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研究生: Vo Ngoc Anh Tuan
Vo Ngoc Anh Tuan
論文名稱: 開發PDMS和PMMA基板之高黏合強度,進而製造以慣性力為基礎之微型系統,用於高效率之血漿分離
Maximizing interfacial bonding strength between PDMS and PMMA substrates for manufacturing microvalve/micropump system for efficient blood plasma separation with inertial particle focusing technique
指導教授: 陳品銓
Pin-Chuan Chen
口試委員: 曾修暘
Hsiu-Yang Tseng
田維欣
Wei-Hsin Tien
陳品銓
Pin-Chuan Chen
曹嘉文
Chia-Wen Tsao
饒達仁
Da-Jeng Yao
陳珮珊
Pai-Shan Chen
學位類別: 博士
Doctor
系所名稱: 工程學院 - 機械工程系
Department of Mechanical Engineering
論文出版年: 2022
畢業學年度: 110
語文別: 英文
論文頁數: 101
外文關鍵詞: Microvalve, Micropump, Blood Plasma Separation, Inertial Microfluidics
相關次數: 點閱:173下載:0
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Polydimethylsiloxane (PDMS) and polymethylmethacrylate (PMMA) are commonly utilized in microfluidics due to their high optical transparency, good biocompatibility, and ease of manufacture. However, conventional bonding techniques cannot produce sufficient bonding strength, which limits their applicability. This thesis represents a method for optimizing the interfacial bonding strength between PDMS and PMMA. Using the Taguchi approach, fabrication parameters were investigated by evaluating bonding strength (i.e., burst test pressure). Under ideal bonding circumstances, the microchannel assembly withstood air pressure greater than 770 kPa, liquid pressure greater than 622 kPa, and a tensile test greater than 3000 kPa. The bonding strength was sufficient to withstand liquid entry at a rate 6800 times greater than the microchannel's volume per minute. This indicates that the interfacial bonding was permanent, as the microdevices could tolerate such severe pressure without damage. Then, the proposed manufacturing technology was utilized to manufacture microfluidic devices that could handle an extraordinarily high liquid pressure of 402 kPa, high flow rates surpassing 120 mL/min, and dense microchannels with a spacing of only 30 µm. This proposed bonding approach was used to manufacture a functioning valve system with a high-density layout that may be used in microfluidics-based assays requiring high precision, rapid response, and the efficient management of liquid transportation.
Moreover, we successfully developed a novel integrated microfluidic device to separate blood plasma from human blood without using external valves or pumps. The concept is based on using a pneumatic peristaltic micropump (PPMs) integrated with a trapezoidal cross-section for blood plasma separation. First, we proposed a fabrication process of PPM with high pumping rate by combining rigidly of PMMA and elasticity of PDMS. Following the procedure to achieve excellent bonding strength of PDMS/PMMA, the PPMs could be operated under high pressure. Then, the dynamic deflection test of PDMS membrane actuator under high pulsation frequency was performed. We proved that the PPMs have excellent actuator diaphragm dynamic behavior without any mechanical fatigue or dead volume, achieving the highest pumping rate of 3,500 µL/min. Then the micropump was integrated with a spiral microchannel with trapezoidal cross-section area and used to rapidly extract plasma from human blood within 3 minutes and with a small blood volume of 200μL, with the efficient separation up to 97%.

Chapter 1.Introduction 1.1 Motivation for maximizing bonding strength of PDMS/PMMA for fabrication of hybrid microfluidic devices. 1.2 Microvalve and Micropump 1.3 Blood plasma separation 1.4 Objective and significance of this dissertation 1.5 Organization of the dissertation Chapter 2. Literature review 2.1 Bonding PDMS/PMMA by surface modification 2.2 Microvalve 2.3 Micropump 2.4 Separation of blood plasma using size-based particle separation with spiral microchannels Chapter 3. Maximizing bonding strength of PDMS/PMMA 3.1 Materials 3.2 Bonding procedure 3.3 Experimental setup 3.4 Design of experiment 3.5 Factor analysis 3.6 Conformation test Chapter 4. Microvalve and micropump system for efficient blood plasma separation 4.1 Design and fabrication of microvalve 4.2 Characterization of microvalve 4.3 Design and fabrication of micropump 4.4 Extraction of blood plasma from human blood by integrated PPM device Chapter 5.Conclusion, limitations, and recommendation 5.1 Conclusion 5.2 Limitation of the dissertation 5.3 Recommendations

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