No description available.

No description available.

No description available.

No description available.

付記する学位プログラム名: 充実した健康長寿社会を築く総合医療開発リーダー育成プログラム / 京都大学 / 新制・課程博士 / 博士(工学) / 甲第23915号 / 工博第5002号 / 新制||工||1781(附属図書館) / 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 大江 浩一, 教授 近藤 輝幸, 教授 浜地 格 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM

<p> This thesis focuses on the use of time-resolved fluorescence anisotropy (TRF A) for the analysis of peptide-silica and protein-silica interactions. Previous studies from our group have shown that strong ionic binding of the cationic probe rhodamine 6G (R6G) to the anionic surface of silica particles in water provides a convenient labeling procedure to study both particle growth kinetics and surface modification by time-resolved fluorescence anisotropy (TRF A). The decays for R6G dispersed in diluted Ludox silica sols usually fit to a sum of picosecond and nanosecond decay components, along with a significant residual anisotropy component. The first objective of my work was to assess the nature of the R6G:silica interaction to determine the origin of the nanosecond decay component, and ultimately validate the model used to fit the TRFA data and gain further insight into the physical meaning of the anisotropy decay parameters. Our results show the origin of the nanosecond decay component ( ¢2) is due to the presence of a subpopulation of small nanoparticles in the Ludox sol. </p> <p> With the correct physical model in place, we have been able use TRFA ofR6G in aqueous Ludox to monitor peptide adsorption onto the silica particles in situ. Steady-state anisotropy and TRF A of R6G in Ludox sols were measured to characterize the extent of the ionic binding of the probe to silica particles in the presence of varying levels of tripeptides of varying charge, including Lys-Trp-Lys (KWK), N-acetylated Lys-Trp-Lys (Ac-KWK), Glu-Trp-Glu (EWE) and N-acetylated Glu-Trp-Glu (Ac-EWE). R6G showed significant decreases in anisotropy in the presence of cationic peptides, consistent with the addition of cationic peptides blocking the adsorption of the dye to the silica surface. The study shows that the competitive binding method can be used to assess the binding of various biologically relevant compounds onto silica surfaces, and demonstrates the potential of TRF A for probing peptide: silica and protein: silica interactions. </p> <p> We have also extended the application of TRF A to monitor protein adsorption onto plain and modified silica particles using a recently reported cationic long-lifetime quinolinium dye, CG437, which strongly binds to anionic silica particles through electrostatic interactions. In this case, alterations in the rotational correlation time of Ludox particles resulting from increases in the diameter of the rotating body upon binding of protein to the silica surface were monitored. The study shows that TRFA analysis of long-lived cationic probes such as CG437 can provide an effective method to investigate interactions between proteins and modified silica surfaces, extending the utility of the TRF A method. </p> / Thesis / Master of Science (MSc)

It is well known that lead is toxic. Since the full effects, particularly of long term, low level exposure are not well understood, further knowledge of lead metabolism has significant public health implications. Traditionally, clinical studies of lead's effect on health have relied heavily on blood lead levels as an indicator of lead exposure. However, this is unsatisfactory, because blood lead levels principally reflect only recent exposure and lead in serum is more readily bioavailable than whole blood. Over 90% of the lead body burden is in bone, where it has a long residence time. Therefore, bone lead measurements are reflective of cumulative exposure. The bone lead detection system at McMaster University uses a ¹⁰⁹Cd source, which is positioned at the centre of the detector face (HPGE). This arrangement allows great flexibility, since one can sample lead in a range of different bone sites due to a robust normalization technique that eliminates the need to correct for bone geometry, thickness of overlying tissue, and other related factors. Lead in both the tibia and the calcaneus, whole blood lead, and serum lead have been measured in a group of 49 active lead workers (Nova Pb bone lead survey). Before studying the interrelationships between the above measurements, work was done to improve the programs which fit the bone lead spectra. That is, work was done to link the amplitudes of the alpha and beta peaks and to investigate the sensitivity of the analysis on the channel ranges and start parameters. The main goal of this project was to carefully study the interrelationships between the major components of any human lead metabolism model, bone, whole blood, and serum, in order to establish a solid basis for computer modelling of lead metabolism. / Thesis / Master of Science (MSc)

Fluorescence based spectroscopy and imaging techniques provide qualitative and quantitative diagnostic information about biological systems. Some tissue cells have inherent fluorescence characteristics, and when excited with light at a certain frequency, they can emit light of a slightly longer wavelength; a phenomenon known as autofluorescence. Differences in the autofluorescence emission spectra between healthy and diseased tissue may be used as a non-invasive diagnostic tool for the detection of diseases. In this thesis, I describe the design, fabrication, and testing of a miniaturized fluorescence imaging device for non-invasive clinical diagnosis in the gastrointestinal tract. The device is designed such that it can be turned completely wireless. The system includes three sub-modules: optical imaging, electronics control and image acquisition, and information processing and transmission. These modules were individually developed and tested before being integrated into a complete, externally powered device. The final integrated system is small in size (diameter: ~ 2.5 cm; length: ~ 11 cm). The performance of each individual module and the overall integrated system has been evaluated using fluorescent phantoms. It has been demonstrated that the miniaturized device can acquire spectrally-resolved fluorescence images. It has also been separately demonstrated that the image stream can be transmitted wirelessly. An important outcome of this feasibility study is the identification of important technological issues and pathways for future prototype development. / Thesis / Master of Applied Science (MASc)

This thesis explores the use of skin iron concentration, assessed using a portable x- ray fluorescence (PXRF) analyzer, as an indicator of liver iron concentration. Ultrasound images were acquired from four sites on human cadavers: thenar eminence (TE), between the metacarpophalangeal joint 1 and 2 (MJ), patella (P), and plantar arch (PA). Skin thickness was subsequently measured using boundary detection software applied to the ultrasound images. Skin iron concentrations, from the same sites, were obtained directly from 13 cadavers using a PXRF analyzer. As the iron concentrations determined using PXRF may have been impacted due to beam attenuation through the skin, these iron concentrations were subsequently corrected using the Beer-Lambert Law accounting for the skin thickness at each site. Huber XRF is a bulk tissue measurement system that was used to measure iron concentrations from the extracted samples of the four sites. The skin iron concentrations determined using both PXRF and Huber XRF were compared to evaluate the agreement between the two methods. As such, samples from the four sites were extracted and the iron concentrations of the extracted samples were measured using a Huber X-Ray Fluorescence (XRF) analyzer as the control. A statistically significant relationship with a p-value of <0.01 and a strong correlation with a R2 value of 0.87 was seen between the corrected skin iron concentrations determined using PXRF and the skin iron concentrations determined using Huber XRF analysis of the extracted samples. Thus, the skin iron concentrations obtained using PXRF are representative of the skin iron concentrations collected by Huber XRF. For further validation, liver samples were obtained from 6 of the 13 cadavers and the liver iron concentrations were assessed using Huber XRF. The non- corrected PXRF, corrected PXRF and the Huber XRF skin iron concentrations were then compared with the liver iron concentrations. The relationships between iron concentrations measured at the PA site and in the liver were found to be statistically significant with strong correlations (R2 = 0.94 for Huber XRF, R2 = 0.87 for non-corrected PXRF, and R2 = 0.95 for corrected PXRF). Therefore, the skin iron concentrations at the PA site determined by PXRF and determined by Huber XRF analysis of skin samples could be used in the future as a surrogate marker for the liver iron concentrations in humans. / Thesis / Master of Science (MSc)

Yes / A laser induced fluorescence system has been developed to visualise the oil film thickness between the piston ring and cylinder wall of a fired gasoline engine via a small optical window mounted in the cylinder wall. A fluorescent dye was added to the lubricant in the sump to allow the lubricant to fluoresce when absorbing laser radiation. The concentration of the dye did not disturb the lubricant chemistry or its performance. Degraded engine oil samples were used to investigate the influence of lubricant quality on ring pack lubricant film thickness measurements. The results show significant differences in the lubricant film thickness profiles for the ring pack when the lubricant degrades which will affect ring pack friction and ultimately fuel economy.