On the fundamental imaging-depth limit in two-photon microscopy

被引:324
作者
Theer, Patrick [1 ]
Denk, Winfried [1 ]
机构
[1] Max Planck Inst Med Res, D-69120 Heidelberg, Germany
关键词
D O I
10.1364/JOSAA.23.003139
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We have analyzed how the maximal imaging depth of two-photon microscopy in scattering samples depends on properties of the sample and the imaging system. We find that the imaging depth increases with increasing numerical aperture and staining inhomogeneity and with decreasing excitation-pulse duration and scattering anisotropy factor, but is ultimately limited by near-surface fluorescence with slight improvements possible using special detection strategies. (c) 2006 Optical Society of America.
引用
收藏
页码:3139 / 3149
页数:11
相关论文
共 42 条
[1]  
[Anonymous], 2005, MATHEMATICA VERS 5 2
[3]   Epifluorescence collection in two-photon microscopy [J].
Beaurepaire, E ;
Mertz, J .
APPLIED OPTICS, 2002, 41 (25) :5376-5382
[4]   Ultra-deep two-photon fluorescence excitation in turbid media [J].
Beaurepaire, E ;
Oheim, M ;
Mertz, J .
OPTICS COMMUNICATIONS, 2001, 188 (1-4) :25-29
[5]   Efficient analysis of temporal broadening of a pulsed focused Gaussian beam in scattering media [J].
Blanca, CM ;
Saloma, C .
APPLIED OPTICS, 1999, 38 (25) :5433-5437
[6]  
Born M., 1999, PRINCIPLES OPTICS
[7]   COMPUTER-SIMULATION OF LIGHT PULSE PROPAGATION FOR COMMUNICATION THROUGH THICK CLOUDS [J].
BUCHER, EA .
APPLIED OPTICS, 1973, 12 (10) :2391-2400
[8]  
Chandrasekhar S, 1950, RAD TRANSFER
[9]   A REVIEW OF THE OPTICAL-PROPERTIES OF BIOLOGICAL TISSUES [J].
CHEONG, WF ;
PRAHL, SA ;
WELCH, AJ .
IEEE JOURNAL OF QUANTUM ELECTRONICS, 1990, 26 (12) :2166-2185
[10]  
Debye P, 1909, ANN PHYS-BERLIN, V30, P755