Comparative study of fully three-dimensional reconstruction algorithms for lens-free microscopy

被引:29
作者
Berdeu, Anthony [1 ,2 ]
Momey, Fabien [3 ]
Laperrousaz, Bastien [1 ,4 ,5 ]
Bordy, Thomas [1 ,2 ]
Gidrol, Xavier [1 ,4 ,5 ]
Dinten, Jean-Marc [1 ,2 ]
Picollet-D'hahan, Nathalie [1 ,4 ,5 ]
Allier, Cedric [1 ,2 ]
机构
[1] Univ Grenoble Alpes, F-38000 Grenoble, France
[2] Commissariat Energie Atom & Energies Alternat, Lab Elect & Technol Informat, F-38054 Grenoble, France
[3] Univ Jean Monnet, Lab Hubert Curien, F-42100 St Etienne, France
[4] Commissariat Energie Atom & Energies Alternat, Inst Biosci & Biotechnol Grenoble, F-38054 Grenoble, France
[5] INSERM, U1038, F-38054 Grenoble, France
关键词
TOMOGRAPHIC DIFFRACTIVE MICROSCOPY; CELL-CULTURE; 3D; MODELS; CHIP;
D O I
10.1364/AO.56.003939
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We propose a three-dimensional (3D) imaging platform based on lens-free microscopy to perform multiangle acquisitions on 3D cell cultures embedded in extracellular matrices. Lens-free microscopy acquisitions present some inherent issues such as the lack of phase information on the sensor plane and a limited angular coverage. We developed and compared three different algorithms based on the Fourier diffraction theorem to obtain fully 3D reconstructions. These algorithms present an increasing complexity associated with a better reconstruction quality. Two of them are based on a regularized inverse problem approach. To compare the reconstruction methods in terms of artefact reduction, signal-to-noise ratio, and computation time, we tested them on two experimental datasets: an endothelial cell culture and a prostate cell culture grown in a 3D extracellular matrix with large reconstructed volumes up to similar to 5 mm(3) with a resolution sufficient to resolve isolated single cells. The lens-free reconstructions compare well with standard microscopy. (C) 2017 Optical Society of America
引用
收藏
页码:3939 / 3951
页数:13
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