Investigation on the optimal wavelength for two-photon microscopy in brain tissue

被引:1
作者
Tang, Wanyi [1 ]
Boateng, Derrick [1 ]
Cheng, Pan [1 ]
Zhou, Quanyu [1 ]
Wei, Xunbin [1 ]
He, Hao [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Biomed Engn, Shanghai 200031, Peoples R China
[2] Tianjin Univ, Coll Precis Instrument & Optoelect Engn, Ultrafast Laser Lab, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
INTACT MOUSE-BRAIN; IN-VIVO; DEEP;
D O I
10.1063/1.5025808
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Two-photon microscopy (TPM) has been one of the most widely used fluorescent microscopy methods in biological tissue. The femtosecond laser in the near-infrared (NIR) range showed better penetration in tissue due to less scattering and absorption. The method to estimate the optimal wavelength generally according to the scattering and absorption is somehow too rough considering the complex biological property and other factors that influence TPM. In this report, we set up a model to calculate the optimal wavelength in the NIR range for different imaging depths by involving more parameters of TPM. The calculated result suggests the image of brain slice stained with fluorescein isothiocyanate (FITC) can be acquired with the best TPM imaging quality at 780 nm excitation rather than longer wavelengths, which is consistent with our experimental results of TPM at depth of 50-300 mu m in mouse brain tissue. Our results may, therefore, bring a better understanding on TPM in tissue and help to develop a more accurate model for the simulation of TPM. (C) 2018 Author(s).
引用
收藏
页数:7
相关论文
共 17 条
[1]   Effect of excitation wavelength on penetration depth in nonlinear optical microscopy of turbid media [J].
Balu, Mihaela ;
Baldacchini, Tommaso ;
Carter, John ;
Krasieva, Tatiana B. ;
Zadoyan, Ruben ;
Tromberg, Bruce J. .
JOURNAL OF BIOMEDICAL OPTICS, 2009, 14 (01)
[2]   Brain refractive index measured in vivo with high-NA defocus-corrected full-field OCT and consequences for two-photon microscopy [J].
Binding, Jonas ;
Ben Arous, Juliette ;
Leger, Jean-Francois ;
Gigan, Sylvain ;
Boccara, Claude ;
Bourdieu, Laurent .
OPTICS EXPRESS, 2011, 19 (06) :4833-4847
[3]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[4]  
EGGERT HR, 1993, ADV EXP MED BIOL, V333, P47
[5]   Deep tissue two-photon microscopy [J].
Helmchen, F ;
Denk, W .
NATURE METHODS, 2005, 2 (12) :932-940
[6]  
Hoover EE, 2013, NAT PHOTONICS, V7, P93, DOI [10.1038/nphoton.2012.361, 10.1038/nphoton.2013.361]
[7]  
Horton NG, 2013, NAT PHOTONICS, V7, P205, DOI [10.1038/nphoton.2012.336, 10.1038/NPHOTON.2012.336]
[8]   Optical properties of biological tissues: a review (vol 58, pg R37, 2013) [J].
Jacques, Steven L. .
PHYSICS IN MEDICINE AND BIOLOGY, 2013, 58 (14) :5007-5008
[9]   Imaging in vivo:: watching the brain in action [J].
Kerr, Jason N. D. ;
Denk, Winfried .
NATURE REVIEWS NEUROSCIENCE, 2008, 9 (03) :195-205
[10]   In vivo two-photon microscopy to 1.6-mm depth in mouse cortex [J].
Kobat, Demirhan ;
Horton, Nicholas G. ;
Xu, Chris .
JOURNAL OF BIOMEDICAL OPTICS, 2011, 16 (10)