0000000000273994

AUTHOR

Miriam Beneito-cambra

0000-0002-5874-9271

showing 20 related works from this author

Recognition and alignment of variables from UV–vis chromatograms and application to industrial enzyme digests classification

2017

Abstract In the last years, industrial applications of chemometrics have largely increased due to their capacity to extract important information from complex records as chromatograms or spectra data. The use of chemometric methods also can avoid the use of detectors of elevated cost. In this work, a procedure to recognize the relevant chemical information contained in complex UV–vis chromatograms, after a trypsin digestion, to identify the three enzyme main classes (proteases, amylases and cellulases) commonly employed in the cleaning industry, has been developed. In order to recognize the chromatogram peaks, six indices of peak identity or identifiers were defined. A program written in MA…

Peak areaChromatographyChemistrybusiness.industryProcess Chemistry and TechnologySample (material)010401 analytical chemistryPattern recognition010402 general chemistry01 natural sciences0104 chemical sciencesComputer Science ApplicationsAnalytical ChemistryChemometricsUltraviolet visible spectroscopyArtificial intelligenceTrypsin DigestionbusinessSpectroscopySoftwareChemometrics and Intelligent Laboratory Systems
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Determination of non-ionic and anionic surfactants in industrial products by separation on a weak ion-exchanger, derivatization and liquid chromatogr…

2013

Abstract A method for the determination of priority surfactants, including fatty alcohol ethoxylates (FAE), alkylether sulfates (AES) and linear alkylbenzene sulfonates (LAS) is described. The samples were diluted with 50% methanol at pH 4 prior to solid-phase extraction on a weak anionic exchanger (WAX). The AES and LAS surfactant classes were retained, whereas the non-ionic components, including most FAE oligomers were eluted. After washing the WAX cartridge to remove cations, the remaining hydrophobic FAE oligomers were eluted using hot 80% methanol at pH 4 (at ca. 50 °C). These two eluates were combined to constitute the non-ionic fraction. Then, AES and LAS were eluted using 80% MeOH w…

AnionsWaxPhthalic anhydrideChromatographyEsterificationLinear alkylbenzeneElutionOrganic ChemistryExtraction (chemistry)Fatty alcoholGeneral MedicineHydrogen-Ion ConcentrationChromatography Ion ExchangeBiochemistryAnalytical ChemistrySurface-Active Agentschemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumMethanolDerivatizationChromatography High Pressure LiquidJournal of Chromatography A
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Determination of alcohols in essential oils by liquid chromatography with ultraviolet detection after chromogenic derivatization

2013

Abstract An HPLC-UV method to determine compounds having a hydroxyl functional group in plant essential oils is developed. The sample is diluted with 1,4-dioxane and the analytes are derivatized with phthalic anhydride. The derivatives (phthalates hemiesters) are separated on a C8 column using an acetonitrile (ACN)/water gradient. Separation conditions were optimized using the DryLab® method development software. For the alcohols and phenols present in mint and rose essential oils, optimization led to a ca. 40 min gradient time and a column temperature of 8 °C. The alcohol and its derivatives were identified using HPLC with mass spectrometry (MS) detection. A large sensitivity enhancement w…

AlcoholRosaMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionchemistry.chemical_compoundLimit of DetectionlawOils VolatileFlame ionization detectorPhenolsDerivatizationDetection limitPhthalic anhydrideChromatographyOrganic ChemistryTemperatureReproducibility of ResultsGeneral MedicinechemistryAlcoholsPhthalic AnhydridesSpectrophotometry UltravioletChromatography LiquidMenthaJournal of Chromatography A
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Comparison of monolithic and microparticulate columns for reversed-phase liquid chromatography of tryptic digests of industrial enzymes in cleaning p…

2011

Abstract Enzymes of several classes used in the formulations of cleaning products were characterized by trypsin digestion followed by HPLC with UV detection. A polymeric monolithic column (ProSwift) was used to optimize the separation of both the intact enzymes and their tryptic digests. This column was adequate for the quality control of raw industrial enzyme concentrates. Then, monolithic and microparticulate columns were compared for peptide analysis. Under optimized conditions, the analysis of tryptic digests of enzymes of different classes commonly used in the formulation of cleaning products was carried out. Number of peaks, peak capacity and global resolution were obtained in order t…

Peptide analysisChromatography Reverse-PhaseMonolithic HPLC columnChromatographyResolution (mass spectrometry)ChemistryOrganic ChemistryDetergentsReproducibility of ResultsGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyPeptide FragmentsAnalytical ChemistryEnzymesIndustrial enzymesTrypsinTrypsin DigestionUv detectionJournal of chromatography. A
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Enzyme class identification in cleaning products by hydrolysis followed by derivatization with o-phthaldialdehyde, HPLC and linear discriminant analy…

2008

The enzymes present in raw materials of the cleaning industry (enzyme industrial concentrates) and in household cleaners were isolated by precipitation with acetone and hydrolyzed with HCl. The resulting amino acids were derivatized with o-phthaldialdehyde, and the derivatives were separated by HPLC. The peaks of 14 amino acids were observed using a C18 column and a multi-segmented gradient of acetonitrile-water in the presence of a 5 mM citric/citrate buffer of pH 6.5. Using either normalized peak areas (divided by the sum of the peak areas of the chromatogram) or ratios of pairs of peak areas as predictor variables, linear discriminant analysis models, capable of predicting the enzyme cla…

chemistry.chemical_classificationChromatographybiologyChemistryHydrolysisDetergentsDiscriminant AnalysisHousehold ProductsCellulaseHigh-performance liquid chromatographyAnalytical ChemistryEnzymeschemistry.chemical_compoundHydrolysisEnzymeArtificial IntelligenceAcetoneBy-productbiology.proteinAmylaseAmino AcidsDerivatizationChromatography High Pressure Liquido-PhthalaldehydeTalanta
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Comparison on photo-initiators for the preparation of methacrylate monolithic columns for capillary electrochromatography.

2010

The synthesis of lauryl methacrylate monoliths for capillary electrochromatography by UV polymerization using several free-radical initiators (alpha,alpha'-azobisisobutyronitrile, 2,2-dimethoxy-2-phenylacetophenone, dibenzoyl peroxide (BPO) and lauroyl peroxide (LPO)) has been investigated. Using a 1,4-butanediol/1-propanol mixture as porogenic solvent, the influence of each initiator and its content on the morphological and electrochromatographical properties of beds was evaluated. Under their respective optimum content, satisfactory separations of a test mixture of PAHs with similar efficiencies (minimum plate heights of 8.0-12.7 microm obtained from Van Deemter plots) were achieved for t…

Van Deemter equationLipid PeroxidesPhotochemistry22-Dimethoxy-2-phenylacetophenoneBenzoyl peroxideMethacrylateBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary ElectrochromatographyNitrilesmedicineCapillary electrochromatographyChromatographyBenzoyl PeroxideOrganic ChemistryAzobisisobutyronitrileAcetophenonesReproducibility of ResultsGeneral MedicineRepeatabilitychemistryPolymerizationMicroscopy Electron ScanningMethacrylatesmedicine.drugJournal of chromatography. A
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Photo-polymerized lauryl methacrylate monolithic columns for CEC using lauroyl peroxide as initiator

2009

Lauryl methacrylate (LMA)-ester based monolithic columns photo-polymerized using lauroyl peroxide (LPO) as initiator were prepared, and their morphological and CEC properties were studied. The composition of the polymerization mixture (i.e. ratios of monomers/porogenic solvents, 1,4-butanediol/1-propanol and LMA/crosslinker) was optimized. The morphological and chromatographic properties of LMA columns were evaluated by means of SEM pictures and van Deemter plots of PAHs, respectively. The polymerization mixture selected as optimal provided a fast separation of a mixture of PAHs with excellent efficiencies (minimum plate heights of 8.9-11.1 μm). Satisfactory column-to-column (RS D < 4.5%) a…

Van Deemter equationLipid PeroxidesChromatographyResolution (mass spectrometry)PhotochemistryClinical BiochemistryReproducibility of ResultsLauroyl peroxideBiochemistryAnalytical Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationCapillary ElectrochromatographyNitrilesMicroscopy Electron ScanningMethacrylatesAlkylbenzenesPolycyclic Aromatic HydrocarbonsLauryl methacrylateELECTROPHORESIS
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Study of the Fragmentation of D-Glucose and Alkylmonoglycosides in the Presence of Sodium Ions in an Ion-Trap Mass Spectrometer

2009

Abstract Using electrospray ion-trap mass spectrometry, the fragmentation of D-glucose and alkylmonoglycopyranosides (alkyl-GPs) was studied. In the presence of Na+, B1 and 0,2A fragmentations were observed. The alkyl-GPs also showed a 2,5Afragmentation. A cluster containing no carbon atoms and adducts of this cluster with neutral molecules were observed. Standards of alkylmonoglycofuranosides (alkyl-GFs) were not available; however, their fragmentation was studied by high-performace liquid chromatography–mass spectrometry (HPLC-MS) and HPLC-MS2 using an industrial mixture of alkylpolyglycosides. The cluster and its adducts were more easily formed by the alkyl-GPs than by the alkyl-GFs, but…

ElectrosprayCollision-induced dissociationChemistryBiochemistry (medical)Clinical BiochemistryAnalytical chemistryMass spectrometryBiochemistryAnalytical ChemistryAdductIonFragmentation (mass spectrometry)ElectrochemistryMoleculelipids (amino acids peptides and proteins)Ion trapSpectroscopyAnalytical Letters
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Chromium(VI) oxide oxidation of non-ethoxylated and ethoxylated alcohols for determination by electrospray ionization mass spectrometry

2010

A new derivatization procedure to increase the sensitivity of electrospray ionization mass spectrometry (ESI-MS) to non-ethoxylated and ethoxylated alcohols was investigated. The analytes were oxidized with chromium(VI) oxide and the resulting carboxylic and ethoxy-carboxylic acids were isolated by extraction with ethyl acetate; the extracts were alkalinized and infused into the ESI-MS system working in the negative-ion mode. The yields of the combined oxidation-extraction were ca. 100% for non-ethoxylated fatty alcohols dissolved in acetone and they decreased moderately in samples containing increasing amounts of water (e.g., a 75% yield was obtained with 50% water). Ethoxylated alcohols w…

ChromatographyEthylene oxideCetyl alcoholElectrospray ionizationOrganic ChemistryExtraction (chemistry)Ethyl acetateAnalytical Chemistrychemistry.chemical_compoundchemistryStearic acidDerivatizationSpectroscopyStearyl alcoholRapid Communications in Mass Spectrometry
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Characterization of poly(4-vinylpyridine 1-oxide) by free-solution capillary electrophoresis and micellar electrokinetic chromatography

2008

The migration characteristics of poly(4-vinylpyridine 1-oxide) (PVP-NO) in phosphate buffers of acidic pH (20 mM H 3 PO 4 or NaH 2 PO 4 ) have been studied using both free-solution capillary electrophoresis (FSCE) and MEKC. To inhibit adsorption, 250 mM o-phosphoethanolamine (2-aminoethyl dihydrogen phosphate) was used. In FSCE, PVP-NO showed a narrow peak and a broader band, both having anionic behavior. These peak and band were attributed to the free and aggregated or micellized PVP-NO forms, respectively. According to surface tension measurements, the CMC of SDS in the BGE was 1.8 and 0.48 mM in the absence and in the presence of 1000 μpg/mL PVP-NO, respectively, and the association of t…

AnionsDetergentsClinical BiochemistryOxidemacromolecular substancesBuffersBiochemistryMicelleMicellar electrokinetic chromatographyAnalytical ChemistrySurface tensionchemistry.chemical_compoundCapillary electrophoresisAdsorptionSurface TensionMicellesLaunderingchemistry.chemical_classificationChromatographyChromatographytechnology industry and agricultureElectrophoresis CapillaryWaterPolymerPhosphateOrganophosphatesSolutionschemistryPolyvinylpyridine N-OxideELECTROPHORESIS
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γ-Oryzanol and tocopherol contents in residues of rice bran oil refining

2012

Rice bran oil (RBO) contains significant amounts of the natural antioxidants γ-oryzanol and tocopherols, which are lost to a large degree during oil refining. This results in a number of industrial residues with high contents of these phytochemicals. With the aim of supporting the development of profitable industrial procedures for γ-oryzanol and tocopherol recovery, the contents of these phytochemicals in all the residues produced during RBO refining were evaluated. The samples included residues from the degumming, soap precipitation, bleaching earth filtering, dewaxing and deodorisation distillation steps. The highest phytochemical concentrations were found in the precipitated soap for γ-…

chemistry.chemical_classificationChromatographyγ-OryzanolPhenylpropionatesintegumentary systemChemistryRice bran oilFatty acidTocopherolsGeneral MedicineRice Bran Oillaw.inventionAnalytical ChemistryHydrolysisResidue (chemistry)PhytochemicallawRice bran by-productsPlant OilsTocopherolγ oryzanolDistillationRice bran oil refiningFood ScienceFood Chemistry
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Overlapped moving windows followed by principal component analysis to extract information from chromatograms and application to classification analys…

2015

Variable generation from chromatograms is conveniently accomplished using unsupervised rather than manual techniques. With unsupervised techniques, there is no need for selecting a few peaks for manual integration and valuable information is quickly and efficiently collected. The generation of variables can be performed by using either peak searching or moving window (MW) strategies. With a MW approach, the peaks are ignored and many variables, only part of them carrying information, are generated. Thus, variable generation by MWs should be followed by data compression to generate the variables to be further used for classification or quantitation purposes. In this work, unsupervised proces…

Chromatographybusiness.industryGeneral Chemical EngineeringGeneral EngineeringPattern recognitionMoving windowLinear discriminant analysisAnalytical Chemistrylaw.inventionVariable (computer science)Window WidthlawPrincipal component analysisRange (statistics)Flame ionization detectorArtificial intelligencebusinessData compressionMathematicsAnalytical Methods
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Single-pump heart-cutting two-dimensional liquid chromatography applied to the determination of fatty alcohol ethoxylates.

2014

Abstract A setup for heart-cutting bi-dimensional liquid chromatography (LC–LC), constructed with a chromatograph provided with a single pump, an auxiliary 6-port 2-position valve (V 6/2 ) and a column selector valve (V CS ), is described. The possible ways of connecting the two valves for LC–LC, namely with V 6/2 first followed by V CS and vice versa, are compared. The possibility of using the setups for preconcentration followed by the backwards transfer of the preconcentrated solutes to the detector or to a second column is also shown. The V 6/2 -first configuration for LC–LC was applied to the characterization of industrial fatty alcohol ethoxylates (FAEs) using UV–vis detection. For th…

chemistry.chemical_classificationResponse factorChromatographySeries (mathematics)ElutionOrganic ChemistryAnalytical chemistryFatty alcoholWaterGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundHydrocarbonchemistryDimension (vector space)Phase (matter)Gradient elutionFatty AlcoholsChromatography LiquidJournal of chromatography. A
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Evaluation of molecular mass and tacticity of polyvinyl alcohol by non-equilibrium capillary electrophoresis of equilibrium mixtures of a polymer and…

2011

Non-equilibrium capillary electrophoresis of equilibrium mixtures (NECEEM) has been used to characterize polyvinyl alcohol (PVA). Commercial PVA samples with different molecular masses, from M(w)=15 up to 205 kDa, were used. According to the (13)C NMR spectra, the samples also differed in tacticity (stereoregularity). Mixtures of PVA and the anionic azo-dye Congo Red (CR) were injected in the presence of a borate buffer. The electropherograms gave a band and a peak due to the residual PVA-CR complex and the excess dye, respectively, plus a superimposed exponential decay due to the partial dissociation of the complex during migration. The stoichiometry of the PVA-CR complex, q=[monomer]/[dye…

Chromatographyintegumentary systemOrganic ChemistryElectrophoresis CapillaryCongo RedGeneral MedicineBiochemistryPolyvinyl alcoholDissociation (chemistry)Analytical ChemistryMolecular Weightchemistry.chemical_compoundElectrophoresisMonomerCapillary electrophoresischemistryStability constants of complexesPolyvinyl AlcoholTacticityBoratesSpectrophotometry UltravioletAzo CompoundsStoichiometryJournal of Chromatography A
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Separation and determination of alkylglycosides by liquid chromatography with electrospray mass spectrometric detection

2007

The separation of alkylpolyglycosides by liquid chromatography with electrospray mass spectrometric detection, using either an alkylamide or a cyanopropyl column, and acetonitrile/water mixtures as mobile phases, was developed. Using the alkylamide column and isocratic elution, the alpha- and beta-epimers and ring isomers (pyranosides and furanosides) of the alkylmonoglycosides were resolved. The ring isomers were also resolved in a much shorter time using the cyanopropyl column with gradient elution. Using these columns, the isomers of the alkyldiglycosides and alkyltriglycosides were also partially resolved. The equilibration time was much shorter with the cyanopropyl column, which was se…

chemistry.chemical_classificationDetection limitSpectrometry Mass Electrospray IonizationChemical ionizationElectrosprayChromatographyElutionElectrospray ionizationAnalytical chemistryMass spectrometryAnalytical ChemistrychemistryGlycosidesIon trapChromatography High Pressure LiquidAlkylTalanta
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Recent advances in aptamer-based miniaturized extraction approaches in food analysis

2021

Abstract Sample preparation is a relevant step in food analysis to achieve adequate extraction and preconcentration of target analytes before their introduction in the analytical system. Current trends in sample preparation involve moving towards miniaturized extraction devices combined with advanced affinity-based sorbents. Within affinity-based materials, aptamer-based ones have attracted much attention due to their excellent molecular recognition properties, high stability, and the possibility of immobilization onto the surface of different supporting materials, such as nanoparticles, monolithic stationary phases, etc. This review gives an overview of the literature published regarding a…

Molecular recognitionMaterials scienceAptamer010401 analytical chemistryExtraction (chemistry)New materialsNanotechnologySample preparation01 natural sciencesSpectroscopyFood Analysis0104 chemical sciencesAnalytical ChemistryTrAC Trends in Analytical Chemistry
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Characterization and determination of poly(vinylpyrrolidone) by complexation with an anionic azo-dye and nonequilibrium capillary electrophoresis

2009

Using capillary zone electrophoresis in nonequilibrium conditions, the complexes of poly(vinylpyrrolidone) (PVP) with anionic azo-dyes dissociate following a first-order kinetics. Two peaks due to the remaining PVP-dye complexes and the equilibrium concentration of the free dye, plus an exponential region due to the dye liberated by the complexes during the electrophoretic run, are obtained. This behaviour was closely similar to that described in the literature for protein-probe and DNA-protein mixtures, upon application of the technique known as nonequilibrium capillary electrophoresis of equilibrium mixtures or NECEEM. Using Congo Red and Acid Blue 113, information about the maximal stoic…

AnionsDetergentsKineticsmacromolecular substancesBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisColoring Agentschemistry.chemical_classificationChromatographyMolecular massPolymer characterizationOrganic Chemistrytechnology industry and agricultureElectrophoresis CapillaryPovidoneGeneral MedicinePolymerCongo redMolecular WeightKineticsElectrophoresischemistryCalibrationAzo CompoundsStoichiometryJournal of Chromatography A
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Rapid classification of enzymes in cleaning products by hydrolysis, mass spectrometry and linear discriminant analysis

2008

A method for the rapid classification of proteases, lipases, amylases and cellulases used as enhancers in cleaning products, based on precipitation with acetone, hydrolysis with HCl, dilution of the hydrolysates with ethanol, and direct infusion into the electrospray ion source of an ion-trap mass spectrometer, has been developed. The abundances of the ([M+H]+ ions of the amino acids, from the hydrolysates of both the enzyme industrial concentrates and the detergent bases spiked with them, were used to construct linear discriminant analysis models, capable of distinguishing between the enzyme classes. For this purpose, the variables were normalized as follows: (A) the ion abundance of each …

chemistry.chemical_classificationElectrosprayChromatographybiologyHydrolasesChemistryHydrolysisOrganic ChemistryDiscriminant AnalysisCellulaseMass spectrometryMass SpectrometryHydrolysateIon sourceAnalytical ChemistryAmino acidHydrolysisMass spectrumbiology.proteinSpectroscopyRapid Communications in Mass Spectrometry
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Determination of fatty alcohol ethoxylates and alkylether sulfates by anionic exchange separation, derivatization with a cyclic anhydride and liquid …

2011

A method for the separation, characterization and determination of fatty alcohol ethoxylates (FAE) and alkylether sulfates (AES) in industrial and environmental samples is described. Separation of the two surfactant classes was achieved in a 50:50 methanol-water medium by retaining AES on a strong anionic exchanger (SAX) whereas most FAE were eluted. After washing the SAX cartridges to remove cations, the residual hydrophobic FAE were eluted by increasing methanol to 80%. Finally, AES were eluted using 80:20 and 95:5 methanol-concentrated aqueous HCl mixtures. Methanol and water were removed from the FAE and AES fractions, and the residues were dissolved in 1,4-dioxane. In this medium, este…

AnionsEthylene OxideFatty alcoholBiochemistryAnalytical ChemistryDioxanesSurface-Active Agentschemistry.chemical_compoundAcetic acidSeawaterDerivatizationChromatography High Pressure LiquidPhthalic anhydrideAqueous solutionChromatographyEsterificationSulfatesElutionOrganic ChemistryExtraction (chemistry)General MedicineChromatography Ion ExchangechemistryMethanolFatty AlcoholsDibenzoxepinsJournal of Chromatography A
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Analytical methods for the characterization and determination of nonionic surfactants in cosmetics and environmental matrices

2013

Nonionic synthetic surfactants, constituted of an assortment of classes, are common ingredients of industrial, household and body-care products. Alone or in combination with anionic surfactants, they perform a variety of functions including cleaning action, emulsification, skin conditioning, appearance and consistency modification, solubilization and dispersing agents. By far fatty alcohol ethoxylates (AEs) and alkylphenol ethoxylates (APEs) are more extensively used than any other nonionic surfactant class; however, works appearing in the literature making reference to the analysis of other nonionic surfactant classes have also been collected in this review. The production volume worldwide…

AlkylphenolGeneral Chemical Engineeringmedia_common.quotation_subjectGeneral EngineeringFatty alcoholCosmeticsAnalytical ChemistryCharacterization (materials science)chemistry.chemical_compoundchemistrySolubilizationAquatic environmentEnvironmental chemistryNonionic surfactantmedia_commonAnal. Methods
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