Feasibility of using multiphoton excited tissue autofluorescence for in vivo human histopathology.

被引:37
作者
Dela Cruz, Johanna M. [1 ]
McMullen, Jesse D. [1 ,2 ]
Williams, Rebecca M. [1 ]
Zipfel, Warren R. [1 ,2 ]
机构
[1] Cornell Univ, Dept Biomed Engn, Ithaca, NY 14853 USA
[2] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14853 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1364/BOE.1.001320
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Rapid and direct imaging of microscopic tissue morphology and pathology can be achieved by multiphoton imaging of intrinsic tissue fluorophores and second harmonic signals. Engineering parameters for developing this technology for clinical applications include excitation levels and collection efficiencies required to obtain diagnostic quality images from different tissue types and whether these levels are mutagenic. Here we provide data on typical average powers required for high signal-to-noise in vivo tissue imaging and assess the risk potential of these irradiance levels using a mammalian cell gene mutation assay. Exposure times of similar to 16 milliseconds per cell to 760 nm, similar to 200 fs raster-scanned laser irradiation delivered through a 0.75 NA objective produced negligible mutagenicity at powers up to about 50 mW. (C) 2010 Optical Society of America
引用
收藏
页码:1320 / 1330
页数:11
相关论文
共 35 条
[1]  
[Anonymous], 2009, PROC SPIE
[2]   Second harmonic generation imaging via nonlinear endomicroscopy [J].
Bao, Hongchun ;
Boussioutas, Alex ;
Jeremy, Reynolds ;
Russell, Sarah ;
Gu, Min .
OPTICS EXPRESS, 2010, 18 (02) :1255-1260
[3]   Reactive oxygen species generated by thiopurine/UVA cause irreparable transcription-blocking DNA lesions [J].
Brem, Reto ;
Li, Feng ;
Karran, Peter .
NUCLEIC ACIDS RESEARCH, 2009, 37 (06) :1951-1961
[4]   Dynamic imaging of collagen and its modulation in tumors in vivo using second-harmonic generation [J].
Brown, E ;
McKee, T ;
diTomaso, E ;
Pluen, A ;
Seed, B ;
Boucher, Y ;
Jain, RK .
NATURE MEDICINE, 2003, 9 (06) :796-800
[5]  
Dahle J, 2003, CANCER RES, V63, P1464
[6]  
Douki T, 1999, PHOTOCHEM PHOTOBIOL, V70, P184, DOI 10.1111/j.1751-1097.1999.tb07988.x
[7]   Fiber-optic fluorescence imaging [J].
Flusberg, BA ;
Cocker, ED ;
Piyawattanametha, W ;
Jung, JC ;
Cheung, ELM ;
Schnitzer, MJ .
NATURE METHODS, 2005, 2 (12) :941-950
[8]   Fibre-optic nonlinear optical microscopy and endoscopy [J].
Fu, L. ;
Gu, M. .
JOURNAL OF MICROSCOPY, 2007, 226 (03) :195-206
[9]   Nonlinear optical endoscopy based on a double-clad photonic crystal fiber and a MEMS mirror [J].
Fu, L ;
Jain, A ;
Xie, HK ;
Cranfield, C ;
Gu, M .
OPTICS EXPRESS, 2006, 14 (03) :1027-1032
[10]   Miniaturization of fluorescence microscopes using fibre optics [J].
Helmchen, F .
EXPERIMENTAL PHYSIOLOGY, 2002, 87 (06) :737-745