Orientador: Marlus Chorilli / Resumo: A candidíase vulvovaginal (CVV) é o tipo mais comum de vaginite aguda entre as mulheres, causada por fungos do gênero Candida spp. A Candida albicans é a espécie responsável por 80-90% dos casos, contudo nos últimos anos, houve um aumento no número de casos envolvendo outras espécies, sendo a Candida glabrata, a segunda mais reportada e mais resistente aos tratamentos convencionais. As terapias existentes para CVV apresentam desvantagens devido aos efeitos colaterais dos agentes antifúngicos utilizados e resistência fúngica prevalente. Como alternativa, compostos naturais como o ácido p-cumárico (p-AC) vêm sendo estudados devido à sua potencial atividade antifúngica. Todavia, seu caráter lipofílico dificulta sua solubilidade em água, diminuindo sua eficácia. A incorporação do p-AC em um sistema de liberação de fármacos (SLF), como os cristais líquidos (CLs), pode auxiliar na sua administração tópica, e assim aumentar sua solubilidade, eficácia, reduzir efeitos colaterais sistêmicos e potencializar sua ação na mucosa vaginal. Dessa forma, este trabalho teve como objetivo desenvolver sistemas liquido-cristalinos com propriedades mucoadesivas para liberação controlada do ácido p-cumárico no tratamento de candidíase vulvovaginal, via administração tópica. A atividade antifúngica do p-AC foi avaliada a partir dos ensaios de concentração inibitória mínima (CIM), concentração fungicida mínima (CFM) , formação de biofilme e ensaio in vivo contra cepas de C. albicans (SC5314), C. glab... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Vulvovaginal candidiasis (VVC) is the most common type of acute vaginitis among women, caused by fungi of the genus Candida spp. Candida albicans is the species responsible for 80-90% of cases, however in recent years, there has been an increase in the number of cases involving other species, with Candida glabrata being the second most reported and most resistant to conventional treatments. Existing therapies for VVC have disadvantages due to the side effects of the antifungal agents used and the prevailing fungal resistance. As an alternative, natural compounds such as p-cumaric acid (p- CA) have been studied due to their potential antifungal activity. However, its lipophilic character hinders its solubility in water, reducing its effectiveness. The incorporation of p-CA in a drug delivery system (DDS), such as liquid crystals (LCs), can assist in its topical administration, and thus increase its solubility, effectiveness, reduce systemic side effects and enhance its activity on the vaginal mucosa. Thus, this work aimed to develop liquid-crystalline systems with mucoadhesive properties for controlled release of p-cumáric acid in the treatment of vulvovaginal candidiasis, via topical administration. The antifungal activity of p-CA was analysed by assays of minimum inhibitory concentration (MIC), minimum fungicidal concentration (MFC), biofilm formation and in vivo assay against strains of C. albicans (SC5314), C. glabrata (ATCC 2001) and C. krusei (ATCC 6528). For the develop... (Complete abstract click electronic access below) / Mestre

Palynology, the study of organic microfossils, is an important tool for improving our understanding of past environments and landscapes. Palynology provides a wealth of information from which climatic and environmental conditions can be inferred. However, inferred climatic and environmental conditions are often open to interpretation. Assumptions made about past climate conditions from pollen assemblages often rely on qualitative understanding of modern-day vegetation distributions, rather than empirical relationships. Historic anthropogenic impact on the environment must also be inferred, and assessments made as to whether vegetation changes are a result of climate change or human impact. This study seeks to address some of the questions that arise through the interpretation of pollen assemblages, by establishing empirical relationships between the geochemistry of modern pollen and climate or environmental controls. It focuses on the pollen of the climatically sensitive montane conifer Cedrus atlantica, which is distributed across the mountains of Morocco and Algeria. The study investigates aspects of modern pollen geochemistry and morphology and finds a strong relationship between the stable carbon isotope composition of modern pollen and mean annual precipitation (r2 = 0.54, p <0.001) and summer precipitation (r2 = 0.63, p <0.0001). Furthermore, a stronger relationship exists with aridity measured using the self-calibrating Palmer Drought Severity Index (r2 = 0.86, p <0.0001), suggesting that the stable carbon isotope composition of Cedrus atlantica pollen is influenced by environmental moisture availability. The study also finds there is an increased abundance of ultraviolet absorbing compounds (UACs) in modern Cedrus atlantica pollen with increasing summer UV-B flux. This relationship was evident with samples growing in their native range (r2 = 0.84, p <0.0001), but not with samples from outside this range (r2 = 0.00, p = 0.99), suggesting a possible genetic influence. Lastly, the study finds that grain size of Cedrus atlantica pollen is highly variable within and between samples, and we rule out climatic control on pollen grain size. These results suggest that quantitative relationships can be established between the geochemistry of Cedrus atlantica pollen and environmental and climatic influences. Stable carbon isotope analysis of fossil pollen could be used as a proxy for reconstruction of summer moisture availability, while analysis of UACs in fossil pollen could be used as a proxy for the reconstruction of summer UV-B flux. These proxies will enhance our understanding of climatic and environmental change in Northwest Africa and will complement existing palynological techniques for environmental and climate reconstruction. Palynology, the study of organic microfossils, is an important tool for improving our understanding of past environments and landscapes. Palynology provides a wealth of information from which climatic and environmental conditions can be inferred. However, inferred climatic and environmental conditions are often open to interpretation. Assumptions made about past climate conditions from pollen assemblages often rely on qualitative understanding of modern-day vegetation distributions, rather than empirical relationships. Historic anthropogenic impact on the environment must also be inferred, and assessments made as to whether vegetation changes are a result of climate change or human impact. This study seeks to address some of the questions that arise through the interpretation of pollen assemblages, by establishing empirical relationships between the geochemistry of modern pollen and climate or environmental controls. It focuses on the pollen of the climatically sensitive montane conifer Cedrus atlantica, which is distributed across the mountains of Morocco and Algeria. The study investigates aspects of modern pollen geochemistry and morphology and finds a strong relationship between the stable carbon isotope composition of modern pollen and mean annual precipitation (r2 = 0.54, p <0.001) and summer precipitation (r2 = 0.63, p <0.0001). Furthermore, a stronger relationship exists with aridity measured using the self-calibrating Palmer Drought Severity Index (r2 = 0.86, p <0.0001), suggesting that the stable carbon isotope composition of Cedrus atlantica pollen is influenced by environmental moisture availability. The study also finds there is an increased abundance of ultraviolet absorbing compounds (UACs) in modern Cedrus atlantica pollen with increasing summer UV-B flux. This relationship was evident with samples growing in their native range (r2 = 0.84, p <0.0001), but not with samples from outside this range (r2 = 0.00, p = 0.99), suggesting a possible genetic influence. Lastly, the study finds that grain size of Cedrus atlantica pollen is highly variable within and between samples, and we rule out climatic control on pollen grain size. These results suggest that quantitative relationships can be established between the geochemistry of Cedrus atlantica pollen and environmental and climatic influences. Stable carbon isotope analysis of fossil pollen could be used as a proxy for reconstruction of summer moisture availability, while analysis of UACs in fossil pollen could be used as a proxy for the reconstruction of summer UV-B flux. These proxies will enhance our understanding of climatic and environmental change in Northwest Africa and will complement existing palynological techniques for environmental and climate reconstruction.

Les altérations sensorielles des vins dues à la présence des levures du genre Brettanomyces se caractérisent par une augmentation de la teneur en phénols volatils tel que le 4-éthylphénol. Le premier objectif de ce travail était de faire un état des lieux sur le risque « éthylphénol » au Liban en s'intéressant à la présence d'un précurseur (acide p-coumarique), du microorganisme responsable (Brettanomyces) et du produit final (4-éthylphénol) dans les vins élaborés dans ce pays. Une forte hétérogénéité de concentrations en acide p-coumarique a été observée avec des valeurs variant de 0 à 31,4 mg.L-1. Des niveaux importants de 4-éthylphénols de l'ordre de 1,367 mg.L-1 ont été détectés sur certains vins. Un dépistage du contaminant microbien a permis de confirmer pour la première fois la présence de Brettanomyces au Liban, les proportions restant toutefois assez faibles (3 % des échantillons testés). Une étude génétique a caractérisé les souches retenues qui se sont montrées diverses au sein de l'espèce. Le travail a porté ensuite sur l'analyse cinétique des étapes réactionnelles constituant le processus enzymatique de la bioconversion des substrats acide p-coumarique et 4-vinlphénol en 4-éthylphénol pour 5 souches de Brettanomyces bruxellensis d'origines libanaises et françaises. La variabilité entre les souches s'est exprimée aux niveaux génétique et cinétique. Des profils hétérogènes de bioréaction ont été mis en évidence en fonction de la nature des souches. L'analyse du bilan-matière a révélé l'existence probable de phénomènes d'adsorption sur les parois des Brettanomyces qui sont souche-dépendants. La dernière partie a été consacrée à l'évaluation du lien entre quantité de biomasse et production de 4-éthylphénol ainsi qu'à l'influence de quelques paramètres environnementaux (pH, source d'ammonium et milieu de culture) sur la cinétique réactionnelle. / Wine sensory alterations due to the presence of Brettanomyces yeasts are characterized by an increased content of volatile phenols such as 4-ethylphenol. The first aim of this work was to make an inventory of the "ethylphenol" risks in Lebanon by focusing on the presence of one precursor (p-coumaric acid), the microorganism provoking these risks (Brettanomyces) and the final product (4-ethylphenol) in wines produced in this country. High heterogeneity of p-coumaric acid concentration was observed with values ranging from 0 to 31,4 mg.L-1. Significant levels of 4-ethylphenols of about 1,367 mg L-1 have been detected in some wines. Screening of microbial contaminants confirmed the presence of Brettanomyces for the first time in Lebanon, with proportions remaining relatively low (3 % of samples tested). A genetic study has characterized the selected strains which are shown to be various within the species. The second objective of this study was the kinetic analysis of the reaction steps constituting the bioconversion enzymatic process of both substrates p-coumaric acid and 4-vinlphenol into 4-ethylphenol for 5 strains of Brettanomyces bruxellensis of different origins (Lebanon and France). Variability between strains was expressed at both levels, genetic and kinetic. Heterogeneous bioreaction profiles were identified according to strain's nature. The mass balance analysis revealed the possible existence of adsorption phenomena on the cell walls of Brettanomyces which are strain-dependent. The last part was devoted to the evaluation of the relationship between biomass concentration and production of 4-ethylphenol as well as the influence of some environmental parameters (pH, ammonium source and culture medium) on the reaction's kinetic.

Philosophiae Doctor - PhD / The role of phenolic acids in mitigating salt stress tolerance have been well documented. However, there are contradicting reports on the effect of exogenously applied phenolic acids on the growth and development of various plants species. A general trend was observed where phenolic acids were shown to inhibit plant growth and development, with the exception of a few documented cases. One of these such cases is presented in this thesis. This study investigates the role of exogenously applied p-coumaric acid (p-CA) on physio-biochemical and molecular responses of chia seedlings under salt stress. This study is divided into three parts. Part one (Chapter 3) focuses on the impact of exogenous p-coumaric acid on the growth and development of chia seedlings. In this section, chia seedlings were supplemented with exogenous p-CA and the various biochemical and plant growth parameters were measured. The results showed that exogenous p-CA enhanced the growth of chia seedlings. An increase in chlorophyll, proline and superoxide oxide contents were also observed in the p-CA treatment relative to the control. We suggested that the increase in chia seedling growth could possibly be via the activation of reactive oxygen species-signalling pathway involving O2− under the control of proline accumulation (Chapter 3). Given the allopathy, nature of p-coumaric acid it is noteworthy that the response observed in this study may be species dependent, as contrasting responses have been reported in other plant species. Part two (Chapter 4) of this study investigates the influence of piperonylic acid (an inhibitor of endogenous p-coumaric acid) on the growth and development of chia seedlings. In trying to illustrate whether p-CA does play a regulatory role in enhancing pseudocereal plant growth, we treated chia seedlings with the irreversible inhibitor of C4H enzyme, to inhibit the biosynthesis of endogenous p-CA. In this section, chia seedlings were treated with piperonylic acid and changes in plant growth, ROS-induced oxidative damage, p-CA content and antioxidant capacity was monitored. Inhibition of endogenous p-CA restricted chia seedling growth by enhancing ROS-induced oxidative damage as seen for increased levels of superoxide, hydrogen peroxide and the extent of lipid peroxidation. Although an increase in antioxidant activity was observed in response to piperonylic acid, this increase was not sufficient to scavenge the ROS molecules to prevent oxidative damage and ultimate cellular death manifested as reduced plant growth. The results presented in this section support our hypothesis that p-CA play an important regulatory role in enhancing chia seedling growth and development as shown in Chapter 3. Part three (Chapter 5) seeks to identify and functionally characterise p-coumaric acid induced putative protein biomarkers under salt stress conditions in chia seedlings. Previous studies have shown that p-CA reversing the negative effect caused by NaCl-induced salt stress. While these studies were able to demonstrate the involvement of p-CA in promoting plant growth under salt stress conditions, they focussed primarily on the physiological aspect, which lacks in-depth biochemical and molecular analysis (ionomic and proteomic data) which could help in detecting the genes/proteins involved in salt stress tolerance mechanisms. A comparative ionomics and proteomic study was conducted, with the aim of elucidating the pivotal roles of essential macro elements and/or key protein markers involved in p-CA induced salt stress tolerance in chia seedlings. With the exception of Na, all the other macro elements were decreased in the salt treatment. Contrary to what was observed for the salt treatment most of the macro elements were increased in the p-CA treatment. However, the addition of exogenous p-CA to salt stressed seedlings showed an increase in essential macro elements such as Mg and Ca which have been shown to play a key role in plant growth and development. In the proteomic analysis we identified 907 proteins associated with shoots across all treatments. Interestingly, only eight proteins were conserved amongst all treatments. A total of 79 proteins were unique to the p-CA, 26 to the combination treatment (NaCl + p-CA) and only two proteins were unique to the salt stress treatment. The unique proteins identified in each of the treatments were functionally characterised to various subcellular compartments and biological processes. Most of the positively identified proteins were localised to the chloroplast and plays key roles in photosynthesis, transportation, stress responses and signal transduction pathways. Moreover, the protein biomarkers identified in this study (especially in the p-CA treatment) are putative candidates for genetic improvement of salt stress tolerance in plants.

In our pervious study, the ethanol extracts from Eupatorium fortunei Turcz at concentrations of 200 ÷ 500 mg L-1 significantly inhibited the growth of Microcystis aeruginosa, which is the most common species, responsible for toxic cyanobacteria blooming in fresh water. o-Coumaric acid (or 2-hydroxy-cinnamic acid) isolated from E. fortunei was tested its growth-inhibitory effect on M. aeruginosa and Chlorella vulgaris at the concentrations of 1.0, 10.0 and 100.0 mg L-1 in the 96- hour experiment by the optical density and the analytical method of chlorophyll a concentration. Results indicated that the compound strongly affected towards M. aeruginosa at the concentration of 100.0 mg L-1 with the inhibition efficiency (IE) values of 76.76 % and 84.66 %, respectively while those for C. vulgaris were lower just of 60.59%, and 74.53 %, respectively. The obtained data demonstrated that two methods were highly consistent and o- coumaric acid was more toxic to M. aeruginosa than C. vulgaris at all tested concentrations (p<0.05). The images of M. aeruginosa and C. vulgaris cells under the light microscope clearly showed the damage of these cells under the attck of o-coumaric acid. Although o-coumaric compound was widely demonstrated antibacterial properties in previous reports, to the best of our knowledge, our study was the first report about effect of o- coumaric acid on the growth of M. aeruginosa and C. vulgaris. / Những nghiên cứu trước đây đã chỉ ra rằng cao chiết etanol từ cây Mần tưới Eupatorium fortune Turcz tại dải nồng độ 200 ÷ 500 μg mL-1 ức chế mạnh sinh trưởng của Microcystis aeruginosa, - loài phổ biến nhất gây nên sự bùng nổ tảo độc trong hệ sinh thái nước ngọt. o-Coumaric axit (hay 2-hydroxy-cinnamic axit) phân lập từ E. fortune được tiến hành đánh giá ảnh hưởng lên sinh trưởng của hai loài M. aeruginosa và Chlorella vulgaris tại ba nồng độ là 1.0, 10.0 and 100.0 mg L-1 trong thời gian 96 giờ thực nghiệm theo phương pháp đo mật độ quang và phân tích hàm lượng chlorophyll a. Kết quả nghiên cứu cho thấy sau 96 giờ phơi nhiễm tại nồng độ 100 mg L-1 hoạt chất ức chế mạnh tới M. aeruginosa với giá trị ức chế sinh trưởng (IE) tương ứng là 76.76 và 84.66%. Giá trị IE đối với C.vulgaris ghi nhận thấp hơn chỉ là 60.65 và 74.53%, tương ứng. Hai phương pháp phân tích trên có tính nhất quán cao và o-coumaric ức chế sinh trưởng lên loài M.aeruginosa mạnh hơn so với loài C.vulgaris tại tất cả các nồng độ nghiên cứu (p<0.05). Ảnh chụp các tế bào M.aeruginosa và C.vulgaris dưới kính hiển vi điện tử đã chứng minh những tổn thương của tế bào dưới tác động của o-coumaric axit. Mặc dù o- coumaric cho thấy đặc tính chống khuẩn cao trong các công bố trước đây, nhưng theo hiểu biết của chúng tôi đây là nghiên cứu đầu tiên công bố về ảnh hưởng của hoạt chất o-coumaric axit lên sinh trưởng của M. aeruginosa và C. vulgaris.

Biologiska processer hos olika organismer påverkas av ultraviolett-B-strålning (UV-B). Kunskapen om förändringar i UV-B-flödet som nått planetens yta under det geologiska tidsspann sedan flercelligt liv uppstod är dock begränsad. Följaktligen har olika biologiska proxies använts som ett sätt att försöka rekonstruera UV-B-flödet som når jordens yta. Växter reagerar på fluktuationen av UV-B genom att variera produktionen av fenolföreningar såsom parakumarsyra (pCA) och ferulinsyra, och därför kan dessa beståndsdelar användas som UV-B-proxys. UV-B-absorberande föreningar (UAC) finns i växternas yttersta skikt, den så kallade kutikulan men även i pollen och sporer, vilka oftaär välbevarade i det geologiska arkivet. Ändå är användningen av kutikula som UV-B-proxy inte lika undersökt. Därför syftar denna magisteruppsats till att analysera kemiska förändringar i fossila växters från trias – jura-gränsen (c. 200 miljoner år gamla)  och deras potential som UV-B-proxys. Eftersom de fossila löven behövde rengöras från sediment och från förkolnat mesofyll, gjordes också en analys av de kemiska förändringarna som orsakades av de olika rengöringsstegen. Icke-destruktiva tekniker, som mikro-FTIR och konfokalt Raman-mikroskop, användes för analysen. Försöken visade att analysen endast kunde utföras med mikro-FTIR på grund av den höga auto-fluorescensen hos de fossila bladen  vilketförhindrade analys med Raman. Signifikanta förändringar orsakades då Schulzes reagens användes för borttagning av mesofyllet, vilket ledde till nitrering av kutikulan. Ett mindre aggressivt och mer hållbart alternativ till denna process har visat sig vara väteperoxid, vilket orsakade mindre förändringar av den fossila kutikulans kemiska sammansättning. Dessutom upptäcktes indikation på förekomst av UAC endast i Ginkgoites regnellii, vilket indikerar att eventuell nedbrytning av dessa föreningar inträffade under diagenesen av de andra analyserade fossilerna. / Biological processes of different organisms are impacted by ultraviolet-B radiation (UV-B). However, knowledge about alterations in the UV-B flux reaching the planet’s surface during the geological past is limited. Consequently, different biological proxies have been used as an approach to attempt reconstructing the UV-B flux reaching Earth’s surface. Plants respond to the fluctuation of UV-B by varying the production of phenolic compounds such as p-coumaric acid (pCA) and ferulic acid, and therefore these constituents can be used as UV-B proxies. UV-B-absorbing compounds (UACs) can be found in the cuticle, pollen, and spores, which are all well-preserved in the geological record. Nevertheless, the use of cuticles as UV-B proxy is not as explored. Hence, this Master’s thesis aimed to analyse chemical changes in the plant cuticles from the Triassic–Jurassic boundary and their potential as UV-B proxies. Moreover, as the cuticles needed to be cleaned from rocks and isolated from coalified mesophyll, an analysis of the chemical changes caused by the cleaning steps was also done. Non-destructive techniques, as micro-FTIR and confocal Raman microscope, were used for the analysis.  Yet, the analysis could only be conducted with micro-FTIR due to auto-fluorescence of the leaves preventing success with Raman. Main changes during the cleaning steps were caused using Schulze’s reagent, which led to nitration of the cuticles. A less aggressive and more sustainable alternative to this process is shown to be hydrogen peroxide, which caused minor alteration of the fossil cuticle’s chemical composition.  Moreover, indication of the presence of UACs was detected only in Ginkgoites regnellii, indicating that possible degradation of these compounds occurred during diagenesis of the other fossils analysed.

Tesis por compendio / [ES] Se han desarrollado mediante termoprocesado películas multicapa biodegradables activas para el envasado de alimentos, combinando películas de almidón mejoradas y de una mezcla de poliésteres (PLA-PHBV), con diferentes ácidos fenólicos (ferúlico, p-cumárico y protocatecuico). En las películas almidón de yuca o de maíz se incorporaron gomas de origen microbiano (xantana y gelano) (10%) para mejorar sus propiedades funcionales. Las gomas mejoraron las propiedades mecánicas y de barrera al vapor de agua y al oxígeno de los films de almidón. Estos films se combinaron con films mezcla de PLA:PHBV en bicapas almidón-poliésteres por termocompresión. Las bicapas presentaron una alta capacidad barrera al oxígeno y al vapor de agua comparado con sus respectivas monocapas. La capa de poliéster contribuyó al refuerzo mecánico de la bicapa, aportando alta capacidad de barrera al vapor de agua, mientras que la capa de almidón aportó alta capacidad de barrera al oxígeno a la bicapa. La bicapa con almidón de yuca y goma gelano presentó la mejor adhesión entre capas, con propiedades funcionales adecuadas para el envasado de alimentos. Los ácidos ferúlico, p-cumárico y protocatecuico, con propiedades antimicrobianas y antioxidantes, se incorporaron (2%) en los films mezcla de PLA:PHBV para obtener films activos. Los ácidos fenólicos modificaron positivamente las propiedades de la mezcla de poliésteres, incrementando su módulo de elasticidad y resistencia a la fractura y su capacidad de barrera al vapor de agua y al oxígeno, al tiempo que aumentaron levemente la Tg del material. El ácido protocatecuico provocó los mayores efectos, afectando a la cristalización del PHBV. La liberación de estos compuestos en diferentes simulantes alimentarios (con polaridad alta e intermedia) fue muy limitada en cuanto a velocidad y cantidad liberada, lo que disminuyó la capacidad de las películas para inhibir de forma significativa el crecimiento de Listeria innocua inoculada en medio de cultivo. Estos films, con y sin compuestos activos, se desintegraron en condiciones de compostaje, sin efecto significativo de los ácidos fenólicos. Los films sin activos y con ácido ferúlico se biodegradaron completamente después de 20 días de compostaje, mientras que los films que contenían ácido p-cumárico y protocatecuico lo hicieron en 21 y 26 días, respectivamente. Por lo tanto, ninguno de los ácidos fenólicos incorporados inhibió el proceso de biodegradación, pero se retardó el proceso, dependiendo del grado de retención del compuesto en la matriz polimérica. Los films bicapa biodegradables constituidos por una capa de almidón-gelano y otra de PLA:PHBV, con y sin ácidos fenólicos, se caracterizaron en sus propiedades mecánicas y de barrera al vapor de agua y al oxígeno y se utilizaron para el envasado de carne de cerdo, evaluando su calidad durante el almacenamiento a 5 °C. La presencia de ácidos fenólicos disminuyó el módulo elástico y la tensión de fractura de las bicapas y mejoró su capacidad de barrera al vapor de agua y al oxígeno. Esto último, junto al efecto activo de los ácidos, contribuyó a mejorar la conservación de la carne durante el almacenamiento, reduciendo los niveles de oxidación lipídica, cambios de pH y pérdidas de peso de las muestras envasadas, así como el crecimiento microbiano, especialmente coliformes totales y bacterias ácido-lácticas. Los films bicapa biodegradables con ácidos fenólicos, a base de almidón y poliésteres, se muestran como una estrategia adecuada para obtener materiales de envasado activo, con propiedades funcionales próximas a las de algunos plásticos sintéticos comúnmente utilizados en el envasado de alimentos. Estos materiales pueden alargar la vida útil de los alimentos, mitigando el impacto ambiental de los envases plásticos ya que pueden ser compostados. / [CA] S'han desenvolupat, mitjançant termoprocesat, pel·lícules multicapa biodegradables actives per a l'envasament d'aliments, combinant pel·lícules de midó millorades i d'una mescla de polièsters (PLA-PHBV), amb diferents àcids fenòlics (ferúlic, p-cumàric i protocatecuic). En les pel·lícules midó de iuca o de dacsa es van incorporar gomes d'origen microbià (xantana i gellan) (10%) per a millorar les seues propietats funcionals. Les gomes van millorar les propietats mecàniques i de barrera al vapor d'aigua i a l'oxigen dels films de midó. Aquests films es van combinar amb films mescla de PLA:PHBV en bicapes midó-polièsters per termocompresió. Les bicapes van presentar una alta capacitat barrera a l'oxigen i al vapor d'aigua comparat amb les respectives monocapes. La capa de polièster va contribuir al reforç mecànic de la bicapa, aportant alta capacitat de barrera al vapor d'aigua, mentre que la capa de midó va aportar alta capacitat de barrera a l'oxigen a la bicapa. La bicapa amb midó de iuca i goma gellan va presentar la millor adhesió entre capes, amb propietats funcionals adequades per a l'envasament d'aliments. Els àcids ferúlic, p-cumàric i protocatecuic, amb propietats antimicrobianes i antioxidants, es van incorporar (2%) en els films mescla de PLA:PHBV per a obtindre films actius. Els àcids fenòlics van modificar positivament les propietats de la mescla de polièsters, incrementant el seu mòdul d'elasticitat i resistència a la fractura i la seua capacitat de barrera al vapor d'aigua i a l'oxigen, al mateix temps que van augmentar lleument la Tg del material. L'àcid protocatecuic va provocar els majors efectes, afectant la cristal·lització del PHBV. L'alliberament d'aquests compostos en diferents simulants alimentaris (amb polaritat alta i intermèdia) va ser molt limitada en quant a velocitat i quantitat alliberada, la qual cosa va disminuir la capacitat de les pel·lícules per a inhibir de manera significativa el creixement de Listeria innocua inoculada en medi de cultiu. Aquests films, amb i sense compostos actius, es van desintegrar en condicions de compostatge, sense efecte significatiu dels àcids fenòlics. Els films sense actius i amb àcid ferúlic es biodegradaren completament després de 20 dies de compostatge, mentre que els films que contenien àcid p-cumàric i protocatecuic ho van fer en 21 i 26 dies, respectivament. Per tant, cap dels àcids fenòlics incorporats va inhibir el procés de biodegradació, però es va retardar el procés, depenent del grau de retenció del compost en la matriu polimèrica. Els films bicapa biodegradables constituïts per una capa de midó-gellan i una altra de PLA:PHBV, amb i sense àcids fenòlics es van caracteritzar en les seues propietats mecàniques i de barrera al vapor d'aigua i a l'oxigen i es van utilitzar per a l'envasament de carn de porc, avaluant la qualitat a llarg del emmagatzematge a 5 °C. La presència d'àcids fenòlics va disminuir el mòdul elàstic i la tensió de fractura de les bicapes i va millorar la seua capacitat de barrera al vapor d'aigua i a l'oxigen. Això últim, junt a l'efecte actiu dels àcids, va contribuir a millorar la conservació de la carn durant l'emmagatzematge, reduint els nivells d'oxidació lipídica, canvis de pH i pèrdues de pes de les mostres envasades, així com el creixement microbià, especialment coliformes totals i bacteris àcid-làctics. Els films bicapa biodegradables amb àcids fenòlics, a base de midó i polièsters, es mostren com una estratègia adequada per a obtindre materials d'envasament actiu, amb propietats funcionals pròximes a les d'alguns plàstics sintètics comunament utilitzats en l'envasament d'aliments. Aquests materials poden allargar la vida útil dels aliments, mitigant l'impacte ambiental dels envasos plàstics ja que poden ser compostats. / [EN] Active biodegradable multilayer films have been developed by thermoprocessing for food packaging purposes, combining improved starch films and a blend of polyesters (PLA-PHBV), with different phenolic acids (ferulic, p-coumaric and protocatechuic). Into the cassava or maize starch films, gums of microbial origin (xanthan and gellan) were incorporated (10%) to improve their functional properties. The gums improved the mechanical and barrier properties to water vapor and oxygen of the starch films. These films were combined with PLA:PHBV blend films in starch-polyester bilayers by thermocompression. The bilayers exhibited high barrier capacity to oxygen and water vapor compared to their respective monolayers. The polyester layer contributes to the mechanical reinforcement of the bilayer, providing high water vapor barrier capacity, while the starch layer provided high oxygen barrier capacity to the bilayer. The bilayer with cassava starch and gellan gum showed the best interlayer adhesion, with adequate functional properties for food packaging applications. Ferulic, p-coumaric and protocatechuic acids, with antimicrobial and antioxidant properties, were incorporated (2%) in the PLA: PHBV blend films to obtain active films. Phenolic acids positively modified the properties of the polyester blend, increasing its elastic modulus and resistance to break and its barrier capacity to water vapor and oxygen, while slightly increasing the Tg of the material. Protocatechuic acid caused the greatest effects, affecting the crystallization of PHBV. The release of these compounds in different food simulants (with high and intermediate polarity) was very limited in terms of release rate and released amount, which reduced the ability of the films to significantly inhibit the growth of Listeria innocua inoculated in culture medium. These films, with and without active compounds, disintegrated under composting conditions, without significant effect of phenolic acids. Films without active compounds and with ferulic acid biodegraded completely after 20 days of composting, whereas films containing p-coumaric and protocatechuic acids did so in 21 and 26 days, respectively. Therefore, none of the incorporated phenolic acids inhibited the biodegradation process, but the process was delayed, depending on the degree of retention of the compound in the polymeric matrix. The biodegradable bilayer films with a layer of starch-gellan and another of PLA: PHBV, with and without phenolic acids, were characterized as to their mechanical properties and barrier capacity to water vapor and oxygen and were used for packaging of pork meat whose quality development was analysed throughout storage time at 5 °C. The presence of phenolic acids decreased the elastic modulus and resistance to break of the bilayers and improved their barrier capacity to water vapor and oxygen. The latter, together with the active effect of the acids, contributed to improving the preservation of the meat during storage, reducing the levels of lipid oxidation, changes in pH and weight losses of the packed samples, as well as microbial growth, especially total coliforms and lactic acid bacteria. Biodegradable bilayer films with phenolic acids, based on starch and polyesters, appeared as a suitable strategy to obtain active packaging materials, with functional properties close to those of some synthetic plastics commonly used in food packaging. These materials can extend the shelf-life of foods, mitigating the environmental impact of plastic packaging since they can be composted. / The authors would like to thank the Ministerio de Ciencia e Innovación of Spain, for funding this study through the Project AGL2016-76699-R and PID2019-105207RB-I00, and the predoctoral research grant # BES-2017-082040 / Hernández García, E. (2022). Biodegradable Multilayer Films for Active Food Packaging, Based on Starch and Polyesters with Phenolic Acids [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/181473 / TESIS / Compendio

The present Doctoral Thesis focuses on the investigation, characterization and influence of polyacrylic materials in different scientific and technological disciplines via a detailed computer simulation using the Molecular Dynamics (MD) technique, in conjunction with the very accurate, all-atom Dreiding force-field. The main research concepts and objectives are discussed and analyzed in three separate parts. In the first part, atomistic configurations of two model pressure-sensitive acrylic adhesives (PSAs), the atactic homopolymer poly(n-BA) [poly(n-butyl acrylate)] and the atactic copolymer poly(n-BA-co-AA) [poly(n-butyl acrylate-co-acrylic acid)] in the bulk phase or confined between two selected substrates, glassy silica (SiO2) and metallic α-ferrite (α-Fe), were built and simulated by MD in the NPT statistical ensemble. First, an equilibration cycle consisting of temperature annealings and coolings was followed, in order to generate well-equilibrated configurations of the PSA systems. Detailed results from the atomistic simulations are presented concerning their volumetric behavior, glass transition temperature, conformational, structural, viscoelastic and dynamic properties. Particular emphasis was given to the analysis and characterization of the hydrogen bonds that form in the poly(n-BA-co-AA) system. By analyzing the MD trajectories, poly(n-BA-co-AA) was found to exhibit a higher density than poly(n-BA) by about 7% at all temperatures, to be characterized by smaller-size chains for a given molecular weight (MW), to exhibit significantly slower terminal and segmental dynamics properties, and to be characterized by a glass transition temperature that was approximately 40% higher than that of poly(n-BA). We also examined the type and degree of adsorption of the two acrylic systems on the selected substrates by analyzing the MD results for the local mass density as a function of distance from the solid plane and the distribution of adsorbed chain segments in train, loop, and tail conformations, and by computing the work of adhesion at the two substrates. The results revealed a stronger adsorption for both acrylics on the SiO2 surface due to highly attractive interactions between polymer molecules and substrate atoms, and as a consequence a higher value for the work of adhesion compared to that on the α-Fe surface. Furthermore, we have developed a generalized non-equilibrium molecular dynamics (NEMD) algorithm to simulate the mechanical response of the two adhesives under a uniaxial stretching deformation. In the second part of the Thesis, results have been obtained from a hierarchical simulation methodology that led to the prediction of the thermodynamic, conformational, structural, dynamic and mechanical properties of two polymer nanocomposites based on syndiotactic poly(methyl methacrylate) or sPMMA. The first was reinforced with uniformly dispersed graphene sheets and the second with fullerene particles. How graphene functionalization affects the elastic constants of the resulting nanocomposite has also been examined. The phase behavior of the nanocomposite (in particular as we varied the relative size between the sPMMA chains and the diameter of fullerene molecules) has also been studied as a function of fullerene volume fraction. The simulation strategy entailed three steps: 1) Generation of an initial structure, which was then subjected to potential energy minimization and detailed molecular dynamics (MD) simulations at T = 500K and P = 1atm to obtain well relaxed melt configurations of the nanocomposite. 2) Gradual cooling of selected configurations down to room temperature to obtain a good number of structures representative of the glassy phase of the polymer nanocomposite. 3) Molecular mechanics (MM) calculations of its mechanical properties following the method originally proposed by Theodorou and Suter. By analyzing the results under constant temperature and pressure, all nanocomposite systems were found to exhibit slower terminal and segmental relaxation dynamics than the pure polymer matrices. The addition of a small fraction of graphene sheets led in all cases to the enhancement of the elastic constants; this was significantly more pronounced in the case of functionalized graphene sheets. We further mention that, for all polymer/fullerene nanocomposites addressed here, no phase separation or variation of polymer chain dimensions was observed as a function of fullerene size and/or fullerene volume fraction. In the third part of the Thesis, and motivated by the use of acrylic polymers for the design of membranes with aligned carbon nanotubes (CNTs) for several separation technologies (such as water desalination and wastewater treatment), we report results from a detailed computer simulation study for the nano-sorption and mobility of four different small molecules (water, tyrosol, vanillic acid, and p-coumaric acid) inside smooth single-wall CNTs (SWCNTs). Most of the results have been obtained with the molecular dynamics (MD) method, but especially for the most narrow of the CNTs considered, the results for water molecule were further confirmed through an additional Grand Canonical (μVT) Monte Carlo (GCMC) simulation using a value for the water chemical potential μ pre-computed with the particle deletion method. Issues addressed in the Thesis include molecular packing and ordering inside the nanotube for the four molecules, average number of sorbed molecules per unit length of the tube, and mean residence time and effective axial diffusivities, all as a function of tube diameter and tube length. In all cases, a strong dependence of the results on carbon nanotube diameter was observed, especially in the way the different molecules are packed and organized inside the CNT. For water for which predictions of properties such as local structure and packing were computed with both methods (MD and GCMC), the two sets of results were found to be fully self-consistent for all types of SWCNTs considered. Water diffusivity inside the CNT (although, strongly dependent on the CNT diameter) was computed with two different methods, both of which gave identical results. For large enough CNT diameters (larger than about 13 Å), this was found to be higher than the corresponding experimental value in the bulk by about 55%. Surprisingly enough, for the rest of the (phenolic) molecules simulated in this Thesis, the simulations revealed no signs of mobility inside nanotubes with a diameter smaller than the (20, 20) tube. This has been attributed to strong phenyl-phenyl attractive interactions, also to favorable interactions of these molecules with the CNT walls, which cause them to form highly ordered, very stable structures inside the nanotube, especially under strong confinement. The interaction, in particular, of the methyl group (present in tyrosol, vanillic acid, and p-coumaric acid) with the CNT walls seems to play a key role in all these compounds causing them to remain practically immobile inside nanotubes characterized by diameters smaller than about 26 Å. It was only for larger-diameter CNTs that tyrosol, vanillic acid, and p-coumaric acid were observed to demonstrate appreciable mobility. / Η παρούσα Διδακτορική Διατριβή εστιάζει στη μελέτη της σχέσης μεταξύ δομής και μακροσκοπικών φυσικών ιδιοτήτων υλικών από πολυακρυλικά μέσω μίας λεπτομερούς προσομοίωσης στον υπολογιστή με τη μέθοδο της Μοριακής Δυναμικής (ΜΔ), σε συνδυασμό με ένα πολύ επακριβές πεδίο δυνάμεων (το Dreiding) σε ατομιστική λεπτομέρεια. Οι κύριες ερευνητικές έννοιες καθώς και οι στόχοι συζητιούνται και αναλύονται σε τρία ξεχωριστά μέρη. Στο πρώτο μέρος, ατομιστικές απεικονίσεις δύο προτύπων πίεσο-ευαίσθητων συγκολλητικών υλικών (acrylic pressure sensitive adhesives ή PSAs), του ατακτικού πολυ-βουτυλικού-ακρυλικού εστέρα (poly(n-BA)) και του συμπολυμερούς του με ακρυλικό οξύ (poly(n-BA-co-AA)), τόσο μακριά όσο και κοντά σε υποστρώματα σίλικας (SiO2) και α-φερρίτη (α-Fe), μελετήθηκαν στη βάση ενός φάσματος ιδιοτήτων (θερμοδυναμικές, δομικές, ιξωδοελαστικές, δυναμικές, και συγκολλητικές), όπως και η μηχανική τους απόκριση υπό συνθήκες μονοαξονικής εκτατικής παραμόρφωσης. Στο δεύτερο μέρος παρουσιάζονται τα αποτελέσματα που εξήχθησαν από μία ιεραρχική μεθοδολογία προσομοίωσης που οδήγησε στην πρόβλεψη της φασικής συμπεριφοράς και των μηχανικών ιδιοτήτων νανοσύνθετων πολυμερικών υλικών (polymer nanocomposites ή PNCs) βασισμένων στο συνδιοτατκτικό πολυ-μεθακρυλικό μεθυλεστέρα (syndiotactic poly(methyl methacrylate) ή sPMMA), ενισχυμένο με ομοιόμορφα διεσπαρμένα φύλλα γραφενίου (graphene sheets) ή σωματίδια φουλερενίου (fullerene particles). Στο τρίτο μέρος, υποκινούμενοι από τη χρήση των ακρυλικών πολυμερών στο σχεδιασμό μεμβρανών με ενσωματωμένους ευθυγραμμισμένους νανοσωλήνες άνθρακα (ΝΑ, carbon nanotubes ή CNTs) σε διάφορες τεχνολογίες διαχωρισμού μορίων (με έμφαση στον καθαρισμό του νερού), παρουσιάζουμε αποτελέσματα από προσομοιώσεις, για τη νανο-ρόφηση και την κινητικότητα τεσσάρων διαφορετικών μικρών μορίων (water, tyrosol, vanilic acid, και p-coumaric acid) στο εσωτερικό λείων μονο-στρωματικών ΝΑ (single-wall CNTs ή SWCNTs). Τα θέματα που εξετάζονται περιλαμβάνουν τη μοριακή διευθέτηση και τη διάταξη στο εσωτερικό Ν.Α. των τεσσάρων μορίων, το μέσο χρόνο παραμονής τους, καθώς και τους αξονικούς συντελεστές διάχυσής του, συναρτήσει της διαμέτρου και του μήκους των ΝΑ.

The study examined the properties of stalk and cob fibres from recombinant inbred corn lines and their parents, grown at two locations, in a polylactic acid (PLA) matrix. The objectives were to: determine fibre compositions; evaluate the effects of fibres on the functional properties of biocomposites and identify quantitative trait loci (QTLs) and gene markers for fibre performance in biocomposites. Significant Genotype*Location effects were observed. Composites had lower strength (impact, tensile, and flexural) but higher tensile/flexural modulus values than pure PLA. The latter were positively affected by cellulose and hemicellulose but negatively affected by free phenolic levels and 93 fibre QTLs and 62 composite markers were detected. This study identified fibre traits and markers for genes that may be important for the use of corn fibres in biocomposites. / Ontario BioCar Initiative Project funded by Ontario Ministry of Research and Innovation, Agriculture and Agri-Food Canada, The Natural Sciences and Engineering Research Council, The Ontario Ministry of Agriculture, Food and Rural Affairs (OMAFRA) and Ontario Public Sector

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