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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/123456789/77486
完整後設資料紀錄
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dc.contributor.advisor陳建甫
dc.contributor.authorHong-Ting Linen
dc.contributor.author林竑廷zh_TW
dc.date.accessioned2021-07-10T22:04:26Z-
dc.date.available2021-07-10T22:04:26Z-
dc.date.copyright2018-08-21
dc.date.issued2018
dc.date.submitted2018-08-16
dc.identifier.citation[1] E. Engvall and P. Perlmann, 'Enzyme-linked immunosorbent assay (ELISA) quantitative assay of immunoglobulin G,' Immunochemistry, vol. 8, p. 871-874, 1971.
[2] G. J. Kost, 'Point‐of‐Care Testing,' Encyclopedia of Analytical Chemistry, 2006.
[3] J. H. Nichols, 'Point of care testing,' Clin. Lab. Med., vol. 27, p. 893-908, 2007.
[4] N. P. Pai, C. Vadnais, C. Denkinger, N. Engel, and M. Pai, 'Point-of-care testing for infectious diseases: diversity, complexity, and barriers in low-and middle-income countries,' PLoS Med., vol. 9, p. e1001306, 2012.
[5] L. Lafleur, D. Stevens, K. McKenzie, S. Ramachandran, P. Spicar-Mihalic, M. Singhal, et al., 'Progress toward multiplexed sample-to-result detection in low resource settings using microfluidic immunoassay cards,' Lab Chip, vol. 12, p. 1119-1127, 2012.
[6] D. Erickson and D. Li, 'Integrated microfluidic devices,' Anal. Chim. Acta, vol. 507, p. 11-26, 2004.
[7] R. Daw and J. Finkelstein, 'Lab on a chip,' Nature, vol. 442, p. 367, 2006.
[8] M. T. Taylor, P. Nguyen, J. Ching, and K. E. Petersen, 'Simulation of microfluidic pumping in a genomic DNA blood-processing cassette,' J Micromech Microeng, vol. 13, p. 201, 2003.
[9] J. G. Smits, 'Piezoelectric micropump with three valves working peristaltically,' aSens Actuators A Phys l, vol. 21, p. 203-206, 1990.
[10] P. A. Limbach and Z. Meng, 'Integrating micromachined devices with modern mass spectrometry,' Analyst, vol. 127, p. 693-700, 2002.
[11] E. Eteshola and D. Leckband, 'Development and characterization of an ELISA assay in PDMS microfluidic channels,' Sens Actuators B Chem, vol. 72, p. 129-133, 2001.
[12] P. Novo, G. Moulas, D. M. F. Prazeres, V. Chu, and J. P. Conde, 'Detection of ochratoxin A in wine and beer by chemiluminescence-based ELISA in microfluidics with integrated photodiodes,' Sens Actuators B Chem, vol. 176, p. 232-240, 2013.
[13] C. D. Chin, T. Laksanasopin, Y. K. Cheung, D. Steinmiller, V. Linder, H. Parsa, et al., 'Microfluidics-based diagnostics of infectious diseases in the developing world,' Nat. Med., vol. 17, p. 1015-1019, 2011.
[14] T. Laksanasopin, T. W. Guo, S. Nayak, A. A. Sridhara, S. Xie, O. O. Olowookere, et al., 'A smartphone dongle for diagnosis of infectious diseases at the point of care,' Sci. Transl. Med., vol. 7, p. 273re1-273re1, 2015.
[15] A. W. Martinez, S. T. Phillips, M. J. Butte, and G. M. Whitesides, 'Patterned paper as a platform for inexpensive, low‐volume, portable bioassays,' Angew. Chem. Int. Ed, vol. 46, p. 1318-1320, 2007.
[16] Q. He, C. Ma, X. Hu, and H. Chen, 'Method for fabrication of paper-based microfluidic devices by alkylsilane self-assembling and UV/O3-patterning,' Anal. Chem., vol. 85, p. 1327-1331, 2013.
[17] N. Madaboosi, C. R. Pedrosa, M. F. Reis, R. R. Soares, V. Chu, and J. P. Conde, 'Microfluidic ELISA for sensing of prostate cancer biomarkers using integrated a-Si: H pin photodiodes,' in SENSORS, 2014 IEEE, 2014, p. 881-884.
[18] X. Li, J. Tian, T. Nguyen, and W. Shen, 'based microfluidic devices by plasma treatment,' Anal. Chem., vol. 80, p. 9131-9134, 2008.
[19] A. W. Martinez, S. T. Phillips, G. M. Whitesides, and E. Carrilho, 'Diagnostics for the developing world: microfluidic paper-based analytical devices,' ed: ACS Publications, 2009.
[20] C. M. Cheng, A. W. Martinez, J. Gong, C. R. Mace, S. T. Phillips, E. Carrilho, et al., 'paper‐based elisa,' Angew. Chem. Int. Ed, vol. 49, p. 4771-4774, 2010.
[21] S. T. Sanjay, M. Dou, J. Sun, and X. Li, 'A paper/polymer hybrid microfluidic microplate for rapid quantitative detection of multiple disease biomarkers,' Scientific reports, vol. 6, p. 30474, 2016.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/77486-
dc.description.abstract本研究開發一微流體系統,其結合紙張與塑膠材料本身優點,(polymer/paper hybrid enzyme-linked immunosorbent assay,hELISA)。研究係藉由塑膠微流道系統只需微量樣品與試劑反應之特性,以及其高流體變因可控制性,與可事先儲存試劑於流道中來減少使用者操作步驟的優點,並結合紙張提供將抗體長效存放,以及其本身為白色的特性,因此進行免疫反應呈色結果相較於小尺寸透明塑膠微流道能更清楚呈現酵素-受質(enzyme-substrate)反應所產生可見光範圍顏色變化。此外,吾人也使用3D列印技術,製造出可重複使用之攜帶式手動液體幫浦,達到不需要外加電力便可手動驅動液體於微流體晶片內流動之目的。最終研究也利用影像分析技術進行影像紅綠藍(red-green-blue,RGB)三原色數值分析,經過邏輯運算後,可由智慧型手機獲得檢測結果,達到快速疾病檢測分析系統目標。研究結果成功進行人類免疫球蛋白檢測,在16分鐘內時間內,獲得0.03 ng/mL之偵測極限。吾人預期此項檢測系統可輕易置換使用不同抗體,進行其他多樣化疾病檢測,達到於資源匱乏區域疾病篩選與病程監控之目的。zh_TW
dc.description.abstractWe develop a microfluidic system which integrates the advantages of paper and plastic materials to propose a new hybrid microfluidic immunoassay platform. Polymeric microfluidic system possesses advantages such as small sample volume, high fluid controllability, and reagent pre-filling. In this study, we combine the paper device to achieve long-term storage of antibodies and visually much clear colorimetric sensing results than in micro size transparent plastic microchannels. On the other hand, we use 3D printing approaches to fabricate a reusable, portable, and hand-powered liquid pump to drive liquid in microchannels without electricity. In addition, we use image processing to analyze the RGB value to quantify detection results. After logic calculation, the results can be obtained directly by a smart phone, and the rapid disease detection system can be accomplished. As a result, the detection limit of 0.03 ng/mL can be achieved in 20 minutes for the human Immunoglobulin G (IgG) tests. We expect different detection targets can be easily carried out easily by replacing receptors for various disease, and the system possesses the potential for disease screening and monitoring in resource-limited regions.en
dc.description.provenanceMade available in DSpace on 2021-07-10T22:04:26Z (GMT). No. of bitstreams: 1
ntu-107-R05543009-1.pdf: 2148578 bytes, checksum: f05daf08f19f5d2ccbfd67ba8638534d (MD5)
Previous issue date: 2018
en
dc.description.tableofcontents致謝 i
摘要 ii
Abstract iii
圖目錄 iv
表目錄 vi
第1章、前言 1
1.1 研究動機 1
1.2 文獻回顧 1
1.2.1 酵素免疫分析法(Enzyme linked immunosorbent assay,ELISA) 1
1.2.2 定點照護(Point of Care,POC) 2
1.2.3 微流道系統 2
1.2.4 微型幫浦 2
1.2.5 微流道分析檢測平臺 3
1.2.6 微流體試紙分析平臺 5
第2章 實驗材料與方法 8
2.1 實驗藥劑與樣品 8
2.2 儀器設備 8
2.3 卡匣晶片製備 8
2.3.1 蜿蜒流道晶片 8
2.3.2 螺紋針頭 9
2.3.3 存放ELISA試紙張之凹槽 9
2.3.4 清洗液之存放區域 9
2.3.5 卡匣晶片溶劑接合 9
2.3.6 各層晶片設計 10
2.4 ELISA試紙製備 11
2.5 溶液及樣品配置 12
2.5.1 人類免疫球蛋白G抗體修飾辣根過氧化物酶 (aHIgG-HRP)溶液配置 12
2.5.2 人類免疫球蛋白G抗體(aHIgG-Fc)溶液配置 12
2.5.3 山羊免疫球蛋白G抗體(aGoat IgG)溶液配置 12
2.5.4 清洗緩衝溶液(Wash buffer)配置 13
第3章 結果與討論 13
3.1 微流體卡匣製備與步驟 13
3.2 最佳化參數 16
3.2.1 使用不同清洗緩衝溶液(Wash buffer)的呈色結果 16
3.2.2 使用不同濃度的人類免疫球蛋白G抗體修飾辣根過氧化物酶( aHIgG-HRP)的呈色結果 19
3.2.3 使用不同人類免疫球蛋白G抗體濃度的呈色結果(Anti-Human IgG Fc specific)濃度的呈色結果 22
3.2.4 檢測點酵素-受質反應時間 25
3.2.5 使用不同山羊免疫球蛋白G抗體(aGoat IgG)濃度的呈色結果 27
3.2.6 控制點酵素受質反應時間 28
3.3不同裝置的ELISA檢測比較表 30
第四章 結論 31
參考文獻 32
dc.language.isozh-TW
dc.subject塑膠微流體zh_TW
dc.subject紙張分析平台zh_TW
dc.subject酵素免疫分析法zh_TW
dc.subjectPolymeric Microfluidicsen
dc.subjectEnzyme-linked Immunosorbent Assayen
dc.subjectMicrofluidic paper-based analytical devicesen
dc.title攜帶式微流體疾病檢測裝置開發zh_TW
dc.titlePortable Microfluidic Disease Detection Device Developmenten
dc.typeThesis
dc.date.schoolyear106-2
dc.description.degree碩士
dc.contributor.oralexamcommittee林宗宏,余政儒,蔡欣怡,周逸儒
dc.subject.keyword塑膠微流體,紙張分析平台,酵素免疫分析法,zh_TW
dc.subject.keywordPolymeric Microfluidics,Microfluidic paper-based analytical devices,Enzyme-linked Immunosorbent Assay,en
dc.relation.page34
dc.identifier.doi10.6342/NTU201803605
dc.rights.note未授權
dc.date.accepted2018-08-16
dc.contributor.author-college工學院zh_TW
dc.contributor.author-dept應用力學研究所zh_TW
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