Endoscopic en-face optical coherence tomography and fluorescence imaging using correlation-based probe tracking

被引:4
|
作者
Marques, Manuel J. [1 ]
Hughes, Michael R. [1 ]
Uceda, Adrian F. [1 ]
Gelikonov, Grigory [2 ]
Bradu, Adrian [1 ]
Podoleanu, Adrian [1 ]
机构
[1] Univ Kent, Div Nat Sci, Phys & Astron, Appl Opt Grp, Canterbury CT2 7NH, Kent, England
[2] RAS, Inst Appl Phys, Nizhnii Novgorod, Russia
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会; 欧盟地平线“2020”;
关键词
COMPLEX MASTER-SLAVE; ROTATIONAL DISTORTION; SCANNING ENDOSCOPE; OCT; SPEED; CATHETER; NEEDLE; PLATFORM; CAPSULE; SYSTEM;
D O I
10.1364/BOE.444170
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Forward-viewing endoscopic optical coherence tomography (OCT) provides 3D imaging in vivo, and can be combined with widefield fluorescence imaging by use of a double-clad fiber. However, it is technically challenging to build a high-performance miniaturized 2D scanning system with a large field-of-view. In this paper we demonstrate how a 1D scanning probe, which produces cross-sectional OCT images (B-scans) and 1D fluorescence T-scans, can be transformed into a 2D scanning probe by manual scanning along the second axis. OCT volumes are assembled from the B-scans using speckle decorrelation measurements to estimate the out-of-plane motion along the manual scan direction. Motion within the plane of the B-scans is corrected using image registration by normalized cross correlation. En-face OCT slices and fluorescence images, corrected for probe motion in 3D, can be displayed in real-time during the scan. For a B-scan frame rate of 250 Hz, and an OCT lateral resolution of approximately 20 mu m, the approach can handle out-of-plane motion at speeds of up to 4 mm/s. Published by Optica Publishing Group under the terms of the Creative Commons Attribution 4.0 License.
引用
收藏
页码:761 / 776
页数:16
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