京都大学 / 0048 / 新制・課程博士 / 博士(医学) / 甲第21682号 / 医博第4488号 / 新制||医||1036(附属図書館) / 京都大学大学院医学研究科医学専攻 / (主査)教授 妻木 範行, 教授 大森 孝一, 教授 別所 和久 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM

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Residual value is defined as the price for which a used piece of equipment can be sold in the market at a particular time. It is an important element of the owning costs of equipment and needs to be estimated by equipment managers for making investment decisions. The purpose of this study is to gain insights into the residual value of selected groups of heavy construction equipment and to develop a mathematical model for its prediction. Auction sales data were collected from two online databases. Manufacturer publications and an online source provided size parameters and manufacturers suggested retail prices matching the auction records. Macroeconomic indicator values were collected from a variety of sources, including government agencies. The data were brought into the same electronic format and were matched by model name and calendar date, respectively. Data from auctions in the U.S. and in Canada were considered for this study. Equipment from four principal manufacturers of up to 15 years of age at the time of sale was included. A total of 35,542 entries were grouped into 11 different equipment types and 28 categories by size as measured by horse power, standard operating weight, or bucket volume. Equipment types considered were track and wheel excavators, wheel and track loaders, backhoe loaders, integrated toolcarriers, rigid frame and articulated trucks, track dozers, motor graders, and wheel tractor scrapers. Multiple linear regression analyses of the 28 datasets were carried out after outliers had been deleted. Explanatory variables for the regression model were age in years, the indicator variables manufacturer, condition rating, and geographic region, and selected macroeconomic indicators. The response variable was residual value percent, defined as auction price divided by manufacturers suggested retail price. Different first, second, and third-order polynomial models and exponential and logarithmic models of age were examined. A second-order polynomial was selected from these functional forms based on the adjusted coefficient of determination. Coefficients for the 28 models and related statistics were tabulated. A spreadsheet tool incorporating the final regression model and its coefficients was developed. It allows performing the residual value prediction in an interactive and intuitive manner. / Ph. D.

Yes / We report a technique for the fabrication of micropockets within electrospun membranes in which to study cell behavior. Specifically, we describe a combination of microstereolithography and electrospinning for the production of PLGA (Poly(lactide-co-glycolide)) corneal biomaterial devices equipped with microfeatures.

Yes / Our overall aim is to develop a synthetic off-the-shelf alternative to human amniotic membrane which is currently used for delivering cultured limbal stem cells to the cornea in patients who suffer scarring of the cornea because of the loss of limbal stem cells. We have recently reported that both cultured cells and limbal explants grow well on electrospun Poly(D,L-lactide-co-glycolide) (PLGA) (44 kg/mol) with a 50:50 ratio of lactide and glycolide and sterilized with γ-irradiation. Prior to undertaking a clinical study our immediate aim now is to achieve long term storage of the membranes in convenient to use packaging. Membranes were electrospun from Poly(D,L-lactide-co-glycolide) (44 kg/mol) with a 50:50 ratio of lactide and glycolide and sterilized with γ-irradiation and then stored dry (with desiccant) for several months at -80°C and -20°C , Room temperature (UK and India), 37°C and 50°C. We explored the contribution of vacuum sealing and the use of a medical grade bag (PET/Foil/LDPE) to achieve a longer shelf life. Confirmation of membranes being suitable for clinical use was obtained by culturing tissue explants on membranes post storage. When scaffolds were stored dry the rate of breakdown was both temperature and time dependent. At -20°C and -80°C there was no change in fiber diameter over 18 months of storage, and membranes were stable for 12 months at 4°C while at 50°C (above the transition temperature for PLGA) scaffolds lost integrity after several weeks. The use of vacuum packaging and a medical grade bag both improved the storage shelf-life of the scaffolds. The impact of temperature on storage is summarized beneath. We report that this synthetic membrane can be used as an off-the-shelf or-out-of-the freezer alternative to the amniotic membrane for corneal regeneration.

Part of the research described in this thesis is conducted in collaboration with Centre d' étude et de Recherche sur les Macromolécules (CERM), Université de Liège, Sart-Tilman, Belgium / Les copolymères séquencés amphiphiles sont très prometteurs pour des applications de technologie de pointe en raison de leur capacité à s'auto-assembler dans des structures bien organisées à l'échelle du micro– et du nanométre, et de leur sensibilité à des stimulations de différentes natures. La formation des nanomotifs bien ordonnés dans les films et/ou en masse fournit un substitut à la nanolithographie et est utile pour le design et l'ingénierie de nanomembranes et de matériaux nanoporeux. L'auto–assemblage dans des solvants sélectifs, en incluant la sensibilité au pH et à la température, peut être ajusté pour correspondre aux besoins de différentes applications biomédicales, telles que l’encapsulation et/ou relargage de médicaments, l'ingénierie de tissus, etc. Dans ce contexte, des copolymères séquencés de type L–lactide (LLA) et méthacrylate 2–diméthylaminoéthyl (DMAEMA) sont d’un grand intérêt. Comme le contrôle sur l'auto–assemblage des copolymères séquencés est permis au niveau moléculaire, il est très important de préparer des copolymères bien définis avec des longueurs de bloc prévisibles et de faible polydispersité. Ainsi, une partie de cette étude a été consacrée au développement de procédures synthétiques optimales et à la caractérisation détaillée de copolymères di– et triblocs de LLA et de PDMAEMA. Un outil simple pour déterminer la présence d'homo–PLLA résiduel a été développée; cela a permis de déterminer et d'expliquer plusieurs voies de synthèse indésirables. La dernière inclut la participation possible de l'amorceur bifonctionnel utilisé, et nous avons alors proposé un système alternatif d'amorceur bifonctionnel/catalyseur. La racémisation du LLA par les unités amine de (P)DMAEMA a été observée pendant la polymérisation, limitant ainsi l'utilisation première du bloc PDMAEMA pour la préparation des copolymères PLLA–b–PDMAEMA. Les études thermiques et de cristallisation, en incluant les copolymères séquencés partiellement quaternisés, ont révélé un retard significatif de la vitesse de cristallisation, en présence du bloc de PDMAEMA. Nous avons constaté que les blocs sont miscibles pour de faibles masses molaires et que la miscibilité partielle est maintenue après quaternisation. Selon la longueur et le taux de quaternisation du bloc PDMAEMA, la cristallisation du PLLA a été étudiée dans un environnement restreint et confiné, faiblement ou fortement. La torsion des lamelles cristallines observée pour certains copolymères biséquencés a été accentuée dans les copolymères triséquencés, où la formation de sphérolites annelés a été observée dans toutes les conditions thermiques utilisées. / Multi–functional amphiphilic block copolymers have much promise for various high technology applications thanks to the controlled stimuli–responsive self–assembly into well–organized structures on the micro– and nanometer scales. The formation of well–ordered nanopatterns in films and/or in bulk provides a competitive substitute to nanolithography and is useful in the design and engineering of nanomembranes and nanoporous materials. Solution self–assembly in selective solvents, including pH and temperature sensitivity, can be tuned to match the needs of different biomedical applications, such as drug encapsulation/delivery, tissue engineering, etc. In this context, block copolymers of L–lactide (LLA) and 2–dimethylaminoethyl methacrylate (DMAEMA) are of great interest. Since the control over self–assembly of block copolymer systems is enabled on a molecular level, it is of great importance to prepare well–defined block copolymers with predictable block lengths and low polydispersity. Thus, a major part of the research in this study was devoted to developing optimal synthetic procedures with detailed characterization of linear di– and triblock copolymers of LLA and PDMAEMA. A simple tool to determine homo–PLLA impurity was developed, which helped to determine and explain several undesired routes. The latter includes possible involvement of the bifunctional initiator used, and an alternative bifunctional initiator/catalyst system was proposed. Racemization of LLA by (P)DMAEMA moieties was observed during LLA polymerization thus limiting the utilization of PDMAEMA–first approach for the preparation of PLLA–b–PDMAEMA. Thermal and crystallization studies, including on quaternized block copolymers, revealed a significant retardation effect of the PDMAEMA block on the crystallization kinetics. The blocks were found to be miscible in the melt at low molecular weights, and maintained partial miscibility after quaternization. Depending on the length and the quaternization degree of PDMAEMA, PLLA crystallization was studied in a templated, soft or hard confinement environment. Crystalline lamellae twisting observed in certain diblock copolymers was facilitated in triblock copolymers, where the formation of banded spherulites was observed in all thermal conditions used.

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