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Magnetic refrigeration based on the magnetocaloric effect (MCE) is a promising alternative to conventional gas compression based cooling techniques. Understanding impacts of reduced dimensionality on the magnetocaloric response of a material such as Gadolinium (Gd) or its alloys is essential in optimizing the performance of cooling devices, which is also the overall goal of this thesis. We have determined, in the first part of the thesis, that laminate structures of pure Gd produced by magnetron sputtering have several disadvantages. The target material (pure Gd), ultra-high vacuum components, and the electrical energy it takes to run the manufacturing process are all very costly. To produce quality films requires a time and energy consuming chamber preparation (gettering) to produce films with a relative cooling power (RCP) of an order of magnitude smaller (~70 J/kg) than can be obtained with Gd-alloy microwires (~800 J/kg). The increased surface area for an array of wires as compared to a laminate structure allows for more efficient heat transfer. For all of these reasons, we turned the focus onto Gd-alloy microwires. In the latter part of this thesis, we have discussed the Gd-alloy microwires as a function of magnetocaloric parameters of magnetic entropy change, adiabatic temperature change, and refrigerant capacity (RC). We have demonstrated two effective methods for improving the RC of the microwires through creating novel biphase nanocrystalline/amorphous structures via thermal annealing and directly from adjusted melt-extraction. Through studying the effects of chemical doping, as well as studying arrays of microwires with a range of Curie temperature (TC) values, we have designed a new magnetic bed structure that has potential applications as a cooling device for micro-electro-mechanical systems and energy-conversion devices.

L’utilisation de plus en plus fréquente des agents de contraste à base de Gd (AC-Gd) au cours des examens d’Imagerie par Résonnance Magnétique (IRM), engendre le rejet de ces produits pharmaceutiques dans les eaux usées retraitées en STation d’EPuration (STEP). En l’absence de retraitement spécifique de ces AC-Gd en STEP, ils sont rejetés dans le milieu aquatique, où de nombreuses études ont relevé leur présence aussi bien dans les eaux de surface que dans les eaux souterraines et jusqu’à l’eau du robinet. Le manque de connaissances concernant les effets des AC-Gd suite à leur rejet a mis en évidence la nécessité d’étudier leurs impacts environnementaux sur les organismes vivants dans les milieux aquatiques. Dans ce contexte, nous avons choisi de déterminer les concentrations en Gd d’origine anthropique à proximité de rejets de STEP et de zones de captage en eau potable situés en région Lorraine. Nos mesures ont permis de montrer la présence Gd d’origine anthropique sur l’ensemble des échantillons prélevés, avec des concentrations mesurées comprises de quelques ng(Gd)/L à quelques dizaines de µg(Gd)/L. Ces concentrations de Gd anthropique seraient dues à la présence d’AC-Gd. Nous nous sommes plus particulièrement intéressés aux effets de l’AC-Gd le plus stable et l’un des plus fréquemment commercialisé : le Gd-DOTA (Dotarem®). Pour cela, nous avons choisis plusieurs espèces représentatives des taxons rencontrés dans les cours d’eau Lorrains. Des essais ont été menés en conditions contrôlées de laboratoire afin de mesurer l’accumulation du Gd-DOTA dans les tissus et les effets de l’AC-Gd ont été appréhendés au travers de mesures de croissance, de reproduction et de mortalité au niveau individuel chez les microalgues vertes unicellulaires (Chlorella vulgaris et Pseudokirchneriella subcapitata), chez un microcrustacé (Daphnia magna) et chez un vertébré aquatique (Danio rerio) exposés à des concentrations en Gd-DOTA réalistes d’un point de vue environnemental. L’accumulation du Gd-DOTA a aussi été mesurée chez les bivalves (Corbicula fluminea et Dresseina rostriformis bugensis) et comparée à des mesures d’accumulation du Gd in situ. Les réponses physiologiques des bivalves ont été évaluées à l’aide d’une batterie de 11 biomarqueurs dans leurs branchies et leur glande digestive. Les effets de l’AC-Gd ont également été étudiés in vitro sur des fibroblastes de D. rerio (cellules ZF4 - ATCC-2050). Nos travaux ont montré que les AC-Gd et le Gd-DOTA en particulier étaient responsables d’effets écotoxiques indirects à différents niveaux d’organisation biologiques. Seuls les bivalves accumulent le Gd-DOTA mais tous les individus semblent mettre en place des mécanismes de dépuration pour parer à la toxicité de l’AC-Gd. Les résultats obtenus au cours de cette recherche ont confirmé la nécessité d’un suivi des concentrations en AC-Gd dans le milieu aquatique et la nécessité d’approfondir les études de l’écotoxicité de ces produits pharmaceutiques. Ceci pourra aboutir à une évaluation pertinente de leur risque environnemental et de proposer des solutions pour la gestion environnementale de ces composés / The increasing use of Gadolinium-based Contrast Agents (Gd-CA) for Magnetic Resonance Imaging (MRI) results in their rejection in Waste Water Treatment Plants (WWTPs). Due to the lack of specific recycling process in European WWTPs, these pharmaceutical produces enter the aquatic environment from river to tap water. The effects of Gd-CA in aquatic media have been not studied yet. The lack of knowledge about these effects highlighted the need to study their environmental impacts on aquatic organisms. In this context, we decided to measure anthropogenic concentrations of Gd in the aquatic environment in the Lorraine region (France) closed to WWTPs outputs and catchment areas used for drinking water. Our measurements underlined the presence of anthropogenic Gd on all the collected samples at concentrations ranging from few ng/L to several dozen of µg/L. In this research we focused on the effects of the most frequently used Gd-CA, the gadoteric acid (Gd-DOTA - Dotarem®) which is also the most stable one. Several representative species of aquatic environment were selected for ecotoxicological assays: i.e. unicellular green microalgae (Chlorella vulgaris and Pseudokirchneriella subcapitata), microcrustacean (Daphnia magna) and aquatic vertebrate (Danio rerio). Assays were conducted in laboratory under controlled conditions as well as in situ. Gd-DOTA accumulation was measured in the tissues of the different organisms. Environmental realistic concentrations of Gd-CA were used to assess their effects at the individual level by means of growth, reproduction and mortality measurements. The Gd-DOTA accumulation was also measured in bivalves’ tissues (Corbicula fluminea and Dresseina rostriformis bugensis) and compared to Gd ones in situ in these organisms. Physiological responses were assessed based on a battery of 11 complementary biomarkers measured in the digestive gland and in the gills of both bivalve species. At cellular level, the effects of Gd-DOTA were studied in vitro on D. rerio fibroblasts (ZF4 – ATCC-2050). Indirect ecotoxicological effects of Gd-CA and of Gd-DOTA especially have been highlighted at all biological levels. Accumulation of Gd-DOTA was observed in bivalves only, but defense systems were mobilized in all organisms to limit toxicity. Our results demonstrated that following both research on ecotoxicological effects of the Gd-CA and evolution of their concentrations in aquatic ecosystem are necessary to assess more precisely their environmental risk and to propose solutions for their environmental management

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第19738号 / 工博第4193号 / 新制||工||1647(附属図書館) / 32774 / 京都大学大学院工学研究科物質エネルギー化学専攻 / (主査)教授 近藤 輝幸, 教授 辻 康之, 教授 大江 浩一 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM

Gadolinium-based contrast agents (GBCAs) have been used in hospitals worldwide for the past three decades to increase contrast for magnetic resonance imaging (MRI), thus allowing for more accurate diagnoses. When first developed, GBCA complexes were thought to be completely stable, and excreted from the body within hours. However, GBCAs have since been shown to deposit in organs such as bone, suggesting complex dissociation. GBCA safety has now become one of the biggest concerns in the field of radiology, with the clinical implications of retained Gd remaining unknown. A non-invasive technique to measure retained Gd in the body would allow for investigation of the potential negative health effects of GBCAs. In this thesis, the technique of x-ray fluorescence (XRF) to detect retained gadolinium (Gd) in bone following the administration of GBCAs is investigated. The research employs a series of bone phantom measurements to determine the feasibility of using an XRF-based detection system to perform non-invasive in vivo measurements of Gd in human tibia bones. Minimum detection limits (MDLs) of the XRF detection system are calculated to assess the feasibility of performing a human measurement in a realistic time. Through these experiments, the XRF detection system developed in this thesis work is deemed feasible for human measurements of Gd in bone. The second half of this thesis work involves performing the first non-invasive measurements of Gd in bone in a small population: 11 exposed individuals who had previously received GBCA, and 11 controls. The result of this work is promising, as the XRF system is successful in measuring Gd in bone in vivo. Additionally, the Gd bone concentration of the exposed group is significantly higher than the control group. Following this small pilot study, additional measurements are conducted on individuals self-reporting symptoms of Gd toxicity. Gd concentrations in bone and urine are compared for three groups: symptomatic exposed, non symptomatic exposed, and control. The concentration of Gd in bone and urine for the symptomatic exposed group is significantly higher. However, there is no correlation between the amount of Gd in bone and urine, suggesting a secondary storage site for Gd in the body, other than bone. / Thesis / Doctor of Philosophy (PhD)

Dans la foulée des avancées en médecine nucléaire, l’imagerie moléculaire par résonance magnétique a pris son essor ces dernières années car elle constitue un enjeu contemporain en vue d’améliorer le diagnostic et le suivi thérapeutique de pathologies comme le cancer ou la maladie d’Alzheimer. Cependant, cette technique d’imagerie médicale souffre à la fois de la petite quantité de récepteurs disponibles in vivo et de la faible sensibilité de l’IRM pour la détection d’agents de contraste exogènes. De ce fait, la littérature montre un intérêt croissant pour le développement de nouveaux agents de contraste pouvant porter plusieurs milliers de contrastophores et de nouvelles techniques sont nécessaires pour évaluer l’efficacité de ces derniers. Ainsi, lorsqu’un agent de contraste fonctionnalisé est injecté in vivo, ce dernier va subir de nombreux processus biochimiques (extravasation, fixation spécifique sur les récepteurs, internalisation dans les cellules…) qui peuvent rendre les mécanismes de prise de contraste difficile à appréhender. De ce fait, nous avons développé une nouvelle méthode in vitro d’observation cellulaire permettant de caractériser les agents de contraste par IRM en modélisant expérimentalement certains des mécanismes ayant lieu in vivo, tout en s’affranchissant des problèmes liées à l’expérimentation sur petit animal (résolution, Rapport signal sur bruit, reproductibilité inter-animale,…). Notre approche a reposé sur la conception d’un dispositif de microhistologie par IRM qui permet de détecter une monocouche de cellules d’une dizaine de microns d’épaisseur dans un environnement microfluidique. Après avoir totalement caractérisé notre méthode avec des cellules ayant internalisé un agent de contraste commercial (Dotarem), nous l’avons utilisé pour évaluer la capture dynamique d’un nouvel agent de contraste développé à Guerbet : une émulsion paramagnétique fonctionnalisée avec des peptides RGD destinée à l’imagerie de l’angiogénèse tumorale. Dans un canal microfluidique, nous avons préparé une monocouche confluente de cellules endothéliales et appliqué un flux d’agent de contraste au-dessus de ces dernières. Par IRM, nous avons pu réaliser un suivi dynamique de la capture de l’agent de contraste par les récepteurs membranaires des cellules. En plus de démontrer la spécificité de l’agent de contraste comme le font les méthodes traditionnelles, notre technique nous a permis d’évaluer les constante cinétiques d’association et de dissociation et la constante d’affinité de l’agent de contraste pour les récepteurs dans des conditions physiologiques proches de celles existant in vivo, notamment en termes de disposition des cellules et de la vitesse et de la concentration de l’agent de contraste. / Following the recent advances in nuclear medicine, magnetic resonance imaging has rapidly become an emerging technique for molecular imaging since it constitutes a contemporary issue for the improvement of the diagnosis and the post-treatment follow-up of pathologies such as cancer and Alzheimer’s disease. However, this technique suffers from both the weak amount of in vivo receptors and the low sensitivity of MRI for the detection of exogenous contrast agents. Thus, the literature shows an increasing interest for the development of novel contrast agents which can carry several thousands of contrastophores and new techniques are needed to evaluate the efficiency of these contrast agents. Indeed, when a targeted contrast agent is injected intraveneously, many biochemical process can occur simultaneously (extravasation, specific binding on receptors, internalization inside cells, …), which can make the contrast uptake mechanisms difficult to investigate. Hence, we developed a new method of cellular observation allowing to characterize the contrast agent by MRI, by imitating some of the in vitro mechanisms that occur in vivo. Using this technique, we also avoided problems that are linked to the experimentation on small animal in terms of resolution, signal to noise ratio and inter-animal reproducibility.Our approach was based on the design and fabrication of a microhistological device that allows to detect a living cells’ monolayer - whose thickness is above 10 microns - in a microfluidic environment. After having fully characterized our method with cells that had internalized a commercial contrast agent (Dotarem), we used it to evaluate the dynamic uptake of a new contrast agent developed and synthetized in Guerbet : a paramagnetic nanoemulsion functionalized with RGD peptides to target the avb3 integrins that play a capital role in the tumor angiogenesis process. In a microfluidic channel, we prepared an endothelial cell monolayer and applied a flow of contrast agent over the cell layer. We were able to follow-up by MRI the uptake of the contrast agent by the cell surface receptors. Besides demonstrating the specificity of the contrast agent as well as traditional in vitro techniques, our technique provides an additional information level since it is able to evaluate the kinetic constants and the affinity of the contrast agents toward the receptors. These experiments were done under physiological conditions close to the ones existing in vivo in terms of cell arrangement, concentration and flow velocity of the contrast agent.

No description available.

This work presents the development of a GaN-based dilute magnetic semiconductor (DMS) by metal organic chemical vapor deposition (MOCVD) that is ferromagnetic at room temperature (RT), electrically conductive, and possesses magnetic properties that can be tuned by n- and p-doping. The transition metal series (TM: Cr, Mn, and Fe) along with the rare earth (RE) element, Gd, was investigated in this work as the magnetic ion source for the DMS. Single- phase and strain-free GaTMN films were obtained. Optical measurements revealed that Mn is a deep acceptor in GaN, while Hall measurements showed that these GaTMN films were semi-insulating, making carrier mediated exchange unlikely. Hysteresis curves were obtained for all the GaTMN films, and by analyzing the effect of n- and p-dopants on the magnetic properties of these films it was determined that the magnetization is due to magnetic clusters. These findings are supported by the investigation of the effect of TM dopants in GaN nanostructures which reveal that TMs enhance nucleation resulting in superparamagnetic nanostructures. Additionally, this work presents the first report on the development of GaGdN by MOCVD providing an alternate route to developing a RT DMS. Room temperature magnetization results revealed that the magnetization strength increases with Gd concentration and can be enhanced by n- and p-doping, with holes being more efficient at stabilizing the ferromagnetic signal. The GaGdN films obtained in this work are single-phase, unstrained, and conductive making them suitable for the development of multifunctional devices that integrate electrical, optical, and magnetic properties.