TY - JOUR
T1 - Moxifloxacin-Based Extended Depth-of-Field Fluorescence Microscopy for Real-Time Conjunctival Goblet Cell Examination
AU - Lee, Jungbin
AU - Kim, Seonghan
AU - Kim, Jeongho
AU - Son, Byeong Jae
AU - Yoon, Chang Ho
AU - Kim, Hong Kyun
AU - Kim, Ki Hean
N1 - Publisher Copyright:
© 1982-2012 IEEE.
PY - 2022/8/1
Y1 - 2022/8/1
N2 - Conjunctival goblet cells (CGCs) are mucin-secreting cells in the eye and play essential roles for ocular surface homeostasis. Since various ocular surface pathologies are related to CGC dysfunction, CGC examination is important for the evaluation of ocular surface conditions. Recently we introduced moxifloxacin-based fluorescence microscopy (MBFM) for non-invasive CGC imaging. However, the imaging speed was up to 1 frame per second (fps) and needed to be improved for clinical applications. In this study, we developed a high-speed moxifloxacin-based, extended depth-of-field (EDOF) microscopy system that operates at a maximum imaging speed of 15 fps. The system used a deformable mirror for the high-speed axial sweeping of focal plane during single-frame acquisitions. The acquired images contained both in-focus and out-of-focus information, and deconvolution was used to filter the in-focus information. The system had a DOF of 800 $\mu \text{m}$ , field-of-view of 1.2 mm $\times1.2$ mm, and resolution of $2.3~\mu \text{m}$. Its performance was demonstrated by real-time, breathing-motion-insensitive CGC imaging of mouse and rabbit models, in vivo. High-speed EDOF microscopy has potentials for non-invasive, real-time CGC examinations of human subjects.
AB - Conjunctival goblet cells (CGCs) are mucin-secreting cells in the eye and play essential roles for ocular surface homeostasis. Since various ocular surface pathologies are related to CGC dysfunction, CGC examination is important for the evaluation of ocular surface conditions. Recently we introduced moxifloxacin-based fluorescence microscopy (MBFM) for non-invasive CGC imaging. However, the imaging speed was up to 1 frame per second (fps) and needed to be improved for clinical applications. In this study, we developed a high-speed moxifloxacin-based, extended depth-of-field (EDOF) microscopy system that operates at a maximum imaging speed of 15 fps. The system used a deformable mirror for the high-speed axial sweeping of focal plane during single-frame acquisitions. The acquired images contained both in-focus and out-of-focus information, and deconvolution was used to filter the in-focus information. The system had a DOF of 800 $\mu \text{m}$ , field-of-view of 1.2 mm $\times1.2$ mm, and resolution of $2.3~\mu \text{m}$. Its performance was demonstrated by real-time, breathing-motion-insensitive CGC imaging of mouse and rabbit models, in vivo. High-speed EDOF microscopy has potentials for non-invasive, real-time CGC examinations of human subjects.
KW - Extended depth-of-field
KW - conjunctival goblet cell
KW - fluorescence microscopy
KW - high-speed imaging
KW - ocular surface diseases
UR - http://www.scopus.com/inward/record.url?scp=85124812000&partnerID=8YFLogxK
U2 - 10.1109/TMI.2022.3151944
DO - 10.1109/TMI.2022.3151944
M3 - Article
C2 - 35167445
AN - SCOPUS:85124812000
VL - 41
SP - 2004
EP - 2008
JO - IEEE Transactions on Medical Imaging
JF - IEEE Transactions on Medical Imaging
SN - 0278-0062
IS - 8
ER -