Search results for "Analyte"

showing 10 items of 303 documents

NQS-Doped PDMS Solid Sensor: From Water Matrix to Urine Enzymatic Application

2021

The development of in situ analytical devices has gained outstanding scientific interest. A solid sensing membrane composed of 1,2-naphthoquinone-4-sulfonate (NQS) derivatizing reagent embedded into a polymeric polydimethylsiloxane (PDMS) composite was proposed for in situ ammonium (NH4+) and urea (NH2CONH2) analysis in water and urine samples, respectively. Satisfactory strategies were also applied for urease-catalyzed hydrolysis of urea, either in solution or glass-supported urease immobilization. Using diffuse reflectance measurements combined with digital image processing of color intensity (RGB coordinates), qualitative and quantitative analyte detection was assessed after the colorime…

In situAnalyteMaterials scienceUreasePolymersClinical BiochemistrywaterNQS02 engineering and technologyureaurea hydrolysis01 natural sciencesArticlechemistry.chemical_compoundDimethylpolysiloxanesoptical sensorureaseglass supportChromatographyPolydimethylsiloxanebiology010405 organic chemistryGeneral Medicine021001 nanoscience & nanotechnologyurine0104 chemical sciencesin-situ analysisammoniumMembranechemistryReagentUreabiology.proteinColorimetry0210 nano-technologyTP248.13-248.65NaphthoquinonesNQS-PDMS sensorBiotechnologyBiosensors
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Revisited BIA-MS combination: Entire "on-a-chip" processing leading to the proteins identification at low femtomole to sub-femtomole levels

2008

International audience; We present the results of a study in which biomolecular interaction analysis (BIA, Biacore 2000) was combined with mass spectrometry (MS) using entire "on-a-chip" procedure. Most BIA-MS studies included an elution step of the analyte prior MS analysis. Here, we report a low-cost approach combining Biacore analysis with homemade chips and MS in situ identification onto the chips without elution step. First experiments have been made with rat serum albumin to determine the sensitivity and validation of the concept has been obtained with an antibody/antigen couple. Our "on-a-chip" procedure allowed complete analysis by MS-MS of the biochip leading to protein identificat…

In situMALDI-TOFAnalyte[ SDV.BBM.BP ] Life Sciences [q-bio]/Biochemistry Molecular Biology/BiophysicsBiomedical EngineeringBiophysicsAnalytical chemistrySPRBiosensing TechniquesMass spectrometry01 natural sciencesSensitivity and Specificity03 medical and health sciencesProtein Interaction MappingElectrochemistryNanotechnologyBIA-MSBiochipChromatography High Pressure Liquid030304 developmental biology0303 health sciencesChromatographyprotein complexesElutionChemistryMicrochemistry010401 analytical chemistryMs analysisReproducibility of ResultsGeneral MedicineEquipment DesignMicrofluidic Analytical Techniques0104 chemical sciencesEquipment Failure Analysis[SDV.BBM.BP]Life Sciences [q-bio]/Biochemistry Molecular Biology/BiophysicsMatrix-assisted laser desorption/ionizationSAMSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationBiotechnology
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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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Capillary zone electrophoresis of alkaloids

1998

Abstract A comprehensive discussion of important aspects for the analysis of alkaloids by capillary zone electrophoresis (CZE) is given. The influence of structure on the electrophoretic mobility (EM) of indole alkaloids was investigated using a running buffer which is generally applicable to the CZE analysis of alkaloids. The EM, which at the applied conditions was mostly dependent on the size and shape of the solvated analyte ions, was additionally affected by the presence of hydrogen bonds or ion–dipole interactions between protonated and unprotonated alkaloids of the same species. This could be derived from the existence of alkaloidal dimer cluster ions [2M+H]+ when mass spectrometry wa…

Indole testElectrosprayAnalyteChromatographyHydrogen bondDimerOrganic ChemistryGeneral MedicineMass spectrometryBiochemistryAnalytical Chemistrychemistry.chemical_compoundElectrophoresisCapillary electrophoresischemistryJournal of Chromatography A
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Comparison of green sample preparation techniques in the analysis of pyrethrins and pyrethroids in baby food by liquid chromatography–tandem mass spe…

2017

A new selective and sensitive liquid chromatography triple quadrupole mass spectrometry method was developed for simultaneous analysis of natural pyrethrins and synthetic pyrethroids residues in baby food. In this study, two sample preparation methods based on ultrasound-assisted dispersive liquid–liquid microextraction (UA-DLLME) and salting-out assisted liquid–liquid extraction (SALLE) were optimized, and then, compared regarding the performance criteria. Appropriate linearity in solvent and matrix-based calibrations, and suitable recoveries (75–120%) and precision (RSD values ≤ 16%) were achieved for selected analytes by any of the sample preparation procedures. Both methods provided the…

InsecticidesAnalyteMaximum Residue LimitLiquid-Liquid ExtractionFood Contamination010402 general chemistry01 natural sciencesBiochemistryAnalytical ChemistryMatrix (chemical analysis)Baby foodchemistry.chemical_compoundLC–MS/MSTandem Mass SpectrometryLiquid chromatography–mass spectrometryEtofenproxNitrilesPyrethrinsAnimalsHumansSample preparationPesticidesFood contaminantsChromatographyChemistry010401 analytical chemistryOrganic ChemistryInfantGreen Chemistry TechnologyGeneral Medicine0104 chemical sciencesMilkUA-DLLMEGreen chemistryFruitSolventsInfant FoodEdible GrainEnrichment factorBaby foodsChromatography Liquid
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Substitution–dilution method to correct the matrix effect in multi-element quantitative analysis by X-ray fluorescence

2001

Abstract A mathematical model based on the dilution–addition method (DAM) for multi-elemental analysis using an X-ray fluorescence technique is proposed. The conditions for sample preparation do not require both the unknown and standard samples to be similar in composition and mineralogy, and the unknown sample is replaced quantitatively by the standard sample, hence the denomination substitution–dilution method (SDM). This method makes it possible to correct the matrix effect in multi-elemental quantitative analysis by X-ray fluorescence for each analyte. The proposed model presents hyperbolic behaviour of the experimental data when the X-ray fluorescence intensities are represented versus…

Internal standardAnalyteChemistryHyperbolic functionAnalytical chemistryLinear modelDiluentAtomic and Molecular Physics and OpticsAnalytical ChemistryDilutionMatrix (chemical analysis)Sample preparationInstrumentationSpectroscopySpectrochimica Acta Part B: Atomic Spectroscopy
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H-Point standard additions method for resolution of binary mixtures with simultaneous addition of both analytes

1995

Abstract The basis of the H-point standard additions method, HPSAM, with simultaneous addition of both analytes is proposed for the resolution of binary mixtures. It is a modification of the previously described H-point standard additions method that permits the resolution of both species from a unique calibration set by making the simultaneous addition of the two analytes. The method uses as analytical signals the absorbances at pairs of wavelengths where each species shows the same absorbance. The required data to apply the method are the absorbance values at the previously selected wavelengths for the sample alone and spiked with both species at known concentrations. Linear relations bet…

Internal standardAnalyteChromatographyResolution (mass spectrometry)ChemistryAnalytical chemistryBiochemistryIntersection (Euclidean geometry)Analytical ChemistryChemometricsAbsorbanceStandard additionEnvironmental ChemistryAbsorption (electromagnetic radiation)SpectroscopyAnalytica Chimica Acta
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Direct chromatographic study of the enantioselective biodegradation of ibuprofen and ketoprofen by an activated sludge

2018

[EN] The quantification of the enantiomeric fraction (EF) during the biodegradation process is essential for environmental risk assessment. In this paper the enantioselective biodegradation of ibuprofen, IBU, and ketoprofen, KET, two of the drugs most consumed, was evaluated. Biodegradation experiments were performed in batch mode using a minimal salts medium inoculated with an activated sludge (collected from a Valencian Waste Water Treatment Plant) and supplemented with the racemate of each compound. The inoculum activity was verified using fluoxetine as reference compound. The experimental conditions used (analyte concentration and volume of inoculum) were chosen according to OECD guidel…

KetoprofenAnalyteCalibration curveIbuprofenFraction (chemistry)Wastewater010501 environmental sciences01 natural sciencesBiochemistryAnalytical ChemistryPeak area based estimatesEnantioselective biodegradationmedicineChromatography High Pressure Liquid0105 earth and related environmental sciencesChromatographySewageChemistryBatch experiment010401 analytical chemistryOrganic ChemistryStereoisomerismGeneral MedicineBiodegradationIbuprofenChiral separation0104 chemical sciencesKineticsBiodegradation EnvironmentalActivated sludgeKetoprofenCalibrationEnantiomermedicine.drugJournal of Chromatography A
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Determination of non-steroidal anti-inflammatory drugs in water and urine using selective molecular imprinted polymer extraction and liquid chromatog…

2016

Abstract A selective solid-phase extraction was employed for the improvement of the determination of non-steroidal anti-inflammatory drugs (NSAIDs) in continental water and urine samples. Ketoprofen, naproxen, diclofenac, and ibuprofen were selected as target analytes due to they are the most frequently administered and consumed NSAIDs. These compounds were extracted using molecular imprinted polymers and determined by liquid chromatography with diode array (DAD), and tandem-mass spectrometry (MS–MS) detectors. Performance of DAD and MS–MS detectors was evaluated throughout this study. The obtained limits of quantification, after a 50-fold preconcentration solid-phase extraction, varied fro…

KetoprofenAnalyteNaproxenPolymersClinical BiochemistryPharmaceutical Science02 engineering and technologyUrineMass spectrometry01 natural sciencesAnalytical ChemistryMolecular ImprintingTandem Mass SpectrometryDrug DiscoverymedicineSpectroscopyChromatographyChemistryAnti-Inflammatory Agents Non-Steroidal010401 analytical chemistryExtraction (chemistry)Molecularly imprinted polymerWater021001 nanoscience & nanotechnologyIbuprofen0104 chemical sciences0210 nano-technologyWater Pollutants ChemicalChromatography Liquidmedicine.drugJournal of Pharmaceutical and Biomedical Analysis
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The application of molecular imprinting technology to solid phase extraction

2001

In parallel to a long lasting search for universal multi-purpose sorbents, the area of solid phase extraction (SPE) is recently experiencing a rapid development of new types of tailor-made class specific or compound-specific sorbents which are designed to respond to the increasing demand for selectivity and efficiency in sample clean-up prior to quantification. An important issue here is the enrichment and clean-up of complex samples, such as environmental waters, sediments, biofluids and foodstuffs prior to detection. This because the analyte is often present in low concentration in a complex mixture of similar compounds and therefore needs to be isolated and enriched in order to be detect…

Long lastingAnalyteChromatographyChemistryOrganic ChemistryClinical BiochemistrySolid-phase microextractionBiochemistryAnalytical ChemistryAdsorptionSample preparationSolid phase extractionMolecular imprintingSelectivityChromatographia
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