Polarization anisotropy in fiber-optic second harmonic generation microscopy

被引:25
作者
Fu, Ling [1 ,2 ]
Gu, Min [1 ,2 ]
机构
[1] Swinburne Univ Technol, Fac Engn & Ind Sci, Ctr Microphoton, Hawthorn, Vic 3122, Australia
[2] Huazhong Univ Sci & Technol, Wuhan Natl Lab Optoelect, Britton Chance Ctr Biomed Photon, Wuhan 430074, Peoples R China
关键词
D O I
10.1364/OE.16.005000
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We report the investigation and implementation of a compact second harmonic generation microscope that uses a single-mode fiber coupler and a double-clad photonic crystal fiber. Second harmonic polarization anisotropy through the fiber-optic microscope systems is quantitatively measured with KTP microcrystals, fish scale and rat tail tendon. It is demonstrated that the polarized second harmonic signals can be excited and collected through the single-mode fiber coupler to analyze the molecular orientations of structural proteins. It has been discovered that a double-clad photonic crystal fiber can preserve the linear polarization in the core, although a depolarization effect is observed in the inner cladding region. The feasibility of polarization anisotropy measurements in fiberoptic second harmonic generation microscopy will benefit the in vivo study of collagen-related diseases with a compact imaging probe. (C) 2008 Optical Society of America.
引用
收藏
页码:5000 / 5006
页数:7
相关论文
共 26 条
[1]   Polarization-resolved second-harmonic-generation optical coherence tomography in collagen [J].
Applegate, BE ;
Yang, CH ;
Rollins, AM ;
Izatt, JA .
OPTICS LETTERS, 2004, 29 (19) :2252-2254
[2]   Two-photon fluorescence endoscopy with a micro-optic scanning head [J].
Bird, D ;
Gu, M .
OPTICS LETTERS, 2003, 28 (17) :1552-1554
[3]   Second-harmonic imaging microscopy for visualizing biomolecular arrays in cells, tissues and organisms [J].
Campagnola, PJ ;
Loew, LM .
NATURE BIOTECHNOLOGY, 2003, 21 (11) :1356-1360
[4]   Three-dimensional high-resolution second-harmonic generation imaging of endogenous structural proteins in biological tissues [J].
Campagnola, PJ ;
Millard, AC ;
Terasaki, M ;
Hoppe, PE ;
Malone, CJ ;
Mohler, WA .
BIOPHYSICAL JOURNAL, 2002, 82 (01) :493-508
[5]   Studies of x(2)/x(3) tensors in submicron-scaled bio-tissues by polarization harmonics optical microscopy [J].
Chu, SW ;
Chen, SY ;
Chern, GW ;
Tsai, TH ;
Chen, YC ;
Lin, BL ;
Sun, CK .
BIOPHYSICAL JOURNAL, 2004, 86 (06) :3914-3922
[6]   Uniform polarity microtubule assemblies imaged in native brain tissue by second-harmonic generation microscopy [J].
Dombeck, DA ;
Kasischke, KA ;
Vishwasrao, HD ;
Ingelsson, M ;
Hyman, BT ;
Webb, WW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (12) :7081-7086
[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]   In vivo brain imaging using a portable 3.9 gram two-photon fluorescence microendoscope [J].
Flusberg, BA ;
Lung, JC ;
Cocker, ED ;
Anderson, EP ;
Schnitzer, MJ .
OPTICS LETTERS, 2005, 30 (17) :2272-2274
[9]   Fibre-optic nonlinear optical microscopy and endoscopy [J].
Fu, L. ;
Gu, M. .
JOURNAL OF MICROSCOPY, 2007, 226 (03) :195-206
[10]   Polarisation characteristics of a 1x2 fibre coupler under femtosecond pulsed and continuous wave illumination [J].
Fu, L ;
Gan, XS ;
Bird, D ;
Gu, M .
OPTICS AND LASER TECHNOLOGY, 2005, 37 (06) :494-497