Dissertations / Theses on the topic 'Oracy'
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Bousted, Mary. "A socio-political analysis of the personal growth ideology of English teaching." Thesis, University of York, 1999. http://etheses.whiterose.ac.uk/10867/.
Full textHilson, Patricia F., and n/a. "From oracy to literacy via writing : a Montessori approach for the pre-school." University of Canberra. Education, 1987. http://erl.canberra.edu.au./public/adt-AUC20060724.131835.
Full textOlbers, Jenny. "The use of oracy skills when teaching English to Swedish speaking primary school pupils." Thesis, Luleå tekniska universitet, Institutionen för hälsa, lärande och teknik, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-82965.
Full textAxelsson, Erik. "”Vad kaotiskt allt skulle vara utan samtal.” : En fenomenografisk studie över elevers uppfattning om samtal." Thesis, Södertörns högskola, Lärarutbildningen, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:sh:diva-33429.
Full textScanlan, Mary. "My story in a box: linking home and school to explore identity, creative writing and oracy." Thesis, University of Bristol, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.492566.
Full textMcCormack, Brittany. "The Development of Oracy in Students with English as an Additional Language or Dialect Through Music." Thesis, Griffith University, 2017. http://hdl.handle.net/10072/370572.
Full textThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School Educ & Professional St
Arts, Education and Law
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Beaumont, Natasha. "Multimodal language and learning: Drama as EAL/D pedagogy in the early primary classroom." Thesis, University of Sydney, 2020. https://hdl.handle.net/2123/22696.
Full textMannion, James. "Metacognition, self-regulation, oracy : a mixed methods case study of a complex, whole-school 'Learning to Learn' intervention." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/289131.
Full textPerez-Adamson, Clara. "Does an oracy intervention affect the way that teachers cope with students who challenge or worry them in some way?" Thesis, University of Essex, 2018. http://repository.essex.ac.uk/22932/.
Full textKeyser, Dorothy. "Oracy, Literacy and the Music of Adam De La Halle: The Evidence of the Manuscript Paris, BibliothèQue Nationale f.fr. 25566." Thesis, University of North Texas, 1996. https://digital.library.unt.edu/ark:/67531/metadc332454/.
Full textCrerand, Mary E. Lavin. "From first language literacy to second language oracy to second language literacy : the act of writing in a foreign language context." The Ohio State University, 1992. http://rave.ohiolink.edu/etdc/view?acc_num=osu1239369687.
Full textMalherbe, Neil. "A critical analysis of the importance of oracy in the classroom, with particular reference to secondary schools in the Cape Education Department." Thesis, Rhodes University, 1995. http://hdl.handle.net/10962/d1003355.
Full textLilliehöök, David, and Hampus Söderberg. "Säg vad du menar och mena vad du säger! : En diskursanalytisk studie av svenska grundskolans nationella prov, läroplan och kommentarmaterial för årskurs 4-6." Thesis, Södertörns högskola, Lärarutbildningen, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:sh:diva-31648.
Full textSöderberg, Hampus. ""Vad det hela faller på är flera saker..." : En diskursanalytisk studie utifrån mellanstadielärares utsagor om muntlighetsundervisningen i den svenska skolans svenskämne." Thesis, Södertörns högskola, Lärarutbildningen, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:sh:diva-33409.
Full textSmith, Andrew John Alexander. "Microphysical modelling of aerosols in the ORAC retrieval." Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:127ca383-e4bf-44f4-8915-badca16c5016.
Full textSilva, Filipe André Nascimento. "Avaliação antioxidante de 3,5-dimetil isoxazol, pirazóis e tiazóis utilizando o método ORAC (capacidade de absorção de radicais oxigênio)." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/9/9141/tde-27052011-111106/.
Full textFree radicals are chemical species that react rapidly with various compounds and target cells, as they have a very short half life and are highly unstable. The formation of these compounds consists of a continuous, physiological action, which includes essential biological functions and occurs through the loss or addition of a single electron to a non-radical compound. These reactions may occur in biochemical processes of the immune system, or by chemical reactions, causing damage to the cells through the destruction of components such as proteins, lipids, sugars and nucleotides. It is known that compounds exist which are effective against these species, preventing damage caused by oxidative stress. The object of this work was to study heterocyclic compounds that have nitrogen in their structure (azoles), which appear in the literature as exemplary molecules of compounds with a wide spectrum of pharmacological applications. Of these compounds, derivatives of pyrazoles (26 compounds), thiazoles (7 compounds) and 1 isoxazole (3,5-dimethylisoxazole) were analyzed. These 34 compounds were evaluated by the ORAC (Oxygen Radicals Absorption Capacity) in order to determine and/or evaluate its antioxidant potential. The choice of ORAC method is based on the fact that the molecules studied have hydrophilic and lipophilic characteristics, as well as a method validated by the literature, which is available and widely used. The ORAC method evaluates the antioxidant capacity of the sample, measuring its ability to protect the fluorescence (FL) of the oxidation by the AAPH in the reaction medium. AAPH is a generator of free radicals which, at 37°C, removes hydrogen from the medium, promoting the reduction of fluorescence from fluorescein in λ measured by time. Six compounds present good to moderate antioxidant activity: 3,5-dimethyl-1H-pyrazole (2.382 µmol eq.Trolox/g); 3-phenyl-5-(4-fluorphenyl)-1-thiocarbamoyl-4,5-dihydro-1H-pyrazole (6.354 µmol eq.Trolox/g); 3-phenyl-5-(2-methoxyphenyl)-1-thiocarbamoyl-4,5-dihydro-1H-pyrazole (8.739 µmol eq.Trolox/g); 5-(2,4-diclorophenyl)-3-phenyl-1-thiocarbamoyl-4,5-dihydro-1H-pyrazole (6.022,226 µmol eq.Trolox/g); 2-[5-(4-methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazole-1-il]-4-phenylthiazole (3.135 µmol eq.Trolox/g); and finally, 2-[5-(3-nitrophenyl)-3-phenyl-4,5-dihydro-1H-pyrazole-1-il]- 4-phenylthiazole (2.700 µmol eq.Trolox/g). Experiments with the ORAC method for the azoles studied present reproducibility in the experimental execution, and have proven to be a viable alternative for studies of synthetic molecules with antioxidant potential.
Pereira, Gustavo Araujo 1991. "Estudo dos parâmetros de extração de compostos fenólicos e avaliação da atividade antioxidante in vitro da banana (Musa sp.)." [s.n.], 2015. http://repositorio.unicamp.br/jspui/handle/REPOSIP/254206.
Full textDissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos
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Resumo: O objetivo do presente trabalho foi estudar a influência dos parâmetros de extração sólido-liquido e de enzimas fenoloxidases (peroxidase) na recuperação de compostos fenólicos a partir do pó da casca de banana liofilizada (CBL), bem como quantificar o conteúdo de compostos fenólicos totais (FT), flavonoides totais (CF) e a atividade antioxidante da CBL e do pó da polpa de banana liofilizada (PBL). A banana utilizada foi da variedade Prata no estágio 6 de maturação (casca totalmente amarela). Primeiramente, o estudo foi iniciado com a seleção dos parâmetros de extração (temperatura, agitação, solvente e relação sólido-líquido) por meio de um Delineamento Fracionado 24-1 e, em seguida, o método de Superfície de Resposta foi empregado para otimizar os principais fatores do processo de extração (relação sólido-líquido e solvente). A casca da banana apresentou elevada atividade da enzima peroxidase (POD), o que provocou a oxidação dos compostos fenólicos e a redução da capacidade antioxidante do extrato. As melhores condições para a extração de compostos fenólicos a partir da casca de banana foram: relação sólido-solvente de 2,5 g/100 mL (1:40), solvente etanol 54% (v/v etanol:água) e homogeneização com auxílio de Ultra Turrax por 30s a 11.000 rpm. O conteúdo de FT obtido com esse sistema de extração foi de 2,44 g EAG/100 g CBL. A casca de banana apresentou conteúdo de FT (2,44 g EAG/100 g CBL), CF (2,32 g EC/100 g CBL) e atividade antioxidante mensurada pelos métodos de DPPH (380,84 ?mol EQT/g CBL; IC50 = 71,74 ?g/mL), TEAC (325,84 ?mol EQT/g CBL) e ORACFL (ORAC Total = 994,33 ?mol EQT/g CBL) maiores do que a polpa de banana (FT = 0,25 g EAG/100 g PBL; CF = 0,21 g EC/100g PBL; DPPHIC50 = 690,97 ?g/mL; TEAC = 11,05 ?mol EQT/g PBL; ORAC Total = 80,16 ?mol EQT/g PBL). A banana é uma das frutas mais produzidas no mundo, e devido ao seu elevado consumo e abundância pode ser considerada uma importante fonte de compostos antioxidantes. Finalmente, por meio deste estudo foi possível verificar que a polpa e a casca de banana apresentam compostos fenólicos antioxidantes. Mais estudos devem ser realizados para verificar a influência do consumo desse
Abstract: The objective of the present work was to study the influence of solid-liquid extraction parameters and phenoloxidases enzymes in the recovery of phenolic compounds from freeze-dried banana peel powder (BPP), as well as to quantify the total phenolic content (TPC), flavonoid content (FC) and antioxidant activity of BPP and freeze-dried banana pulp powder (BPU). The banana Prata variety was utilized in 6th stage of ripening (fully yellow peel). First of all, the study started with the selection of the extraction parameters (temperature, agitation, solvent and solid-liquid ration) through factionary design (24-1). Subsequently, the Response Surface Methodology (RSM) was employed to optimize the main parameters of the extraction process (solid-liquid ration and solvent). The banana peel showed high peroxidase activity (POD), which led the oxidation of phenolic compounds and the decrease of antioxidant activity of the extract. The best conditions for the extraction of phenolic compound from BPP were solid-liquid ration of 2.5 g/100 mL (1:40), solvent ethanol 54% (v/v ethanol:water) and homogenization using Politron at 11.000 rpm for 30 s. The total phenolic content obtained whit this extraction system was 2.44 g GAE/100 g BPP. The banana peel showed TPC (2.44 g GAE/100 g BPP), FC (2.32 g CE/100 g BPP), and antioxidant activity measured by DPPH (380.84 ?mol TE/g BPP; IC50 = 71.74 ?g/mL), TEAC (325.84 ?mol TE/g BPP) and ORACFL (ORAC Total = 994.33 ?mol TE/g BPP) methods higher than banana pulp (TPC = 0.25 g GAE/100 g BPU; FC = 0.21 g CE/100 g BPU; DPPHIC50 = 690.97 ?g/mL; TEAC = 11.05 ?mol TE/g BPU; ORAC Total = 80.16 ?mol TE/g BPU). The banana is one of the most produced and consumed fruit in the entire world and can be considered as an important source of natural antioxidants. In this sense, this study was to possible found that banana pulp and peel have phenolic compounds with antioxidants properties. More studies should be performed to verify the relationship between banana consumption and human health. Furthermore, research addressing the use of the banana peel by food and pharmaceutical and medical industries. fruto tropical na saúde do corpo humano e também pesquisas abordando o uso da casca na indústria de alimentos e no desenvolvimento de novos produtos
Mestrado
Ciência de Alimentos
Mestre em Ciência de Alimentos
Calomeni, Andressa do Valle. "Utilização de película de amendoim para produção de pigmento natural em pó: estudo do efeito do processo de atomização na estabilidade, propriedades antioxidante e antimicrobiana do material." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/74/74132/tde-03022016-162446/.
Full textThe peanut skin presents intense red color and is rich in phenolic compounds, however the liquid extract is unstable and difficult to commercialize. The aim of this project was to extract the pigments of peanut skin, study the process of spray drying this extract, characterize the powders as well as its antioxidant properties, antimicrobial properties and storage stability, when compared to the control. The extract was characterized measuring the phenolic compounds, pH, moisture, ash, protein, lipids, sugars, aflatoxin and acidity. The extracts were then mixed with the carrier agent at concentrations of 10, 20 and 30%, these were atomized in a spray dryer at inlet air temperatures of 130, 150 and 170 º C. To obtain a control sample, part of the extract was freeze-dried without the presence of maltodextrin. The powders were characterized for moisture, water activity, hygroscopicity, morphology, particle size, color, total phenolic content, solubility, stability, antimicrobial and antioxidant properties by the methods: ORAC, DPPH and ABTS HPLC-online. In the analysis of the liquid extract, the following results were obtained: 0.24% protein, 2.31% sugar, 0.09% ash, 1.41% lipid, 0.91% titratable acidity, 42.88 mg of Galic acid eq. / g extract (phenolic), pH of 5.30, 90.93% moisture and 1.81 ng aflatoxin / mL extract (aflatoxin). In the analysis of the powders, moisture was lower for powders dried at 170ºC and with 10% maltodextrin concentration and was always lower than the control. The hygroscopicity is lower as higher the concentration of maltodextrin, since the last has low hygroscopicity. Higher temperatures generated more hygroscopic powders, because they reduced moisture. In concern to solubility, the values ranged from 85.60 to 91.91%; higher values were obtained for powders with higher concentrations of maltodextrin, since it has high solubility values. The control showed lower solubility of 77.62%. The color parameters were influenced only by the concentration of maltodextrin; the samples with lower concentrations showed more pronounced color, what was to be expected since maltodextrin is white. Therefore, controls have always presented with more intense color than the atomized powders. The temperature of 170 ºC originated powders with smoother surfaces, thus resulting in better flow. In the evaluation of stability, it was found that the atomized sample suffered lower color loss compared to the freeze dried sample, and samples with higher concentrations of maltodextrin (30%) had better preservation of total phenolics, especially at a temperature of 150ºC. In concern to antioxidant activity, the T5 treatment stood out compared to the others, showing the best values of antioxidant activity in all methods studied. The extract of peanut skin in powder also showed antimicrobial activity against Gram-positive bacteria Staphylococcus aureus and Listeria monocytogenes, with bactericidal properties against Staphylococcus aureus. This study clearly showed that peanut skin is a potential natural additive product and may be used as a powdered pigment which has excellent stability, low hygroscopicity and high solubility, besides having biological activities, such as antioxidant and antimicrobial capabilities.
Infante, Juliana. "Composição fenólica e atividade antioxidante de polpa, casca, semente e folha de espécies frutíferas nativas do Brasil." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/11/11141/tde-19122013-165106/.
Full textBrazil has a great biodiversity, in which many bioactive compounds can be found and used to benefit the society. However, environmental degradation processes and introduction of exotic species have contributed to limited use and knowledge of many native plants, reflecting in few studies about chemical composition and biological potential. The prevention of chronic diseases has been constantly associated with the antioxidant activity of plants secondary metabolites, mainly the phenolics. The objective of this study was to evaluate the antioxidant activity and the phenolic composition of five Brazilian native fruitful species (G. brasiliensis, E. leitonii, E. involucrata, E. brasiliensis e E. myrcianthes). The methods of Folin-Ciocalteau reducing capacity, co-oxidation of ?-carotene/linoleic acid system, oxygen radical absorbance capacity (ORAC), DPPH and superoxide free radical scavenging were used to determine the antioxidant activity of ethanolic extracts of leaf, peel, seed and pulp of the selected species. The samples showed significant antioxidant activity and, in some cases, it was superior to fruits commonly consumed by Brazilian population. In general, leaves presented the highest activities, but the seed of E. Leitonii stood out exhibiting the best results in four of the five methods: 120.67 mg GA.g-1 in the Folin reducing; 7.08 Gmol Trolox.g-1 in the ?-carotene; EC50 of 0.26 mg.mL-1 and 0.07 mg.mL-1 in the superoxide and DPPH scavenging, respectively; 514.75 Gmol Trolox.g-1 in the ORAC, for which the E. Involucrata leaf had the highest value (1393.3 GmolTrolox.g-1). The extracts of native species also demonstrate antioxidant effect against radicals of biological relevance, such as peroxyl and superoxide. By GC-MS and HPLC coupled to a photodiode array, the major phenolic compounds found in the plant extracts were catechin, epicatechin and gallic acid. In this study, Brazilian native fruitful presented high antioxidant potential, showing a possible positive effect on biological systems.
Gupta, Elera Gaytri Devi. "Effect of Antioxidants and Oxidative Stress on Different Cancer Cell Types." BYU ScholarsArchive, 2012. https://scholarsarchive.byu.edu/etd/3227.
Full textPazinatto, Caroline. "Avaliação in vitro da capacidade antioxidante de grãos de amaranto (Amatanthus Cruentus)." [s.n.], 2008. http://repositorio.unicamp.br/jspui/handle/REPOSIP/256393.
Full textDissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos
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Resumo: O amaranto se destaca por seu perfil protéico, rico em aminoácidos essenciais e pela presença de outros compostos tais como: fibras, esqualeno, tocoferóis, tocotrienóis e compostos fenólicos, que lhe confere propriedades especiais, incluindo propriedade antioxidante. A fácil adaptação da planta a diferentes condições climáticas, juntamente com as suas qualidades nutricionais e funcionais, aumentam o interesse em introduzir a cultura do amaranto no Brasil. Apesar de bem caracterizado quimicamente e de apresentar compostos com potencial fisiológico, poucos estudos foram realizados para avaliar o potencial do grão de amaranto como alimento funcional. O presente trabalho tem como objetivo avaliar a capacidade antioxidante dos diferentes produtos obtidos a partir do grão integral de amaranto (Amaranthus cruentus). Após a moagem e o desengorduramento dos grãos para a obtenção da farinha desengordurada, diferentes processos, incluindo a hidrólise com Alcalase, foram utilizados na produção dos diversos produtos de amaranto que foram posteriormente digeridos in vitro com as enzimas pepsina e pancreatina. Os efeitos dos processos e da digestão in vitro das frações protéicas, e o efeito dos compostos fenólicos totais na capacidade antioxidante, em extrato aquoso e metanólico, foram avaliados utilizando o ensaio da capacidade seqüestradora de radicais DPPH e o ensaio de ORAC. O teor de fenóis totais apresentou elevada correlação com a capacidade antioxidante quando avaliada no extrato metanólico. Entretanto, a correlação foi menor quando avaliada no extrato aquoso, sugerindo que os compostos hidrossolúveis podem interferir nas avaliações. A hidrólise com Alcalase elevou significativamente o potencial antioxidante das amostras, de 2 a 4 vezes a capacidade seqüestradora de radicais DPPH e de 13 a 15 vezes os valores de ORAC. A digestão in vitro aumentou a capacidade antioxidante medida por ambos os ensaios (até 7 vezes para a capacidade seqüestradora de radicais DPPH e 12 para o valor de ORAC), especialmente para o concentrado protéico e seus hidrolisados. O elevado teor de fenóis totais liberados e o aumento da capacidade antioxidante dos produtos de amaranto após a digestão in vitro sugerem que o mesmo ocorre após a digestão fisiológica. Os resultados sugerem que a inclusão de produtos de amaranto na dieta, especialmente concentrado protéico e seus hidrolisados, pode promover benefícios à saúde
Abstract: Amaranth is well known for its protein profile, rich in essential amino acids and the presence of other compounds such as fiber, squalen, tocols (tocopherols and tocotrienols) and phenolic compounds that are responsible for its special properties, including antioxidant capacity. The easy adaptation of the plant to different climate conditions, together with its nutritional qualities and functional properties, increase the interest to introduce the culture of amaranth in Brazil. Despite being well characterized chemically and exhibiting compounds with physiological potential, few studies have been conducted to evaluate the potential of amaranth grain, as a functional food. This study aims to evaluate the antioxidant capacity of different products obtained from amaranth grain (Amaranthus cruentus). After milling and defatting the grain to obtain deffated amaranth flour, different processes, including Alcalase hydrolysis, were used to produce a variety of products that were digested in vitro with pepsin and pancreatin. The effects of the processes and of the digestion in vitro of the protein fractions, and the effect of the total content of phenolic compounds on the antioxidant capability in aqueous and methanolic extracts were evaluated using scavenging capacity of DPPH radical and ORAC assays. Total phenolic compounds content showed high correlation with the antioxidant capacity, when evaluated in methanolic extract. However, the correlation was lower when using the aqueous extract, suggesting that water soluble compounds may interfere in these evaluations. Hydrolysis with Alcalase increased significantly the antioxidant potencial, from 2 to 5 times the scavenging DPPH capacity and 13 to 15 the ORAC values. In vitro digestion increased the antioxidant capacity measured by both assays (up to 7 times for scavenging DPPH capacity and 12 times for ORAC assays), especially for protein concentrate and its hydrolysates. The high content of phenolic compounds released and the increase in antioxidant capacity after in vitro digestion of the amaranth products suggests that the same occurs after the physiological digestion. These results suggest that the inclusion of these products, especially concentrate and its hydrolysates, in the diet should promote health benefits
Mestrado
Nutrição Experimental e Aplicada à Tecnologia de Alimentos
Mestre em Alimentos e Nutrição
Hosseini-Beheshti, Elham. "Characterization of antioxidant activities from fruits rich in delphinidin or malvidin anthocyanins." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/912.
Full textOracz, Joanna [Verfasser], Stefan [Akademischer Betreuer] Hell, Stefan [Gutachter] Hell, and Tim [Gutachter] Salditt. "Coordinate-targeted optical nanoscopy: molecular photobleaching and imaging of heterostructured nanowires / Joanna Oracz ; Gutachter: Stefan Hell, Tim Salditt ; Betreuer: Stefan Hell." Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2018. http://d-nb.info/1172071942/34.
Full textLeite, Alice Vieira. "Avaliação da composição e da capacidade antioxidante "in vivo" e "in vitro"de antocianinas da casca de jabuticaba (Myrciaria jaboticaba (Vell.) Berg) liofilizada em ratos Wistar." [s.n.], 2010. http://repositorio.unicamp.br/jspui/handle/REPOSIP/255063.
Full textDissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos
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Resumo: O objetivo do presente estudo foi avaliar a produção de casca de jabuticaba em pó, sua composição de antocianinas e efeito antioxidante em animais de laboratório. Muitas frutas tropicais são ricas em antocianinas e existem poucos dados disponíveis sobre a caracterização e quantificação destas antocianinas. A identificação e quantificação de antocianinas de casca de jabuticaba liofilizada foram realizadas por HPLC-PDA e HPLC-ESI-MS/MS e revelaram a presença de dois compostos, delfinidina-3-glicosídeo e cianidina-3- glicosídeo (635,3 e 1964 mg/100 de peso seco), respectivamente. Para as análises do potencial antioxidante foram utilizados os ensaios de ORAC, DPPH e ABTS. Para estes ensaios foram encontrados os seguintes valores, respectivamente, 25514,25±3037,24 YMTEAC.g-1, 45,38 Yg.ml-1, 9457,74±54,29 YMTEAC.g-1. Foram quantificados também os fenólicos totais por Folin-Ciocalteau, e encontrado 556,28±20,37 gGAEb.kg-1 .Neste estudo, a casca de jabuticaba liofilizada mostrou uma grande capacidade antioxidante comprovada por todos os métodos antioxidantes analisados, pela quantidade de compostos fenólicos encontrada e principalmente pela concentração de cianidina-3-glicosídeo e delfinidina-3- glicosídeo. Diante dos dados descritos acima, o efeito antioxidante da ingestão de pó casca de jabuticaba liofilizada no plasma de ratos foi investigado em dois experimentos. No primeiro foi realizado um teste de cinética de absorção, no qual trinta e cinco ratos machos, divididos em 5 grupos, receberam por gavagem 7 mg de antocianinas/ 100 g de peso. A coleta de sangue foi realizada nos tempos 0, 30, 60 e 120 minutos. O potencial antioxidante foi quantificado no plasma por ORAC e TEAC. Neste experimento não ocorreu diferença significativa no potencial antioxidante plasmático quando comparados os diversos tempos. No segundo experimento, 40 ratos machos foram divididos em 4 grupos que consumiram, respectivamente, 0, 1, 2 e 4% de pó de casca de jabuticaba liofilizada acrescido a dieta. Foi observado um aumento no potencial antioxidante plasmático (1.7 vezes pelo método de TEAC e 1.3 vezes por ORAC), porém a concentração de 4% não apresentou efeito antioxidante. A partir dos resultados do potencial antioxidante in vivo, e diante do fato de que a ingestão de uma dieta rica em antioxidantes e com pouca quantidade de gorduras pode reduzir o risco de obesidade e resistência à insulina, investigou-se o efeito da casca de jabuticaba liofilizada sobre as concentrações plasmáticas de glicose, frações lipídicas, aspartato aminotransferase e alanina aminotrasferase em ratos Wistar machos adultos. Os animais foram distribuídos nos seguintes grupos: G0, o grupo controle e G1, G2 e G4, os grupos que receberam 1, 2 e 4%, respectivamente, do pó de casca de jabuticaba liofilizada adicionado à dieta AIN-93M. A suplementação reduziu as concentrações de glicose nos grupos G1 e G2, porém no grupo G3 esse efeito não foi encontrado. O colesterol total sofreu redução para os animais tratados com 1% de cascas de jabuticabas em relação ao grupo controle, mas os animais tratados com 2 e 4% de cascas de jabuticabas sofreram aumento no colesterol total e da fração LDL-colesterol, porém, o valor para colesterol total apresenta-se dentro da faixa normal para ratos Wistar. Os triacilgliceróis e a fração HDL-colesterol não sofreram alterações significativas. Os resultados indicam um possível benefício da suplementação da casca de jabuticaba na redução da glicemia plasmática, dos níveis de LDL e colesterol total e a possível existência de uma dose recomendada
Abstract: The objective of this study was to evaluate the antioxidant effects of anthocyanin and the antioxidant effects of peel jabuticaba powder in laboratory animals. Many tropical fruits are rich in anthocyanins, but there are few data available on the characterization and quantification of these anthocyanins. The identification and quantification of anthocyanins from bark jabuticaba was performed by HPLC-PDA and LC-ESI-MS/MS Q-TOF. The analysis revealed the presence of two compounds, delphinidin-3-glucoside and cyanidin-3-glucoside (635, 3 and 1964 mg/100 dry weight, respectively). ORAC, DPPH and ABTS methods were used for antioxidant analysis and the results were, 25514,24±3037,24 µMTEAC.g-1, 45.38 Yg.ml-1, 9457,74±54,29 µMTEAC.g-1, respectively. The total phenolics (Folin-Ciocalteau method) revealed that the jabuticaba powder contained 556,28±20,37 gGAEb.kg-1. In this study, freezedried peel jabuticaba showed great antioxidant proven by all methods antioxidants tested. The effects of the ingestion of jabuticaba peel in the antioxidant capacity of plasma of rats was investigated in two 'in vivo¿ experiments. In the first test, the absorption kinetics were evaluated. The male rats were divided into 5 groups received, by gavage, 7 mg anthocyanins / 100 g of body weight. Blood collection was performed at 0, 30, 60 and 120 minutes. The antioxidant potential was quantified in plasma by ORAC and TEAC. In this experiment there was no significant difference in plasma antioxidant potential when comparing the different times. In the second experiment, 40 rats were divided into 4 groups that consumed, respectively, 0, 1, 2 and 4% powdered peel jabuticaba lyophilized plus diet. We observed an increase in plasma antioxidant potential (1.7 times by the method of TEAC and ORAC by 1.3 4 times), but the concentration of 4% had no antioxidant effect. We investigated the effect of freeze-dried peel jabuticaba on plasma glucose, lipid fractions, aminotransferase and aspartate aminotransferase alanian in adult male Wistar rats. The animals assigned to groups G0, the control group, G1, G2 and G4 groups receiving 1, 2 and 4%, respectively, of freeze-dried peel jabuticaba added to the AIN-93M diet. Supplementation reduced the concentration of glucose in G1 and G2, but in G4 this effect was not found. Total cholesterol was reduced in animals treated with 1% bark jabuticabas in the control group, but animals treated with 2 and 4% experienced an increase in total cholesterol and LDL cholesterol, but the value for cholesterol total amount is within the normal range for rats. Triglycerides and HDL-cholesterol did not change significantly. The results indicate the possible benefit of supplementing with bark jabuticaba in reducing plasma glucose, LDL cholesterol and total cholesterol and the possible existence of a dose
Mestrado
Nutrição Experimental e Aplicada à Tecnologia de Alimentos
Mestre em Alimentos e Nutrição
Furuhagen, Sara. "Application and interpretation of biomarkers in ecotoxicology - from molecular to individual level responses." Doctoral thesis, Stockholms universitet, Institutionen för miljövetenskap och analytisk kemi, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-120161.
Full textAt the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Manuscript. Paper 4: Manuscript.
Livingston, Justin Ryan. "The Antioxidant and DNA Repair Capacities of Resveratrol, Piceatannol, and Pterostilbene." BYU ScholarsArchive, 2015. https://scholarsarchive.byu.edu/etd/5525.
Full textHunt, Spencer Philip. "Whole-Genome Assembly of Atriplex hortensis L. Using OxfordNanopore Technology with Chromatin-Contact Mapping." BYU ScholarsArchive, 2019. https://scholarsarchive.byu.edu/etd/8580.
Full textAndreae, Mary Christine. "Value of Raisins for Reduction of Oxidative Stress, Endothelial Dysfunction, and Inflammation in Obesity." Thesis, Virginia Tech, 2009. http://hdl.handle.net/10919/34102.
Full textMaster of Science
Arraki, Kamel. "Les stilbénoïdes chez les Cypéracées : isolation, identification et étude de leurs activités biologiques : identification et dosage des stilbènes dans des vins Tunisiens." Thesis, Bordeaux, 2014. http://www.theses.fr/2014BORD0481/document.
Full textStilbenes are phenolic compounds of plant secondary metabolism, whosedistribution within the plant kingdom is limited to species that have acquired during theevolution the ability to synthesize these molecules. Their impacts and their biologicalactivities such as neuroprotective, anticarcinogenic, antioxidant effects have already touchedseveral topics. It is in this context that the purpose of our work arose. First, we have isolatedand identified these molecules in some species of the sedge family. Phytochemical studieswere performed using a set of analytical and preparative strategies by means of analytical andpreparative HPLC and CPC (Centrifugal Partition Chromatography) for obtaining puremolecules and LC-Mass and NMR for identification of compound isolated. In a second step,we investigated the in vitro biological properties of these products such as antioxidantactivities by three methods (ORAC, DPPH and MCA) and their effect on neuronalcytotoxicity induced by β-amyloid peptide with PC12 cells. We isolated a new molecule, forthe first time, carexinol A, that showed strong anti-amyloid activity. The last part of this thesisrefers to the analysis and determination of stilbenes in Tunisian wines including Sidi Zahiawine that gave the best results
Massaretto, Isabel Louro. "Características químicas e nutricionais de arroz-preto, vermelho e selvagem e comparação por análise estatística multivariada." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/9/9131/tde-04062014-152239/.
Full textRice (Oryza sativa L.) is mostly consumed in its milled form; however there is an increasing demand for whole non-pigmented and pigmented rice, such as black, red, and wild rice, which the latter belongs to the genus Zizania. Pigmented rice has particular nutritional composition and sensory characteristics, and in addition high amounts of phenolic compounds, which not only confer color but also has been linked to beneficial effects on human health. To date, little is known about the nutritional and bioactive contents of these grains. The aim of this study was to compare the chemical composition, including the total phenolic compounds (TPC), the majoritarian polyphenols and the antioxidant radical efficiency of the following accessions: three black rice from the state of São Paulo, two black rice from the state of Rio Grande do Sul, eleven black rice genotypes from Santa Catarina state, nine red rice from those states and six wild rice, imported from Canada and marketed in São Paulo. All samples were cultivated and/or marketed from 2009 to 2011. Data were evaluated by uni- and multivariate statistical analysis. The effect of cooking on the stability of TPC and antioxidant capacity was also evaluated. In addition, a preliminary comparison of γ- oryzanol, tocopherols and tocotrienols was carried out between two groups: seven black rice and four red rice samples, all of them cultivated in 2013. Based on chemical results and multivariate statistical analysis it was possible to cluster the various types of rice in four groups, significantly different among themselves: wild rice, black long grain rice, black medium grain rice, and red rice. Wild rice was the most dissimilar group due to its highest contents of protein (12.9 g/100g) and α-linolenic acid (0.12 g/100g), and the lowest amounts of lipids (0.9 g/100g), TPC, and antioxidant capacity. Black long grain rice was characterized mainly by its high contents of TPC, especially anthocyanins and by its elevated antioxidant capacity. Cyanidin-3-O-glycoside was identified by HPLC-DAD-MS/MS as being the main anthocyanin. The protein and lipid mean contents in these groups were respectively, 9.8 and 3.6 g/100g and were higher than the amounts in the other next two types of rice. The black medium grain rice and red rice were similar in terms of nutrient composition and TPC. The average amount of protein in both groups was about 8.8 g/100g. However, in black rice prevails anthocyanins, while in red rice coloration is provided by proanthocyanidins, which results in differences in antioxidant activity. Medium and long black grain rice showed a 2-fold higher antioxidant activity than red rice. These findings indicate that the high content of anthocyanins, independent of the grain shape, is responsible for the high antioxidant capacity in black rice. The multivariate analysis demonstrated that the grain shape is fundamental to differentiate black rice in terms of nutrient composition, like protein and lipids, but not in relation to amounts of phytochemicals and antioxidant capacity. ORAC was more suitable than DPPH· methodology to evaluate the antioxidant activity of black rice, due to its high correlation to anthocyanin contents. Conversely, DPPH· can be a consistent method to evaluate antioxidant capacity of red and wild rice. Cooking resulted in significant loss on TPC contents and on the antioxidant capacity of black and red rice. In black rice, 26% of TPC was reduced on average, while the loss of anthocyanins was 50%. The reason may be that during cooking, part of the anthocyanins is converted into protocatechuic acid, which is quantified as TPC. The reduction in TPC in red rice was 60%, possibly due to a partial insolubilization of proanthocyanidins. In wild rice, cooking caused no significant loss of TPC. The antioxidant capacity of different types of cooked rice was dependent on the method used, being strongly correlated with the remaining levels of TPC. Thus, black rice even after cooking showed the highest antioxidant capacity, followed by red and wild rice. From a preliminary evaluation, the contents of lipophilic phytochemicals, γ-orizanol and vitamin E homologues were similar in black and red rice, which indicates that the contents of these compounds are not dependent of the pericarp color.
Aikman, Matthew Andrew. "Exercise and DNA damage and repair in middle aged men / Andrew Aikman." Thesis, North-West University, 2007. http://hdl.handle.net/10394/1490.
Full textGarrett, Andrew Robert. "Antioxidants in Cancer Research and Prevention: Assay Comparison, Structure-Function Analysis, and Food Product Analysis." BYU ScholarsArchive, 2011. https://scholarsarchive.byu.edu/etd/2735.
Full textScheffler, Thomas. "Privacy enforcement with data owner-defined policies." Phd thesis, Universität Potsdam, 2013. http://opus.kobv.de/ubp/volltexte/2013/6793/.
Full textIm Rahmen der Dissertation wurde ein Framework für die Durchsetzung von Richtlinien zum Schutz privater Daten geschaffen, welches darauf setzt, dass diese Richtlinien oder Policies direkt von den Eigentümern der Daten erstellt werden und automatisiert durchsetzbar sind. Der Schutz privater Daten ist ein sehr wichtiges Thema im Bereich der elektronischen Kommunikation, welches durch die fortschreitende Gerätevernetzung und die Verfügbarkeit und Nutzung privater Daten in Onlinediensten noch an Bedeutung gewinnt. In der Vergangenheit wurden verschiedene Techniken für den Schutz privater Daten entwickelt: so genannte Privacy Enhancing Technologies. Viele dieser Technologien arbeiten nach dem Prinzip der Datensparsamkeit und der Anonymisierung und stehen damit der modernen Netznutzung in Sozialen Medien entgegen. Das führt zu der Situation, dass private Daten umfassend verteilt und genutzt werden, ohne dass der Datenbesitzer gezielte Kontrolle über die Verteilung und Nutzung seiner privaten Daten ausüben kann. Existierende richtlinienbasiert Datenschutztechniken gehen in der Regel davon aus, dass der Nutzer und nicht der Eigentümer der Daten die Richtlinien für den Umgang mit privaten Daten vorgibt. Dieser Ansatz vereinfacht das Management und die Durchsetzung der Zugriffsbeschränkungen für den Datennutzer, lässt dem Datenbesitzer aber nur die Alternative den Richtlinien des Datennutzers zuzustimmen, oder keine Daten weiterzugeben. Es war daher unser Ansatz die Interessen des Datenbesitzers durch die Möglichkeit der Formulierung eigener Richtlinien zu stärken. Das dabei verwendete Modell zur Zugriffskontrolle wird auch als Owner-Retained Access Control (ORAC) bezeichnet und wurde 1990 von McCollum u.a. formuliert. Das Grundprinzip dieses Modells besteht darin, dass die Autorität über Zugriffsentscheidungen stets beim Urheber der Daten verbleibt. Aus diesem Ansatz ergeben sich zwei Herausforderungen. Zum einen muss der Besitzer der Daten, der Data Owner, in die Lage versetzt werden, aussagekräftige und korrekte Richtlinien für den Umgang mit seinen Daten formulieren zu können. Da es sich dabei um normale Computernutzer handelt, muss davon ausgegangen werden, dass diese Personen auch Fehler bei der Richtlinienerstellung machen. Wir haben dieses Problem dadurch gelöst, dass wir die Datenschutzrichtlinien in drei separate Bereiche mit unterschiedlicher Priorität aufteilen. Der Bereich mit der niedrigsten Priorität definiert grundlegende Schutzeigenschaften. Der Dateneigentümer kann diese Eigenschaften durch eigene Regeln mittlerer Priorität überschrieben. Darüber hinaus sorgt ein Bereich mit Sicherheitsrichtlinien hoher Priorität dafür, dass bestimmte Zugriffsrechte immer gewahrt bleiben. Die zweite Herausforderung besteht in der gezielten Kommunikation der Richtlinien und deren Durchsetzung gegenüber dem Datennutzer (auch als Data User bezeichnet). Um die Richtlinien dem Datennutzer bekannt zu machen, verwenden wir so genannte Sticky Policies. Das bedeutet, dass wir die Richtlinien über eine geeignete Kodierung an die zu schützenden Daten anhängen, so dass jederzeit darauf Bezug genommen werden kann und auch bei der Verteilung der Daten die Datenschutzanforderungen der Besitzer erhalten bleiben. Für die Durchsetzung der Richtlinien auf dem System des Datennutzers haben wir zwei verschiedene Ansätze entwickelt. Wir haben einen so genannten Reference Monitor entwickelt, welcher jeglichen Zugriff auf die privaten Daten kontrolliert und anhand der in der Sticky Policy gespeicherten Regeln entscheidet, ob der Datennutzer den Zugriff auf diese Daten erhält oder nicht. Dieser Reference Monitor wurde zum einen als Client-seitigen Lösung implementiert, die auf dem Sicherheitskonzept der Programmiersprache Java aufsetzt. Zum anderen wurde auch eine Lösung für Server entwickelt, welche mit Hilfe der Aspekt-orientierten Programmierung den Zugriff auf bestimmte Methoden eines Programms kontrollieren kann. In dem Client-seitigen Referenzmonitor werden Privacy Policies in Java Permissions übersetzt und automatisiert durch den Java Security Manager gegenüber beliebigen Applikationen durchgesetzt. Da dieser Ansatz beim Zugriff auf Daten mit anderer Privacy Policy den Neustart der Applikation erfordert, wurde für den Server-seitigen Referenzmonitor ein anderer Ansatz gewählt. Mit Hilfe der Java Reflection API und Methoden der Aspektorientierten Programmierung gelang es Datenzugriffe in existierenden Applikationen abzufangen und erst nach Prüfung der Datenschutzrichtlinie den Zugriff zuzulassen oder zu verbieten. Beide Lösungen wurden auf ihre Leistungsfähigkeit getestet und stellen eine Erweiterung der bisher bekannten Techniken zum Schutz privater Daten dar.
Chung, Hyun. "Characterization of antioxidant activities of soybeans and assessment of their bioaccessibility after in vitro digestion." Diss., Virginia Tech, 2009. http://hdl.handle.net/10919/29638.
Full textPh. D.
Cacchi, Mattia. "Qualita di nuove accessioni di fragola (fragaria x ananassa) in funzione del tipo di materiale di propagazione: Aspetti analitici e sensoriali." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2014. http://amslaurea.unibo.it/7877/.
Full textChase, Jennifer Leigh. "Utah Red Raspberry Jam: The Effects of Formulation, Heating, and Time on Color, Flavor, Texture, and Antioxidant Capacity." BYU ScholarsArchive, 2013. https://scholarsarchive.byu.edu/etd/4278.
Full textSilva, Fernanda Guimarães Drummond e. 1983. "Atividade antioxidante de produtos proteicos de linhaça (Linum usitatissimum L.)." [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/256383.
Full textDissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos
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Resumo: Existem evidências numerosas sobre o papel dos radicais livres em uma série de condições patológicas, incluindo envelhecimento, câncer, esclerose múltipla, doenças cardiovasculares. Hidrolisados protéicos de diferentes fontes têm sido estudados por seu potencial antioxidante. A atuação antioxidante da proteína, na maioria das vezes, encontra-se limitada devido à conformação espacial, que concentra resíduos capazes de neutralizar radicais livres no interior da molécula, dificultando o acesso das espécies reativas aos centros nucleofílicos. A hidrólise da proteína contribui para aumentar a exposição desses resíduos de aminoácidos, aumentando sua atuação como antioxidante. Compostos fenólicos podem estar presentes em hidrolisados proteicos de origem vegetal, devido a sua associação com as proteínas. Métodos in vitro que simulam as condições do trato gastrointestinal permitem estudar como a digestão pode interferir na atividade antioxidante de peptídeos e compostos fenólicos. O presente trabalho tem como objetivos obter hidrolisados proteicos com capacidade antioxidante a partir da farinha de linhaça e avaliar o efeito da digestão in vitro pode interferir nessa atividade. A farinha de linhaça marrom foi desengordurada, obtendo-se a farinha de linhaça marrom desengordurada (FLMD). O concentrado proteico de linhaça (CPL) foi obtido a partir da FLMD por extração alcalina e precipitação no ponto isoelétrico seguida de neutralização. Para obtenção dos hidrolisados proteicos (HPL), a partir do CPL, com Alcalase, foi realizado um delineamento composto central rotacional (DCCR) 2². As variáveis independentes foram pH que variou entre 7,5 a 9,5 e relação enzima: substrato (E:S) que variou de 1:150 a 1:30. As variáveis dependentes foram grau de hidrólise (GH), teor de substâncias redutoras do reagente de Folin-Ciocalteau e atividade antioxidante, determinada por FRAP e ORAC. Teor de substâncias redutoras e atividade antioxidante foram avaliados a partir dos extratos aquosos e metanólico (metanol 70%). Os hidrolisados de maior atividade antioxidante, a FLMD e o CPL foram submetidos à digestão in vitro, simulando as condições da digestão gastrintestinal. As amostras antes e após a digestão in vitro foram caracterizadas por eletroforese em sistema SDS-PAGE Tricina e por cromatografia liquida de alta eficiência de fase reversa (HPLC- RP). O teor de substâncias redutoras e da atividade antioxidante das amostras FLMD, CPL e HPL foram avaliados antes e após a digestão in vitro. As condições ótimas para obtenção de HPL de maior GH (21,0%) são pH entre 7,5 e 8,0 e E:S entre 1:60 e 1:30, indicando que a faixa de pH ótimo da enzima e a alta E:S favorecem maior hidrólise do CPL. Para obtenção de HPL com maior teor de substâncias redutoras para os extratos aquoso (24 mg EAG/ g HPL) e metanólico (20 mg EAG/ g HPL) as condições ótimas são pH ~ 8,5 /E:S 1:30. Este resultado parece estar relacionado à liberação de compostos fenólicos ligados a proteína e também de peptídeos durante a hidrólise. Açúcares e aminoácidos aromáticos presentes no hidrolisado podem interferir na reação e superestimar o teor de fenóis dos HPL. A maior atividade antioxidante determinada pelo método de FRAP para o extrato aquoso (42 mg SF/ g HPL) se dá nas condições de pH ~ 9,5/E:S ~1:150 e para o extrato metanólico (40 mg SF/ g HPL) pH entre 8,5 e 9,0/E:S entre 1:90 a 1:150. Para o método de ORAC, as condições ótimas para maior atividade antioxidante no extrato aquoso (300 µmol TE/ g HPL) são pH entre 7,5 a 9,5/E:S ~ 1:30 ou ~1:150 e para o extrato metanólico (330 µmol TE/ g HPL) são pH ~ 8,5/E:S entre 1:150 e 1:30. Os hidrolisados de maior atividade antioxidante foram os obtidos em pH 8,5/E:S 1:90, e em pH 9,2/E:S 1:133 denominados HPL 0 e HPL 3, respectivamente. Para a FLMD, CPL e os hidrolisados, após a digestão in vitro, observou-se que o teor de substâncias redutoras totais aumentou (9 a 20 vezes) para todas as amostras. O teor de substâncias redutoras do CPL (~24 mg EAG/ g amostra), em ambos os extratos, após a digestão in vitro se igualou ao teor dos hidrolisados (~23 mg EAG/ g amostra). Este resultado sugere que tanto a hidrólise com Alcalase quanto o processo digestório liberam compostos redutores, dentre eles fenólicos da proteína de linhaça. A atividade antioxidante dos extratos de FLMD e CPL, determinada por FRAP, também aumentou (de 3 a 10 vezes) após a digestão, mas não se igualou à atividade antioxidante dos hidrolisados (48 mg SF/g amostra). No entanto, o CPL apresentou atividade antioxidante determinada por ORAC semelhante à dos hidrolisados no extrato aquoso (~420,24 µmol TE/ g amostra) e 10 % maior que o encontrado para os hidrolisados (~365 µmol TE/ g amostra) no extrato metanólico. Após a digestão in vitro, os hidrolisados apresentaram a maior atividade antioxidante medida por FRAP (50 mg SF/ g amostra), e o CPL, a maior atividade determinada pelo método de ORAC (~430 µmol TE/ g amostra). Estes resultados sugerem o processo digestório é tão ou mais eficiente que a Alcalase em liberar os compostos com atividade redutora no CPL. Uma vez que a metodologia de determinação da atividade antioxidante por ORAC tem maior proximidade com o mecanismo de oxirredução que ocorre in vivo, esses resultados sugerem o uso do CPL como melhor produto protéico da linhaça com maior potencial antioxidante para a formulação de nutracêuticos e alimentos funcionais
Abstract: There are several evidences which indicate the role of free radicals on a series of pathological conditions, including aging, cancer, multiple sclerosis and cardiovascular disease. Hydrolysates from different sources have been studied because of their antioxidant potential. The antioxidant activity of the protein, in most cases, is limited due to their conformation, which concentrates residues capable of neutralize free radicals in the molecule¿s core, hampering the access of the reactive species to nucleophilic sites. The protein hydrolysis contributes to increasing the exposure of these amino acid residues, increasing their role as antioxidants. Phenolic compounds may also be present in vegetable protein hydrolysates because of their association with proteins. In vitro methods that simulate the conditions of the gastrointestinal digestion are an important way to evaluate how the digestion affects the antioxidant activity of phenolic compounds and peptides. This study aims at obtaining hydrolysates with antioxidant capacity from defatted flaxseed flour and evaluate the effect of the in vitro digestion on this activity. The brown flaxseed flour was defatted, resulting in the brown defatted flaxseed meal (BDFM). The flaxseed protein concentrate (FPC) was obtained from the BDFM by alkaline extraction and precipitation at the isoelectric point followed by neutralization. To obtain the flaxseed protein hydrolysates (FPL), using FPC and Alcalase, a central composite rotational design (DCCR) was performed. The independent variables were pH ranging from 7.5 to 9.5 and enzyme: substrate ratio (E: S) that ranged from 1:150 to 1:30. The dependent variables were the degree of hydrolysis (DH), total phenolic content and antioxidant activity, determined by FRAP and ORAC. Phenolic and antioxidant activity were evaluated from the aqueous and methanol (70% methanol). The hydrolysates with the highest antioxidant activity, the CPL FLMD were submitted to the in vitro digestion. The samples obtained before and after the in vitro digestion were characterized by electrophoresis SDS-PAGE- tricine and HPLC. The total phenolic content and antioxidant activity of FLMD, CPL and HPL were evaluated before and after in vitro digestion. The optimum conditions to obtain HPL with the highest GDH (21.0%) are pH (7.5-8) and E:S ratio (1:60-1:30), which indicates that the Alcalase optimum pH and highest E:S ratio collaborates to highest hydrolysis of CPL. To obtain HPL with higher content of Folin-Ciocalteau reducing compounds content in aqueous (EAG 24 mg / g HPL) and methanol (20 mg EAG / g HPL) extracts, the optimum conditions were pH ~ 8.5 / E: S 1:30. This result seems to be related to the release of phenolic compounds bound to protein and also of peptides during hydrolysis. The highest antioxidant activity determined by the FRAP method in the aqueous extract (42 mg SF / g HPL) occurs under pH ~ 9.5 / E: S ~ 1:150 and the methanol extract (40 mg SF / g HPL) pH 8.5-9.0 / E: S 1:90-1:150. For the ORAC method, optimum conditions for increased antioxidant activity in aqueous extract (300 µmol TE / g HPL) are pH 7.5-9.5 / E: S ~ 1:30 or 1:150 and the methanol extract (330 µmol TE / g HPL) are pH ~ 8.5 / E: S 1:30-1:150. The hydrolysates with the highest antioxidant activities were obtained at pH 8.5 / E: S 1:90, and at pH 9.2 / E: S 1:133 denominated HPL ) and HPL 3, respectively. For FLMD, CPL and hydrolysates, after in vitro digestion, the content increased (9-20 times) for all samples. The Folin-Ciocalteau reducing capacity of the CPL (EAG ~ 24 mg / g sample) in both extracts after in vitro digestion equaled the content of hydrolysates (EAG ~ 23 mg / g sample). This result suggests that both hydrolysis with Alcalase and the digestion process are able to release phenolic compounds from the flaxseed products. The antioxidant activity of extracts of FLMD, CPL determined by FRAP, also increased (from 3 to 10 times) after digestion, but did not reached the antioxidant activity of hydrolysates (48 mg SF / g sample). However, when the activity was determined by ORAC, the FPC showed value similar to the hydrolysates, measured on the aqueous extract (~ 420.24 µmol TE / g sample) and 10% higher than on the methanol extract (~ 365 µmol TE / g sample). After in vitro digestion, hydrolysates showed the highest antioxidant activity measured by FRAP (SF 50 mg / g sample), and the FPC, the highest activity determined by ORAC method (~ 430 micromol TE / g sample). These results suggest that digestive process are equally or more effective than Alcalase in releasing peptides and phenolic compounds present in the FPC. Since the methodology for determining the antioxidant activity by ORAC utilizes a biologically relevant radical source, these results suggest the use of FPC as the best protein product of flaxseed with potential antioxidant in the formulation of nutraceuticals and functional foods
Mestrado
Nutrição Experimental e Aplicada à Tecnologia de Alimentos
Mestre em Alimentos e Nutrição
Ibarra, Sixto Alvin. "OBTENTION AND CHARACTERIZATION OF ROSEMARY AND ASH TREE SEED EXTRACTS AND STUDY OF THEIR PREVENTIVE EFFECTS ON METABOLIC DISORDERS." Doctoral thesis, Universitat Politècnica de València, 2011. http://hdl.handle.net/10251/10795.
Full textIbarra, SA. (2011). OBTENTION AND CHARACTERIZATION OF ROSEMARY AND ASH TREE SEED EXTRACTS AND STUDY OF THEIR PREVENTIVE EFFECTS ON METABOLIC DISORDERS [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/10795
Palancia
Pretorius, Corlea. "Antioxidant properties of Lippia javanica (Burm.f.) Spreng. / C. Pretorius." Thesis, North-West University, 2010. http://hdl.handle.net/10394/4726.
Full textThesis (M.Sc. (Pharmaceutical Chemistry))--North-West University, Potchefstroom Campus, 2011.
Matrose, Albertina Neliswa. "Evaluation of the antioxidant and anti-diabesity potential of cyclopia maculata using in vitro non-cell based screening models." Thesis, University of the Western Cape, 2014. http://hdl.handle.net/11394/4262.
Full textThe aim of this study was therefore to evaluate the antioxidant and anti-diabesity potential of a hot water extract of C. maculata in non-cell based assays and correlate the activities with phenolic composition. Total antioxidant capacity (TAC) was assessed in terms of free radical scavenging and iron reducing ability. The DPPH, ABTS, ORAC and FRAP assays were employed. Anti-diabesity potential was assessed in terms of the inhibition of the digestive enzymes, α-glucosidase and pancreatic lipase
Techer, Sophie. "Criblage d’activités biologiques de plantes endémiques ou indigènes de La Réunion - Recherche de molécules antivirales ciblant le virus du chikungunya." Thesis, La Réunion, 2013. http://www.theses.fr/2013LARE0014/document.
Full textThe aims of this PhD work were to identify plants and/or molecules with cytotoxic, antioxidant, anti-inflammatory or antiviral (chikungunya virus , CHIKV) activities in order to find therapeutic alternatives towards oxidative stress and inflammation, mechanisms involved in chronic noncommunicable diseases (diabetes, obesity ...), and chikungunya disease, reemerging vector-borne disease. The first part of this work presents the results obtained from a biological screening carried out on a selection of eighteen endemic and indigenous plants of La Réunion. The targeted activities were cytotoxicity on a human cell line (THP-1), antioxidant activities evaluated using an in cellulo hemolysis assay and four chemical tests (TEAC / DPPH / FRAP / ORAC) together with an evaluation of the content of phenolic compounds (FOLIN test) and anti-inflammatory activity tested in murine macrophages (RAW cells-BlueTM). The results allowed to highlight activities of different extracts in particular : cytotoxic for Carissa spinarum, antioxidant for Dryopteris wallichiana and Agarista buxifolia and anti-inflammatory for Stillingia lineata and Indigofera ammoxylum.The second part of this work is devoted to the phytochemical study of Stillingia lineata, an indigenous species of La Réunion chosen because of the results obtained in this preliminary biological screening and those carried out in Phytochik programme. Bioassay-guided fractionation performed on Vero cells (green monkey kidney cells Cercopithecus aethiops) infected with CHIKV led to the isolation of three rare macrocycle-type diterpenes called tonantzitlolone and a new pimarane. The 4'-acetoxytonantzitlolone was identified as a candidate molecule against CHIKV (EC50 = 7 μM). Structure-activity relationships have been defined, the presence of an oxygenated group on the side chain of tonantzitlolones seems to play an important role in the antiviral response of the diterpene skeleton
Waldron, Sarah Winona. "Children's responses to culturally relevant oracy practices." Thesis, 2014. http://hdl.handle.net/1828/5667.
Full textGraduate
0727
0524
winona.waldron@shaw.ca
Tichapondwa, Stanslaus Modesto. "The effects of a course in classroom text and discourse on oracy in high school classrooms." Thesis, 2008. http://hdl.handle.net/10500/2015.
Full textLinguistics
D.Litt. et Phil. (Linguistics)
Wang, Jhih-Jheng, and 王至正. "Measurement of Antioxidant Capacity of Horticultural Crops Using Oxygen Radical Absorbance Capacity (ORAC) Assay." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/66084342143435244719.
Full text國立臺灣大學
園藝學研究所
94
Abstract Oxygen radical absorbance capacity (ORAC) assay is regarded as the recommended method for representing the total hydrophilic antioxidant capacity in fruits and vegetables. This method measures the decay of fluorescence as the fluorescent probe is oxidized by the peroxy radicals generated from AAPH (2,2-Azobis(2-amidinopropane) dihydrochloride). At present, there are two fluorescent probes being used in the ORAC assay, the β-phycoerythrin (β-PE), an fluorescent algae protein; and fluorescein (FL), an organic fluorescent molecule. The object of this paper is to compare the fluorescence stability, influence of solvent on free radical reaction, and the responses of different antioxidants in the ORAC assay by using these two probes. Results showed that under excitation irradiation, FL remained stable during the assay period, while β-PE lost its fluorescence intensity with time. Using phosphate buffer or methanol as solvent did not influence the fluorescence change of the free radical reaction, but using acetone or ethanol as solvent would affect the reaction. Both β-PE and FL probes have shown linear correlation at the concentration range of 0~10 μΜ for the water-soluble vitamin E analog trolox. Similar linearity and sensitivity were obtained with other antioxidants, including glutathione, ascorbic acid, sodium ascorbate, uric acid, rutin, catechin and catechol. The relative antioxidant capacity (with respect to trolox) of various antioxidants were further compared, the antioxidant value of glutathione obtained with β-PE was similar to that of FL. For ascorbic acid, Sodium ascorbate and uric acid, the antioxidant values obtained with β-PE was higher than that of the FL. While for phenolic compounds including rutin, catechin and catechol, the antioxidant values obtained with β-PE was lower than that of FL. These results indicated that interactions between free radicals, antioxidants and fluorescence probes were different among various antioxidants. Since the relative antioxidant capacity of all the phenolic compounds was much higher than trolox in both assays, it is a good indication that phenolic compounds possess high antioxidation capacity against peroxy radicals. The total oxyradical scavenging capacity (TOSC) assay is another method for total hydrophilic antioxidant capacity, which is based on the oxidation of α-keto-γ-methylthiobutyric acid by 2,2’-azobis-amidino -propane (ABAP) with the evolution of ethylene as the quantifiable end product. Linear correlations were observed between TOSC antioxidant capacity and concentration of various antioxidants. The antioxidants being tested include trolox, ascorbic acid, glutathione, rutin, catechin and catechol. The antioxidant capacity of ascorbic acid and glutathione were similar to the ORACFL assay, and antioxidant capacity of all the phenolics, rutin, catechin and catechol are lower than that of the ORACFL assay. Fourteen horticulture crops were analyzed for their antioxidant capacity by both the TOSC assay and the ORACFL assay. The results of ORACFL and TOSC assay had rather poor correlation, indicating the difficulty of comparing results of two different assays. When using mixtures of two or more antioxidant standards, both ORACFL and TOSC assays gave linear regression curve between measured and calculated values, but the ORACFL had better correlation coefficients. Based on the accuracy and reliability of the assay methods, the ORAC assay was considered the better method to be chosen. In the last part, the antioxidant capacity of 24 vegetables and 5 fruits grown in Taiwan was measured by the ORACFL assay. The total hydrophilic antioxidant capacity of all the fruits and vegetables analyzed ranged between 2.08 ± 1.11 to 58.19 ± 1.48 μmole Trolox equiv./g. Among them, ‘Taiwan’ cutting lettuce, ‘Kaiya’, ‘C×Y cross’ and ‘Siashan’ cabbages all had relative high amount of antioxidant capacity, that is, higher than 40 μmole Trolox equiv./g. There are significant differences in antioxidant capacity among cultivars of the same crop, and there are differences among vegetables grown in different locations and by different growers. But there were no difference between vegetables grown by the same grower at the same location but harvested at different time. It is concluded that in addition to the differences among cultivars, antioxidant capacity of crops may be influenced by environmental factors as well as cultivation styles.
Cheng, Yu-Hsuan, and 鄭又瑄. "Measurement of Antioxidant Capacity of Vegetables Using Oxygen Radical Absorbance Capacity(ORAC)and Folin-Ciocalteu Reagent Reducing Capacity(FCR)Assay." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/55207036073793414144.
Full text國立臺灣大學
園藝學研究所
99
Fruits and vegetables are rich in compounds that possess antioxidative capacity, such as carotenoids, flavonoids and phenolics, and these compounds act as the major source of antixidants in our daily diet. A number of methods, that were based on different principles, had been developed to determine the antioxidant capacity in our food. In this research, two of the major methods for antioxidant capacity assay: the Oxygen radical absorbance capacity assay(ORAC)and the Folin-Ciocalteo reagent reducing capacity assay(FCR)were studied in detail. First, standard assay procedures were established for these two assays and the relative antioxidant capacity of ten phytochemicals representing antioxidants commonly found in vegetables were obtained and the differences between these two assays were compared. Then, the most effective way of extracting antioxidant components from vegetable tissue was studied and the antioxidant capacities of sixteen vegetables sold in local market were assayed and the correlation between the antioxidant capacity and the antioxidant compounds were further analyzed. The ORAC assay utilizes Fluorescein as the fluorescent probe, its optimum excitation and emission wavelengths were 490 nm and 510 nm respectively. During the assay, the sample and the probe were mixed first and incubated at 37℃for 5 min in darkness, then the free radical generating compound AAPH was added to initiate the reaction. The changes in fluorescence with time were monitored with a spectro- fluorometer until the fluorescence dropped to less than 1% of the initial value. The area under the fluorescence curve(AUC)was then used to calculate the antioxidant capacity of the sample. The ORAC assay system was not affected by the presence of 5% methanol or 2% acetone; however, the decline of fluorescence was strongly interfered by the presence of 0.5% ethanol in the system. Ten phytochemicals commonly found in vegetables, including ascorbic acid, chlorogenic acid, gallic acid, catechin, luteolin, myricetin, rutin, kaempferol, apigenin, and quecertin were assayed by the ORAC method and all of them gave good linear correlations between concentration and AUC, indicating the validity of the ORAC assay. Based on the curves of fluorescence decline obtained from these ten compounds, three types of pattern could be distinguished, probably representing different mode of antioxidation reaction by these compounds. The FCR assay utilize the Folin-Ciocalteu reagent as reactant, it undergo oxidation reaction with phenolics or other compounds having reducing capacities under alkaline condition. Both gallic acid and Trolox gave good linear correlations by the FCR assay, indicating the method was suitable for antioxidant assay. By using Trolox as the mutual reference compound, the ten phytochemicals were assayed by three antioxidant capacity assays: the FCR, the ORAC and the DPPH assay; and the resulting relative antioxidant capacities were compared for consistency. The ORAC assay was found to be able to react with different types of antioxidant, and the results were highly representative of the antioxidant capacity of the system. The FCR assay showed preference for water soluble compounds, but also gave comparable results with the ORAC assay. The DPPH assay was less consistent with the other two assays and was less responsive to compounds with higher antioxidant capacity. Onion powders extracted with methanol containing 1.2 N HCl at 90℃for two hours gave the highest antioxidant capacity by all three assay methods. This extraction condition was used to obtain extracts from 16 vegetables commonly found in local market, and they were assayed for antioxidant capacity by the ORAC, the FCR and the DPPH assay. In the DPPH assay, over 95% free radical scavenging capacity was obtained for all vegetable samples, suggesting the inability of this assay in distinguishing the antioxidant capacities among different vegetables. On the other hand, both the FCR and the ORAC assay gave different results for different vegetables. Vegetables that showed the highest antioxidant capacity were okra, sweetpotato leaf and Chinese parsley by the FCR assay; and sweetpotato, Chinese parsley and leaf lettuce by the ORAC assay. The absolute antioxdant capacity were between 300~1500 μmol TE・g-1,by the FCR assay and between 100~800 μmol TE・g-1 by the ORAC assay. Statistical analyses were carried out with data from the results of antioxidant capacity assay of 16 vegetables and the contents of ascorbic acid and 6 individual flavonoids. The result showed that there was a significant correlation, r=0.77, between the ORAC assay and the FCR assay, indicating the consistency of these two assays in measuring the antioxidant capacity of the sample. The correlation coefficient between ascorbic acid content and the ORAC assay and the FCR assay were 0.73 and 0.62 respectively, indicating the dominant role of ascorbic acid played in the antioxidant capacity of vegetables. The relationship between antioxidant capacity and antioxidant compounds were further analyzed with multiple linear regression. The best multiple linear regression equation for the ORAC assay showed that ascorbic acid was the major component, and the best multiple linear regression equation for the FCR assay showed that ascorbic acid, quecertin and apigenin were the important factors. The result also showed that ascorbic acid was involved in the antioxidant capacity in all 16 vegetable studied. Results of this study indicated that both the ORAC assay and the FCR assay could distinguish the antioxidant capacity of different vegetable correctly and therefore were considered as the recommended method for antioxidant capacity assay for horticultural products in the future.
Harrington, Whitney Leigh. "The Effects of Roasting Time and Temperature on the Antioxidant Capacity of Cocoa Beans from Dominican Republic, Ecuador, Haiti, Indonesia, and Ivory Coast." 2011. http://trace.tennessee.edu/utk_gradthes/976.
Full textRanamukhaarachchi, Sahan. "Production and fractionation of antioxidant peptides from soy protein isolate using sequential membrane ultrafiltration and nanofiltration." Thesis, 2012. http://hdl.handle.net/10012/6620.
Full textHambira, Chipo. "Proanthocyanidins, anthocyanins and phenolic acids in food barleys of diverse origin." 2010. http://hdl.handle.net/1993/3841.
Full textEversley, Tiffany C. "Le potentiel antioxydant de l’alimentation tel qu'estimé par le score ORAC : une comparaison des apports des personnes âgées avec démence du type Alzheimer avec ceux des témoins sans problèmes cognitifs." Thèse, 2012. http://hdl.handle.net/1866/8489.
Full textOxidative stress and the formation of free radicals are involved in several mechanisms of neuronal death that are characteristic of Alzheimer's disease. Antioxidants are known to help defend against oxidative stress and may protect against the development of Alzheimer's disease. This study aims to evaluate the antioxidant potential, using the “oxygen radical absorbance capacity” (ORAC) score of the diet of older adults people with Alzheimer's disease compared with cognitively-intact age-matched controls. It was hypothesized that the antioxidant potential of the diet of elderly people with Alzheimer's disease will be lower than that of controls without cognitive problems. The current study is a secondary analysis of data obtained from the "Nutrition-Memory study" (NMS). The NMS study recruited forty-two patients with probable Alzheimer’s disease, and their caregivers, and followed them over a period of eighteen months. The current study focuses on three days of dietary data collection, compiled at the beginning (T0) of the NMS study. The antioxidant potential of the diet was determined using the list of ORAC scores highlighted in the USDA database for the oxygen radical absorbance capacity of selected foods. Our results showed that the diet of patients (13784.07 ± 7372.70 μmol TE/100g) had a lower antioxidant potential than that of controls (± 23220.54 10862.55 μmol TE/100g). Moreover, BMI, education and group-status were factors that influenced the total ORAC score. Eating foods rich in antioxidants is a low risk preventative behaviour that could benefit individuals susceptible to developing Alzheimer’s disease.
Duro, Lia Susana Lourenço Simões. "Métodos para a determinação do potencial antioxidante dos frutos." Master's thesis, 2016. http://hdl.handle.net/10451/34615.
Full textAs polpas e os extratos de frutos têm sido identificados como fontes potenciais de grande atividade antioxidante. Tendo em conta que o stress oxidativo foi descrito como estando envolvido em patologias degenerativas, tais como o cancro, Parkinson, Alzheimer, doenças cardiovasculares e doenças autoimunes, atualmente efetuam-se diversos estudos, a fim de verificar e comprovar a atividade antioxidante de frutos e de outros alimentos na prevenção dessas doenças. Para avaliar a atividade antioxidante dos frutos, podem ser utilizados, individualmente ou em conjunto, diversos métodos. Neste contexto, apresenta-se uma revisão dos métodos mais utilizados na avaliação do potencial antioxidante dos frutos, nomeadamente por remoção de um radical peroxil (ORAC, Oxygen Radical Absorbance Capacity e TRAP, Total Reactive Antioxidant Potential), pela capacidade de redução de um metal (FRAP, Ferric Reducing Antioxidant Power e CUPRAC, Cupric ion Reducing Antioxidant Capacity), pela capacidade de remoção de um radical orgânico (ABTS, método do ácido 2,2'-azino-bis-3-etilbenzotiazolina-6-sulfónico e DPPH, método do 2,2-difenil-1-picril-hidrazil) e pela quantificação de produtos formados durante a oxidação de lípidos (TBARS, Thiobarbituric Acid Reactive Substances, oxidação das lipoproteínas de baixa densidade (LDL, Low Density Lipoprotein) e co-oxidação do β-caroteno). Apresentam-se também as vantagens e as desvantagens de cada um dos métodos.
Fruit pulp and fruit extracts have been identified as potential great sources of antioxidant activity. Although oxidative stress has been previously described as being involved in degenerative diseases such as cancer, Parkinson's, Alzheimer's, cardiovascular diseases and autoimmune diseases, there are currently several studies being performed in order to verify and confirm the antioxidant activity of fruits and other foods for the prevention of these diseases. Several methods may be used, individually or together, to evaluate the antioxidant activity in fruits. In this report, the author comprehensively reviews the literature regarding the methods used in the evaluation of the fruit antioxidant potential, namely by removal of a peroxyl radical (ORAC, Oxygen Radical Absorbance Capacity and TRAP, Total Reactive Antioxidant Potential), by the capacity of reduction of a metal (FRAP, Ferric Reducing Antioxidant Power and CUPRAC, Cupric ion Reducing Antioxidant Capacity), by the ability to remove an organic radical (ABTS, 2,2′-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid method and DPPH, 2,2- diphenyl-1-picril – hydrazyl method) and by the quantification of the products formed during the oxidation of lipids (TBARS, Thiobarbituric Acid Reactive Substances, LDL oxidation and Co-oxidation of β-carotene). The author also presents advantages and disadvantages of each method.