Search results for "ferulic acid"

showing 10 items of 48 documents

Assessment of pro-oxidant activity of natural phenolic compounds in bio-polyesters

2018

Abstract In this work, natural phenolic compounds, such as Vanillic Acid (VA), Ferulic Acid (FA) and Thymol (Th), at very high concentrations, have been considered as pro-oxidant agents for Polylactic acid (PLA). Specifically, thin films of neat PLA and PLA-based systems containing 2 and 3 wt% of VA, FA and Th have been produced and subjected to accelerated degradation in different environmental conditions. Preliminary characterizations, through rheological, mechanical, optical and morphological analysis, of the formulated PLA-based systems show that the VA and FA, even less the Th, are able to exert a plasticizing action during the processing and subsequently, the PLA crystallinity and rig…

Photo-and thermo-oxidationNatural phenolic compoundPolymers and Plastics02 engineering and technology010402 general chemistry01 natural sciencesPolylactic acidFerulic acidHydrolysischemistry.chemical_compoundCrystallinitystomatognathic systemPolylactic acidPro-oxidant activityMaterials ChemistryVanillic acidrespiratory system021001 nanoscience & nanotechnologyCondensed Matter PhysicsPro-oxidantHydrolysi0104 chemical sciencesPolyesterSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryMechanics of MaterialsDegradation (geology)lipids (amino acids peptides and proteins)0210 nano-technologyNuclear chemistryPolymer Degradation and Stability
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Tributyltin(IV) ferulate, a novel synthetic ferulic acid derivative, induces autophagic cell death in colon cancer cells: From chemical synthesis to …

2020

Ferulic acid (FA) is a natural phenolic phytochemical that has low toxicity and exhibits therapeutic effects against various diseases, behaving as an antioxidant. FA also displays modest antitumor properties that have been reported at relatively high concentrations. With the aim of improving the anti-tumor efficacy of FA, we synthesized the novel compound tributyltin(IV) ferulate (TBT-F). The coordination environment at the tin center was investigated spectroscopically. Following synthesis, chemical characterization and computational analysis, we evaluated TBT-F effects in colon cancer cells. The results showed that TBT-F, at nanomolar range concentrations, was capable of reducing the viabi…

Programmed cell deathAntioxidantCoumaric AcidsAutophagic Cell Deathmedicine.medical_treatmentAntineoplastic AgentsOrganotin(IV)VacuolePharmacology010402 general chemistry01 natural sciencesBiochemistryInorganic ChemistryFerulic acidchemistry.chemical_compoundColon cancer cytotoxicityLC3medicineHumansViability assay010405 organic chemistryChemistryp62AutophagyFerulic acidHCT116 Cells0104 chemical sciencesApoptosisCell Death ProcessColonic NeoplasmsCaco-2 CellsTrialkyltin CompoundsHT29 CellsJournal of Inorganic Biochemistry
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Controlled release of tyrosol and ferulic acid encapsulated in chitosan–gelatin films after electron beam irradiation

2016

Abstract This work deals with the study of the release kinetics of antioxidants (ferulic acid and tyrosol) incorporated into chitosan–gelatin edible films after irradiation processes. The aim was to determine the influence of electron beam irradiation (at 60 kGy) on the retention of antioxidants in the film, their release in water (pH=7) at 25 °C, in relation with the barrier and mechanical properties of biopolymer films. The film preparation process coupled to the irradiation induced a loss of about 20% of tyrosol but did not affect the ferulic acid content. However, 27% of the ferulic acid remained entrapped in the biopolymer network during the release experiments whereas all tyrosol was …

Radiationfood.ingredientKinetics04 agricultural and veterinary sciencesengineering.material040401 food scienceGelatinControlled releaseChitosanTyrosolFerulic acidchemistry.chemical_compound0404 agricultural biotechnologyfoodchemistryengineeringOrganic chemistryBiopolymerIrradiationNuclear chemistryRadiation Physics and Chemistry
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Visible-light-induced oxidation of trans-ferulic acid by TiO2 photocatalysis

2012

Abstract The oxidation of trans-ferulic acid (C10H10O4) in aqueous TiO2 dispersion occurs via the formation of a charge-transfer complex on the TiO2 surface that is able to absorb visible light (λ ⩾ 400 nm). The main product is CO2, whereas secondary oxidation products are organic species such as vanillin, caffeic acid, homovanillic acid, and vanillylmandelic acid. Oxidation through the formation of a charge-transfer complex occurs only in the presence of specific TiO2 samples. Experiments in the absence of oxygen, in the presence of bromate ions and by using a phosphate-modified TiO2, have been carried out for investigating the reaction mechanism. In order to study the interaction between …

Reaction mechanismAqueous solutiontrans-Ferulic acid photo-oxidationChemistryVanillinInorganic chemistryCharge-transfer complexPhotochemistryBromateCatalysisCatalysisFerulic acidchemistry.chemical_compoundtrans-Ferulic acid photo-oxidation Visible-light photocatalysis TiO2 Charge-transfer complexVisible-light photocatalysiPhotocatalysisCaffeic acidTitanium dioxideSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical ChemistryJournal of Catalysis
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Meat production from dairy breed lambs due to slaughter age and feeding plan based on wheat bran

2019

This experiment aimed to investigate the possibility to increase the carcass weight of dairy breed lambs and produce moderate-fat meat by applying inexpensive feeding strategies based on restriction and through the use of a fibrous byproduct such as the durum wheat bran (DWB). Sixty-five 45-day-old lambs of the Valle del Belice breed, divided into 6 groups, were fed alfalfa hay supplemented with concentrate feeds including DWB at 0% or 20% (DWB0, DWB20), supplied ad libitum (L) or restricted at 75% (R), and slaughtered at 90 or 120 days of age. The groups were as follows: DWB0-90L (n = 14), DWB20-90L (n = 14), DWB0-120R (n = 10), DWB20-120R (n = 9), DWB0-120L (n = 9), DWB20-120L (n = 9). Th…

Settore AGR/19 - Zootecnica Speciale030309 nutrition & dieteticsDurum wheat branGrowthBiologyfatty acidsArticle03 medical and health sciencesAnimal scienceFeed restrictionlcsh:ZoologyLamb meatmedicineDry matterlcsh:QL1-9912. Zero hungerchemistry.chemical_classification0303 health scienceslcsh:Veterinary medicineGeneral VeterinaryBranCarca0402 animal and dairy sciencePolyphenols04 agricultural and veterinary sciencesFerulic acidFatty acid040201 dairy & animal scienceBreedAntioxidant capacitySettore AGR/02 - Agronomia E Coltivazioni ErbaceeTendernessAntioxidant capacitychemistrylcsh:SF600-1100Animal Science and ZoologyIntramuscular fatmedicine.symptomWeight gaincarcassPolyunsaturated fatty acid
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Improvement of Oxidative Status, Milk and Cheese Production, and Food Sustainability Indexes by Addition of Durum Wheat Bran to Dairy Cows’ Diet

2019

Durum wheat bran (DWB) is a by-product mostly used in feeding ruminants, contributing to decrease in the utilization of feeds suitable as foods for human consumption, thus improving the sustainability of livestock production. However, the potential benefits of DWB, due to its content in phenolic acids, mainly consisting of ferulic acid with antioxidant properties, have not been well clarified yet. Accordingly, in this experiment, 36 lactating cows divided into three groups received, over a period of 100 days, one of three concentrates including DWB at 0% (DWB0), 10% (DWB10), or 20% (DWB20). The concentrates were formulated to be isoproteic and isoenergetic and, to balance the higher fiber c…

Settore AGR/19 - Zootecnica SpecialeBy-productBiologyFeed conversion ratioArticleFerulic acid03 medical and health scienceschemistry.chemical_compoundantioxidant powerCaseinlcsh:ZoologySettore AGR/18 - Nutrizione E Alimentazione AnimaleDry matterdurum wheat branFood sciencelcsh:QL1-991by-products030304 developmental biology2. Zero hunger0303 health scienceslcsh:Veterinary medicineGeneral VeterinaryBranbusiness.industrydairy products0402 animal and dairy sciencefood and beverages04 agricultural and veterinary scienceshuman-edible feed conversion efficiency040201 dairy & animal scienceSettore AGR/02 - Agronomia E Coltivazioni ErbaceeDairy productchemistryHayFood processinglcsh:SF600-1100Animal Science and ZoologyFermentationbusinessphenolic acidsSettore AGR/16 - Microbiologia AgrariaAnimals
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FERULIC ACID LOADED SOLID LIPID NANOPARTICLES PROTECTS LAN5 NEUROBLASTOMA CELL LINE BY Ab-AMYLOID OXIDATIVE STRESS

2008

Settore CHIM/09 - Farmaceutico Tecnologico Applicativosolid lipid nanoparticles ferulic acid
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Ferulic Acid Oxidation Through Visible Light Induced TiO2 Photocatalysis

2012

Settore ING-IND/24 - Principi Di Ingegneria ChimicaFerulic acid TiO2Settore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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Visible Light Induced Oxidation of Ferulic Acid by TiO2 Photocatalysis

2012

Oxidation of ferulic acid (C10H10O4) in aqueous medium occurs by using both commercial and home prepared TiO2 samples under visible light irradiation. Among the oxidation products vanillin was found with a selectivity ranging from 1 to 2% with respect to the converted substrate. By considering that TiO2 is unable to absorb visible light and ferulic acid does not react in the absence of TiO2, the observed photoactivity may be explained by the formation of a charge-transfer complex between ferulic acid and TiO2, being the complex able to absorb visible light. Among all the tested semiconductor oxides, only Merck anatase TiO2 does not perform the oxidation of ferulic acid under visible light i…

Settore ING-IND/24 - Principi Di Ingegneria ChimicaPhotocatalysiCharge transferVanillinFerulic acid TiO2 charge transfer complexSettore CHIM/07 - Fondamenti Chimici Delle TecnologieVisible light
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Preparation of ferulic acid derivatives and evaluation of their xanthine oxidase inhibition activity.

2007

Several ferulic acid ethyl esters (3a-h) were synthesized under the Knoevengel reaction condition and they were further reduced to afford the respective allylic alcohol derivatives (4a-g). Some of them were evaluated for the xanthine oxidase (XO) inhibitory activity. Among them, 3h exhibited a significant inhibitory activity with an IC50 value of 1.35 x 10(-5) M, while the IC50 value of allopurinol used as the positive control was 1.49 x 10(-5) M. The study suggested that the higher acidity of the phenolic OH group in the ferulic acid derivatives might result in improved XO inhibitory activity.

Xanthine OxidaseMagnetic Resonance SpectroscopyCoumaric Acidsmedicine.drug_classAllopurinolPositive controlPlant ScienceIn Vitro TechniquesInhibitory postsynaptic potentialBiochemistryAnalytical ChemistryFerulic acidElectron Transportchemistry.chemical_compoundmedicineOrganic chemistryAnimalsEnzyme InhibitorsXanthine oxidaseXanthine oxidase inhibitorIC50ChemistryOrganic ChemistryEstersNuclear magnetic resonance spectroscopyRatsLiverBenzaldehydesIndicators and Reagentsmedicine.drugNatural product research
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