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  1. NTU Theses and Dissertations Repository
  2. 理學院
  3. 物理學系
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/36675
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DC 欄位值語言
dc.contributor.advisor董成淵(Chen-Yuan Dong)
dc.contributor.authorChun-Chin Wangen
dc.contributor.author王俊欽zh_TW
dc.date.accessioned2021-06-13T08:10:35Z-
dc.date.available2005-07-22
dc.date.copyright2005-07-22
dc.date.issued2005
dc.date.submitted2005-07-20
dc.identifier.citation[1.1] M.H. Ross, L.J. Romrell, and G.I. Kaye, “Histology: A text and atlas,” third edition, Williams&Wilkins, Baltimore, MD, USA ( 1995 )
[1.2] M. Göppert-Mayer, “Über elementarakte mit zwei quantensprüngen,” Annalen der Physik ( 9 ), 273-295 ( 1931 )
[1.3] P.A. Franken, A.E. Hill, C.W. Peter, and G. Weinreich, “Generation of optical harmonics,” Physical Review Letters ( 7 ), 118-119 ( 1961 )
[1.4] W. Kaiser, and C.G.B. Garrett, “Two-photon excitation in CaF2:Eu2+,” Physical review letters ( 7 ), 229-231 ( 1961 )
[1.5] S. Singh, and L.T. Bradley, “Three-photon absorption in naphthalene crystals by laser excitation,” Physical Review Letters ( 12 ), 162-164 ( 1964 )
[1.6] P.M. Rentzepis, C.J. Mitschele, and A.C. Saxman, “Measurement of ultrashort laser pulses by three-photon fluorescence,” Applied Physics Letters ( 17 ), 122-124 ( 1970 )
[1.7] J.N. Gannaway, and C.J.R. Sheppard, “Second harmonic imaging in the scanning optical microscope,” Optical and Quantum Electronics ( 10 ), 435-439 ( 1978 )
[1.8] W. Denk, J.H. Strickler, and W.W. Webb, “Two-photon laser scanning fluorescence microscopy,” Science ( 248 ), 73-76 ( 1990 )
[1.9] Edited by A. Diaspro, “Confocal and two-photon microscopy,” John Wiley & Sons, NY, USA ( 2002 )
[1.10]P.N. Prasad “Introduction to biophotonics ,” John Wiley & Sons, Hoboken, NJ, USA ( 2003 )
[1.11]P.J. Campagnola, A.C. Millard, M. Terasaki, et al., “Three-dimensional high-resolution second-harmonic generation imaging of endogenous structural proteins in biological tissues,” Biophysical journal ( 81 ), 493-508 ( 2002 )
[1.12]A. Schönle, and S. Hell, “Heating by absorption in the focus of an objective lens,” Optics Letters ( 23 ), 325-327 ( 1998 )
[1.13]K. König, U. Simon, and K.J. Halbhuber, “3D resolved two-photon fluorescence microscopy of living cells using a modified confocal laser scanning microscope,” Cellular and Molecular Biology ( 42 ), 1181-1194 ( 1996 )
[1.14]S.J. Lin, C.Y. Hsiao, Y. Sun, et al., “Monitoring the thermally induced structural transitions of collagen by use of second-harmonic generation microscopy,” Optics Letters 30( 6 ), 622-624 ( 2005 )
[1.15]J.M. Squirrell, D.L. Wokosin, J.G. White, and B.D. Bavister, “Long-term two-photon fluorescence imaging of mammalian embryos without compromising viability,” Nature Biotechnology ( 17 ), 763-767 ( 1999 )
[1.16]C.K. Sun, S.W. Chu, S.Y. Chen, et al., “Higher harmonic microscopy for developmental biology,” Journal of Structural Biology ( 147 ), 19-30 ( 2004 )
[1.17]D.A. Dombeck, M. Blanchard-Desce, and W.W. Webb, “Optical recording of action potentials with second-harmonic generation microscopy,” The Journal of Neuroscience 24( 4 ), 999-1003 ( 2004 )
[1.18] J.C. Jung, A.D. Mehta, E.Aksay, R. Stepnoski, and M.J. Schnitzer, “In vivo mammalian brain imaging using one- and two-photon fluorescence microendoscopy,” Journal of Neurophysiology ( 92 ), 3121-3133 ( 2004 )
[2.1] H.A. Haus, “Waves and fields in optoelectronics,” Prentice-Hall, Englewood Cliffs, NJ, USA ( 1984 )
[2.2] R.W. Boyd, “Nonlinear optics,” second edition, Academic Press, Boston, MA, USA ( 2003 )
[2.3] M. Born, and E. Wolf, “Principles of optics,” seventh edition, Cambridge University Press, Cambridge, UK ( 2002 )
[2.4] P.A. Franken, A.E. Hill, C.W. Peters, and G.. Weinreich, “Generation of optical harmonics,” Physical Review Letters ( 7 ), 118-119 ( 1961 )
[2.5] C.Y. Dong, K. Koenig, P. So, “Characterizing point spread functions of two-photon fluorescence microscopy in turbid,” Journal of Biomedical Optics 8(3), 450-459 ( 2003 )
[2.6] P. Stoller, K.M. Reiser, P.M. Celliers, and A.M. Rubenchik, “Polarization modulated second harmonic generation in collagen,” Biophysical Journal ( 82 ), 3330-3342 ( 2002 )
[2.7] G.H. Algire, “An adaptation of the transparent chamber technique to the mouse,” Journal of National Cancer Institute ( 4 ), 1-11 ( 1943 )
[3.1]「民國九十年癌症登記報告」,行政院衛生署,中華民國九十三年十一月
十八日,台灣 ( 2004 )
[3.2] M.H. Ross, L.J. Romrell, and G.I. Kaye “Histology: A text and atlas,” third edition, Williams&Wilkins, Baltimore, MD, USA ( 1995 )
[3.3] F.H. Netter, “Atlas of human anatomy,” second edition, ICON Learning Systems, Teterboro, NJ, USA ( 1997 )
[3.4] G.J. Tortora, “Principles of Human Anatomy,” eight edition, John Wiley & Sons, New York, NY, USA ( 1999 )
[3.5] 台大皮膚科部編著, “實用皮膚醫學,” 國立台灣大學醫學院出版, 台北市, 台灣 ( 2003 )
[3.6] L.H. Kligman, R. Elenitsas, “Melanoma induction in a hairless mouse with short-term application of dimethylbenz[a]anthracene,” Melanoma Research 11( 4 ), 319-324 ( 2001 )
[4.1] M.H. Ross, L.J. Romrell, and G.I. Kaye “Histology: A text and atlas,” third edition, Williams&Wilkins, Baltimore, MD, USA ( 1995 )
[4.2] R.W. Boyd, “Nonlinear optics,” second edition, Academic Press, Boston, MA, USA ( 2003 )
[4.3] Edited by C.D.M. Fletcher, “Diagnostic histopathology of tumors,” second edition, Churchill Livingstone, London, UK ( 2002 )
[4.4] K. König, K. Schenke-Layland, I. Riemann, and U.A. Stock, “Multiphoton autofluorescence imaging of intratissue elastic fibers,” Biomaterials ( 26 ), 495-500 ( 2005 )
[4.5] K. König, P.T.C. So, W.W. Mantulin, and E. Gratton, “Cellular response to near-infrared femtosecond laser pulses in two-photon microscopes,” Optics Letters 22( 2 ), 135-136 ( 1997 )
[4.6] 朱士維, “倍頻光學顯微影像術之原理及應用,”國立台灣大學光電工程研究
所博士論文, 147-152 ( 2004 )
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/36675-
dc.description.abstract在台灣癌症是一項嚴重的疾病,而發展最低侵入式的技術來診斷膀胱癌是相當具有癌症診斷價值的。在這個研究中,我們利用非線性光學顯微術,對正常與癌症膀胱組織進行影像與分析。為了觀察癌症細胞早期的發展,我們也提出了皮膚固定裝置,以求在活體情況下擁有高解析度的觀察影像。
我們的結果顯示:結合二倍頻與雙光子自體螢光的影像,可以取得分子與結構的資訊,以區分膀胱癌和正常組織。藉由ASI(自體螢光對二倍頻的指數),我們可得到定性與定量的資訊,用以區分正常與罹癌的膀胱組織。
運用自體螢光與二倍頻訊號的消長,我們也對在活體環境中扁平細胞與結締組織的交互作用有了一定的了解。
zh_TW
dc.description.abstractTumor is a major disease in Taiwan and the development of minimally invasive techniques to diagnose bladder tumor will be of tremendous values for cancer diagnosis. In this investigation, we used nonlinear optical microscopy to image and analyze normal and cancerous bladder tissues. In order to monitor the early development of cancer cells, we also implemented a skin-fold chamber system for high resolution observation in vivo.
Our results show that a combination of second harmonic generation and two-photon autofluorescence imaging can be used to acquire molecular and structural information in distinguishing bladder carcinoma from normal tissues. With the application of ASI ( Autofluorescence versus Second harmonic generation Index ), we can obtain the qualitative and quantitative information for distinguishing normal and cancerous bladder tissues.
Utilizing the variation of autofluorescence and second harmonic generation signal, we can also visualize the interaction between squamous cells and connective tissue in vivo.
en
dc.description.provenanceMade available in DSpace on 2021-06-13T08:10:35Z (GMT). No. of bitstreams: 1
ntu-94-R92222042-1.pdf: 2420077 bytes, checksum: 4710b16bc0c526745e712e09f9107bf6 (MD5)
Previous issue date: 2005
en
dc.description.tableofcontents致謝 1
Abstract 4
摘要 5
目錄 6
圖目錄 8
表目錄 9
第一章 緒論
1.1 研究動機 10
1.2 非線性光學顯微術的發展與生醫應用 10
1.2.1 歷史回顧 10
1.2.2 生醫應用 11
第二章 實驗原理與儀器
2.1 非線性光學顯微術原理
2.1.1 雙光子螢光 16
2.1.2 二倍頻 18
   2.1.3 顯微術原理 20
點擴函數、數值孔徑與解析度 22
2.2 實驗儀器架構 24
2.2.1 多光子顯微系統 24
雷射光源、光路元件、顯微系統、訊號接收 25
2.2.2 皮膚固定裝置 26
第三章 樣品與處理方法
3.1 實驗樣品選擇 29
3.1.1 膀胱 29
3.1.2 裸鼠 29
3.2 生物樣品構造    30
3.2.1 上皮、結締與肌肉組織 30
3.2.2 膀胱構造 31
3.2.3 皮膚構造        32
3.3 處理方法         33
3.3.1 膀胱樣品處理  33
3.3.2 裸鼠癌症模式 34
第四章 結果與討論
4.1 人類組織病變研究 36
4.1.1 正常與癌症配對組織影像 36
4.1.2 螢光與倍頻訊號分析與討論 40
4.2 裸鼠活體研究 44
4.2.1 活體細胞影像 44
4.2.2 光學訊號分析與討論 46
第五章 總結與展望 49
附錄:動物實驗許可證明 50
dc.language.isozh-TW
dc.subject二倍頻zh_TW
dc.subject非線性光學zh_TW
dc.subject雙光子zh_TW
dc.subject癌症zh_TW
dc.subject活體zh_TW
dc.subjectin vivoen
dc.subjectcanceren
dc.subjectsecond harmonic generationen
dc.subjecttwo-photonen
dc.subjectnonlinear opticsen
dc.title運用非線性光學顯微術於診斷人類膀胱癌與活體裸鼠早期癌症影像技術之發展zh_TW
dc.titleUtilizing nonlinear optical microscopy to diagnose human bladder tumor and the development of early cancer
imaging techniques in nude mice in vivo
en
dc.typeThesis
dc.date.schoolyear93-2
dc.description.degree碩士
dc.contributor.oralexamcommittee孫啟光(Chi-Kuang Sun),林啟萬(Chii-Wann Lin),李宣書(Hsuan-Shu Lee)
dc.subject.keyword非線性光學,雙光子,二倍頻,癌症,活體,zh_TW
dc.subject.keywordnonlinear optics,two-photon,second harmonic generation,cancer,in vivo,en
dc.relation.page50
dc.rights.note有償授權
dc.date.accepted2005-07-21
dc.contributor.author-college理學院zh_TW
dc.contributor.author-dept物理研究所zh_TW
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