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Encapsulação de carotenoides em matrizes de amilose por diferentes processos: formação de criogéis, ultrassom e precipitação em meio ácido / Encapsulación de carotenoides en matrices de amilosa por diferentes procesos: formación de criogeles, ultrasonido y precipitación en medio ácidoPérez-Monterroza, Ezequiel José 26 February 2018 (has links)
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Previous issue date: 2018-02-26 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / O amido é ideal como material de parede na preparação de sistemas de liberação controlada, é barato e considerado GRAS. O amido está constituído por dois biopolímeros de D-glicose, a amilose e a amilopectina, as quais representam 99 % da matéria seca do grânulo. A amilose tem a capacidade de formar complexos com algumas moléculas hidrofóbicas como flavors e ácidos graxos, os quais são capazes de resistir a variações de pH e temperaturas elevadas, tornando-se interessante para a formulação de sistemas de liberação controlada de nutrientes. O objetivo inicial deste projeto foi a utilização de amilose extraída da mandioca e do amido de milho com alto teor de amilose comercial (Hylon VII, 72% de amilose) com o intuito de encapsular bixina e avaliar a formação de complexos de inclusão de V-amilose, bem como a sua caracterização usando difração de raios X (DRX), calorimetria exploratória de varredura, espectroscopia de infravermelho, microscopia eletrônica de varredura (MEV), cor, teor de bixina encapsulado, ensaios reológicos oscilatórios e capacidade de liberação. Foram estudados os efeitos das condições de processo de encapsulação por precipitação em solução ácida e através do tratamento com ultrassom sobre as interações entre a bixina e o amido. O efeito da proteína de soro de leite sobre o processo de encapsulação por precipitação em solução ácida também foi estudado. Finalmente, foi realizado um estudo de otimização usando a metodologia de superfície de resposta para selecionar as melhores condições em ambos os métodos, maximizando a capacidade de carga interior da matriz de amido. Além disso, pelo fato de que os xerogéis e criogéis de amido têm ganhado interesse na indústria como sistemas para a microencapsulação de compostos bioativos, este trabalho também explora a capacidade da amilose de mandioca para encapsular carotenoides usando essas metodologias. Nesse caso foram usados como moléculas-hóspedes os carotenoides presentes no óleo de abacate, luteína e neoxantina. Os resultados da encapsulação da bixina usando Hylon VII e proteína por precipitação de uma solução ácida mostraram que existe interação entre a proteína de soro de leite, o Hylon VII e a bixina, como foi observado na análise por FT-IR, no entanto, os padrões de difração e a análise por DSC não confirmaram a formação de complexos de inclusão do tipo V-amilose com a bixina. Porém, transições endotérmicas com ponto de fusão em 117,2, 105 e 104 °C foram observadas nas amostras preparadas a 90 °C com 0%, 10% e 20% de proteína, respectivamente. Cabe ressaltar que um aumento no conteúdo de proteína causou uma diminuição na entalpia de fusão desta estrutura, assim como um decréscimo em sua cristalinidade relativa, o qual foi causado provavelmente pela interação entre a bixina e a proteína. No grupo das amostras preparadas a 90 °C, o aumento no conteúdo de proteína resultou em uma tendência a aumentar o conteúdo e bixina encapsulado. Os resultados de FT-IR mostraram que as bandas de absorção associadas com as vibrações do grupo -C=C- desaparecem, indicando restrição da cadeia da bixina na matriz, assim como o aumento da disponibilidade para interagir com a proteína, embora, essas interações pareçam ser poucas a altas temperaturas. Os padrões de liberação da bixina foram afetados pelo conteúdo de proteína e a temperatura usada no processo de encapsulação, resultando em diferentes porcentagens de liberação. Nos ensaios de encapsulação da bixina com ultrassom foi avaliado o efeito do tratamento sobre as interações amido-bixina. Os resultados por DSC e DRX não confirmaram a formação de complexos de inclusão tipo V-amilose, no entanto, a análise por FT-IR indicou que as bandas de absorção do grupo funcional -C=O da bixina desapareceram depois do processo de encapsulação, o que sugere a existência de interação entre a bixina e o amido. Aparentemente esta não foi encapsulada eficientemente dentro da cavidade de amilose, provavelmente pelo seu tamanho molecular. Os espectros mecânicos dos géis formados durante o processo de encapsulação por ultrassom mostraram uma leve variação dos módulos de armazenamento (G’) e de perda (G’’), com G’>G’’, indicando tratar-se de géis fracos. O maior teor de bixina encapsulado no interior da matriz foi obtido com potência de ultrassom de 150 W por 60 minutos de tratamento. As amostras submetidas ao ultrassom foram menos susceptíveis à ação do fluido intestinal simulado, provavelmente devido ao aumento das interações entre a bixina e o amido em comparação à amostra controle. Em ambos os métodos de encapsulação a morfologia das partículas apresentou superfície irregular e erodida, com protrusões provocadas pela agregação de amilose. Através da análise estatística, observou-se que nos dois métodos de preparação todos os fatores tiveram efeito significativo (p<0,05) sobre o teor de bixina, tanto na superfície como no interior da matriz de amido. Na encapsulação por precipitação em meio ácido, o maior teor de bixina na matriz foi encontrado com o tratamento a 90 °C usando amilose de mandioca junto com proteína. De forma geral, com o uso de amilose de mandioca obteve se um maior teor de bixina encapsulado no interior da matriz e este sempre aumentou com o uso de proteína. Em relação ao tratamento com ultrassom, o maior teor de bixina encapsulado no interior da matriz foi alcançado com 2% de Hylon 150 W e 20 minutos de tratamento. A eficiência de encapsulação alcançada variou de 13,1% a 62,1% e de 17,3% a 94,5% usando tratamento com ultrassom e precipitação em meio ácido, respectivamente. As condições ótimas foram de 2% Hylon, 150 W e 20 minutos para o tratamento com ultrassom. Em relação ao método por precipitação em meio ácido foram 2% amilose de mandioca com proteína, a 68 °C. Os resultados obtidos no processo de encapsulação de luteína e neoxantina usando xerogéis e criogéis de amilose de mandioca indicaram que não houve formação de complexos de inclusão do tipo V-amilose. Entanto, os padrões de difração de raios X observados são característicos deste tipo de complexos. Foi observado um leve aumento na capacidade de encapsulação nas amostras retrodegradadas a -18°C e liofilizadas. / The starch is considered safe and cheap, ideal as wall material in the formulation of delivery systems. Starch granule consists of two major types of α-glucans, amylose, and amylopectin, which represent about 99% of dry matter. Amylose and some hydrophobic molecules such as flavors and fatty acids, form amylose inclusion complexes. Amylose complexes resist to variations of pH and elevated temperature, being good candidates for the formulation of nutrient delivery systems. The initial objective of this thesis was to use high-amylose corn starch (Hylon VII, 72 % amylose) and amylose from cassava starch as wall material for the encapsulation of bixin, evaluating the formation of V-amylose inclusion complexes, and performing their characterization by using X-ray diffractometry, FT-IR spectrometry, scanning electron microscopy, oscillatory rheological tests, color, encapsulated bixin content, and release profile. The effects of process parametres used in the methods based on ultrasound treatment and precipitation in acid solution on the interaction between amylose and bixin were studied, as well as the effect of whey protein on the encapsulation process by precipitation in acid solution. The process conditions that would maximize the encapsulate bixin content inside of the starch matrix were determined by using desirability function. In addition, considering that xerogels and cryogels have gained interest as potential systems for microencapsulation of bioactive compounds and the use of silica aerogels as delivery systems has been demonstrated with success, this thesis explores the capacity of amylose from cassava starch to encapsulate carotenoids using these methodologies. In this case, the guest molecules were the carotenoids present in the avocado oil, lutein and neoxanthin. The results of FT-IR indicated that there was an interaction between protein, Hylon, and bixin in the encapsulation process by precipitation in acid medium. However, the diffraction patterns and the DSC analysis indicated no formation of V-amylose complexes. Nevertheless, although the set of samples prepared at 90°C with 0%, 10% e 20% of protein respectively, showed endothermal transitions with a melting point about 117,2º, 105º and 104°C The increase in protein content decreased the melting enthalpy and relative crystallinity, probably due to the interaction between bixin and protein. In the set of samples prepared at 90°C, the increase in protein content led to a tendency to increase the encapsulate bixin content inside the matrix. The FT-IR analysis indicated that adsorption bands associated with the vibration of the group -C=C- disappeared due to the restriction of bixin chain into starch matrix and increase in the availability to interacting with the protein. However, these interactions seem to be fewer at the higher temperature. The bixin delivery patterns were affected by protein content and temperature used in the encapsulation process, resulting in different delivery amounts. In the encapsulation of bixin by ultrasound treatment, the effect of sonication power level on the interaction between starch and bixin was studied, nevertheless, the results of DSC and Xray diffraction indicated no formation of amylose inclusion complex. The FT-IR analysis showed that adsorption bands of the -C=O group in bixin disappeared after the encapsulation process, which confirms the interaction between starch and bixin, in spite of bixin having not be entrapped efficiently inside of the amylose cavity, probably due to its molecular size. Frequency sweep tests of gels formed during ultrasound encapsulation process showed a slight frequency dependence of G’ and G” moduli with G’>G’’, with patterns correponding to weak gels. The highest bixin encapsulated content inside of matrix was reached using the combination of ultrasound power of 150 W and 60 min of treatment. The sonicated samples were less susceptible to action of simulated intestinal fluid, probably due to increases interaction between starch and bixin as compared to control sample. The particle morphology of samples prepared by both methods showed protrusions of aggregates of amylose, as well as irregular and eroded surfaces. Statistical analysis showed that in both methods, all factors had a significant effect (p<0.05) on bixin encapsulated content inside or on the surface of the matrix. In the encapsulation by precipitation in acid solution, the combination of 90 °C using amylose from cassava starch and protein leaded to the highest bixin encapsulated content. In general, amylose from cassava starch encapsulated a greater bixin content inside of matrix compared to Hylon, and the presence of protein increased this effect even more. Regarding ultrasound treatment, the combination of 2% of amylose from Hylon, and 20 min of treatment showed the highest bixin encapsulated content inside of matrix. Encapsulation efficiency ranged from 13.1% to 62.1% and 17.3% to 94.5% using ultrasound treatment and precipitation in acid solution respectively. The optimum conditions were 2% amylose, 150 W, and 20 min in the ultrasound treatment, whereas in the method by precipitation in acid solution the best conditions were 2% amylose from cassava starch with protein at 68 °C. The results obtained from DSC and FT-IR spectroscopy in the encapsulation using cryogels and xerogels indicated no formation of inclusion complexes V-type of amylose. Nevertheless, the diffraction patterns were characteristic of this type of complexes. The samples retrograded at -18 °C and dried using freeze-drying had a slightly higher encapsulation degree than the samples retrograded at 8 °C.
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Biochemistry and genetics of carotenoid composition in potato tubersOthman, Rashidi January 2009 (has links)
Potato cultivars exhibit a wide variation in skin and flesh colour due to the presence of pigments. This study established that potato cultivars differ greatly with respect to types and concentrations of carotenoids in tubers. A total of 46 cultivars were evaluated for quantitative and qualitative carotenoid composition in different growing seasons, locations, storage conditions and disease symptoms. Factors controlling carotenoid accumulation were also tested by developing an in vitro minituber system as a new high-throughput model system for carotenogenesis in potato tubers. Tuber flesh colour was found to correlate with total carotenoid content in potato cultivars grown in both New Zealand and Netherlands. The main carotenoids identified in 32 potato cultivars in New Zealand were lutein, neoxanthin, violaxanthin and β-carotene. The ratio of these carotenoids varies between cultivars. Neoxanthin was detected in only 13 cultivars (10.59 to 69.21µg/g DW); violaxanthin was found only in 1 cultivar (32.76 µg/g DW). Whereas lutein and β-carotene were found in most of the cultivars but the concentration varied from (0.00 to 160.63 µg/g DW) and (0.00 to 13.62 µg/g DW) respectively. The main carotenoids identified in 12 cultivars grown in the Netherlands were neoxanthin, violaxanthin and lutein, whereas zeaxanthin was not found in any of the cultivars analysed. Marked differences were observed between the same potato cultivars grown in New Zealand and the Netherlands. Therefore cultivars were analysed over a second growing season to assess stability in carotenoids composition. The carotenoid profiles of the potato tubers grown for two different seasons showed highly significant differences between the cultivars, the seasons, the carotenoid pigments, and all combinations of interactions, indicating the complex nature of factors influencing carotenoid composition. Reflectance colorimeter measurement of yellow hue component in this study confirmed that the higher the total carotenoid content, the greater the yellow intensity colour. Eight cultivars were grown at three locations in New Zealand and Agria and Desiree were grown at eight locations in the Netherlands to further investigate the stability of carotenoid composition. Highly significant differences were observed between the cultivars, the locations, the carotenoid pigments, and all combinations of interactions, which emphasises that changes in carotenoid composition are complex and the responses are not consistent across cultivars. Reflectance colorimeter measurement of yellow hue component confirmed the relationship between the yellow colour intensity of tuber flesh, as well as confirming the interaction between colour and locations. Disease and post harvest storage conditions markedly influenced the levels of total carotenoid, neoxanthin, violaxanthin, zeaxanthin, lutein and β-carotene in potatoes. The magnitude of these effects depends on the cultivar, time of storage, and the intensity of powdery scab symptoms. Results showed that long term storage resulted in the accumulation of neoxanthin, violaxanthin and zeaxanthin with a concomitant decreased of lutein, β-carotene and total carotenoid content. Genotypes infected with disease (lower and higher scab score) resulted in accumulation of violaxanthin, β-carotene and total carotenoid with a concomitant decreased in neoxanthin and lutein. A high-throughput model system for investigating carotenoid biogenesis in potato tubers was developed. This involved in vitro potato minitubers and was validated by assessing the effects of environmental variables, such as drought stress, light intensity and nutrient availability on carotenoid accumulation. Light influenced the presence of zeaxanthin, whereas water stress and nutrient strength influenced the accumulation of neoxanthin and violaxanthin. Although these factors had an effect on the carotenoid content and profile, the most influential factor appeared to be cultivar selection.
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Optimalizace extrakce bioaktivních látek z bylin do různých druhů méně známých olejových základů / Optimalization of the extraction of bioactive compounds from herbs into different kind of oil basesChytil, Dalibor January 2020 (has links)
This diploma thesis deals with the optimization of processes for extraction of bioactive lipophilic compounds from fruits of sea buckthorn (Hippophae Rhamnoides) into various types of plant oil bases using simple maceration. The theoretical part of this thesis deals with the characterization of this herb, its botanical classification, traditional use, chemical composition and medicinal effects. Increased attention is also paid to the characterization of individual types of plant oils used, namely camellia, camellia organic, passionflower, kukui and kiwi oil. The experimental part of the thesis deals with application of theoretical knowledge. The profile of total and free fatty acids for individual plant oil bases was determined by GC/FID, furthet the basic fat numbers were also determined. When optimizing the extraction, emphasis was placed not only on the effect of the extraction agent used, but also on the extraction time (1, 3, 5, 7, 10, 14, 21 and 66 days). The macerates were continuously subjected to the determination of selected parameters (total amount of carotenoids, total amount of phytosterols, lutein, neoxanthin, astaxanthin, stigmasterol, -sitosterol and vitamin E) using UV-VIS spectroscopy and HPLC/PDA. Likewise, the peroxide number was monitored during maceration to assess the degree of oxidative degradation of macerates. The recovery of selected total parameters in individual oils did not differ significantly in most cases. On the contrary, the yield of individual monitored parameters differed significantly. At the same time, static maceration under our conditions was not very suitable for the extraction of vitamin E, stigmasterol and total phytosterols.
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