請用此 Handle URI 來引用此文件:
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/18808
完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 陳炳煇 | |
dc.contributor.author | Hong-Zheng Yang | en |
dc.contributor.author | 楊宏政 | zh_TW |
dc.date.accessioned | 2021-06-08T01:27:41Z | - |
dc.date.copyright | 2014-08-14 | |
dc.date.issued | 2014 | |
dc.date.submitted | 2014-07-30 | |
dc.identifier.citation | [1]Saiki, R. K., Scharf, S., Faloona, F., Mullis, K. B., Horn, G.T., Erlich, H. A., and Arnheim, N., 'Enzymatic amplification of β-Globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia,' Science, vol. 230, pp. 1350-1354, 1985.
[2]Higuchi, R., Dollinger, G., Walsh, P. S., and Griffith, R., 'Simultaneous amplification and detection of specific DNA-sequences,' Bio-Technology, vol. 10, pp. 413-417, 1992. [3]謝一帆,單一溫控熱對流聚合酶連鎖反應系統之開發與研究,碩士,機械工程學研究所,國立臺灣大學,台北市,2007。 [4]周文彬,一種新式核酸擴增系統之研究-毛細管熱對流聚合酶連鎖反應,博士,機械工程學研究所,國立臺灣大學,台北市,2011。 [5]Wittwer, C. T., Herrmann, M. G., Moss, A. A., and Rasmussen, R. P., 'Continuous fluorescence monitoring of rapid cycle DNA amplification,' Biotechniques, vol. 22, pp. 130-138, 1997. [6]Wittwer, C. T., Ririe, K. M., Andrew, R. V., David, D. A., Gundry, R. A., and Balis, U. J., 'The LightCycler(TM) a microvolume multisample fluorimeter with rapid temperature control,' Biotechniques, vol. 22, pp. 176-181, 1997. [7]Lyon, E.,and Wittwer, C. T., ' LightCycler technology in molecular diagnostics,' Journal of Molecular Diagnostics, vol. 11, pp. 93-101, 2009. [8]Krishnan, M., Ugaz, V. M., and Burns, M. A., 'PCR in a Rayleigh-Benard convection cell,' Science, vol. 298, pp. 793-793, 2002. [9]Ugaz, V. M. and Krishnan, M., 'Novel convective flow based approaches for high-throughput PCR thermocycling,' JALA, vol. 9, pp. 318-323, 2004. [10]Krishnan, N., Agrawal, N., Burns, M. A., and Ugaz, V. M., 'Reactions and fluidics in miniaturized natural convection systems,' Analytical Chemistry, vol. 76, pp. 6254-6265, 2004. [11]Chen, Z., Qian, S., Abrams, W. R., Daniel, Malamud, D., and Bau, H. H., 'Thermosiphon-based PCR reactor: experiment and modeling,' Analytical Chemistry, vol. 76, pp. 3707-3715, 2004. [12]Qiu, X., and J. Yuan.,'Temperature control for PCR thermocycles based on peltier-effect thermoelectric,' Conf. Proc. IEEE Eng. Med. BiolSoc., vol.7, pp.7509-7512, 2005. [13]Agrawal, N., and Ugaz, V. M., 'A buoyancy-driven compact thermocycler for rapid PCR,' JALA, vol. 11, pp. 217-221, 2006. [14]Gill, P., and A. Ghaemi., 'Nucleic acid isothermal amplification technologies,' Nucleotides Nucleic Acids, vol.27, pp. 224-243,2008. [15]Hennig, M. and Braun, D., 'Convective polymerase chain reaction around micro immersion heater,' Applied Physics Letters, vol. 87, pp. 183901, 2005. [16]Lee, D. S., Wu, M. H., Ramesh, U., Lin, C. W., Lee, T. M., and Chen, P. H., 'A novel Real-time PCR machine with a miniature spectrometer for fluorescence sensing in a micro liter volume glass capillary,' Sensors and Actuators B-Chemical, vol. 100, pp. 401-410, 2004. [17]Lee, D. S., Chang, B. H., and Chen, P. H., 'Development of a CCD-based fluorimeter for Real-time PCR machine,' Sensors and Actuators B-Chemical, vol. 107, pp. 872-881, 2005. [18]李達生,即時偵測同步定量聚合脢連鎖反應器研究與開發,博士 ,機械工程學研究所,國立臺灣大學,台北市,2004。 [19]Tsai, Y. L., Wang, H. T. T., Chang, H. F. G., Tsai, C. F., Lin, C. K., Teng, P. H., Su, C., Jeng, C. C., and Lee, P. Y., 'Development of TaqMan Probe-Based Insulated Isothermal PCR (iiPCR) for Sensitive and Specific On-Site Pathogen Detection,' Plos One, vol. 7, 2012. [20]Tsai, Y. L., Lin, Y. C., Chou, P. H., Teng, P. H., and Lee, P. Y., 'Detection of white spot syndrome virus by polymerase chain reaction performed under insulated isothermal conditions,' Journal of Virological Methods, vol. 181, pp. 134-137, 2012. [21]Chang, H. F. G., Tsai, Y. L., Tsai, C. F., Lin, C. K., Lee, P. Y., Teng, P. H., Su, C., and Jeng, C. C., 'A thermally baffled device for highly stabilized convective PCR,' Biotechnology Journal, vol. 7, pp. 662-666, 2012. [22]張維真,兩種新型毛細管熱對流聚合酶連鎖反應機台的開發與研究,碩士,機械工程學研究所,國立臺灣大學,台北市,2011。 [23]蘇丁亮,利用光學模擬設計即時定量聚合酶連鎖反應的光學檢測機制,碩士,機械工程學研究所,國立臺灣大學,台北市,2013。 [24]Hsieh, Y. F., Lee, D. S., Chen, P. H., Liao, S. K., Yeh, S. H., Chen, P. J., Yang, A. S., “A Real-time convective PCR machine in a capillary tube instrumented with a CCD-based fluorometer.” Sensors and Actuators B-Chemical, vol. 183, pp. 434-440, 2013. [25]Chien, A., Edgar, D. B., and Trela, J. M., 'Deoxyribonucleic acid polymerase from the extreme thermophile thermus aquaticus,' Journal of Bacteriology, Vol. 127, pp. 1550-1557, 1976 [26]張玉瓏、徐乃芝、許素菁著,生物技術,新文京開發出版股份有限公司,台北,2008。 [27]http://www.invitrogen.com [28]http://www.originlab.com [29]http://www.hamamatsu.com [30]http://www.unice.com.tw [31]http://www.logitech.com [32]楊子正,毛細管熱對流聚合酶連鎖反應產物專一性檢測機制,碩士,機械工程學研究所,國立臺灣大學,台北市,2013 | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/18808 | - |
dc.description.abstract | 本論文以開發新式聚合酶連鎖反應(Polymerase Chain Reaction,PCR)之機台為基礎,進行光學感測器的選用與數據分析,達到低成本,高準確度之目標,並希望未來能將此機台普及至一般診所進行即時的疾病檢測。
傳統PCR必須經過約四十次95℃、60℃、72℃三種溫度循環達到核酸擴增。本機台結合毛細管熱對流聚合酶連鎖反應(Capillary Convective Polymerase Chain Reaction,CCPCR)與即時定量聚合酶連鎖反應(Real-time Polymerase Chain Reaction,Real-time PCR)。僅透過底部95℃單一溫控進行加熱,在試管中試劑經由自然對流達到所需的三種溫度,並隨時間觀測試管內螢光強度變化。即時顯示擴增情形,使核酸擴增約在30分鐘完成。 首先更換試劑容器,以單支25NTD之玻璃毛細管改為低於1NTD之塑膠毛細管,大幅降低耗材成本。但塑膠材質透光度比起玻璃減少42.7%,故需針對光學感測器進行改善。本機台使用鎳鉻絲加熱,紅銅塊傳導熱使試管底部維持在95℃左右,並且溫控準確,標準差約在0.2℃。光學機制採取一藍色發光二極體(Light-Emitting Diode,LED)從下方往上打光,再從側面收取試管內被激發之螢光。 本研究因更換毛細管材質降低透光度,故選用三種光學感測器進行實驗,分別為color sensor、silicon detector與webcam影像分析。首先進行靈敏度實驗,可得50copies/tube的B型肝炎核酸能成功擴增。再選用三種核酸濃度進行重複性實驗,分別為5×105copies/tube、5×103copies/tube和5×101copies/tube,螢光擴增結果可經由曲線擬合公式,繪製出各感測器之標準曲線。作為本機台初始濃度之定量分析。 | zh_TW |
dc.description.abstract | A new polymerase chain reaction (PCR) machine is developed for discussing the optical sensor selection and analyzing the fluorescence data in this study. The goal is to achieve low cost and high accuracy. In the future, we hope to popularize this machine at clinics for immediate disease detection.
General PCR nucleic acid amplification test must be controlled to the three temperature, which are 95℃, 60℃and72℃. This machine combines two technologies that are capillary convective polymerase chain reaction (CCPCR)and Real-time polymerase chain reaction(Real-time PCR). By single temperature control, the capillary will be heated to 95℃. Then, observing the change of fluorescence intensity in a capillary continuously when the reagent in the tube reaches the desired three temperatures by natural convection. Finally, Nucleic acid amplification completed within 30 minutes. At the first, this study replace the reagent container from a glass capillary cost 25NTD to a plastic capillary cost lower than 1NTD. This change greatly reduce the cost of tubes. However, compared to plastic and glass, the transmittance decreased by approximately 40%, so the optical sensors must be improved. This research used a nickel-chromium wire as a heater for CCPCR. The copper block is heated to temperature 95℃ fixedly by the nickel-chromium wire at the bottom of the capillary and the temperature standard deviation is 0.2℃. About the optical mechanism, blue light-emitting diodes (LED) is used to light the capillary from below and collect the fluorescence signal from the side. This study selects three kinds of optical sensors to experiment, namely color sensor, silicon detector and webcam. Sensitivity test with nucleic acid of HBV initial concentration of 50 copies/tube was amplified successfully. Repeatability test with three kinds of concentration of 5×105copies/tube, 5×103copies/tube and 5×101copies/tube was plot fluorescence curves. By curve fitting, we can draw the standard curve of this CCPCR machine to find the initial concentration of virus. | en |
dc.description.provenance | Made available in DSpace on 2021-06-08T01:27:41Z (GMT). No. of bitstreams: 1 ntu-103-R01522401-1.pdf: 4775738 bytes, checksum: a45fbbfac3e4e82ec0f81249ae723d61 (MD5) Previous issue date: 2014 | en |
dc.description.tableofcontents | 誌謝 i
中文摘要 ii ABSTRACT iii 符號說明 v 目錄 vi 圖目錄 ix 表目錄 xi 第一章 緒論 1 1.1 前言 1 1.2 研究目的與動機 2 1.3 文獻回顧 3 1.4 論文架構 7 第二章 研究原理與方法 19 2.1 聚合酶連鎖反應 19 2.1.1 發展歷史背景 19 2.1.2 基本原理 20 2.1.3 影響聚合酶連鎖反應之因素 21 2.2 即時定量聚合酶連鎖反應 23 2.3 毛細管熱對流聚合酶連鎖反應 24 2.4 數據分析 25 第三章 實驗設備 31 3.1 實驗試劑與化學藥品 31 3.1.1 聚合酶連鎖反應的試劑 31 3.1.2凝膠電泳分析的化學藥品 33 3.2 實驗設備 34 3.2.1 實驗容器 34 3.2.2 傳統聚合酶連鎖反應機台 35 3.2.3 溫度量測系統 35 3.2.4 凝膠電泳分析系統 35 3.2.5 毛細管熱對流聚合酶連鎖反應的檢測機制 36 3.2.6 毛細管熱對流聚合酶連鎖反應的光學感測器選用 37 第四章 實驗結果 47 4.1 溫度量測結果 47 4.1.1 單孔溫度量測結果 47 4.1.2 多孔溫度量測結果 48 4.2 實驗機台核酸擴增結果 48 4.2.1 試劑有無汙染確認 48 4.2.2 核酸擴增結果與靈敏度測試 49 4.3 螢光擴增結果 49 4.3.1 Color sensor螢光訊號分析 50 4.3.2 Silicon detector 螢光訊號分析 50 4.3.3 Webcam 螢光訊號分析 51 4.4 定量分析結果 52 第五章 結論與未來展望 65 5.1 結論 65 5.1.1 機台檢測結果 65 5.1.2 感測器擴增結果比較 66 5.2 未來展望 67 參考文獻 70 | |
dc.language.iso | zh-TW | |
dc.title | 不同的光學機制對即時定量聚合酶連鎖反應檢測之影響 | zh_TW |
dc.title | Effects of Different Optical Mechanism on Real-time Polymerase Chain Reaction Detection | en |
dc.type | Thesis | |
dc.date.schoolyear | 102-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 陳志臣,李達生 | |
dc.subject.keyword | 聚合?連鎖反應,熱對流,光學感測器,即時定量核酸檢測, | zh_TW |
dc.subject.keyword | Polymerase chain reaction,Convection,Optical sensor,Real-time nucleic acid detection, | en |
dc.relation.page | 73 | |
dc.rights.note | 未授權 | |
dc.date.accepted | 2014-07-30 | |
dc.contributor.author-college | 工學院 | zh_TW |
dc.contributor.author-dept | 機械工程學研究所 | zh_TW |
顯示於系所單位: | 機械工程學系 |
文件中的檔案:
檔案 | 大小 | 格式 | |
---|---|---|---|
ntu-103-1.pdf 目前未授權公開取用 | 4.66 MB | Adobe PDF |
系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。