Coherent control improves biomedical imaging with ultrashort shaped pulses

被引:29
作者
Dela Cruz, Johanna M.
Lozovoy, Vadim V.
Dantus, Marcos [1 ]
机构
[1] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
[2] Michigan State Univ, Dept Phys & Astron, E Lansing, MI 48824 USA
基金
美国国家科学基金会;
关键词
coherent control; phase modulation; shaped pulses; femtosecond; two-photon imaging; three-photon;
D O I
10.1016/j.jphotochem.2006.02.020
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Although ultrashort pulses are advantageous for multiphoton excitation microscopy, they can be difficult to manipulate and may cause increased sample damage when applied to biological tissue. Here we present a method based on coherent control that corrects phase distortions introduced by high numerical aperture (NA) microscope objectives, thereby achieving the full potential of ultrashort pulses. A number of useful phase functions are recommended to gain selectivity that is similar to that which can be achieved by tuning a longer laser pulse; however this one involves no moving parts and maintains perfect optimization. This capability is used to demonstrate functional imaging by selective two-photon excitation of a pH-sensitive chromophore. Finally, we show that phase functions can also be introduced to minimize multiphoton excitation damage, while maintaining a high efficiency of two-photon excitation. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:307 / 313
页数:7
相关论文
共 24 条
[1]   Multiphoton intrapulse interference 6; binary phase shaping [J].
Comstock, M ;
Lozovoy, VV ;
Pastirk, I ;
Dantus, M .
OPTICS EXPRESS, 2004, 12 (06) :1061-1066
[2]   Quantitative mass spectrometric identification of isomers applying coherent laser control [J].
Dela Cruz, JM ;
Lozovoy, VV ;
Dantus, M .
JOURNAL OF PHYSICAL CHEMISTRY A, 2005, 109 (38) :8447-8450
[3]   Use of coherent control methods through scattering biological tissue to achieve functional imaging [J].
Dela Cruz, JM ;
Pastirk, I ;
Comstock, M ;
Lozovoy, VV ;
Dantus, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (49) :16996-17001
[4]   Multiphoton intrapulse interference 3: Probing microscopic chemical environments [J].
Dela Cruz, JM ;
Pastirk, I ;
Lozovoy, VV ;
Walowicz, KA ;
Dantus, M .
JOURNAL OF PHYSICAL CHEMISTRY A, 2004, 108 (01) :53-58
[5]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[6]   Photon upmanship: Why multiphoton imaging is more than a gimmick [J].
Denk, W ;
Svoboda, K .
NEURON, 1997, 18 (03) :351-357
[7]  
Denk W, 1996, J Biomed Opt, V1, P296, DOI 10.1117/12.242945
[8]   Highly nonlinear photodamage in two-photon fluorescence microscopy [J].
Hopt, A ;
Neher, E .
BIOPHYSICAL JOURNAL, 2001, 80 (04) :2029-2036
[9]   Ca2+ fluorescence imaging with pico- and femtosecond two-photon excitation:: Signal and photodamage [J].
Koester, HJ ;
Baur, D ;
Uhl, R ;
Hell, SW .
BIOPHYSICAL JOURNAL, 1999, 77 (04) :2226-2236
[10]   Pulse-length dependence of cellular response to intense near-infrared laser pulses in multiphoton microscopes [J].
König, K ;
Becker, TW ;
Fischer, P ;
Riemann, I ;
Halbhuber, KJ .
OPTICS LETTERS, 1999, 24 (02) :113-115