Search results for "Fruit"

showing 10 items of 859 documents

Bioaccessibility of bioactive compounds after non-thermal processing of an exotic fruit juice blend sweetened with Stevia rebaudiana

2017

Abstract A comparative study of the bioaccessibility of bioactive compounds and antioxidant capacity in a fruit juice-Stevia rebaudiana mixture processed by pulsed electric fields (PEF), high voltage electrical discharges (HVED) and ultrasound (USN) technology at two equivalent energy inputs (32–256 kJ/kg) was made using an in vitro model. Ascorbic acid was not detected following intestinal digestion, while HVED, PEF and USN treatments increased total carotenoid bioaccessibility. HVED at an energy input of 32 kJ/kg improved bioaccessibility of phenolic compounds (34.2%), anthocyanins (31.0%) and antioxidant capacity (35.8%, 29.1%, 31.9%, for TEAC, ORAC and DPPH assay, respectively) compared…

DPPHBiological AvailabilityAscorbic AcidHealth benefitsAntioxidantsAnalytical ChemistryIn vitro modelAnthocyaninschemistry.chemical_compound0404 agricultural biotechnologyElectricityPhenolsSteviaUltrasonicsFood scienceCarotenoidchemistry.chemical_classification04 agricultural and veterinary sciencesGeneral MedicineIntestinal digestionAscorbic acidCarotenoids040401 food scienceFruit and Vegetable JuicesStevia rebaudianachemistrySweetening AgentsFruit juiceFood AnalysisFood ScienceFood Chemistry
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Direct Peel Monitoring of Xenobiotics in Fruit by Direct Analysis in Real Time Coupled to a Linear Quadrupole Ion Trap–Orbitrap Mass Spectrometer

2013

Study of xenobiotics present in fruit peel by exposing it (without any pretreatment) to direct analysis in real time coupled to a high-resolution orbitrap mass spectrometer (DART-HRMS) is reported for the first time. Variables such as DART gas heater temperature and pressure, source-to-MS distance, and sample velocity are investigated. The analysis of one sample by DART-MS lasts ca. 1 min, and the benefits of both high-resolution and tandem mass spectrometry to elucidate nontarget or unknown compounds are combined. Identification of postharvest fungicides, antioxidants, and sugars in fruit peel is performed in the positive ion mode. A possible elemental formula is suggested for marker compo…

DartTime FactorsMaximum Residue LimitChromatographyChemistryAnalytical chemistryFood ContaminationMass spectrometryOrbitrapTandem mass spectrometryDART ion sourceMass SpectrometryPlant EpidermisXenobioticsAnalytical Chemistrylaw.inventionlawFruitPostharvestFeasibility StudiesQuadrupole ion trapcomputerFood Analysiscomputer.programming_languageAnalytical Chemistry
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A Simple and Efficient Deep Learning-Based Framework for Automatic Fruit Recognition

2022

Accurate detection and recognition of various kinds of fruits and vegetables by using the artificial intelligence (AI) approach always remain a challenging task due to similarity between various types of fruits and challenging environments such as lighting and background variations. Therefore, developing and exploring an expert system for automatic fruits’ recognition is getting more and more important after many successful approaches; however, this technology is still far from being mature. The deep learning-based models have emerged as state-of-the-art techniques for image segmentation and classification and have a lot of promise in challenging domains such as agriculture, where they can …

Deep LearningGeneral Computer ScienceArticle SubjectArtificial IntelligenceGeneral MathematicsGeneral NeuroscienceFruitGeneral MedicineNeural Networks ComputerVDP::Teknologi: 500::Informasjons- og kommunikasjonsteknologi: 550Algorithms
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Determination of fungicide residues in fruits and vegetables by liquid chromatography–atmospheric pressure chemical ionization mass spectrometry

2002

Abstract A liquid chromatography (LC) method for the quantitative determination of five fungicide residues (dichloran, flutriafol, o -phenylphenol, prochloraz and tolclofos methyl) in oranges, lemons, bananas, peppers, chards and onions is described. The residues were extracted by matrix solid-phase dispersion (MSPD) using C 8 . Quantitative analysis was performed by isocratic LC coupled to quadrupole mass spectrometer using atmospheric pressure chemical ionization in the negative ionization mode. The limit of quantification was 0.01 mg kg −1 for flutriafol, o -phenylphenol and dichloran, and 0.1 mg kg −1 for prochloraz and tolclofos methyl. The MSPD method is also suitable for LC–UV analys…

Detection limitChemical ionizationChromatographyChemistryOrganic ChemistryReproducibility of ResultsAtmospheric-pressure chemical ionizationGeneral MedicineMass spectrometrySensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyMass SpectrometryFungicides IndustrialAnalytical ChemistryAtmospheric PressureFruitVegetablesSpectrophotometry UltravioletSample preparationSolid phase extractionQuadrupole mass analyzerChromatography LiquidJournal of Chromatography A
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Determination of carbamate residues in fruits and vegetables by matrix solid-phase dispersion and liquid chromatography-mass spectrometry.

2000

Abstract Thirteen carbamates were analysed in orange, grape, onion and tomatoes by matrix solid-phase dispersion (MSPD) followed by liquid chromatography–mass spectrometry (LC–MS). Electrospray (ES) and atmospheric pressure chemical ionisation (APCI) were compared and both gave similar results in terms of sensitivity and structural information because at 20 V fragmentor voltages the fragmentation is minimal. The efficiency of different solid-phases (C18, C8, cyano, amine and phenyl) for the MSPD was compared. Mean recoveries using C8 varied from 64 to 106% with relative standard deviations of 5–15% in the concentration range of 0.01–10 mg kg−1. Matrix constituents did not interfere signific…

Detection limitChemical ionizationInsecticidesChromatographyChemistryOrganic ChemistryPesticide ResiduesAtmospheric-pressure chemical ionizationGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityMass SpectrometryAnalytical ChemistryLiquid chromatography–mass spectrometryFruitVegetablesmedia_common.cataloged_instanceSolid phase extractionCarbamatesEuropean unionChromatography High Pressure Liquidmedia_commonJournal of chromatography. A
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Analysis of post-harvest fungicides by micellar electrokinetic chromatography.

2001

A method based on solid-phase extraction (SPE) and micellar electrokinetic chromatography (MEKC) was developed for the simultaneous determination of carbendazim, imazalil, methylthiophanate, O-phenylphenol, prochloraz, procimidone, thiabendazole and triadimefon residues in grape, lettuce, orange and tomato. Selectivity and resolution were studied changing the pH and the concentration of the buffer, the type and concentration of surfactant and the methanol content in the mobile phase. A buffer consisting of 4 mM borate with 75 mM sodium cholate (pH 9.2) gave the best results. The recoveries of the fungicides in spiked fruit and vegetable samples ranged from 30 to 105%, and the limits of dete…

Detection limitChromatographyCarbendazimOrganic ChemistryReproducibility of ResultsSodium Dodecyl SulfateGeneral MedicineBuffersSodium CholateBiochemistryMicellar electrokinetic chromatographyAnalytical ChemistryFungicides IndustrialFungicidechemistry.chemical_compoundSurface-Active AgentsTriadimefonchemistryFruitSample preparationSolid phase extractionSodium CholateChromatography Micellar Electrokinetic CapillaryJournal of chromatography. A
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Analysis of Chlorpyrifos in Water, Fruit Juice, and Honeybee Extract by Chemiluminescent Elisa

2008

Abstract The suitability of competitive enzyme-linked immunosorbent assays (ELISAs) with chemiluminescent detection-based immobilized antigen (indirect assay) for rapid and accurate determination of chlorpyrifos in various food matrices was tested. The limit of detection (LOD) values were 1–1.75 ng mL−1, the standard curve midpoint (IC50) was 3.5 ng mL−1, and the assay duration was 1.5 h. Assay application to the analysis of honeybee extract resulted in chlorpyrifos recoveries varying between 62 and 83% in 5–15 ng mL−1 herbicide concentration range.

Detection limitChromatographyChemistryBiochemistry (medical)Clinical BiochemistryFOOD/FRUIT JUICESBiochemistryCHEMILUMINESCENCECHLORPYRIFOSAnalytical Chemistrylaw.inventionStandard curveHONEYBEEchemistry.chemical_compoundlawChlorpyrifosElectrochemistryELISAFruit juiceIC50SpectroscopyChemiluminescenceAnalytical Letters
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On-line preconcentration strategies for analyzing pesticides in fruits and vegetables by micellar electrokinetic chromatography.

2007

Five pesticides (fludioxonil, procymidone, pyriproxyfen, dinoseb and carbendazim) were separated in reversed migration micellar electrokinetic chromatography (RM-MEKC) using 20 mmol l(-1) phosphate buffer at pH 2.3, containing 25 mmol l(-1) sodium dodecylsulfate and 10% methanol. Three on-line concentration strategies, sweeping (SW), normal stacking with reversed migration and a water plug (SRW) and stacking with reverse migration and removal of sample matrix using polarity switching (SRMM), were compared. About 10-, 30- and 50-fold increases in detection sensitivity, compared with standard hydrodynamic injection (5 s at 0.5 psi), were observed with SW, SRW and SRMM, respectively. Limits of…

Detection limitChromatographyChemistryCarbendazimOrganic ChemistryAnalytic Sample Preparation MethodsElectrophoresis CapillaryGeneral MedicineBiochemistryOnline SystemsMicellar electrokinetic chromatographyAnalytical ChemistryFungicides Industrialchemistry.chemical_compoundElectrophoresisFruitDinosebVegetablesSample preparationSolid phase extractionProcymidonePesticidesFood AnalysisChromatography Micellar Electrokinetic CapillaryJournal of chromatography. A
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Solid-Phase Microextraction Liquid Chromatography/Tandem Mass Spectrometry To Determine Postharvest Fungicides in Fruits

2003

A method to determine five postharvest fungicides (dichloran, flutriafol, o-phenylphenol, prochloraz, tolclofos methyl) in fruits (cherries, lemons, oranges, peaches) has been developed using solid-phase microextraction (SPME) coupled to liquid chromatography (LC) with photodiode array (DAD), mass spectrometry (MS), or tandem mass spectrometry (MS/MS) with ion trap detection. Extraction involved sample homogenization with an acetone/water solution (5:1), filtration, and acetone evaporation prior to fiber extraction. The pesticides were isolated with a fused-silica fiber coated with 50-microm Carbowax/template resin. The effects of pH, ion strength, sample volume, and extraction time were in…

Detection limitChromatographyChemistryPesticide ResiduesReference StandardsSolid-phase microextractionMass spectrometryTandem mass spectrometryMass SpectrometryFungicides IndustrialAnalytical ChemistryLiquid chromatography–mass spectrometryFruitDesorptionCalibrationIndicators and ReagentsSpectrophotometry UltravioletSample preparationIon trapChromatography LiquidAnalytical Chemistry
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Off-line solid-phase microextraction and capillary electrophoresis mass spectrometry to determine acidic pesticides in fruits.

2003

A method based on solid-phase microextraction (SPME) and capillary electrophoresis/mass spectrometry (CE/ MS) is described for determining simultaneously five acidic pesticides (o-phenylphenol, ioxynil, haloxyfop, acifluorfen, picloram) in fruits. The CE device is coupled to an electrospray interface by a commercial sheath-flow adapter. Emphasis is placed on fulfillment of the speed and sensitivity requirements. The best separation is achieved using 32 mM ammonium formate/acid formic buffer at pH 3.1, with a working voltage of 25 kV. The MS detection of the five pesticides was performed in negative ionization mode. Full-scan spectra with base peaks corresponding to [M-H]- were obtained exce…

Detection limitChromatographyChemistryPlant ExtractsAnalytical chemistryElectrophoresis CapillaryFood ContaminationAcifluorfenMass spectrometrySolid-phase microextractionCapillary electrophoresis–mass spectrometryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisFruitAmmonium formateSample preparationPesticidesAnalytical chemistry
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