Microelectrophoresis analysis with a rapid impulse measurement

碩士 === 國立臺灣大學 === 電子工程學研究所 === 93 === Electrophoresis is a technique has long been used to separate biomolecule fragments with different e/m ratios in accordance with medical diagnosis. But there were some shortcomings have long been existed but still cannot be overcome in traditional electrophoresi...

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Main Authors: Kung-Chu Ho, 何恭竹
Other Authors: Chieh-Hsiung Kuan
Format: Others
Language:en_US
Published: 2005
Online Access:http://ndltd.ncl.edu.tw/handle/48982426538850517948
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spelling ndltd-TW-093NTU054280732015-12-21T04:04:14Z http://ndltd.ncl.edu.tw/handle/48982426538850517948 Microelectrophoresis analysis with a rapid impulse measurement 快速脈衝式量測之微電泳分析 Kung-Chu Ho 何恭竹 碩士 國立臺灣大學 電子工程學研究所 93 Electrophoresis is a technique has long been used to separate biomolecule fragments with different e/m ratios in accordance with medical diagnosis. But there were some shortcomings have long been existed but still cannot be overcome in traditional electrophoresis. Most of which could be analyzed and be taken innovation in a point of view of nanoelectronic technology. First, the buffer medium used in traditional electrophoresis leads to decrease the biomolecular separation efficiency because of thermal diffusion, convection and perturbation motion. That is why high applied electric field could not suitable for old type electrophoresis. Besides, we also want to exclude some poor properties like time-consuming, low repeatability, and use of dangerous carcinogenic fluorescent dye, etc. In this thesis, we bring up a concept base on semiconductor physics to analysis the movement of DNA macroions under an applied impulse voltage. We can obtain the DNA composition with different molecular weights rapidly with just feeding an impulse with high-frequency instead of really “separating” them. By observing RC transient response of different bases, molecular weights and concentrations, we expect that the response curve under the same measuring condition can be repeated. Then we import Ambipolar equations in semiconductor physics to elucidate DNA movement and distribution under applied impulses. And we got an I-V characteristic after sufficient times for measuring, analyzing current component and the reasons of current difference among different DNA sequences. We preliminary confirmed the novel analysis technique is practicable and repeatable. After sufficient data are being acquired, we decide to establish a theoretical model to analyze biomolecular rapid mechanism, and then making a breakthrough for biomedical diagnosis and identification. Chieh-Hsiung Kuan 管傑雄 2005 學位論文 ; thesis 68 en_US
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description 碩士 === 國立臺灣大學 === 電子工程學研究所 === 93 === Electrophoresis is a technique has long been used to separate biomolecule fragments with different e/m ratios in accordance with medical diagnosis. But there were some shortcomings have long been existed but still cannot be overcome in traditional electrophoresis. Most of which could be analyzed and be taken innovation in a point of view of nanoelectronic technology. First, the buffer medium used in traditional electrophoresis leads to decrease the biomolecular separation efficiency because of thermal diffusion, convection and perturbation motion. That is why high applied electric field could not suitable for old type electrophoresis. Besides, we also want to exclude some poor properties like time-consuming, low repeatability, and use of dangerous carcinogenic fluorescent dye, etc. In this thesis, we bring up a concept base on semiconductor physics to analysis the movement of DNA macroions under an applied impulse voltage. We can obtain the DNA composition with different molecular weights rapidly with just feeding an impulse with high-frequency instead of really “separating” them. By observing RC transient response of different bases, molecular weights and concentrations, we expect that the response curve under the same measuring condition can be repeated. Then we import Ambipolar equations in semiconductor physics to elucidate DNA movement and distribution under applied impulses. And we got an I-V characteristic after sufficient times for measuring, analyzing current component and the reasons of current difference among different DNA sequences. We preliminary confirmed the novel analysis technique is practicable and repeatable. After sufficient data are being acquired, we decide to establish a theoretical model to analyze biomolecular rapid mechanism, and then making a breakthrough for biomedical diagnosis and identification.
author2 Chieh-Hsiung Kuan
author_facet Chieh-Hsiung Kuan
Kung-Chu Ho
何恭竹
author Kung-Chu Ho
何恭竹
spellingShingle Kung-Chu Ho
何恭竹
Microelectrophoresis analysis with a rapid impulse measurement
author_sort Kung-Chu Ho
title Microelectrophoresis analysis with a rapid impulse measurement
title_short Microelectrophoresis analysis with a rapid impulse measurement
title_full Microelectrophoresis analysis with a rapid impulse measurement
title_fullStr Microelectrophoresis analysis with a rapid impulse measurement
title_full_unstemmed Microelectrophoresis analysis with a rapid impulse measurement
title_sort microelectrophoresis analysis with a rapid impulse measurement
publishDate 2005
url http://ndltd.ncl.edu.tw/handle/48982426538850517948
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