Analytical model to describe fluorescence spectra of normal and preneoplastic epithelial tissue: comparison with Monte Carlo simulations and clinical measurements

被引:80
作者
Chang, SK
Arifler, D
Drezek, R
Follen, M
Richards-Kortum, R [1 ]
机构
[1] Univ Texas, Dept Biomed Engn, Austin, TX 78712 USA
[2] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Gynecol Oncol, Houston, TX 77030 USA
[4] Ctr Biomed Engn, Houston, TX 77030 USA
关键词
fluorescence spectroscopy; cancer diagnosis;
D O I
10.1117/1.1695559
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescence spectroscopy has shown promise for the detection of precancerous changes in vivo. The epithelial and stromal layers of tissue have very different optical properties; the albedo is relatively low in the epithelium and approaches one in the stroma. As precancer develops, the optical properties of the epithelium and stroma are altered in markedly different ways: epithelial scattering and fluorescence increase, and stromal scattering and fluorescence decrease. We present an analytical model of the fluorescence spectrum of a two-layer medium such as epithelial tissue. Our hypothesis is that accounting for the two different tissue layers will provide increased diagnostic information when used to analyze tissue fluorescence spectra measured in vivo. The Beer-Lambert law is used to describe light propagation in the epithelial layer, while light propagation in the highly scattering stromal layer is described with diffusion theory. Predictions of the analytical model are compared to results from Monte Carlo simulations of light propagation under a range of optical properties reported for normal and precancerous epithelia[ tissue. In all cases, the mean square error between the Monte Carlo simulations and the analytical model are within 15%. Finally, model predictions are compared to fluorescence spectra of normal and precancerous cervical tissue measured in vivo; the lineshape of fluorescence agrees well in both cases, and the decrease in fluorescence intensity from normal to precancerous tissue is correctly predicted to within 5%. Future work will explore the use of this model to extract information about changes in epithelial and stromal optical properties from clinical measurements and the diagnostic value of these parameters. (C) 2004 Society of Photo-Optical Instrumentation Engineers.
引用
收藏
页码:511 / 522
页数:12
相关论文
共 43 条
[1]   Accuracy of the diffusion approximation in determining the optical properties of a two-layer turbid medium [J].
Alexandrakis, G ;
Farrell, TJ ;
Patterson, MS .
APPLIED OPTICS, 1998, 37 (31) :7401-7409
[2]   Light scattering from normal and dysplastic cervical cells at different epithelial depths: finite-difference time-domain modeling with a perfectly matched layer boundary condition [J].
Arifler, D ;
Guillaud, M ;
Carraro, A ;
Malpica, A ;
Follen, M ;
Richards-Kortum, R .
JOURNAL OF BIOMEDICAL OPTICS, 2003, 8 (03) :484-494
[3]   Cost-effectiveness analysis of diagnosis and management of cervical squamous intraepithelial lesions [J].
Cantor, SB ;
Mitchell, MF ;
Tortolero-Luna, G ;
Bratka, CS ;
Bodurka, DC ;
Richards-Kortum, R .
OBSTETRICS AND GYNECOLOGY, 1998, 91 (02) :270-277
[4]   Optimal excitation wavelengths for discrimination of cervical neoplasia [J].
Chang, SK ;
Follen, M ;
Malpica, A ;
Utzinger, U ;
Staerkel, G ;
Cox, D ;
Atkinson, EN ;
MacAulay, C ;
Richards-Kortum, R .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2002, 49 (10) :1102-1111
[5]  
CHENG WF, 1995, OPTICAL THERMAL RESP, pCH8
[6]   Determination of epithelial tissue scattering coefficient using confocal microscopy [J].
Collier, T ;
Arifler, D ;
Malpica, A ;
Follen, M ;
Richards-Kortum, R .
IEEE JOURNAL OF SELECTED TOPICS IN QUANTUM ELECTRONICS, 2003, 9 (02) :307-313
[7]   Near real-time confocal microscopy of amelanotic tissue: Detection of dysplasia in ex vivo cervical tissue [J].
Collier, T ;
Lacy, A ;
Richards-Kortum, R ;
Malpica, A ;
Follen, M .
ACADEMIC RADIOLOGY, 2002, 9 (05) :504-512
[8]   Angiogenesis in cervical neoplasia: Microvessel quantitation in precancerous lesions and invasive carcinomas with clinicopathological correlations [J].
Dellas, A ;
Moch, H ;
Schultheiss, E ;
Feichter, G ;
Almendral, AC ;
Gudat, F ;
Torhorst, J .
GYNECOLOGIC ONCOLOGY, 1997, 67 (01) :27-33
[9]   Light scattering from cervical cells throughout neoplastic progression: influence of nuclear morphology, DNA content, and chromatin texture [J].
Drezek, R ;
Guillaud, M ;
Collier, T ;
Boiko, I ;
Malpica, A ;
Macaulay, C ;
Follen, M ;
Richards-Kortum, R .
JOURNAL OF BIOMEDICAL OPTICS, 2003, 8 (01) :7-16
[10]  
Drezek R, 2001, PHOTOCHEM PHOTOBIOL, V73, P636, DOI 10.1562/0031-8655(2001)073<0636:AMOFCT>2.0.CO