Real-time optical coherence microscopy in biological tissues

1999 ◽  
Author(s):  
A. Dubois ◽  
L. Vabre ◽  
M. Lebec ◽  
S. Lévêque ◽  
A. C. Boccara ◽  
...  
Photonics ◽  
2021 ◽  
Vol 8 (12) ◽  
pp. 527
Author(s):  
Vladimir Y. Zaitsev ◽  
Sergey Y. Ksenofontov ◽  
Alexander A. Sovetsky ◽  
Alexander L. Matveyev ◽  
Lev A. Matveev ◽  
...  

We present a real-time realization of OCT-based elastographic mapping local strains and distribution of the Young’s modulus in biological tissues, which is in high demand for biomedical usage. The described variant exploits the principle of Compression Optical Coherence Elastography (C-OCE) and uses processing of phase-sensitive OCT signals. The strain is estimated by finding local axial gradients of interframe phase variations. Instead of the popular least-squares method for finding these gradients, we use the vector approach, one of its advantages being increased computational efficiency. Here, we present a modified, especially fast variant of this approach. In contrast to conventional correlation-based methods and previously used phase-resolved methods, the described method does not use any search operations or local calculations over a sliding window. Rather, it obtains local strain maps (and then elasticity maps) using several transformations represented as matrix operations applied to entire complex-valued OCT scans. We first elucidate the difference of the proposed method from the previously used correlational and phase-resolved methods and then describe the proposed method realization in a medical OCT device, in which for real-time processing, a “typical” central processor (e.g., Intel Core i7-8850H) is sufficient. Representative examples of on-flight obtained elastographic images are given. These results open prospects for broad use of affordable OCT devices for high-resolution elastographic vitalization in numerous biomedical applications, including the use in clinic.


2007 ◽  
Vol 32 (16) ◽  
pp. 2375 ◽  
Author(s):  
Linbo Liu ◽  
Cheng Liu ◽  
Wong Chee Howe ◽  
C. J. R. Sheppard ◽  
Nanguang Chen

2017 ◽  
Vol 8 (2) ◽  
pp. 608 ◽  
Author(s):  
Samuel Choi ◽  
Keita Sato ◽  
Takeru Ota ◽  
Fumiaki Nin ◽  
Shogo Muramatsu ◽  
...  

2017 ◽  
Author(s):  
Cristina Canavesi ◽  
Andrea Cogliati ◽  
Adam Hayes ◽  
Patrice Tankam ◽  
Anand Santhanam ◽  
...  

1997 ◽  
Vol 3 (S2) ◽  
pp. 795-796
Author(s):  
Joseph A. Izatt ◽  
Manish Kulkarni ◽  
Hsing-Wen Wang ◽  
Michael V. Sivak

Optical coherence microscopy (OCM) is a novel technique complementary to optical coherence tomography (OCT) which combines low-coherence interferometry with confocal microscopy to achieve micron-scale resolution imaging in highly scattering media. OCM may be implemented using a single-mode fiber-optic low-coherence interferometer (See Fig. 1). A high numerical aperture objective is used to focus sample-arm light into the specimen, and the reference arm length of the interferometer is adjusted to match the sample arm focal plane optical depth. The sample arm of the interferometer comprises a scanning confocal microscope, in which either the sample or the probe beam is laterally scanned in a raster pattern, and the optical fiber acts as a single-mode confocal aperture for combined light illumination and collection. The reference arm length of the interferometer establishes the depth position of an interferometric “coherence gate” in the sample, from which backscattered light is preferentially collected. Initial studies of OCM in scattering phantoms have demonstrated that this technique provides increased optical sectioning depth compared to confocal microscopy alone.


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