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Miniaturized light-field endoscope via a GRIN lens array

光学 镜头(地质) 内窥镜 物理 医学 放射科
作者
Yixuan Zhao,Jian Liu,Cheng Guo,Weisong Zhao,Guo Ye,Jing Liu
出处
期刊:Optics Communications [Elsevier]
卷期号:528: 129016-129016 被引量:4
标识
DOI:10.1016/j.optcom.2022.129016
摘要

Endoscopy provides an intuitive observation of the internal organ structures for surgeons. Most clinical 3D endoscopes generally rely on visual parallax to create a stereoscopic vision, which is incapable of obtaining quantitative depth information for precise diagnosis. Hence a compact probe-type 3D quantitative imaging remains a challenging task for the endoscopic system. In this work, we propose an integrated light-field endoscope that realizes 3D morphology observation with cellular-level resolution from a single-frame data record. In our prototype, a compact customized GRIN lens array (GLA) is used as an objective lens to capture the spatio-angular information directly from object space, as well as maintain consistent spatial measurements. In data processing, we employ a calibration method to estimate the 3D point spread function. After decoupling the spatio-angular information, the 3D morphology of sample can be reconstructed by a deconvolution operation. The system has a lateral resolution of about 15 ∼ 40 μ m and an axial resolution of 100 ∼ 200 μ m over an axial operating range of 10 mm. In experiment, we demonstrate the 3D imaging capacity of our platform via fixed structures and living worms. • A new miniaturized light-field endoscope to obtain quantitative depth information with cellular-level resolution from a single-frame data record for precise diagnosis. We utilize a GRIN lens array to capture the spatio-angular information directly from object space, as well as maintain consistent spatial measurements. • A new PSF calibration method is proposed. We employ a nonlinear curve fitting method to estimate the 3D PSF which can obtain high-quality PSF quickly and robustly. • The experimental results including sets of samples (USAF target, ductile fiber mesh, mint leaf, and living worms) demonstrate the superiority of our method.
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