簡易檢索 / 詳目顯示

研究生: 江振榮
Jiang, Jhen-Rong
論文名稱: 設計多通道高頻功能性近紅外光譜系統
Design of multi-channel high frequency functional near-infrared spectroscopy system
指導教授: 陳家進
Chen, Jia-Jin
學位類別: 碩士
Master
系所名稱: 工學院 - 醫學工程研究所
Institute of Biomedical Engineering
論文出版年: 2006
畢業學年度: 94
語文別: 英文
論文頁數: 54
中文關鍵詞: 近紅外光譜神經活動IQ解調高頻系統
外文關鍵詞: IQ demodulator, near-infrared spectroscopy, high frequency system, neural activity
相關次數: 點閱:71下載:3
分享至:
查詢本校圖書館目錄 查詢臺灣博碩士論文知識加值系統 勘誤回報
  • 關於人體大腦活動的近紅外光譜研究中,伴隨大腦活動時,有兩種主要的光學訊號可以被發現到;分別是較緩慢的血氧濃度變化與快速的神經訊號。其中快速的神經訊號根據推測可能與神經活動有關,但是訊號較微小而且比較難去偵測的到。本研究的目的,去建立一套可以同時去測量血氧濃度變化訊號與神經活動訊號的多通道高頻近紅外光譜系統;利用高頻強度調變光源經由光纖打入物質內,延伸先前的研究將調變頻率從10 KH提升到125 MHz,再使用靈敏度高的光電倍增管偵測微弱的散射光源並將以轉化成電訊號,最後透過類比IQ解調變的方式,將高頻訊號混波,取其低頻成分經由運算得到高頻成分的振幅與相位資訊。
    透過假體實驗對架設好的系統做校準的測試,而假體的成分包含具有散射特性物質的 Intralipid 與吸收特性物質的Ink溶液。在不同的變因,例如:調變頻率,光源到接收器的距離以及調配不同的溶液濃度,同時量測訊號的強度衰減與相位平移的變化來驗證系統。。在未來本系統可進一步應用在動物與細胞的研究上,用以檢測神經活動地情形。

    Two major types of optical signals following functional brain activation can be observed, the slow hemodynamic signal and the fast neuronal signal. The fast neuronal signal is supposedly related to neuronal activity, but its intensity is small and difficult to detect. The aim of this study was to set up a multi-channel high frequency fNIRS system for detecting the slow hemodynamic as well as the fast neuronal signals. We utilized high-frequency intensity-modulated light source through optical fiber to illuminate the medium. The modulated frequency was changed from 10 KHz up to 125 MHz used in our previous study. Instead of photodiode, high sensitivity photomultiplier tube (PMT) with Peltier cooling system was applied to detect scattering light and transform optical signal into electrical signal. The low frequency I and Q components from mixed signals were acquired from the analog in-phase and quadrature (IQ) demodulator for deriving the amplitude and phase information.
    The designed high frequency fINRS system was first calibrated in phantom in which the intralipid was used as scatter for varied amount of ink absorber. Under the phantom setup, we varied the modulated frequencies, the source-to-detector distance, and the concentration of intralipid-ink solution for validation purposes. Our observations on the amplitude attenuation and phase shift coincided with those of previous studies. The designed high frequency fNIRS system could be applied to brain activities of animal experiments and neuronal activities of cultured neurons in future studies.

    Chapter 1 Introduction 1 1.1 Introduction to neuroimaging techniques 1 1.2 Measurement methods for fNIRS 3 1.3 Applications of fNIRS systems 5 1.3.1 Slow hemodynamic signal 6 1.3.2 Fast neuronal signal 7 1.3.3 Comparison between slow and fast fNIRS signals 9 1.4 Motivations and the aims of this study 10 Chapter 2 Materials and Methods 11 2.1 Overall structure of multi-channel fNIRS system 11 2.2 The optical source unit, light intensity modulated output 12 2.2.1 Multiplexer for driving multichannel sources 13 2.2.2 Laser diode module and optical probe 14 2.3 The fNIRS detection system 15 2.3.1 Photo-detector components 16 2.3.2 Peltier modules and cooling system 18 2.4 Data acquisition unit and signal processing 19 2.4.1 Signal preprocessing 20 2.4.2 Homodyne IQ demodulation and low-pass filter 22 2.5 Calibration experiments for fast signal fNIRS system 25 Chapter 3 Results 28 3.1 Specifications of multi-channel high frequency fNIRS 28 3.1.1 Current source with multiplexing circuit 30 3.1.2 Configuration of photo-detector module 32 3.1.3 High frequency band-pass filter 32 3.1.4 Homodyne IQ demodulation 34 3.1.5 Measured amplitude value versus theoretical values after IQ demodulation 35 3.2 Validation tests of direct optical coupling 37 3.2.1 Validation test of high frequency intensity modulation 37 3.2.2 Performance of cooling effect on PMT module 38 3.2.3 Attenuation in intensity at high frequency modulation 39 3.2.4 Effect of source-detector distance 40 3.2.5 Effect of ink concentration in intralipid 41 3.3 Calibration experiments Observed from IQ demodulation 42 3.3.1 Effect of source-detector distance and ink concentration after IQ demodulation 42 3.3.2 Measured and theoretical values of phase shift for varied source-to-detector distances 43 3.4 The system flow chart with example signal 47 Chapter 4 Discussion and Conclusion 49 References 51

    [1] G. Strangman, D. A. Boas, and J. P. Sutton, "Non-invasive neuroimaging using near-infrared light," Biol. Psychiatry., vol. 52, pp. 679-93, 2002.
    [2] T. Vo-Dinh, Photon migration spectroscopy frequency-domain techniques. Boca Raton, Fla. : CRC, 2003.
    [3] J. B. Fishkin, S. Fantini, M. J. vandeVen, and E. Gratton, "Gigahertz photon density waves in a turbid medium: Theory and experiments," Phys. Rev. E., vol. 53, pp. 2307-19, 1996.
    [4] M. Wolf, U. Wolf, J. H. Choi, R. Gupta, L. P. Safonova, L. A. Paunescu, A. Michalos, and E. Gratton, "Functional frequency-domain near-infrared spectroscopy detects fast neuronal signal in the motor cortex," NeuroImage., vol. 17, pp. 1868-75, 2002.
    [5] M. Wolf, U. Wolf, J. H. Choi, V. Toronov, L. A. Paunescu, A. Michalos, and E. Gratton, "Fast cerebral functional signal in the 100-ms range detected in the visual cortex by frequency-domain nearinfrared spectrophotometry," Psychophysiology., vol. 40, pp. 521-8, 2003.
    [6] G. Morren, M. Wolf, P. Lemmerling, U. Wolf, J. H. Choi, E. Gratton, L. D. Luthauwer, and S. V. Huffel, "Detection of fast neuronal signals in the motor cortex from functional near infrared spectroscopy measurements using independent component analysis," Med. Biol. Eng. Comput., vol. 42, pp. 92-9, 2004.
    [7] E. Gratton, V. Toronov, U. Wolf, M. Wolf, and A. Webb, "Measurement of brain activity by near-infrared light," J. Biomed. Opt., vol. 10, pp. 0110081-9, 2005.
    [8] M. A. Franceschini and D. A. Boas, "Noninvasive measurement of neuronal activity with near-infrared optical imaging," NeuroImage., vol. 21, pp. 372-86, 2004.
    [9] R. A. Stepnoski, A. LaPorta, F. Raccuia-Behling, G. E. Blonder, R. E. Slusher, and D. Kleinfeld, "Noninvasive detection of changes in membrane potential in cultured neurons by light scattering," Proc. Natl. Acad. Sci. U.S.A., vol. 88, pp. 9382-86, 1991.
    [10] X. C. Yao, D. M. Rector, and J. S. George, "Optical lever recording of displacements from activated lobster nerve bundles and Nitella internodes," Appl. Opt., vol. 42, pp. 2972-76, 2003.
    [11] S. Fantini, M. A. Franceschini-Fantini, J. S. Maler, S. A. Walker, B. Barbieri, and E. Graton, "Frequency-demain multichannel optical detector for noninvasive tissue spectroscopy and oximetry," Opt. Eng., vol. 34, pp. 32-42, 1995.
    [12] V. Tuchin, Time- and frequency-domain sepectorscopy and tompgraphy of tisuue. Bellingham, Wash.: SPIE-International Society for Optical Engine 2000.
    [13] N. Ramanujam, C. Du, H. Y. Ma, and B. Chance, "Sources of phase noise in homodyne and heterodyne phase modulation deviced used for tissue oximetry studies," Rev. Sci. Instrum., vol. 69, pp. 3042-54, 1998.
    [14] S. Fantini, M. A. Franceschini, J. B. Fishkin, B. Barbieri, and E. Gratton, "Quantitative determination of the absorption spectra of chromophores in strongly scattering media: a light-emitting-diode based technique," Appl. Opt., vol. 33, pp. 5204-13, 1994.
    [15] J. Lai, Z. Li, C. Wang, and A. He, "Experimental measurement of the refractive index of biological tissues by total internal reflection," Appl. Opt., vol. 44, pp. 1845-9, 2005.
    [16] R. Frostig, Noninvasive imaging of cerebral activation with diffuse optical tomography. Boca Raton CRC, 2002.
    [17] K. Michielsen, H. D. Raedt, J. Przeslawski, and N. Garcia, "Computer simulation of time-resolved optical imaging of objects hidden in turbid media," Phys. Rep., vol. 304, pp. 89-144, 1998.
    [18] H. J. v. Staveren, C. J. M. Moes, J. v. Marie, S. A. Prahl, and G. M. J. C. v., "Light scattering in Intralipid -10% in the wavelength range of 400-1100 nm," Appl. Opt., vol. 30, pp. 4507-14, 1991.
    [19] B. Chance, M. Cope, E. Gratton, N. Ramanujam, and B. Tromberg, "Phase measurement of light absorption and scatter in human tissue," Rev. Sci. Instrum., vol. 69, pp. 3451-81, 1998.
    [20] E. Graton, M. W. W., and M. J. vandeVen, "Frequency domain optical imaging using diffusion of intensity modulated radiation," in Time-resolved spectroscopy of hemoglobin and myoglobin in resting and ischemic muscle, vol. 5,213,105. United States: Research corporation technologies, Inc., Tucson, Ariz, 1993.

    下載圖示 校內:2009-07-24公開
    校外:2009-07-24公開
    QR CODE