A high sensitivity multi-spectral three-dimensional fluorescence optical tomography system for small animal imaging

2009 ◽  
Author(s):  
Changqing Li ◽  
Gregory S. Mitchell ◽  
Joyita Dutta ◽  
Sangtae Ahn ◽  
Richard M. Leahy ◽  
...  
2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Zi-Jing Lin ◽  
Haijing Niu ◽  
Lin Li ◽  
Hanli Liu

We report the feasibility of three-dimensional (3D) volumetric diffuse optical tomography for small animal imaging by using a CCD-camera-based imaging system with a newly developed depth compensation algorithm (DCA). Our computer simulations and laboratory phantom studies have demonstrated that the combination of a CCD camera and DCA can significantly improve the accuracy in depth localization and lead to reconstruction of 3D volumetric images. This approach may present great interests for noninvasive 3D localization of an anomaly hidden in tissue, such as a tumor or a stroke lesion, for preclinical small animal models.


2013 ◽  
Vol 24 (10) ◽  
pp. 105405 ◽  
Author(s):  
James A Guggenheim ◽  
Hector R A Basevi ◽  
Jon Frampton ◽  
Iain B Styles ◽  
Hamid Dehghani

2014 ◽  
Vol 19 (4) ◽  
pp. 046002 ◽  
Author(s):  
Changqing Li ◽  
Arnulfo Martínez-Dávalos ◽  
Simon R. Cherry

2008 ◽  
Author(s):  
John Gamelin ◽  
Andres Aguirre ◽  
Anastasios Maurudis ◽  
Fei Huang ◽  
Diego Castillo ◽  
...  

2007 ◽  
Vol 29 (3) ◽  
pp. 155-166 ◽  
Author(s):  
Ai-Ho Liao ◽  
Li-Yen Chen ◽  
Wen-Fang Cheng ◽  
Pai-Chi Li

Small-animal models are used extensively in disease research, genomics research, drug development and developmental biology. The development of noninvasive small-animal imaging techniques with adequate spatial resolution and sensitivity is therefore of prime importance. In particular, multimodality small-animal imaging can provide complementary information. This paper presents a method for registering high-frequency ultrasonic (microUS) images with small-animal positron-emission tomography (microPET) images. Registration is performed using six external multimodality markers, each being a glass bead with a diameter of 0.43–0.60 mm, with 0.1 μl of [18F]FDG placed in each marker holder. A small-animal holder is used to transfer mice between the microPET and microUS systems. Multimodality imaging was performed on C57BL/6J black mice bearing WF-3 ovary cancer cells in the second week after tumor implantation and rigid-body image registration of the six markers was also performed. The average registration error was 0.31 mm when all six markers were used and increased as the number of markers decreased. After image registration, image segmentation and fusion are performed on the tumor. Our multimodality small-animal imaging method allows structural information from microUS to be combined with functional information from microPET, with the preliminary results showing it to be an effective tool for cancer research.


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