The Study of the Preconcentration for Diluted Biochemical Samples

碩士 === 國立成功大學 === 工程科學系碩博士班 === 100 === In this experiment, we demonstrate production of a microfluidic chip through a micro-electromechanical technique and, by use of Nafion instead of a nanochannel, we produce integrated micro-nano chips for use in sample preconcentration. By applying an electri...

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Main Authors: Chen-ChiaoChao, 趙晨喬
Other Authors: Ruey-Jen Yang
Format: Others
Language:en_US
Published: 2012
Online Access:http://ndltd.ncl.edu.tw/handle/97967694555066053233
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spelling ndltd-TW-100NCKU50280702015-10-13T21:33:37Z http://ndltd.ncl.edu.tw/handle/97967694555066053233 The Study of the Preconcentration for Diluted Biochemical Samples 稀薄濃度的生化樣品預濃縮之研究 Chen-ChiaoChao 趙晨喬 碩士 國立成功大學 工程科學系碩博士班 100 In this experiment, we demonstrate production of a microfluidic chip through a micro-electromechanical technique and, by use of Nafion instead of a nanochannel, we produce integrated micro-nano chips for use in sample preconcentration. By applying an electric field to the chips, the Nafion becomes ion selective as a result of inner electric double layer overlapping. More specifically, when a difference in flux exists between positive and negative ions in the nanochannels, it results in a concentration polarization phenomenon at the micro and nano interface. Concentration polarization phenomena cause a concentration gradient to occur near the membrane. This study used an ion-selective membrane in which the flux of the cation is larger than the flux of the anion. When we applied an electric field, the effect caused a partial depletion at the anodic side and ion enrichment at the cathodic side. The ion accumulation is induced by the difference in electromigration at the border between the depletion zone and electroosmosis flow. In the end, it creates a high concentration interface in the channel. In this experiment, we will discuss how geometric factors influence preconcentration through a straight microchannel and a convergent microchannel. A convergent channel is in the middle of a channel and narrows the width, so that the sample can be concentrated in smaller areas by the impact of different flow rates. As a result, the fluorescence concentration increases in this reduced unit area. We hypothesized relatively faster and more efficient concentration at higher voltages, and thus used the potential difference to study ways to enhance the feasibility of the preconcentration effect in this device, thereby optimizing the device. Based on the experimental result, we took the applied voltage of 50 V in this experiment. To confirm how it works in the preconcentration process, a fluorescein dye was used. To explore its applications in biomedical detection, we used FITC-labeled bovine serum albumin samples to observe the cumulative effect in the same device. In the experiment using a straight microchannel, FITC-labeled bovine serum albumin accumulated up to 100-fold in 360 s. With a convergent microchannel whose middle was 50 μm wide, the result showed that one can achieve a 200-fold increase in preconcentration factor within 840 s. With a convergent microchannel whose middle was 25 μm wide, the result showed that a preconcentration factor of at least a 400 had been achieved within 240 s. Ruey-Jen Yang 楊瑞珍 2012 學位論文 ; thesis 62 en_US
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description 碩士 === 國立成功大學 === 工程科學系碩博士班 === 100 === In this experiment, we demonstrate production of a microfluidic chip through a micro-electromechanical technique and, by use of Nafion instead of a nanochannel, we produce integrated micro-nano chips for use in sample preconcentration. By applying an electric field to the chips, the Nafion becomes ion selective as a result of inner electric double layer overlapping. More specifically, when a difference in flux exists between positive and negative ions in the nanochannels, it results in a concentration polarization phenomenon at the micro and nano interface. Concentration polarization phenomena cause a concentration gradient to occur near the membrane. This study used an ion-selective membrane in which the flux of the cation is larger than the flux of the anion. When we applied an electric field, the effect caused a partial depletion at the anodic side and ion enrichment at the cathodic side. The ion accumulation is induced by the difference in electromigration at the border between the depletion zone and electroosmosis flow. In the end, it creates a high concentration interface in the channel. In this experiment, we will discuss how geometric factors influence preconcentration through a straight microchannel and a convergent microchannel. A convergent channel is in the middle of a channel and narrows the width, so that the sample can be concentrated in smaller areas by the impact of different flow rates. As a result, the fluorescence concentration increases in this reduced unit area. We hypothesized relatively faster and more efficient concentration at higher voltages, and thus used the potential difference to study ways to enhance the feasibility of the preconcentration effect in this device, thereby optimizing the device. Based on the experimental result, we took the applied voltage of 50 V in this experiment. To confirm how it works in the preconcentration process, a fluorescein dye was used. To explore its applications in biomedical detection, we used FITC-labeled bovine serum albumin samples to observe the cumulative effect in the same device. In the experiment using a straight microchannel, FITC-labeled bovine serum albumin accumulated up to 100-fold in 360 s. With a convergent microchannel whose middle was 50 μm wide, the result showed that one can achieve a 200-fold increase in preconcentration factor within 840 s. With a convergent microchannel whose middle was 25 μm wide, the result showed that a preconcentration factor of at least a 400 had been achieved within 240 s.
author2 Ruey-Jen Yang
author_facet Ruey-Jen Yang
Chen-ChiaoChao
趙晨喬
author Chen-ChiaoChao
趙晨喬
spellingShingle Chen-ChiaoChao
趙晨喬
The Study of the Preconcentration for Diluted Biochemical Samples
author_sort Chen-ChiaoChao
title The Study of the Preconcentration for Diluted Biochemical Samples
title_short The Study of the Preconcentration for Diluted Biochemical Samples
title_full The Study of the Preconcentration for Diluted Biochemical Samples
title_fullStr The Study of the Preconcentration for Diluted Biochemical Samples
title_full_unstemmed The Study of the Preconcentration for Diluted Biochemical Samples
title_sort study of the preconcentration for diluted biochemical samples
publishDate 2012
url http://ndltd.ncl.edu.tw/handle/97967694555066053233
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