Search results for "Maillard"

showing 10 items of 30 documents

Evaluation of carotenoids and furosine content in air dried carrots and parsnips pre-treated with pulsed electric field (PEF)

2019

Carrot and parsnip slices were subjected to hot drying at 50, 60 and 70 °C with or without pulsed electric field (PEF) pre-treatment at 0.9 kV/cm and 1000 and 10,000 pulses. The effect of drying on processed samples was assessed by analysis of carotenoids, the furosine value, total phenols and the Whiteness Index (WI). PEF pre-treatment is effective in reducing drying times, but the degree of cellular breakdown makes the compounds more susceptible to chemical and enzymatic reactions. In our condition PEF pre-treatment increased the carotenoid degradation and promoted the Maillard reaction above all at the highest temperature of 70 °C. The assessment of carotenoid stability, together with th…

Pre treatment030309 nutrition & dieteticsCarotenoid degradationBiochemistryIndustrial and Manufacturing Engineering03 medical and health sciencessymbols.namesake0404 agricultural biotechnologyCarrotElectric fieldFood scienceParsnipCarotenoidchemistry.chemical_classification0303 health sciencesDried foodCarotenoids; Carrot; Maillard reaction; Parsnip; PEF; Pre-treatment04 agricultural and veterinary sciencesGeneral ChemistryPEFPre-treatmentCarotenoids040401 food scienceMaillard reactionMaillard reactionchemistryPre-treatment PEF Carotenoids Maillard reaction Carrot ParsnipsymbolsThermal damageCellular breakdownFood ScienceBiotechnologyEuropean Food Research and Technology
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Simultaneous analysis of lysine, Nɛ-carboxymethyllysine and lysinoalanine from proteins

2007

Protein quality was assayed by simultaneous measurement of lysine (Lys), carboxymethyllysine (CML) and lysinoalanine (LAL). GC-FID analysis of N-tert-butyl dimethylsilyl (tBDMSi) derivatives of these amino acids was undertaken. tBDMSi derivates were separated on a CP-SIL 5CB commercially fused silica capillary column (25 m × 0.25 mm i.d., 0.25 μm film thickness) employing a thermal gradient programmed from 200 to 300 °C. The identity of tBDMSi derivatives of Lys, CML and LAL was established by GC–MS while FID detection was employed for quantification. Analytical parameters such as linearity (lysine 350–4200 μM, LAL 3–81 μM, CML 16–172 μM), precision (1–13% variation coefficients), accuracy …

Chromatography GasG proteinEggsFluoroacetatesClinical BiochemistryLysineLysinoalanineBiochemistryAnalytical Chemistrysymbols.namesakeCaseinAcetamidesOrganosilicon CompoundsNɛ-CarboxymethyllysineLysinoalanineSoy proteinchemistry.chemical_classificationGas chromatographyChromatographyChemistryLysineProteinProteinsCell BiologyGeneral MedicineGlutenMaillard ReactionMaillard reactionsymbolsInfant FoodProtein qualityFood Analysis
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High-performance liquid chromatographic determination of furfural compounds in infant formulas during full shelf-life

2005

Abstract In order to evaluate the extent of the Maillard reaction in adapted and follow-up infant formulas (IF), a study was made of the evolution of furfural compound (2-furaldehyde, 5-hydroxymethyl-2-furfuraldehyde, 2-furylmethylketone and 5-methyl-2-furaldehyde) in these products, along with their relation to available lysine during the shelf-life period (two years at 20 and 37 °C). Total and free furfural contents were measured by RP-HPLC and UV detection, heating or not the sample in boiling water to free the furfurals bound to proteins and the furfurals formed from precursors. Only 2-furylmethylketone and 5-hydroxymethyl-2-furfuraldehyde were detected. Adapted and follow-up IF showed …

ChromatographyChemistryAdvanced stageFood preservationGeneral MedicineShelf lifeFurfuralHigh-performance liquid chromatographyAnalytical ChemistryWarehouseMaillard reactionsymbols.namesakechemistry.chemical_compoundBoilingsymbolsFood ScienceFood Chemistry
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Effect of storage conditions on furosine formation in milk-cereal based baby foods

2008

[EN] The effect of storage during 9 months at 25, 30 and 37 degrees C on furosine formation in three milk-cereal based baby foods was studied to evaluate development of the Maillard reaction. Furosine was measured by HPLC-UV. Immediately after the manufacturing process, furosine contents were 310-340 mg/100 g protein and at the 9th storage month were 426-603 mg/100 g protein. Storage time and temperature have a significant increase (p < 0.05) of furosine content during storage. Furosine contents were higher in sample containing honey than in those without honey. Interactions (p < 0.05) between storage time and temperature or type of sample were found. A predictive model equation of the evol…

ChromatographyChemistryManufacturing processESTADISTICA E INVESTIGACION OPERATIVAFood preservationStorageGeneral MedicineAnalytical ChemistryWarehouseMaillard reactionMaillard reactionsymbols.namesakeFurosinesymbols; Maillard reactionFood scienceBaby foodsFood ScienceLysine blockage
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The chemistry of death--Adipocere degradation in modern graveyards.

2015

The formation of adipocere slows further decomposition and preserves corpses for decades or even centuries. This resistance to degradation is a serious problem, especially with regard to the reuse of graves after regular resting times. We present results from an exhumation series in modern graveyards where coffins from water-saturated earth graves contained adipocere embedded in black humic material after resting times of about 30 years. Based on the assumption that this humic material resulted from in situ degradation of adipocere, its presence contradicts the commonly held opinion that adipocere decomposition only occurs under aerobic conditions. To test our hypothesis, we collected black…

chemistry.chemical_classificationMagnetic Resonance SpectroscopyAutoxidationBurialCarboxylic acidFatty AcidsCarbohydratesFatty acidExhumationAdipocereDecompositionChemical reactionLipidsPathology and Forensic MedicineMaillard reactionsymbols.namesakeSoilchemistryPostmortem ChangessymbolsOrganic chemistryHumansCemeteriesLawVan Krevelen diagramForensic science international
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High-performance liquid chromatographic determination of Maillard compounds in store-brand and name-brand ultra-high-temperature-treated cows' milk.

2000

Furosine and furfural products of the Maillard reaction are used as specific indicators of the effect of heating treatments on milk quality. Their contents were measured in representative samples of store- and name-brand ultra-high-temperature-treated milks using RP-HPLC with UV detection. Furosine contents ranged from 40.32 to 50.67 and from 65.48 to 310.58 mg/100 g protein in name- and store-brand milks, respectively. Of the furfurals, only hydroxymethylfurfural was detected. The free hydroxymethylfurfural contents of store-brand milks ranged from 0.22 to 1.70 mg/100 g protein. Total hydroxymethylfurfural contents ranged from 0.29 to 0.41 and from 0.72 to 2.21 mg/100 g protein, for name- …

ChromatographyHot TemperatureOrganic ChemistryFood composition dataGeneral MedicineReversed-phase chromatographyFurfuralBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMaillard Reactionchemistry.chemical_compoundMaillard reactionsymbols.namesakeMilkchemistrysymbolsAnimalsCattleSpectrophotometry UltravioletUv detectionQuantitative analysis (chemistry)HydroxymethylfurfuralChromatography High Pressure LiquidJournal of chromatography. A
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Nonenzymatic glycation reaction of folate with reducing sugars: A case study on [6S]-5-methyltetrahydrofolate and fructose

2006

In the Maillard reaction, free amino groups react with reducing sugars to form nonenzymatic glycation products. It has recently been shown that in the presence of reducing sugars (i.e. fructose) folic acid is subjected to a non-enzymatic glycation reaction, which may represent an important pathway of folate degradation besides the established oxidative degradation pathways. In the current study, the thermal stability of [6S]-5-methyltetrahydrofolic acid ([6S]-5-CH3H4PteGlu, 0.4µM), the predominant naturally occuring folate derivate, was investigated on a qualitative and kinetic basis in the presence of different fructose concentrations (0-3M) in milliQ water (8.11ppm O2). Samples were isoth…

ChromatographyChemistryFirst-order reactionKineticsFructoseMaillard reactionsymbols.namesakechemistry.chemical_compoundReaction rate constantGlycationsymbolsOrganic chemistryThermal stabilityDestabilisation13th World Congress of Food Science &amp; Technology
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Formation of fumonisin B(1)-glucose reaction product, in vitro cytotoxicity, and lipid peroxidation on kidney cells.

2010

Fumonisin B(1) (FB(1)) content in corn products decreases during the heating process in foods containing reducing sugars, mainly because of the formation of N-(carboxymethyl)fumonisin B(1). In this study, a rapid method has been developed for the determination of both compounds in corn products using a high-speed blender, Ultra-Turrax, for solvent extraction and liquid chromatography-tandem mass spectrometry. The kinetics of FB(1) degradation and the formation of the Maillard adduct were studied in a model system constituted by corn bread spiked with FB(1) and heated at 160, 180, and 200 degrees C for 3, 6, 10, 15, and 20 min. FB(1) decreased from 0.96 to 0.3 mg/kg and N-(carboxymethyl)fumo…

Neutral redFood HandlingKidneyFumonisinsZea maysLipid peroxidationsymbols.namesakechemistry.chemical_compoundfumonisinFumonisinChlorocebus aethiopskidney cellAnimalsIC50Vero CellsFumonisin B1ChromatographyChemistryfood and beveragesGeneral ChemistryCarbohydrateMalondialdehydeMaillard reactionKineticsGlucosesymbolsLipid PeroxidationGeneral Agricultural and Biological SciencesJournal of agricultural and food chemistry
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High-performance liquid chromatographic determination of furfural compounds in infant formulas

2002

Furfural contents in adapted and follow-up infant formulas were measured by RP-HPLC. The evolution of furfural compound contents during storage (a year at 20 and 37 °C) was studied. 2-Furylmethylketone and 5-methyl-2-furaldehyde were not detectable in analysed samples. The differences in the furfural compounds at point zero between both infant formulas has to be ascribed to the differences in protein and iron contents. An increase in free 5-hydroxymethyl-2-furfuraldehyde (HMF), 2-furaldehyde (F) and HMF+F contents was observed in all samples, although the differences were not statistically significant. The storage temperature affected the total HMF content and the storage time affected the …

ChromatographyChemistryOrganic ChemistryPasteurizationGeneral MedicineReversed-phase chromatographyFurfuralBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionMaillard reactionsymbols.namesakechemistry.chemical_compoundInfant formulalawBrowningsymbolsQuantitative analysis (chemistry)Journal of Chromatography A
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Chemical messages in 170-year-old champagne bottles from the Baltic Sea: Revealing tastes from the past

2015

International audience; Archaeochemistry as the application of the most recent analytical techniques to ancient samples now provides an unprecedented understanding of human culture throughout history. In this paper, we report on a multiplatform analytical investigation of 170-y-old champagne bottles found in a shipwreck at the bottom of the Baltic Sea, which provides insight into winemaking practices used at the time. Organic spectroscopy-based nontargeted metabolomics and metallomics give access to the detailed composition of these wines, revealing, for instance, unexpected chemical characteristics in terms of small ion, sugar, and acid contents as well as markers of barrel aging and Maill…

Magnetic Resonance SpectroscopyArchaeochemistryMass Spectrometryddc:630Furaldehyde[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology14. Life underwaterwine[SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory OrgansWinemakingMultidisciplinaryChemistryChromatography liquidCarbon DioxidemetabolomicsArchaeologyMaillard Reactionddc:Archaeochemistry ; Champagne ; Metabolomics ; WineArchaeologyBaltic seaSpectrophotometryHuman cultureTasteEnvironmental chemistryPhysical SciencesChampagneWine tasting[SDV.AEN]Life Sciences [q-bio]/Food and NutritionChromatography LiquidProceedings of the National Academy of Sciences
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