Spectrally resolved bioluminescence tomography using the reciprocity approach

被引:59
作者
Dehghani, Hamid [1 ]
Davis, Scott C. [2 ]
Pogue, Brian W. [2 ]
机构
[1] Univ Exeter, Sch Phys, Exeter EX4 4QL, Devon, England
[2] Dartmouth Coll, Thayer Sch Engn, Hanover, NH 03755 USA
基金
英国工程与自然科学研究理事会;
关键词
molecular imaging; optical tomography; image reconstruction; inverse problems;
D O I
10.1118/1.2982138
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Spectrally resolved bioluminescence optical tomography is an approach to recover images of, for example, Luciferase activity within a volume using multiwavelength emission data from internal bioluminescence sources. The underlying problem of uniqueness associated with nonspectrally resolved intensity-based bioluminescence tomography is demonstrated and it is shown that using a non-negative constraint inverse algorithm, an accurate solution for the source distribution can be calculated from the measured data. Reconstructed images of bioluminescence are presented using both simulated complex and heterogeneous small animal models as well as real multiwavelength data from a tissue-simulating phantom. The location of the internal bioluminescence source using experimental data is obtained with 0.5 mm accuracy and it is shown that small (2.5 mm diameter) sources of up to 12.5 mm deep, within a complex mouse model, can be resolved accurately using a single view data collection strategy. Finally, using the reciprocity approach for image reconstruction, a dramatic improvement in computational time is shown without loss to image accuracy with both experimental and simulated data, potentially reducing computing time from 402 to 3.75 h. (C) 2008 American Association of Physicists in Medicine. DOI: [10.1118/1.2982138]
引用
收藏
页码:4863 / 4871
页数:9
相关论文
共 25 条
[1]   Tomographic bioluminescence imaging by use of a combined optical-PET (OPET) system: a computer simulation feasibility study [J].
Alexandrakis, G ;
Rannou, FR ;
Chatziioannou, AF .
PHYSICS IN MEDICINE AND BIOLOGY, 2005, 50 (17) :4225-4241
[2]   PHOTON-MEASUREMENT DENSITY-FUNCTIONS .2. FINITE-ELEMENT-METHOD CALCULATIONS [J].
ARRIDGE, SR ;
SCHWEIGER, M .
APPLIED OPTICS, 1995, 34 (34) :8026-8037
[3]   Optical tomography in medical imaging [J].
Arridge, SR .
INVERSE PROBLEMS, 1999, 15 (02) :R41-R93
[4]  
CHU KM, 2008, BIOM OPT TOP M 2008
[5]   Bioluminescence imaging of point sources implanted in small animals post mortem: evaluation of a method for estimating source strength and depth [J].
Comsa, D. C. ;
Farrell, T. J. ;
Patterson, M. S. .
PHYSICS IN MEDICINE AND BIOLOGY, 2007, 52 (17) :5415-5428
[6]   It's not just about anatomy: In vivo bioluminescence imaging as an eyepiece into biology [J].
Contag, CH ;
Ross, BD .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2002, 16 (04) :378-387
[7]   Advances in vivo bioluminescence imaging of gene expression [J].
Contag, CH ;
Bachmann, MH .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 :235-260
[8]   Spinal muscular atrophies - distinctions and therapeutic progress [J].
Davies, SL ;
Moral, MA .
DRUGS OF THE FUTURE, 2006, 31 (04) :365-371
[9]   Image-guided diffuse optical fluorescence tomography implemented with Laplacian-type regularization [J].
Davis, Scott C. ;
Dehghani, Hamid ;
Wang, Jia ;
Jiang, Shudong ;
Pogue, Brian W. ;
Paulsen, Keith D. .
OPTICS EXPRESS, 2007, 15 (07) :4066-4082
[10]   The effects of internal refractive index variation in near-infrared optical tomography: a finite element modelling approach [J].
Dehghani, H ;
Brooksby, B ;
Vishwanath, K ;
Pogue, BW ;
Paulsen, KD .
PHYSICS IN MEDICINE AND BIOLOGY, 2003, 48 (16) :2713-2727