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  1. NTU Theses and Dissertations Repository
  2. 工學院
  3. 應用力學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/35647
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor胡文聰(Andrew M. Wo)
dc.contributor.authorKuan-Ying Luen
dc.contributor.author呂冠瑩zh_TW
dc.date.accessioned2021-06-13T07:02:53Z-
dc.date.available2005-08-01
dc.date.copyright2005-08-01
dc.date.issued2005
dc.date.submitted2005-07-27
dc.identifier.citation[1] S. W. Lee and Y. C. Tai, “A Micro cell Lysis Device,” Sensors and Actuators A-Physical, Vol 73, no 1-2, pp. 74-79, 1999
[2] Hang Lu, Martin A. Schmidt and Klavs F. Jensen, “A microfluidic electroporation device for cell lysis,” Lab on a chip, 5, pp. 23-29, 2005
[3] Yong Huang, Boris Rubinsky, “Flow-through micro-electroporation chip for high efficiency single-cell genntic manipulation,” Sensors and Actuators A, 104, 205-212, 2003
[4] Yu-Cheng Lin and Ming-Yuan Huang, “Electroporation microchips for in vitro gene transfection,” J. Micromech. Microeng, 11, 542-547, 2001
[5] Michelle Khine, Adrian Lau, Cristian Ionescu-Zanetti, Jeonggi Seo and Luke P. Lee, “A single cell electroporation chip,” Lab on a chip, 5, pp. 38-43, 2005
[6] H. Lu, S. Gaudet, P. K. Sorger, M. A. Schmidt, and K. F. Jensen, “Miniaturized Electroporation Device for Controlled Cell Lysis,” Micro Total Analysis Systems, 5-9, 2003
[7] Hang Lu, Rebecca J. Jackman, Suzanne Gaudet, Michael Cardone, Martin A. Schmidt, and Klavs F. Jensen, “Microfluidic Devices for Cell Lysis and Isolation of Organelles,” Micro Total Analysis Systems, 297-298, 2001
[8] Chia-Yen Lee, Gwo-bin Lee, Jr-Lung Lin, Fu-Chun Huang and Chia-Sheng Liao, “Integrated microfluidic systems for cell lysis, mixing/pumping and DNA amplification,” J. Micromech. Microeng. 15, 1215-1223, 2005
[9] Dino Di Carlo, Ki-Hun Jeong and Luke P. Lee, “Regenless mechanical cell lysis by nanoscale barbs in microchannels for sample preparation,” Lab on a chip, 3, 287-291, 2003
[10] U. Zimmermann, “Electrical breakdown, electropermeabilization and electrofusion,” Rev. Physiol. Biochem. Pharmacol, 105, 175-256, 1986
[11] E. Neumann, A. E. Sowers, C. A. Jordan (Eds), “Electroporation and Electrofusion in Cell Biology,” Plenum, New York, 1989
[12] K.J. Muller, V.L. Sukhorukov, U. Zimmermann, “Reversilbe Electropermeabilization of Mammalian Cells by High-Intensity, Ultra-Short Pulses of submicrosecond Duration,” J. Membrane Biol, 184, 161-170, 2001
[13] 莊達仁,“VLSI 製造技術”, 高立出版 民國90年2月 20日
[14] Kirt R. Williams, Senior Member, IEEE, Kishan Gupta, Student Member, IEEE and Matthew Wasilik, “Etch Rates for Micromachining Processing-Part Ⅱ,” Journal of microelectromechanical systems, 12, 6, 761-778, 2003
[15] 楊啟榮, 游智勝, 黃奇聲, 胡一君, “微機電系統技術與應用”, 4.4節 精密電鑄技術, 行政院國家科學委員會 精密儀器發展中心出版, 225-246, 民國 92 年 七月
[16] Younan Xia and George M. Whitesides, “Soft Lithography,” Annu. Rev. Mater. Sci., 28, 153-184, 1998
[17] Y. S. Chen, “A Study on Micro-Pump with PDMS,” Master thesis, Institute of Applied Mechanics, National Taiwan University, 2002
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/35647-
dc.description.abstract本論文發表了應用電穿孔技術(electroporation)在具有平面和3D電極的細胞裂解微流體晶片,此研究的目標在對於探討平面及3D電極兩種設計在電穿孔晶片的性能上的差別。 平面電極的形狀為尖頭設計,其中兩電極距離為20 ,寬度為50 ,3D電極刑狀為圓柱形,電極間距同為20 ,直徑及高度都是50 。 實驗所用的電訊號為電脈衝,其中的電壓為10V持續時間為100 ,而這持續時間相較於細胞膜的電容充電時間10-1000ns是相當長的。 同時也應用商用軟體FEMLAB及MABLAB做為電場的模擬計算,而實驗所用的細胞為白血球。
對於電穿孔技術,電極的設計注重的是一個能產生足夠強度且分佈廣電場的電極,而不是一個能產生強度很大但分佈在小區域的電極。 經由FEMLAB的電場模擬以及MATLAB計算有效體積比率,結果顯示3D電極電場不會隨著微流道的高度而衰減且具有較均勻的分佈,另外3D電極的有效體積比率也優於平面電極。
在實驗方面,可發現細胞在3D 電極的形況下,是有多個破孔出現,有別於在平面電極的單個破洞,也發現當細胞出現破孔時,經由Trypan blue的輔助觀察以及在食鹽水稀釋情況下,細胞內液是往外流出的,另外由裂解比率的結果,3D電極也是優於平面電極。
zh_TW
dc.description.abstractThis thesis presents microfluidic devices to perform cell lysis using electroporation with planar and 3D electrode designs. The goal of the study is to compare the lysis performance of the two electrode geometries. The planar electrode design is pointed in shape (gap is 20μm, width of base 50μm) and that of 3D electrode are circular cylinders (diameter and height are 50μm, gap between cylinders 20μm), which are fabricated by electroforming. Pulse signal is used for electroporation, with amplitude of 10V and duration of 100μs – long compared to membrane charging time of 10-1000ns. The commercial software FEMLAB and MATLAB are used for simulation of electric field. In the experiment, leukocyte is used as lysis element.
Computational results show that the electric field of 3D electrode geometry is, indeed, more uniform than that of planar configuration, resulting in effective volume ratio — volume which electric field is sufficient for cell lysis to net volume — of the 3D geometry is substantially larger than that of the planar design. Also, the efficacy of lysing depends not only on the electric field but, more importantly, on the temporal extend which the cell is exposed to the field strength required for lysis as the cell proceeds downstream.
Experimentally, multi-pores are observed on leukocyte lysed with 3D electrodes and just single pore with planar electrodes. This is believed to be due to more uniform electric field of 3D electrodes than that of planar electrodes. Intracellular elements are extracted through the membrane as observed by increased intensity of Trypan blue when diluted by saline solution. We also demonstrate the lysing percentages at same flow velocity to explain the performance of 3D electrode is superior to that of planar electrode.
en
dc.description.provenanceMade available in DSpace on 2021-06-13T07:02:53Z (GMT). No. of bitstreams: 1
ntu-94-R92543021-1.pdf: 964854 bytes, checksum: ae40d959ccbd48c413a0175d449534d5 (MD5)
Previous issue date: 2005
en
dc.description.tableofcontentsAbstract………………………………………………………………………………..3
中文摘要…………………………………………………………………………….4
Chapter1. Introduction and Literature Review………………………………...5
1.1 Microfluidic system and MEMS technology………………………………….5
1.2 Mechanisms of cell lysis………………………………………………………5
1.3 Literature review………………………………………………………………6
1.4 Motivation and Goal…………………………………………………………..8
Chapter 2. Theory…………………………………………………………………10
2.1 Properties of cell membrane………………………………………………….10
2.2 Electroporation……………………………………………………………….10
2.3 Device Design and Computation of Electric Field...…………………………14
Chapter 3. Chip Fabrication……………………………………………………..19
3.1 Fabrication of planar electrodes and 3D electrodes………………………….19
3.1.1 Surface preparation…………………………………………………...20
3.1.2 Metal deposition……………………………………………………...20
3.1.3 Electrode patterning and protection coating………………………….20
3.1.4 Fabrication of 3D electrodes…………………………………………23
3.2 Microchannel fabrication…………………………………………………….26
Chapter 4. Experimental Setup…………………………………………………29
4.1 Cells preparations…………………………………………………………….29
4.2 Apparatus, procedure and experimental setup………………………………..30
4.2.1 Apparatus……………………………………………………………..30
4.2.2 Procedure and experimental setup……………………………………32
Chapter 5. Experimental Results……………………………………………….34
5.1 Cell lysis by planar electrode at no flow velocity…………………………….34
5.2 Cell lysis by planar and 3D electrodes at low flow velocity………………….38
Chapter 6. Conclusions and Future work……………………………………..40
6.1 Conclusions…………………………………………………………………...40
6.1 Future work…………………………………………………………………...40
Reference…………………………………………………………………………...41
dc.language.isoen
dc.subject電穿孔zh_TW
dc.subject細胞裂解zh_TW
dc.subject微流zh_TW
dc.subjectPDMSen
dc.subjectelectroporationen
dc.subjectcell lysisen
dc.subjectmicrofluidicen
dc.title3D電極應用於細胞裂解晶片之研究zh_TW
dc.titleA 3D ELECTRODE CHIP FOR CELL LYSIS BY ELECTROPORATIONen
dc.typeThesis
dc.date.schoolyear93-2
dc.description.degree碩士
dc.contributor.oralexamcommittee李雨(U Lei),沈弘俊(Horn-Jiunn Sheen)
dc.subject.keyword電穿孔,細胞裂解,微流,zh_TW
dc.subject.keywordelectroporation,cell lysis,microfluidic,PDMS,en
dc.relation.page42
dc.rights.note有償授權
dc.date.accepted2005-07-27
dc.contributor.author-college工學院zh_TW
dc.contributor.author-dept應用力學研究所zh_TW
顯示於系所單位:應用力學研究所

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