The emergence of organic semiconductors is exciting since it promises to open up for straightforward and low-cost fabrication of a wide range of efficient and novel electronic devices. However, in order for this promise to become reality it is critical that new and functional fabrication techniques are developed. This thesis demonstrates the conceptualization, development, realization and implementation of a particularly straightforward and scalable fabrication process: the photo-induced and resist-free imprint patterning technique.Initial experiments revealed that some members of a group of carbon-cage molecular semiconductors – termed fullerenes – can be photochemically modified into dimeric or polymeric structures during exposure to laser light, and, importantly, that the exposed fullerene material retains its good electron-transport property while its solubility in common organic solvents is drastically lowered. With this information at hand, it was possible to design and create well-defined patterns in a solution-deposited fullerene film by exposing selected film areas to laser light and then developing the entire film in a tuned developer solution. An electronically active fullerene pattern emerges at the locations defined by the incident laser beam, and the patterning technique was successfully utilized for the fabrication of arrays of efficient field-effect transistors.In a later stage, the capacity of the photo-induced and resist-free imprint technique was demonstrated to encompass the fabrication of ubiquitous and useful CMOS circuits. These are based on a combination of p-type and n-type transistors, and a blend between a p-type organic semiconductor and an n-type fullerene compound was designed so that the latter dominated. By solution-depositing the blend film on an array of transistor structures, exposing selected transistors to laser light, and then developing the entire transistor array in a developer solution, it was possible to establish a desired combination of (non-exposed) p-type transistors and (exposed) n-type transistors. We finally utilized this combination of transistors for the fabrication of a CMOS circuit in the form of well a-functional organic inverter stage.

L’utilisation des adhésifs dans le domaine médical prend de plus en plus de place jusqu’à leur utilisation par le grand public pour refermer certaines plaies superficielles. Les adhésifs les plus courants pour applications médicales sont formulés à partir d’hydrogel voire de silicone, prêts à l’emploi, très peu étant associés à une préparation particulière avant application comme c’est le cas dans le domaine dentaire avec l’utilisation de la photo-polymérisation. Notre travail de recherche a consisté à formuler des adhésifs photo-polymérisables permettant un collage résistant sur les tissus biologiques internes et à comprendre les mécanismes permettant d’aboutir à un collage de bonne qualité en tenant compte des contraintes fortes liées à l’application visée : (i) milieu humide dans lequel sera disposé l’adhésif, (ii) nature viscoélastique des tissus biologiques et (iii) facilité de mise en œuvre. L’ensemble des expériences a été mené sur un substrat considéré comme « modèle », le péricarde bovin, dont il a été montré que les propriétés mécaniques sont similaires à celles du péricarde humain. Ce travail a démontré que l’adhésion sur un tissu interne est dépendante de plusieurs paramètres. Pour assurer un bon collage, il est nécessaire que l’adhésif mouille le tissu biologique et pénètre suffisamment pour assurer un bon ancrage mécanique. De ce fait, des formulations adhésives à base d’acrylates de faible viscosité ont été réalisées. Nous avons montré que l’énergie d’adhésion développée diminue linéairement avec la viscosité de l’adhésif avant photo-polymérisation. Ce résultat a mené à l’hypothèse de la pénétration de l’adhésif dans le péricarde, validée par plusieurs techniques. Nous avons ainsi démontré le lien entre une adhésion forte sur un tissu biologique, la viscosité initiale de la solution adhésive et sa capacité à pénétrer le substrat. L’ensemble de ce travail a mené à la compréhension des mécanismes induits par le dépôt d’un monomère sur un substrat vivant et à des hypothèses sur la polymérisation de la couche adhésive et son interaction avec le substrat. Des expériences in-vivo sur différents organes de souris et de lapins ont permis de montrer des résultats prometteurs qui ne demandent qu’à être confirmés par une étude systématique à plus grande échelle. Enfin, une description phénoménologique est proposée au travers d’une équation simplifiée tenant compte de différents paramètres essentiels pour décrire les mécanismes en jeu. / Adhesives are more and more used by the public to seal superficial wounds. The current adhesives for medical use are formulated on the basis of hydrogels, silicon and are ready to use. Only a few of them are associated to a particular preparation before application as the dental adhesives. The main goals of this research were to formulate some photo-polymerizable adhesives which induce a permanent strong anchorage into the internal biological tissues and to understand the mechanisms leading to a good quality adhesion and respecting the high constraints of the application: (i) the wetness of the media in which the adhesive is deposited, (ii) the viscoelasticity of the biological tissues and (iii) the easiness of the set up. The whole experiments were done onto a substrate considered as a “model”, the bovine pericardium, which was demonstrated to have the same mechanical properties as the human pericardium. This study showed that the adhesion onto internal tissue depends on several parameters. To create the adhesion, the adhesive has to wet and penetrate deep enough the tissue to get a strong mechanical anchorage. Thus, some low viscous acrylate-based adhesive formulations were realized. A linear correlation was found between the viscosity of the formulation before photo-polymerization and the adhesion energy: as the viscosity increases, the adhesion energy decreases. This result led to the hypothesis of the penetration of the adhesive into the tissue, which was proven by different techniques. Finally, it was proven that a strong adhesion onto a biological tissue depends on the viscosity and its capability to penetrate the substrate. This whole work led to the understanding of the mechanisms induced by the deposit of a monomer onto a living substrate and to some hypotheses about the polymerization of the adhesive layer and its interaction with the substrate. Some in-vivo experiments onto internal organs of mice or rabbits have shown promising results which are to be confirmed by multiple other experiments. Finally, a phenomenological description is proposed through a simplified equation takin into account different essential parameters to describe the mechanisms taking part into this phenomenon.

No description available.

No presente trabalho produzimos microestruturas, através da técnica de fotopolimerização via absorção de dois fótons, dopadas com nanofios de ZnO, um material que vem sendo amplamente explorado devido as suas interessantes propriedades ópticas e elétricas. Para a fabricação das microestruturas, utilizamos um oscilador laser de Ti:safira que produz pulsos de aproximadamente 100 fs em 800 nm. A intensidade dos pulsos de femtossegundos é alta o suficiente para induzir a absorção¬ de dois fótons em torno do volume focal, localizando a polimerização a esta região. Portanto, através da varredura do feixe na resina polimérica fabrica-se a estrutura desejada. Neste trabalho, desenvolvemos uma metodologia para introduzir nanofios de ZnO às microestruturas fabricadas, a partir da mistura do pó de nanofios de ZnO à resina acrílica. A resina utilizada é uma combinação de duas resinas, o etoxilated(6)trimethylolpropane triacrylate (SR-499) e tris(2-hydroxy ethyl)isocyanurate triacrylate (SR-368). Como fotoiniciador utilizamos o Lucirin TPO-L (2,4,6-trimetilbenzoiletoxifenil phosphine oxide). As microestruturas produzidas foram caracterizadas pelas técnicas de microscopia óptica, microscopia eletrônica de varredura, espectroscopia de energia dispersiva, difração de Raios X e espectroscopia de espalhamento micro-Raman. Através destas técnicas, foi possível observar a presença dos nanofios nas microestruturas, bem como caracterizar suas propriedades morfológicas que se mostram adequadas para o desenvolvimento de microdispositivos. Observamos também a emissão de fluorescência das microestruturas excitadas por um e dois fótons. Sendo assim, a metodologia de fabricação descrita aqui pode ser usada como mais uma opção na concepção de novos dispositivos tecnológicos. / In this study we fabricated microstructures, using the two-photon polymerization technique, containing ZnO nanowires, a material that has been widely exploited due to their interesting optical and electrical properties. For the microstructures fabrication, we used Ti:Sapphire laser oscillator operating at 800 nm with 100 fs pulses. The intensity of the fs-pulses is high enough to induce two-photon absorption, confining the excitation and thus the polymerization to the focal volume. By scanning the beam across the resin the desired microstructure is fabricated. In this work, we developed a method to introduce ZnO nanowires in the fabricated microstructure by mixing the ZnO nanowires powder to the acrylic resin. The used resin is a combination of two compounds, etoxilated(6)trimethylolpropane triacrylate (SR-499) and tris(2-hydroxy ethyl)isocyanurate triacrylate (SR-368). As a photoinitiator we have used Lucirin TPO-L (2,4,6-trimetilbenzoiletoxifenil phosphine oxide).The produced samples were characterized by optical microscopy, scanning electron microscopy, energy dispersive spectroscopy, X-ray diffraction spectroscopy and micro-Raman scattering. From these techniques it was possible to observe the presence of nanowires in the microstructures, as well as to characterize the morphological properties, which has been shown to be interesting for developing microdevices. We have also observed fluorescent emission of the microstructures excites by one and two-photons absorption. Therefore, the methodology described here can be used as an alternative in the design of new optical devices.

No presente trabalho produzimos microestruturas, através da técnica de fotopolimerização via absorção de dois fótons, dopadas com nanofios de ZnO, um material que vem sendo amplamente explorado devido as suas interessantes propriedades ópticas e elétricas. Para a fabricação das microestruturas, utilizamos um oscilador laser de Ti:safira que produz pulsos de aproximadamente 100 fs em 800 nm. A intensidade dos pulsos de femtossegundos é alta o suficiente para induzir a absorção¬ de dois fótons em torno do volume focal, localizando a polimerização a esta região. Portanto, através da varredura do feixe na resina polimérica fabrica-se a estrutura desejada. Neste trabalho, desenvolvemos uma metodologia para introduzir nanofios de ZnO às microestruturas fabricadas, a partir da mistura do pó de nanofios de ZnO à resina acrílica. A resina utilizada é uma combinação de duas resinas, o etoxilated(6)trimethylolpropane triacrylate (SR-499) e tris(2-hydroxy ethyl)isocyanurate triacrylate (SR-368). Como fotoiniciador utilizamos o Lucirin TPO-L (2,4,6-trimetilbenzoiletoxifenil phosphine oxide). As microestruturas produzidas foram caracterizadas pelas técnicas de microscopia óptica, microscopia eletrônica de varredura, espectroscopia de energia dispersiva, difração de Raios X e espectroscopia de espalhamento micro-Raman. Através destas técnicas, foi possível observar a presença dos nanofios nas microestruturas, bem como caracterizar suas propriedades morfológicas que se mostram adequadas para o desenvolvimento de microdispositivos. Observamos também a emissão de fluorescência das microestruturas excitadas por um e dois fótons. Sendo assim, a metodologia de fabricação descrita aqui pode ser usada como mais uma opção na concepção de novos dispositivos tecnológicos. / In this study we fabricated microstructures, using the two-photon polymerization technique, containing ZnO nanowires, a material that has been widely exploited due to their interesting optical and electrical properties. For the microstructures fabrication, we used Ti:Sapphire laser oscillator operating at 800 nm with 100 fs pulses. The intensity of the fs-pulses is high enough to induce two-photon absorption, confining the excitation and thus the polymerization to the focal volume. By scanning the beam across the resin the desired microstructure is fabricated. In this work, we developed a method to introduce ZnO nanowires in the fabricated microstructure by mixing the ZnO nanowires powder to the acrylic resin. The used resin is a combination of two compounds, etoxilated(6)trimethylolpropane triacrylate (SR-499) and tris(2-hydroxy ethyl)isocyanurate triacrylate (SR-368). As a photoinitiator we have used Lucirin TPO-L (2,4,6-trimetilbenzoiletoxifenil phosphine oxide).The produced samples were characterized by optical microscopy, scanning electron microscopy, energy dispersive spectroscopy, X-ray diffraction spectroscopy and micro-Raman scattering. From these techniques it was possible to observe the presence of nanowires in the microstructures, as well as to characterize the morphological properties, which has been shown to be interesting for developing microdevices. We have also observed fluorescent emission of the microstructures excites by one and two-photons absorption. Therefore, the methodology described here can be used as an alternative in the design of new optical devices.

No description available.

Mechanical stimulation plays a crucial role in promoting cell differentiation. However, applying physical force directly to cells requires complex equipment and a sterile environment, posing challenges. To overcome this, stimuli-responsive biomaterials or 4D scaffolds can serve as an alternative platform for mechanical stimulation. These scaffolds, fabricated using advanced 3D printing techniques, can apply the necessary force to cells. To optimize their functionality, bioactive molecules or extracellular matrices can be incorporated or decorated on their surfaces. This thesis proposal focuses on developing a versatile material platform that allows customization through systematic composition adjustment and on-demand printing, while also offering surface modification capabilities. The primary objective is to create a novel cell carrier platform using thermo-responsive polymers. By manipulating the additive monomer compositions, we can finely adjust properties such as the transition temperature of the polymers, tailoring them to specific requirements. Furthermore, this platform will enable the fabrication of complex three-dimensional biomaterial structures with controllable porosity, a critical aspect of biomaterial design. Leveraging the capabilities of three-dimensional printing technology, we can program and achieve desired porosity levels in the printed structures, providing enhanced flexibility for biomaterial design. The development of thermo-responsive scaffolds involved three distinct stages aimed at designing an optimized platform that effectively operates within the physiological range while ensuring cell viability. One of the key challenges was to achieve a balance between thermoresponsive behavior and biocompatibility. In the initial stage, we investigated the interplay between a crosslinkable three-armed macromer (trimethylolpropane triacrylate-TMPTA) and various monomers (N-isopropylacrylamide-NiPAAm, methyl methacrylate-MMA, dimethylaminoethyl acrylate-DMAEA, 4-acryloylmorpholine-AMO) using thermally induced solution polymerization. NiPAAm, known for its thermoresponsive properties, was selected despite its limited biocompatibility. DMAEA was chosen to adjust the polymer network transition temperature by introducing cationic charge, which disrupts the coil-globule effect of PNiPAAm and provides cell adhesiveness of the composition. Additionally, the hydrophilic monomer AMO was incorporated to further fine-tune the polymeric network. We examined the behavior of these components within the physiological range and their integration into the PNiPAAm network, establishing significant correlations between the transition temperature of the polymer and the crosslinker and monomers in their soluble condition. In the second stage of our research, we introduced photo-induced polymerization to enhance the crosslinking ratio. By utilizing this method, we successfully fabricated photo-polymerized mixtures (photoresists) into thermo-responsive discs, enabling us to study their swelling behavior between 37℃ and 25℃. Our findings revealed that the swelling behavior could be adjusted by varying the ratios of the crosslinker and monomers in the experimental groups. Through careful experimentation, we identified a suitable composition (3% w/w TMPTA, 80% w/w NiPAAm, 15% w/w DMAEA, 5% w/w AMO, and 4% w/w photo-initiator(PI)) that required minimal crosslinking incorporation while still retaining thermo-responsiveness. Furthermore, we conducted a preliminary biocompatibility study by fabricating the mixture into thin-films and cultivating them with L929 fibroblast cells. In the third and final stage, we utilized the optimized formulations from the previous stage to build thermo-responsive 3D scaffolds using continuous Digital Light Processing (cDLP) printing. We investigated the effects of various parameters, such as curing time and monomer composition, on the swelling property of the scaffolds. Additionally, we introduced glycofurol (GF) as a photo-polymerization solvent, which allowed us to produce scaffolds with improved resolution and reduced printing time. The resulting optimized scaffolds, with a composition of 3% w/w TMPTA, 80% w/w NiPAAm, 15% w/w DMAEA, 5% w/w AMO, 4% w/w PI, and 10 seconds per layer, exhibited the desired thermo-responsiveness. To further understand the mechanical properties and thermal dependencies of these scaffolds, we conducted rheological analysis. This analysis helped establish a relationship between the mechanical properties of the scaffolds and their response to temperature changes. To investigate the potential of cell stimulation through periodic changes, we conducted an experiment involving the seeding of L929 fibroblasts and C2C12 myoblasts on thermo-responsive 3D scaffolds. Our objective was to assess the ability of cells to proliferate on scaffolds with different compositions. Specifically, we examined two types of scaffolds: lattice scaffolds, characterized by a porous structure with a periodic network that enables cells to inhabit a 3D environment, and raft scaffolds, which feature a dense 3D structure designed for cells to reside on the surface for observation and evaluation. The lattice scaffolds were composed of ≥2% w/w DMAEA, while the raft scaffolds consisted of ≥5% w/w DMAEA. To evaluate cell proliferation, we conducted direct contact experiments and employed live/dead assays, subjecting the scaffolds to temperature switching conditions at 31℃ and 37℃. These experimental setups aimed to provide insights into the response and behavior of cells in the presence of thermo-responsive scaffolds with varying compositions. The results revealed favorable adhesion and spreading of the cells on the scaffolds. Interestingly, in our dynamic temperature experiment, we observed that myoblasts seeded on the scaffolds exhibited both proliferation and spreading, whereas myoblasts subjected to constant-temperature conditions did not show the same behavior. This suggests that the expansion and contraction of the scaffold, observed in previous experiments, may impact cell viability. Further investigation is needed to better understand this phenomenon. Additionally, we enhanced cell adhesiveness of the scaffolds by impregnating the scaffolds with poly-L-lysine and tested them with hASCs (human adipose-derived stem cells). Significant differences were observed between scaffolds with and without poly-L-lysine, highlighting the effectiveness of this approach. In conclusion, we have successfully developed a thermo-responsive 3D scaffold that exhibits a transition temperature within the physiological range, ensuring cell survival, and provides mechanical stimulation to the cells through the coil-globule effect without causing cell detachment. Among the formulations tested, the GF-printed formulation (3% w/w TMPTA, 80% w/w NiPAAm, 15% w/w DMAEA, 5% w/w AMO, and 4% w/w photo-initiator) with an exposure time of 10 seconds per layer showed the most promising results for cell cultivation under periodic changes in temperature, with a transition temperature of 36.3 °C ± 0.9 °C. Furthermore, we conducted direct cell contact experiments and confirmed the biocompatibility of the thermo-responsive macromer-based scaffolds. These findings demonstrate that this material platform offers a versatile and responsive material for mechanical stimulation of cells on three-dimensional scaffolds. These promising results suggest that this approach holds significant potential for tissue engineering applications and can be utilized to develop mechanical stimulation devices for various biomedical applications.:CHAPTER 1……………………..……………...…………………………..…4 Introduction CHAPTER 2……………………..…………………………..……………….29 Material and Methods CHAPTER 3……………………………………..…..……………………….52 Thermo-Responsive Polymer from Thermal Synthesis Studies CHAPTER 4…………………………………..……………………………...70 An Adjustable Thermo-Responsive Polymer from Photo Synthesis CHAPTER 5……………………………………………………………....….88 Fabrication of Thermo-Responsive Scaffolds from DLP Printing CHAPTER 6…………………...…………………………………………....107 3D Scaffold Biocompatibility Studies CHAPTER 7…………………...……………………………………………139 Discussions CHAPTER 8…………………...……………………………………………161 Summery APPENDIX…………………...………………………………………….…166 Bibliography, List of Publications, CV, Declaration of Authorship, Acknowledgements, Related publication