Swept source optical coherence microscopy using a 1310 nm VCSEL light source

被引:36
作者
Ahsen, Osman O. [1 ,2 ]
Tao, Yuankai K. [1 ,2 ]
Potsaid, Benjamin M. [1 ,2 ,3 ]
Sheikine, Yuri [4 ]
Jiang, James [3 ]
Grulkowski, Ireneusz [1 ,2 ]
Tsai, Tsung-Han [1 ,2 ]
Jayaraman, Vijaysekhar [5 ]
Kraus, Martin F. [1 ,2 ,6 ,7 ]
Connolly, James L. [4 ]
Hornegger, Joachim [6 ,7 ]
Cable, Alex [3 ]
Fujimoto, James G. [1 ,2 ]
机构
[1] MIT, Dept Elect Engn & Comp Sci, Cambridge, MA 02139 USA
[2] MIT, Elect Res Lab, Cambridge, MA 02139 USA
[3] Thorlabs Inc, Adv Imaging Grp, Newton, NJ USA
[4] Harvard Univ, Sch Med, Dept Pathol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[5] Praevium Res Inc, Santa Barbara, CA USA
[6] Univ Erlangen Nurnberg, Pattern Recognit Lab, Nurnberg, Germany
[7] Univ Erlangen Nurnberg, Grad Sch Adv Opt Technol, Nurnberg, Germany
来源
OPTICS EXPRESS | 2013年 / 21卷 / 15期
关键词
IN-VIVO; MULTIPHOTON MICROSCOPY; HIGH-SPEED; TOMOGRAPHY; RESOLUTION; TISSUES; LASER; CONTRAST; MARGIN;
D O I
10.1364/OE.21.018021
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We demonstrate high speed, swept source optical coherence microscopy (OCM) using a MEMS tunable vertical cavity surface-emitting laser (VCSEL) light source. The light source had a sweep rate of 280 kHz, providing a bidirectional axial scan rate of 560 kHz. The sweep bandwidth was 117 nm centered at 1310 nm, corresponding to an axial resolution of 13.1 mu m in air, corresponding to 8.1 mu m (9.6 mu m spectrally shaped) in tissue. Dispersion mismatch from different objectives was compensated numerically, enabling magnification and field of view to be easily changed. OCM images were acquired with transverse resolutions between 0.86 mu m - 3.42 mu m using interchangeable 40X, 20X and 10X objectives with similar to 600 mu m x 600 mu m, similar to 1 mm x 1 mm and similar to 2 mm x 2 mm field-of-view (FOV), respectively. Parasitic variations in path length with beam scanning were corrected numerically. These features enable swept source OCM to be integrated with a wide range of existing scanning microscopes. Large FOV mosaics were generated by serially acquiring adjacent overlapping microscopic fields and combining them in post-processing. Fresh human colon, thyroid and kidney specimens were imaged ex vivo and compared to matching histology sections, demonstrating the ability of OCM to image tissue specimens. (C) 2013 Optical Society of America
引用
收藏
页码:18021 / 18033
页数:13
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