocyanin and Non-Anthocyanin Phenolic Levels in Pomegranate Juices by High Resolution Mass Spectrometry Approach

2020

Quali-quantitative analyses of anthocyanins and non-anthocyanin phenolic compounds performed with the use of liquid chromatography coupled with high resolution mass spectrometry, were evaluated in juice of pomegranate fruits (&lsquo

0106 biological sciencesHealth (social science)Fruit weightPlant SciencephenolsHealth benefitslcsh:Chemical technology01 natural sciencesHealth Professions (miscellaneous)MicrobiologyArticlechemistry.chemical_compound0404 agricultural biotechnologyAntimicrobial effectUltra High Performance Liquid Chromatography -Orbitrap-Mass Spectrometrylcsh:TP1-1185Food scienceHPLC MSpomegranate juicessolar exposurepolyphenolsSunlightPunica granatumChemistryfungihydrolysable tanninsfood and beverages04 agricultural and veterinary sciences040401 food sciencecarbohydrates (lipids)PolyphenolAnthocyaninflavonoidsUltra High Performance Liquid Chromatography-Orbitrap-Mass Spectrometry010606 plant biology & botanyFood ScienceFoods
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Guava: phytochemical composition of a potential source of antioxidants for cosmetic and/or dermatological applications

2017

Made available in DSpace on 2018-11-28T14:21:45Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-01-01. Added 1 bitstream(s) on 2019-10-09T18:26:25Z : No. of bitstreams: 1 S1984-82502017000200612.pdf: 803011 bytes, checksum: 199524e8d40cccb25490594ec61b3ed8 (MD5) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) PADC-FCF-UNESP Fundação para o Desenvolvimento da UNESP (FUNDUNESP) Guava (Psidium guajava L.) is a native fruit of the American tropics with commercial applications for its taste, flavor and aroma. Numerous pharmacological uses have been described for it, such as the antiseptic effect of it…

0301 basic medicineAntioxidantP. guajava L./use in cosmeticsmedicine.medical_treatmentlcsh:RS1-44101 natural scienceslcsh:Pharmacy and materia medica03 medical and health scienceschemistry.chemical_compoundmedicineOrganic chemistryFood scienceGeneral Pharmacology Toxicology and PharmaceuticsP.guajava L./use in cosmeticsAromaFlavorPsidiumP. guajava L./antioxidant/chemical compositionABTSbiologyP.guajava L./antioxidant/chemical compositionP.guajava L./phytochemistrybiology.organism_classificationFree radical scavengerP.guajava L/chemical stabilityHigh Performance Liquid Chromatography0104 chemical sciences010404 medicinal & biomolecular chemistry030104 developmental biologychemistryP. guajava L./phytochemistryQuercetinKaempferolP. guajava L/chemical stability
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Science based calibration for the extraction of 'analyte-specific' HPLC-DAD chromatograms in environmental analysis

2010

Multivariate science based calibration (SBC) has been applied to the resolution of overlapped peaks in liquid chromatography with diode array detection (LC-DAD). Complex river water samples spiked with 11 pharmaceutical substances resulted in poorly resolved chromatograms containing additional peaks from interfering matrix compounds and a change in the background absorbance due to the mobile phase gradient. Applying the present multivariate approach it was possible to resolve all 11 analytes from overlapping peaks, obtaining linear calibration lines (R2 > 0.96). Recovery percentages on spiked samples ranged between 74.6 and 113.5%, which are quite satisfactory taking into account the low co…

AnalyteResolution (mass spectrometry)Adrenergic beta-AntagonistsStatistics as TopicAnalytical chemistryEnvironmentHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)AbsorbanceRiversSCIENCE BASED CALIBRATIONSample preparationLeast-Squares AnalysisElectrodesChromatography High Pressure LiquidAnalgesicsENVIRONMENTAL ANALYSISChromatographyChemistryOtras Ciencias QuímicasExtraction (chemistry)Ciencias QuímicasDrug ResiduesStandard curveHIGH PERFORMANCE LIQUID CHROMATOGRAPHY-DIODE ARRAY DETECTION (HPLC-DAD)CalibrationMultivariate AnalysisEnvironmental PollutantsCIENCIAS NATURALES Y EXACTAS
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Application of a low transition temperature mixture for the dispersive liquid–liquid microextraction of illicit drugs from urine samples

2021

© 2021 by the authors.

BioanalysisLiquid Phase MicroextractionProductes biològicsIllicit drugsDispersive liquid–liquid mi-croextractionPharmaceutical ScienceOrganic chemistryUrineUrineHigh-performance liquid chromatographyBiological samples; Deep eutectic solvents; Dispersive liquid–liquid mi-croextraction; Drugs; High performance liquid chromatography; Illicit drugs; Low transition temperature mixtures; UrineArticleLow transition temperature mixturesAnalytical Chemistrychemistry.chemical_compoundBiological samplesQD241-441Limit of DetectionDrug DiscoveryHumansTransition TemperatureSample preparationPhysical and Theoretical ChemistryChromatographyChemistryExtraction (chemistry)Deep eutectic solventsDrugsSolventCold TemperatureChemistry (miscellaneous)Dispersive liquid–liquid microextractionMolecular MedicineDroguesGlass transitionCholine chlorideHigh performance liquid chromatography
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Application of molecularly imprinted polymers in analytical chiral separations and analysis

2018

Over the last two decades the process of development and application of a new types of molecular imprinted polymer (MIP) sorbents in the field of analytical chemistry have been widely described in the literature. One of the new trends in analytical chemistry practice is the use of new types of MIP sorbents as specific sorption materials constituting the stationary phase in advanced separation techniques. The following review paper contains comprehensive information about the application of a specific and well defined MIP sorbents (with the data base in the paper about the reagents used in MIP preparation process) as stationary phases in separation techniques including high performance liqui…

Capillary electrochromatographychiral separationMaterials sciencehigh performance liquid chromatography010401 analytical chemistryMolecularly imprinted polymerEnantioselective synthesisNanotechnologySorptionenantiomers02 engineering and technologycapillary electrochromatography021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryStationary phasemolecularly imprinted polymers0210 nano-technologySpectroscopyTrac-Trends in Analytical Chemistry
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Modulation of the growth and metabolic response of cyanobacteria by the multifaceted activity of naringenin

2017

The interactions between the plant-derived bioflavonoid, naringenin, and prokaryotic microalgae representatives (cyanobacteria), were investigated with respect to its influence on the growth and metabolic response of these microorganisms. To achieve reliable results, the growth of cyanobacteria was determined based on measurements of chlorophyll content, morphological changes were assessed through microscopic observations, and the chemical response of cells was determined using liquid and gas chromatography (HPLC; GC-FID). The results show that micromolar levels of naringenin stimulated the growth of cyanobacteria. Increased growth was observed for halophilic strains at naringenin concentra…

ChlorophyllPigments0301 basic medicineCyanobacteriaNaringeninExopolysaccharidesChloroplastsMicroorganismCellGlycobiologyMarine and Aquatic Scienceslcsh:MedicineFresh WaterPlant ScienceBiochemistrychemistry.chemical_compoundElectron MicroscopyNostoclcsh:ScienceLiquid ChromatographyMicroscopyMultidisciplinarybiologyChemistryChromatographic Techniquesfood and beveragesHalophilemedicine.anatomical_structureBiochemistryFlavanonesPhysical SciencesScanning Electron MicroscopyCellular Structures and OrganellesCellular TypesResearch ArticleFreshwater EnvironmentsChromatography GasPlant Cell BiologyMaterials Science030106 microbiologyCyanobacteriaResearch and Analysis MethodsCell wallExcretion03 medical and health sciencesPolysaccharidesPlant CellsmedicineMaterials by AttributeBacteriaOrganic PigmentsEcology and Environmental Scienceslcsh:ROrganismsBiology and Life SciencesAquatic EnvironmentsCell Biologybiology.organism_classificationAnabaenaHigh Performance Liquid Chromatography030104 developmental biologyEarth Scienceslcsh:QBacteriaChromatography LiquidNostoc muscorumPLOS ONE
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HPLC determination of oxadiazon in commercial pesticide formulations

2008

A simple, fast and precise high performance liquid chromatographic (HPLC) procedure has been developed for the determination of oxadiazon in emulsifiable concentrated pesticide formulations. 20 µL of diluted sample in acetonitrile were injected in a Kromasil C18 (250 ×am injetados em uma coluna Kromasil C18 4.6 mm, 5 µm) column, using acetonitrile:water (80:20) as mobile phase at 1 mL min-1 flow rate and oxadiazon determined by absorbance measurement at 292 nm. A theoretical limit of detection of 0.02 µg mL-1, a limit of quantification of 0.047 µg mL-1, corresponding to a 0.02 and 0.07% m/v in the original sample, and a relative standard deviation of 0.08% for three replicate analysis of sa…

Detection limitChromatographymedicine.diagnostic_testhigh performance liquid chromatographyChemistryRelative standard deviationUV-Vis detectionGeneral ChemistryPesticideHigh-performance liquid chromatographyoxadiazonAbsorbancechemistry.chemical_compoundSpectrophotometrymedicineFourier transform infrared spectroscopyAcetonitrilepesticide formulations
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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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Light-induced Changes in the Dimerization Interface of Bacteriophytochromes

2015

Phytochromes are dimeric photoreceptor proteins that sense red light levels in plants, fungi, and bacteria. The proteins are structurally divided into a light-sensing photosensory module consisting of PAS, GAF, and PHY domains and a signaling output module, which in bacteriophytochromes typically is a histidine kinase (HK) domain. Existing structural data suggest that two dimerization interfaces exist between the GAF and HK domains, but their functional roles remain unclear. Using mutational, biochemical, and computational analyses of the Deinococcus radiodurans phytochrome, we demonstrate that two dimerization interfaces between sister GAF and HK domains stabilize the dimer with approximat…

Histidine KinaseLightProtein ConformationMutantCrystallography X-RayBiochemistryProtein structureBacterial Proteinsx-ray scatteringcell signalingDeinococcusMolecular BiologybiologyPhytochromeHistidine kinaseMutagenesista1182Photoreceptor proteinDeinococcus radioduransCell Biologybiology.organism_classificationphotoreceptormolecular dynamicsProtein Structure TertiaryBiochemistryhigh performance liquid chromatography (HPLC)BiophysicsDeinococcusPhytochromeDimerizationProtein KinasesmutagenesisMolecular BiophysicsJournal of Biological Chemistry
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In vitro evaluation of poloxamer in situ forming gels for bedaquiline fumarate salt and pharmacokinetics following intramuscular injection in rats

2019

Graphical abstract

In situPO Propylene oxideIV IntravenousP338 Poloxamer 338lcsh:RS1-441Pharmaceutical Sciencechemistry.chemical_compoundn Sample sizeSD Standard deviationIM Intramuscularchemistry.chemical_classificationC0 Analyte plasma concentration at time zeroDoE Design of experimentsUV UltravioletPharmacology. TherapyK2.EDTA Potassium ethylenediaminetetraacetic acidLC–MS/MS Liquid chromatography-tandem mass spectrometryH&E Hematoxylin and eosintmax Sampling time to reach the maximum observed analyte plasma concentrationIn situ forming gelsCMC Critical micellar concentrationCmax Maximum observed analyte plasma concentrationIntramuscular injectionDN Dose normalizedGPT Gel point temperaturePLGA Poly-(DL-lactic-co-glycolic acid)TFA Trifluoroacetic acidCAN AcetonitrileATP Adenosine 5′ triphosphateSalt (chemistry)Polyethylene glycolPoloxamerArticlelcsh:Pharmacy and materia medicaPharmacokineticsIn vivoUHPLC Ultra-high performance liquid chromatographyPharmacokineticsAUClast Area under the analyte concentration versus time curve from time zero to the time of the last measurable (non-below quantification level) concentrationEO Ethylene oxideNMP N-methyl-2-pyrrolidoneComputingMethodologies_COMPUTERGRAPHICSAUC∞ Area under the analyte concentration vs time curve from time zero to infinite timeP407 Poloxamer 407In vitro releasePoloxamerCMT Critical micellar temperatureGel erosionIn vitrot1/2 Apparent terminal elimination half-lifechemistryMDR-TB Multi-drug resistant tuberculosisAUC80h Area under the analyte concentration versus time curve from time zero to 80 htlast Sampling time until the last measurable (non-below quantification level) analyte plasma concentrationMRM Multiple reaction monitoringNuclear chemistrySustained releaseInternational Journal of Pharmaceutics: X
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