Time multiplexing and parallelization in multifocal multiphoton microscopy

被引:66
作者
Egner, A [1 ]
Hell, SW [1 ]
机构
[1] Max Planck Inst Biophys Chem, High Resolut Opt Microscopy Grp, D-37070 Gottingen, Germany
来源
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION | 2000年 / 17卷 / 07期
关键词
D O I
10.1364/JOSAA.17.001192
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We investigate the imaging properties of high-aperture multifocal multiphoton microscopy on the basis of diffraction theory. Particular emphasis is placed on the relationship between the sectioning property and the distance between individual foci. Our results establish a relationship between the degree of parallelization and the axial resolution for both two- and three-photon excitation. In addition, we show quantitatively that if a matrix of temporal delays is inserted between the individual foci, it is, for the first time to our knowledge, possible to solve the classical conflict between the light budget and the sectioning property in three-dimensional microscopy and to provide a virtually unlimited density of foci at best axial resolution. (C) 2000 Optical Society of America [S0740-3232(00)01906-2] OCIS codes: 180.6900, 350.5730, 320.7080, 350.2950, 180.1790, 190.4180.
引用
收藏
页码:1192 / 1201
页数:10
相关论文
共 24 条
[1]   Multifocal multiphoton microscopy [J].
Bewersdorf, J ;
Pick, R ;
Hell, SW .
OPTICS LETTERS, 1998, 23 (09) :655-657
[2]  
Bewersdorf J, 1998, J MICROSC-OXFORD, V191, P28
[3]   SELF-IMAGING PROPERTIES OF A PERIODIC MICROLENS ARRAY - VERSATILE ARRAY ILLUMINATOR REALIZATION [J].
BONET, E ;
ANDRES, P ;
BARREIRO, JC ;
PONS, A .
OPTICS COMMUNICATIONS, 1994, 106 (1-3) :39-44
[4]  
Born M., 1993, PRINCIPLES OPTICS
[5]  
Buist AH, 1998, J MICROSC-OXFORD, V192, P217, DOI 10.1046/j.1365-2818.1998.00431.x
[6]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[7]  
Fujita K, 1999, J MICROSC-OXFORD, V194, P528, DOI 10.1046/j.1365-2818.1999.00493.x
[8]   Optical sectioning fluorescence spectroscopy in a programmable array microscope [J].
Hanley, QS ;
Verveer, PJ ;
Jovin, TM .
APPLIED SPECTROSCOPY, 1998, 52 (06) :783-789
[9]   Two-photon near- and far-field fluorescence microscopy with continuous-wave excitation [J].
Hell, SW ;
Booth, M ;
Wilms, S ;
Schnetter, CM ;
Kirsch, AK ;
Arndt-Jovin, DJ ;
Jovin, TM .
OPTICS LETTERS, 1998, 23 (15) :1238-1240
[10]  
Ichihara A., 1996, Bioimaging, V4, P52