Filtration and separation technologies remain as one of the biggest challenges humanity currently faces. The separation of different elements such as bacteria, viruses, heavy metals, particles, and chemical agents require the development of multifunctional membranes. In membrane technology, one of the most promising fabrication techniques is electrospinning, which can produce highly tailored non-woven fibrous multifunctional membranes with a high surface area. On the other hand, cellulose derivatives, like cellulose acetate, have many beneficial properties for filtering technology such as high availability and easy functionalization. Likewise, cellulose nanocrystals are used to improve mechanical properties and functionalize membranes. In this project, a cellulose nanocrystal (CNCs) functionalized cellulose acetate electrospun multifunctional membrane is developed for adsorption and separation of nanosized particles. In this work, cellulose acetate (CA) fibers with an average fiber diameter of approximately 900 nm were electrospun and tested as membranes for size and affinity based filtration. First, the electrospinning process was optimized regarding solution and process parameters. As a result, solution parameters were found to be 12 wt% solid content CA dissolved in a 1:1 acetone:acetic acid solution. Regarding process parameters, the suitable electrospinning parameters were found to be 18 kV applied voltage, a feeding rate of 5 mL/h, and a tip-to-collector distance of 20 cm.   The electrospun CA membrane was coated with cationic (+) and anionic (-) cellulose nanocrystals up to a 25 wt% concentration. The incorporation of CNCs, of either anionic or cationic surface charge, affected membrane wettability. The neat CA membrane had a hydrophobic behavior with a contact angle of 110°. The addition of CNCs decrease contact angle, to 31.5° for CA-CNCs(-) and 50° for CA-CNCs(+), which resulted in functionalized membranes with a hydrophilic behavior. Both functionalized membranes managed to maintain high flux values. CA-CNCs(-) maintained a flux of 9500 Lm−2h−1, while CA-CNCs(+) maintained a flux of 6700 Lm−2h−1. The addition of cellulose nanocrystals improved the mechanical properties of the CA membranes. The tensile strength increases from 410 kPa to 4990 kPa for CA-CNCs(-) membranes and 3010 MPa for CA-CNCs(+) membranes, and is accompanied by an increase in Young’s modulus as well. To evaluate the adsorption efficiency and size-exclusion filtration, an anionic dye (Congo red), a cationic dye (Victoria blue), and 500 nm model particles were used. CA-CNC(-) membranes achieved a removal efficiency of 96% of 500 nm particles with an affinity-based dye removal of 63% of Victoria blue dye. On the other hand, CA-CNC(+) membranes achieved a removal efficiency of 43% of 500 nm particles with a dye removal of 27% of Congo red dye. In this regard, CA-CNC(-) membranes were the best candidate for size-exclusion filtration, while also maintaining a good level of adsorption. Cellulose based composite membranes were successfully produced as multifunctional filters that could act in both size-exclusion regime and affinity-based regime. A cellulose acetate fibrous membrane was produced by electrospinning, tuning for fiber size and porosity, while the incorporation of cellulose nanocrystals functionalizes the membranes and enhance mechanical properties, and wettability.

Natural composites, in particular nacre, often combine high strength and toughness thanks to highly ordered architectures and controlled geometries of the reinforcement components. However, combining strength, toughness and resorbability in synthetic materials remains a challenge in particular in the field of bone graft substitutes. In the present study, calcium phosphate-(CaP-)based materials with designed architectures inspired from natural composite materials were achieved. CaP platelets obtained by precipitation in organic medium were first aligned in chitosan matrices by solvent casting in ambient conditions. Efficient strengthening was obtained with 15 vol-% ceramic, reaching cortical bone strength (150 MPa) and preserving good ductility (5 % deformation). In a weak magnetic field, high spatial arrangement without percolation was maintained up to 20 vol-%. With directional freezing, good alignment of the platelets could be pushed up to 50 vol-%. In parallel, in situ recrystallization of CaP blocks in hydrothermal conditions led to hierarchical structures. The strength and the work-of-fracture were enhanced (300%) thanks to a change of failure mode.

<p>Xyloglucans are polysaccharides found as storage polymers in seeds and tubers, and as cross-linking glycans in the cell wall of plants. Their structure is complex with intricate branching patterns, which contribute to the physical properties of the polysaccharide including its binding to and interaction with other glycans such as cellulose.</p><p>Xyloglucan is widely used in bulk quantities in the food, textile and paper making industries. With an increasing interest in technically more advanced applications of xyloglucan, such as novel biocomposites, there is a need to understand and control the properties and interactions of xyloglucan with other compounds, to decipher the relationship between xyloglucan structure and function, and in particular the effect of different branching patterns. However, due to the structural heterogeneity of the polysaccharide as obtained from natural sources, relevant studies have not been possible to perform in practise. This fact has stimulated an interest in synthetic methods to obtain xyloglucan mimics and analogs with well-defined structure and decoration patterns.</p><p>Glycosynthases are hydrolytically inactive mutant glycosidases that catalyse the formation of glycosidic linkages between glycosyl fluoride donors and glycoside acceptors. Since its first conception in 1998, the technology is emerging as a useful tool in the synthesis of large, complex polysaccharides. This thesis presents the generation and characterisation of glycosynthases based on xyloglucanase scaffolds for the synthesis of well-defined homogenous xyloglucan oligo- and polysaccharides with regular substitution patterns.</p>

L’accroissement de l’espérance de vie s’accompagne d’une détérioration de l’état de santé général des seniors et d’une recrudescence des maladies chroniques. Parmi les manifestations de la sénescence, l’atteinte de l’appareil locomoteur est particulièrement invalidante et accélère considérablement l’entrée en dépendance. C’est également le cas chez les plus jeunes lors d’atteintes traumatiques ou pathologiques. Ainsi, au niveau mondial 2,2 millions de greffes osseuses sont pratiquées chaque année, mais le taux de complications post-opératoires demeure élevé et est estimé à 15 % des interventions. Ces faits dessinent les contours d’un enjeu sociétal majeur ; les matériaux d’origine animale posent des problèmes d’histocompatibilité, de pathogénicité et donc de rejet. C’est pourquoi les efforts de recherche ciblent prioritairement le développement de biomatériaux synthétiques aptes à promouvoir la régénération osseuse. Actuellement les principaux substituts osseux sur le marché sont les « céramiques » bioactives (phosphates de calcium, verres bioactifs) qui présentent comme caractéristiques d’être biocompatibles, de se lier spontanément aux tissus osseux, de promouvoir l’adhésion des cellules osseuses et enfin d’être biorésorbables. Cependant, malgré cet ensemble de caractéristiques très satisfaisantes, la fragilité de ces matériaux en limite les applications. Pour pallier ce défaut, une solution ingénieuse est de s’inspirer de la structure particulière du tissu osseux. Celle-ci mêle intimement une phase inorganique, le minéral osseux constitué de cristaux d’apatite (phosphate de calcium résorbable), à une phase organique qui est majoritairement du collagène. De manière remarquable, une telle structure associe la rigidité de la partie inorganique à la ténacité des fibres de collagène. Pour obtenir des implants aux propriétés mécaniques proches du tissu osseux, la stratégie consiste donc à combiner céramiques bioactives et matière organique. À cette fin, l’équipe Biomatériaux du Laboratoire de Physique de Clermont (LPC) a récemment mis au point un procédé innovant qui permet la synthèse de matrices tridimensionnelles d’hybrides organique-inorganique à base de verre bioactif et de polymère biocompatible aux caractéristiques variées. Dans la continuité des travaux, il était alors question d’exploiter ce procédé afin de développer un substitut osseux hybride aux propriétés optimisées. Il s’agissait tout d’abord de sélectionner le polymère le plus adéquat pour la régénération osseuse, qui s’est avéré être le polycaprolactone, puis d’optimiser la synthèse (notamment la source de calcium), la structure macroporeuse et la proportion organique-inorganique. Le matériau hybride résultant a ensuite été dopé en éléments thérapeutiques à faible dose (< 5 % de la masse totale) avec des ions strontium ou des nutriments tels que la fisétine et l’hydroxytyrosol qui possèdent un effet ostéogénique. Les mousses hybrides ainsi développées ont finalement été caractérisées in vitro afin de déterminer leurs propriétés physico-chimiques et biologiques, et in vivo afin d’évaluer leur performance. Après 3 mois d’implantation dans un défaut critique de la calvaria de souris, les résultats démontrent le potentiel de ce substitut osseux: comparé au matériau commercial de référence (os bovin traité) qui conduit à une reconstruction osseuse de 16% (± 5%), l’hybride permet une reconstruction allant de 32% (± 3%) lorsqu’il n’est pas dopé, jusqu’à 55% (± 7%) voire 58% (± 7%) lorsqu’il est dopé respectivement en fisétine ou en strontium. Ces travaux de thèse laissent entrevoir des perspectives prometteuses telles que l’association des dopants et l’impression 3D des mousses hybrides polycaprolactone-verre bioactif. / The increase in life expectancy results in the decline of seniors’ health conditions and the resurgence of chronic diseases. Among the expressions of senescence, disorders of the musculoskeletal system are particularly disabling and considerably accelerate the state of dependency. This is also the case for young people who suffer from traumatic injuries or pathologic conditions. Thus, about 2.2 million bone grafts are performed worldwide every year. Yet, the level of postoperative complications remains high and is estimated at 15% of surgical operations. These facts outline a major societal concern: animal-based materials present a risk of histocompatibility issues and pathogenicity that may lead to implant failure. This is the reason why research efforts focus on the development of synthetic biomaterials capable of promoting bone regeneration. Currently, commercialised bone substitutes are mainly made of bioactive “ceramics” (calcium phosphates, bioactive glass) that are known to be biocompatible, to spontaneously bond to bone tissues, to promote bone cell adhesion and finally to be bioresorbable. However, despite these remarkable properties, the brittleness of these materials limits their applications. An ingenious solution to this brittleness can be learned from the particular structure of bone tissue. Bone tissue intimately blends an inorganic phase, the bone mineral, which is made of apatite crystals (resorbable calcium phosphates), with an organic phase that is mainly collagen. Such a structure associates the stiffness of the inorganic part with the toughness of collagen fibres. Therefore, in order to obtain implants with mechanical properties similar to that of bone, the strategy consists in combining bioactive ceramics with organic matter. To this end, the Biomatériaux team from the Laboratoire de Physique de Clermont (LPC) recently developed an innovative process that allows the synthesis of tridimensional organic-inorganic hybrids comprised of bioactive glass and biocompatible polymer. The objective of the thesis was to exploit this process in order to develop a hybrid bone substitute with optimal properties. First of all, polycaprolactone was selected as the polymer, especially because of its adequate degradation rate for long-term applications such as bone regeneration. Then, the synthesis process was improved (in particular, the calcium source was changed), the macroporous structure was optimised and the organic-inorganic ratio was chosen. Afterwards, elements that are known to induce an osteogenic effect were incorporated in the hybrid at low doses (< 5% of total weight): an inorganic doping was performed using strontium ions and an organic doping was performed using nutrients such as fisetin or hydroxytyrosol. The resultant hybrid scaffolds were eventually characterised in vitro in order to determine their physicochemical and biological properties and in vivo in order to evaluate their performance. After 3 months of implantation in a mouse calvarial critical defect, results demonstrate the potential of this bone substitute: compared to the reference commercial material (treated bovine bone) that leads to a bone reconstruction of 16% (± 5%), the hybrid allows a reconstruction going from 32% (± 3%) when it is not doped, to 55% (± 7%) and even 58% (± 7%) when it is doped respectively with fisetin or strontium. This thesis paves the way to promising perspectives like the association of doping agents and the 3D printing of polycaprolactone-bioactive glass hybrid scaffolds.

L’absence de croissance en monocouche des cellules endothéliales sur la paroi des prothèses vasculaires est une des causes d’échec de leur implantation chez l’humain. Des études précédentes ont montré que le recouvrement de ces prothèses par un échafaudage de nanofibres d’acide polylactique (PLA), fabriqué par un système de filage par jet d’air innovant, peut être utilisé pour promouvoir la croissance des cellules endothéliales de façon adéquate. Ainsi, le caractère dégradable d’un matériau comme le PLA permettrait son remplacement graduel par la matrice extra-cellulaire produite par les cellules. D’autre part, la réussite d’une transition entre les nanofibres dégradables et la matrice extra-cellulaire nécessite un remplacement contrôlé et approprié. Or, la dégradation des nanofibres de PLA, dépendant de ses séquences stéréochimiques, est généralement trop longue et peut induire une cytotoxicité relative pendant sa dégradation. Dans ce contexte, les études de cette thèse ont pour objectifs de mieux comprendre la formation des fibres lors du filage, d’optimiser la fabrication des échafaudages permettant ainsi la création de nanofibres d’autres polymères, puis, de concevoir des nanofibres provenant d’un polymère mieux adapté à nos besoins, d’évaluer leur mécanisme de dégradation et sa cytotoxicité durant sa dégradation. Les travaux d’optimisation du système de filage ont démontré que la concentration avec un effet prépondérant. Ainsi, la mesure de la viscosité permet de trouver les paramètres adéquats pour le filage de polymère. Ensuite, un poly(L-lactide) semi-cristallin (PLLA) et un terpolymère de poly(lactide-co-ε-caprolactone) (PLCL) dédié pour des applications vasculaires ont été synthétisés et filés par jet d’air. Ces échantillons ont été dégradés en solution aqueuse et caractérisés par des méthodes physico-chimiques afin de mieux comprendre leurs mécanismes de dégradation et mis en présence de cellules endothéliales pour évaluer leur cytotoxicité. La comparaison entre les échafaudages des deux polymères a montré des comportements singuliers en dégradation, dépendants des caractéristiques thermiques des polymères. De plus, ces mécanismes de dégradation des nanofibres ont une influence directe sur la sensibilité des cellules endothéliales face aux produits de dégradation. En conclusion, ces travaux de doctorat présentent une solution prometteuse pour améliorer les prothèses vasculaires et qui pourrait être appliquée pour résoudre plusieurs problématiques en médecine régénératrice. / The absence of neo-endothelium on the intimal surface of vascular substitutes is known to be one cause of failure upon implantation of these prostheses in humans. Previous studies have shown that the coating of these substitutes with a nanofiber scaffold, made with an innovative air spinning device, can be used to promote a suitable endothelial cells growth. On one hand, the degradable feature of material as PLA enable the progressive replacement of the scaffold by the extracellular matrix of cells. On the other hand, the success of this replacement between degradable nanofibers and the extracellular matrix requires to be appropriate and controlled. Yet, the PLA nanofiber degradation process, which depends on its stereosequences, is generally too long for this application and could involve cell sensitivity during the degradation. In this context, studies from this thesis aim to understand the fibers formation during spinning, optimizing the scaffold fabrication as well as to promote the making of novel polymer scaffolds, then, design solution to polymeric nanofiber scaffolds for vascular application, evaluate its degradation mechanism and cytotoxicity during degradation process. The work on spinning device optimisation has demonstrated that the concentration had a dominant effect. Thus, viscosity measurements enable to find suitable parameters for polymer spinning. Then, a semi-cristalline poly(L-lactide) (PLLA) and a poly(lactide-co-ε-caprolactone) (PLCL) terpolymer specifically made for vascular application have been synthesized and air-spun. These samples were degraded in aqueous solution and characterized by physical and chemical methods to better understand their degradation mechanisms and seeded with endothelial cells to evaluate their cytotoxicity. The comparison between the two polymers scaffolds have shown surprising degradation behaviors depending on thermal properties of polymers. Moreover, these nanofiber degradation mechanisms have a direct influence on endothelial cells sensitivity with degradation by-products. To conclude, these works of doctorate display a promising solution to improve vascular prostheses and which could be applied to solve several issues in regenerative medicine field.

A liga Ti-6Al-4V tem sido usada com sucesso como biomaterial com aplicações nos campos da odontologia e ortopedia. As características da liga Ti-6Al-4V que a tornaram um material interessante são sua boa resistência à corrosão em meio biológico, combinada com um excelente grau de biocompatibilidade. Os efeitos biológicos a longo prazo dos íons metálicos resultantes da lenta lixiviação dos implantes de titânio não estão completamente entendidos. É conhecido que os íons titânio são considerados agentes químicos cancerígenos, os íons alumínio causam desordem neurológicas e os íons vanádio estão associados com distúrbios enzimáticos, entre outros problemas. O recobrimento das ligas de titânio por óxido de titânio (TiO2) pode atuar como uma barreira química para os íons lixiviados da superfície metálica da liga, além deste óxido ser um bom osseoindutor. O processo de aspersão térmica é amplamente empregado na aplicação de recobrimentos por óxidos. Uma vez que este processo acontece em altas temperaturas, onde partículas fundidas ou semi-fundidas aderem ao substrato, pode ocorrer difusão localizada. O objetivo deste estudo é caracterizar a interdifusão dos elementos de liga através das camadas superficiais do sistema Ti-6Al-4V/TiO2. Os recobrimentos de TiO2 foram preparados pela técnica de aspersão por plasma. A zona recoberta mostrou pequena porosidade distribuída por toda a camada e algumas trincas radiais. Adicionalmente, uma grande quantidade de buracos foi observada na região entre-camadas. Neste trabalho, a interface Ti-6Al-4V/TiO2 foi estudada por microscopia eletrônica de varredura. Os perfis de difusão do Ti, Al, V e O nas camadas superficiais da amostra recoberta foram obtidos por microanálise semi-quantitativa por energia dispersiva de raios-X. A caracterização química superficial do lado substrato depois da deposição de TiO2 mostrou a formação localizada de TiO. Na região entre-camadas foram observados os perfis de difusão característicos com forma de S para o Ti, V e O. O perfil de difusão do Al mostrou um pico na região entre-camadas indicando um acúmulo de Al2O3 nos buracos presentes nesta zona. O TiO2 foi identificado como o maior constituinte no lado revestimento. Pequenas quantidades de Al e V foram também detectadas homogeneamente distribuídas dentro do depósito. A presença do Al e V (metais tóxicos) na superfície externa do depósito indica que estes metais não competem com a oxidação da camada depositada indicando um efeito desmascarante da superfície da liga metálica pelo óxido superficial TiO2. / Ti-6Al-4V alloy has been used with some success as biomaterial with applications in the field of dentistry and orthopaedics. The features with make the Ti-6Al-4V alloy such an interesting material are its good corrosion resistance in the biological environment, combined with an excellent degree of biocompatibility. The long-term biological effects of the slowly leaching of metal ions from titanium implants are not completely understood. It is known that the titanium ions are considered chemical carcinogen, aluminium ions cause neurological disorders and, vanadium ions are associated with irreversible enzymatic disturbance, among other problems. Titanium oxide (TiO2) coatings on titanium alloys can act as a chemical barrier for ions leaching from the metallic alloy surface, beside the fact that this oxide is a very good osteoinductor. The thermal spray process is widely used to apply oxide coatings. Once this is a high temperature process where molten or semi-molten particles impinge upon the substrate, localized diffusion can occur. The aim of this study is characterize the inter-diffusion of the alloying elements through the surface layers of the system Ti-6Al-4V/TiO2. The TiO2 coatings were prepared by the plasma spray technique. The coated zone showed some porous distributed in all layer and a few radial cracks. Additionally, large amount of holes were observed in the interlayer region. In this work, the interface Ti-6Al-4V/TiO2 was studied by scanning electron microscopy. Diffusion profiles of Ti, Al, V and O in the surface layers of coated samples were measured by semi-quantitative energy dispersive X-ray microanalysis. Chemical surface characterization of the substrate side after the TiO2 deposition showed the localized formation of TiO. At the interlayer region was observed the characteristic S shape diffusion profiles for Ti, V and O. The Al diffusion profile showed a peak in the interlayer region indicating anaccumulation of Al2O3 into the holes present in this zone. TiO2 was identified as the major component in the coating side. Small amounts of Al and V were also detected homogeneously distributed inside the deposit. Presence of Al and V (toxic metals) on the external surface of the deposit indicated that these metals did not compete with the oxidation of the deposited layer indicating a non-masking effect of metallic alloy surface by the TiO2- surface oxide.

Ce travail a pour objet de déterminer les conditions optimales de production de substituts allogéniques capables de combler les lésions cartilagineuses dans le cadre du traitement de l’arthrose. Il s’oriente particulièrement sur la composante cellulaire de ces substituts. L’usage de cellules souches mésenchymateuses issues de cordons ombilicaux (CSM-GW) implique de déterminer quels facteurs obstétricaux, liés à l’environnement direct et indirect des CSM-GW, peuvent influencer leur prolifération ainsi que leur différenciation chondrocytaire. Dans une première partie de ce travail, trois types de facteurs ont été étudiés : les facteurs liés à l’enfant donneur, au déroulement de l’accouchement et de la délivrance, à la grossesse et à la mère. Nos données montrent que les CSM-GW ont des capacités prolifératives améliorées lorsque l’accouchement s’est déroulé à terme et sans complication, avec utilisation de Syntocinon® pendant le travail. Sur la base de ces résultats, nous avons utilisé les CSM-GW les plus efficaces dans le cadre de l’ingénierie du cartilage. Il a ensuite été essentiel d’élucider le profil d’action des CSM-GW dans un contexte allogénique. Le deuxième temps de ce travail a donc consisté à chercher le profil de stimulation le plus performant, au regard de la viabilité des cellules et de l’évolution de la sécrétion des facteurs solubles responsables des propriétés immunomodulatrices des CSM-GW au cours de la différenciation chondrocytaire. Nous avons alors mimé, in vitro et en biomatériaux d’Alginate/Acide hyaluronique (Alg/HA) une telle situation en stimulant les CSM-GW avec différentes doses d’IFN-γ et de TNF-α. Selon nos résultats, la stimulation par IFN-γ et TNF-α sur les CSM-GW en biomatériaux d’Alg/HA est plus efficace lorsque ces deux cytokines sont utilisées conjointement et n’est pas délétère pour la viabilité cellulaire aux concentrations respectives de 20 et 30 ng/mL. Cette double stimulation induit une augmentation de la sécrétion d’IL-6 et de PGE-2 par les CSM-GW, ne modifie pas leur sécrétion de TGF-β, et diminue la sécrétion de VEGF. Nous avons confirmé ces données lors d’une mise en situation fonctionnelle : des cocultures avec des cellules mononucléées de sang périphérique (PBMC) de donneurs sains nous ont permis d’évaluer la réponse des CSM-GW lors d’une situation allogénique. Ces mises en situations allogéniques ont été étudiées à différents temps afin d’évaluer les propriétés immunologiques des CSM-GW au cours du temps passé en biomatériaux. Nos résultats montrent que les CSM-GW peuvent exprimer des molécules HLA-G ainsi qu’IDO, mais ces expressions sont limitées en biomatériaux d’Alg//HA. Les CSM-GW en biomatériaux d’Alg/HA en situation allogénique ne sont pas immunogènes, quel que soit le temps de différenciation. En revanche, leurs capacités immunomodulatrices décroissent au cours du temps et sont plus fortes à J0 et J3 de la différenciation chondrocytaire, ce qui oriente vers une utilisation précoce de ces cellules. Les conclusions de ce travail permettent de (i) sélectionner les cordons idoines à l’ingénierie cellulaire et l’ingénierie du cartilage, (ii) définir les conditions permettant de mimer une situation allogénique in vitro, (iii) connaitre les propriétés immunomodulatrices des CSM-GW au cours de la culture en biomatériaux d’Alg/HA, y compris en situation allogénique / The purpose of this work is to determine the optimal conditions for allogeneic substitutes production, adapted to filling the cartilaginous lesions in osteoarthritis treatment. It focuses on the cellular component of these substitutes. The use of mesenchymal stem cells from umbilical cords (WJ-MSC) involves determining which factors, related to direct and indirect environment of the WJ-MSC, can influence their proliferation and chondrogenic differentiation. In a first part of our work, three types of factors were studied: related to the donor child, the course of labor and delivery, pregnancy and the mother. Our results show that WJ-MSC have enhanced proliferative capacities when coming from full-term birth and without complications, with the use of Syntocinon® during labor. On this basis, we used the most effective WJ-MSC for cartilage engineering. It was then essential to elucidate their action profile in allogeneic context. We stimulated WJ-MSC embedded in Alginate/Hyaluronic Acid (Alg/HA) scaffolds with different concentrations of IFN-γ and TNF-α in order to determine the most effective stimulation profile, with regard to viability of the cells and evolution of immunomodulatory soluble factors secretion. According to our results, the stimulation by IFN-γ and TNF-α on WJ-MSC in Alg/HA scaffolds is more effective when these two cytokines are used together and is not deleterious for cell viability at the concentrations of 20 and 30 ng/mL, respectively. This double stimulation induces an increase in the secretion of IL-6 and PGE-2 by the WJ-MSC, a decrease in the secretion of VEGF and does not modify the secretion of TGF-β. We confirmed these data during a functional study: cocultures with peripheral blood mononuclear cells (PBMC) from healthy donors allowed us to evaluate the response of WJ-MSC in an allogeneic situation. These allogeneic situations have been studied at different times to evaluate the immunological properties of WJ-MSC during the time of chondrogenic differentiation. Our results show that WJ-MSC can express HLA-G molecules as well as IDO, but these expressions are limited in Alg/HA biomaterials. Finally, the WJ-MSC in Alg/HA biomaterials in allogeneic conditions are not immunogenic, regardless of the time of differentiation. On the other hand, their immunomodulatory capacities decrease over time and are stronger at day 0 and day 3 of chondrogenic differentiation, which leads to an early use of these cells. Finally, this work allows us to (i) select the umbilical cords suitable for cellular and cartilage engineering, (ii) define the conditions mimicking in vitro an allogeneic situation, (iii) elucidate the immunomodulatory properties of WJ-MSC during Alg/HA biomaterials chondrogenic differentiation, including allogeneic situations

Submitted by Kelren Mota (kelrenlima@ufpa.br) on 2019-01-17T17:13:33Z No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Tese_SinteseCaracterizacaoceramicas.pdf: 2239585 bytes, checksum: e376a3f04b743253d03e174e22df4df9 (MD5) / Approved for entry into archive by Kelren Mota (kelrenlima@ufpa.br) on 2019-01-17T17:14:43Z (GMT) No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Tese_SinteseCaracterizacaoceramicas.pdf: 2239585 bytes, checksum: e376a3f04b743253d03e174e22df4df9 (MD5) / Made available in DSpace on 2019-01-17T17:14:43Z (GMT). No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Tese_SinteseCaracterizacaoceramicas.pdf: 2239585 bytes, checksum: e376a3f04b743253d03e174e22df4df9 (MD5) Previous issue date: 2018-10-31 / Os remanescentes do agronegócio do açaí (Euterpe oleracea Mart.) são fontes de materiais lignocelulósicos. A extração de nanocelulose a partir do tegumento do açaí constitui matéria-prima viável para a síntese de cerâmicas bifásicas (HA / β-TCP) por hidrólise ácida. Após o despolpamento da fruta é encontrada uma biomassa que é dividida em três frações: borra (parênquima), fibra (monostelo) e endocarpo. O tegumento é analisado por MEV / EDS, através do endocarpo de açaí de terra firme e de várzea apresentando nutrientes essenciais, para obter cerâmicas de fosfatos de cálcio. O biocompósito (NC / HA / β-TCP) foi caracterizado por MEV, apresentando espécies cristalinas na superfície da nanocelulose; Difração de raios-X apresentando nucleação de HA atribuída a celulose tipo I e fosfato tricálcico (β-TCP) na superfície de celulose tipo II; mostrando o crescimento de cristais de HA na superfície da nanocelulose. A análise por FTIR mostrou picos característicos de PO4-3, deformação glicosídica C1-H em 897 cm-1 atribuída à celulose, forte ligação conjugada C-C em 1609 cm-1 atribuída à lignina que mostra uma diminuição no conteúdo durante o processo. Os resultados de tamanho de partícula estão na dimensão nanométrica apresentando 643,50 nm como valor mais comum relacionados aos resultados do potencial zeta apresentando partículas instáveis produzindo agregação das partículas e partículas estáveis com valor em módulo maior que 20 mV. Devido às características apresentadas pela cerâmica bifásica sintetizada neste trabalho sugere-se sua aplicação como biomaterial. / The remnants of the açaí agribusiness (Euterpe Oleracea Mart) are sources of lignocellulosic materials. The extraction of nanocellulose from the açaí integument constitutes viable raw material for the synthesis of biphasic ceramics (HA / β-TCP) by acid hydrolysis. After the fruit pulp is obtained a biomass that is divided into three fractions: sludge (parenchyma), fiber (monostelo) and endocarp. The integument is analyzed by MEV / EDS, through the endocarp of açaí of terra firme and of várzea presenting essential nutrients, to obtain ceramics of phosphates of calcium. The biocomposite (NC / HA / β-TCP) was characterized by MEV, presenting crystalline species on the surface of the nanocellulose; X-ray diffraction presenting HA nucleation attributed to type I cellulose and tricalcium phosphate (β-TCP) on the surface of cellulose type II; showing the growth of HA crystals on the surface of the nanocellulose. The FTIR analysis showed characteristic peaks of PO4-3, C1-H glycosidic deformation at 897 cm -1 attributed to cellulose, strong C-C conjugate binding at 1609 cm -1 attributed to lignin showing a decrease in content during the process. The results of particle size are in the nanometric dimension showing 643.50 nm as the most common value related to the results of the zeta potential presenting unstable particles producing particles aggregation and stable particles with modulus value greater than 20 mV. Due to the characteristics presented by the biphasic ceramic synthesized in this work it is suggested its application as biomaterial. / SEDUC - Secretaria de Estado de Educação do Pará

O elevado número de cirurgias de enxertia óssea impulsiona o desenvolvimento de novos biomateriais de preenchimento. Materiais a base de hidroxiapatita sintética e tendão bovino mineralizado foram preparados para servirem de arcabouço para regeneração óssea. Este estudo teve como objetivo avaliar a osteocondutibilidade desses materiais, comparando-os ao Bio-Oss/Geistlich. Foram criados defeitos de tamanho crítico (circular / 8 mm) na calvária de ratos Wistar, preenchidos com os biomateriais e, após 30 dias, ocorreu o sacrifício, análise não invasiva por microtomografia computadorizada (micro-CT/ microtomógrafo SkyScan 100kV - 100\'mü\'A) com reconstituição de imagem em três dimensões (3D) e análise histológica convencional para avaliar a neoformação óssea e comparar os métodos. Os resultados da micro-CT mostraram que o Bio-Oss apresentou maior volume, densidade e porcentagem de tecido ósseo que os demais grupos. Nas imagens reconstituídas em 3D notou-se no grupo Bio-Oss as menores taxas de reabsorção, permanecendo em maior quantidade no interior do defeito aos trinta dias. No grupo da hidroxiapatita sintética notou-se uma intensa reabsorção do material e uma leve neoformação óssea nas margens do defeito, deixando-o com um contorno irregular. O grupo do tendão bovino mineralizado apresentou discretíssima neoformação óssea e o material foi totalmente reabsorvido. Já na avaliação da presença do material, de vasos sanguíneos e das células osteoblásticas no interior do defeito obtidos através da análise histológica, os grupos Bio-Oss e hidroxiapatita sintética obtiveram resultados semelhantes e maiores que o tendão bovino mineralizado. Constatou-se através da análise histológica que a hidroxiapatita sintética mostrou-se presente no interior do defeito exibindo propriedades osteocondutoras semelhantes a marca comercial Bio-Oss. Já o tendão bovino mineralizado não teve boa osteocondução, sendo contra-indicado na manutenção do espaço ósseo. Na comparação dos dois métodos, constatou-se que a micro-CT apresenta baixa especificidade, ou seja, não foi capaz de distinguir o tecido ósseo do Bio-Oss e alta sensibilidade, pois quantifica de uma forma muito precisa os valores com alta resolução. Já a análise histológica consegue distinguir com precisão os materiais e o tecido adjacente, porém não consegue quantificá-los de maneira fácil e precisa. Portanto, conclui-se que a hidroxiapatita sintética tem grande potencial de ser utilizada no preenchimento de defeitos ósseos, diferentemente do tendão bovino mineralizado. Quanto aos métodos de avaliação, eles são complementares e novos aprimoramentos devem ser feitos na técnica de micro-CT para melhorar sua capacidade de distinguir diferentes materiais. / Biodegradable bone grafts have been widely employed on bone regeneration. The purpose of this study was to evaluate the osteoconductive potential of hydroxyapatite, mineralized bovine tendon and Bio-Oss/Geistlich in a rat critical-size calvaria defect model through non-destructive three-dimensional (3D) micro-tomographic (\'mü\'CT) imaging and histological evaluation. Two experimental biomaterials were developed: synthetic hydroxyapatite (particles size < 0,2 mm) and mineralized bovine tendon. Bio-Oss/Geistlich was employed as a control group. A critical size defect (8 mm) was created in the skull of Wistar rats (weight 200 - 300 g) and treated with the biomaterials and one group was left untreated in the control group (n = 5). After 30 days, the animals were killed and the calvaria removed for \'mü\'CT and histological analysis. No adverse reactions were noted. No bone repair was observed in untreated surgical defects. The results of micro-CT showed that BioOss showed higher volume, density and percentage of bone tissue than the other groups. In the images reconstructed in 3-D was noted in the group Bio-Oss the lowest rates of resorption, staying in larger quantities within thirty days of the defect. In the group of synthetic hydroxyapatite noticed an intense resorption of the material and a slight bone formation at the margins of the defect, leaving him with an irregular contour. The bovine tendon mineralized group presented discreet bone formation and the material was completely resorbed. In the evaluation of the presence of the material, blood vessels and osteoblastic cells within the defect obtained by histological analysis, the groups Bio-Oss and synthetic hydroxyapatite showed similar results and larger than the mineralized bovine tendon. We verified by histological analysis that the synthetic hydroxyapatite is present within the defect displaying osteoconductive properties similar to trademark BioOss. Already the mineralized bovine tendon, again, did not have good osteoconduction and is contraindicated in maintaining the bone. When comparing the two methods observed that the micro-CT has low specificity, ie, was not able to distinguish the bone tissue to Bio-Oss and high sensitivity, as quantified in a very accurate values with high resolution. Already histological analysis can accurately distinguish materials and tissues, but can not quantify them easily and accurately. Therefore, we conclude that the synthetic hydroxyapatite has great potential to be used to fill bone defects, unlike mineralized bovine tendon. When comparing the methods, we found that still are complementary and new enhancements must be made in micro-CT technique to improve their ability to distinguish different materials.

Les microsphères polymériques, biodégradables et biocompatibles sont prometteuses comme échafaudages pour fournir des cellules aux tissus sans dommage et améliorer la réponse des cellules souches. Il a été montré que les microparticules à base de PLGA à base de protéines ECM préparées par une technique d'extraction par solvant en émulsion améliorent l'adhésion et la prolifération des cellules souches. Bien qu'un certain effet biologique du revêtement protéique sur les microparticules de polymère soit établi, il n'est pas bien compris car des informations détaillées sur l'interaction entre les propriétés de surface des particules chimiques et physiques, l'adsorption protéique et la réponse cellulaire restent floues. Le but de cette étude est d'établir une relation entre les propriétés de surface des particules qui proviennent des variables utilisées lors des formulations, l'adsorption des protéines et la réponse des cellules souches pour permettre une conception plus rationnelle des microparticules. Deux types de polymères différents (PLGA et PLGA-P188-PLGA) et deux stabilisants d'émulsion différents; un polymérique PVA et une huile polaire Propylène glycol ont été utilisés pour préparer quatre types de particules dans un procédé en émulsion. Les particules ont été caractérisées en termes de taille, charge, topographie et morphologie et chimie de surface Identification des effets des variables dans la chimie et l'émulsifiant des polymères Des surfaces de polymère plat recouvertes de spins sont générées pour comprendre les interactions entre les polymères et les molécules d'adhésion de la fibronectine et de la poly-D-Lysine pour la fonctionnalisation des microparticule. / Polymeric, biodegradable and biocompatible microspheres are promising as colloidal scaffolds to deliver cells to tissues without damage and to enhance stem cell survival. It has been shown that PLGA (poly(lactic-co-glycolic acid)) based microparticles prepared by an emulsion solvent extraction technique and functionalised with ECM proteins improves stemcell adhesion and proliferation. While it is established that the presence of proteins in these systems has abiological effect, the interplay between microparticle properties and cells is poorly understood because there lationship between chemical and physical particle surface properties, protein adsorption and cell response remain unclear. Protein adsorption on a polymer particle surface is a complex phenomenon that is affected by different interfacial mechanisms/forces (e.g. DLVO and non-DLVO forces) and inherents tructural properties of macromolecules (e.g. polymers, surfactants, peptides and proteins) present on surface, establishing the parameters that involves inprotein/peptide adsorption on microparticles insights the logical design of the particles as a biomaterial useby contributing the understanding of another related complex phenomenon of the colloidal biomaterial-cell interface interaction in tissue engineering where limited study available to fully understand the concept.The purpose of this study is to investigate the impact of different formulation approaches on the physicochemical properties of the microparticles and identify connections between the particle properties, protein adsorption and ensuing cell response on these materials. To examine these, two different polymertypes (PLGA and PLGA-P188-PLGA) and two different emulsion stabilizers; a polymeric surfactant (PVA(Polyvinyl alcohol) and a polar oil propylene glycol were used to prepare four different types of particles in an emulsion process (O/W). Particles were characterized in terms of size, charge, topography, morphology and surface chemistry to identify the effect of the variables of polymer chemistry and use of surfactant on particle properties in first part of the study. Spin coated flatpolymer surfaces were generated to understand the interactions between the polymers and the proteins (fibronectin /poly-d-Lysine).