| Project/Area Number |
11554032
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 展開研究 |
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| Research Field |
分離・精製・検出法
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| Research Institution | The University of Tokyo (2000-2001)
Hokkaido University (1999) |
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Principal Investigator |
KIM Haeng-boo The University of Tokyo, School of Engineering, Assc. Prof., 工学部・附属総合試験所, 助教授 (40186367)
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| Co-Investigator(Kenkyū-buntansha) |
HISAMOTO Hideaki The University of Tokyo, School of Engineering, Lecturer, 大学院・工学系研究科, 講師 (00286642)
KITAMORI Takehiko The University of Tokyo, School of Engineering, Prof., 大学院・工学系研究科, 教授 (60214821)
セルゲイ クラユシュキン (株)東京インスツルメンツ, レーザー計測開発課, 係長(研究職)
SATOH Kiichi The University of Tokyo, School of Engineering, Res.Assc., 大学院・工学系研究科, 助手 (50321906)
KRAYUSHKIN Sergey V. Tokyo Instruments, Inc., Assistant Manager
石坂 昌司 北海道大学, 大学院・理学研究科, 助手 (80311520)
八尾 浩史 北海道大学, 大学院・理学研究科, 助手 (20261282)
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| Project Period (FY) |
1999 – 2001
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| Project Status |
Completed (Fiscal Year 2001)
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| Budget Amount *help |
¥12,400,000 (Direct Cost: ¥12,400,000)
Fiscal Year 2001: ¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 2000: ¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 1999: ¥6,300,000 (Direct Cost: ¥6,300,000)
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| Keywords | microspectroscopy / laser-trapping / flow cell / extraction / solid phase concentration / microparticle / dye staining of living cell / イオン交換樹脂 |
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| Research Abstract |
Microspectroscopy and microelectrochemical systems combined with a fluid manifold were developed to manipulate : and analyze single microparticles such as polymer beads, oil droplets, living cells, and so forth. By using a flow cell set on a microscope stage, an aqueous solution containing microparticles is introduced to the cell. With a single particle being fixed by laser-trapping for polymer beads, on the top end of a microcapillary for oil-droplets, or on the wall by adhesion for living-cells, other non-fixed particles are pumped out completely by flow of sufficient amount of water to the cell. These procedures can hold exclusively the single particle in the cell. By using an appropriate fluid manifold, furthermore, an arbitrary reagent can be introduced to the cell, so that a temporal profile of chemical/physical responses of the particle would be monitored by microspectroscopic and/or microelectrochemical method(s) without interference by other particles. Three different chemical/biochemical processes were studied under solution-flow conditions :
1) Ion-exchange dynamics of a single ion-exchange-resin bead by laser trapping-absorption microspectroscopy.
2) Liquid/liquid extraction dynamics of a single oil-droplet by microinjection - microspectroscopy.
3) Dye-staining dynamics of a single living-cell (Saccharomyces cerevisiae)
The ion-exchange, the extraction, or the staining rate and efficiency were discussed in terms of the solution flow rate and the particle diameter.
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