Imaging volumes with arbitrary geometries in contact and non-contact tomography

a technology of arbitrary geometries and images, applied in the field of clinical imaging modality, can solve the problems of inability to implement a limited number of detector channels, inapplicability, and significant disadvantages of fiber guides, and achieve the effect of retaining accuracy and capacity, achieving computational simplicity and efficiency of analytical methods

Inactive Publication Date: 2005-12-22
VISEN MEDICAL INC
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AI Technical Summary

Benefits of technology

[0006] There is a need for fast computational methods for real-time optical tomographic diagnostics and other research and clinical uses that can deal with arbitrary sizes, shapes and boundaries that (1) attain the computational simplicity and efficiency of analytical methods while (2) retaining the accuracy and capacity of numerical methods to model arbitrary shapes and boundaries, and (3) can be applied both to contact and non-contact measurements of diffuse and diffuse-like medium.
[0013] The approach described herein provide several advantages over the existing art, including (1) the ability to image volumes with 2D or 3D geometries of arbitrary size, shape and boundaries using fast and accurate analytical methods, and (2) the application of these new methods for both contact and non-contact tomography of diffuse and diffuse-like medium. These new imaging methods can have broad applications in a wide variety of areas in research and clinical imaging. Importantly, these methods significantly improve existing tomographic imaging techniques and make possible the use of these imaging techniques in real-time animal and human subject imaging and clinical medical diagnostics by allowing the implementation of practical systems with unprecedented capacity for data collection.

Problems solved by technology

The use of fiber guides, however, has significant disadvantages.
The most significant is that only a limited number of detector channels can be implemented since scaling up requires a large number of fibers (usually fiber bundles) that have to be coupled to the tissue, which in many cases is not practical.
In addition, it is also very difficult to control or measure the exact coupling conditions of each individual fiber or fiber bundle, which can vary quite significantly from fiber to fiber.
In either case, the use of fiber guides and / or optical matching fluids and fixed geometries impedes the experimental practicality and severely limits the tomographic capacity of the imaging system.
These constraints result in significant limitations to the use of these systems either in research or in the clinic.
Numerical methods, such as the finite element method (FEM), finite differences (FD) or the boundary element method (BEM), are used for complex geometries of air / tissue boundaries and are extremely computationally costly and therefore are currently non-viable in a real-time three-dimensional research and clinical setting.
Analytical methods are much faster (for example, an analytical-based 3D reconstruction case of the breast ranges between 2-15 minutes), but are available only for simple geometries of air / tissue boundary such as a slab, a cylinder or a sphere, and often lack adequate accuracy for imaging complex objects such as a human breast.
Although in contact imaging applications the KA can achieve relatively good computational efficiency (Ripoll et al., Opt. Lett. 27:333-335, 2002), it has several significant limitations that would restrict its use in real research and clinical settings.

Method used

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  • Imaging volumes with arbitrary geometries in contact and non-contact tomography
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  • Imaging volumes with arbitrary geometries in contact and non-contact tomography

Examples

Experimental program
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example 1

KA is Several Orders of Magnitude Faster Than More Rigorous Numerical Methods Such as FD or ET

[0081] Referring to FIG. 4, the computing times achieved by using the KA as defined by equation (12) is compared to the extinction theorem (ET) and finite-differences solution (FD). While both ET and FD methods have a strong non-linear dependence as the area of the surface and the volume investigated increases, the KA method scales linearly with the size of the problem and more importantly it is faster than the ET and FD methods by almost three-orders of magnitude.

[0082] By way of a practical example, the number of discretization points for a sphere of radius 2 cm needed in order to maintain a one transport mean free path (ltr=D / 3) distance between points (N˜5000) was used to compare the speed of the KA and ET methods. In this case, it takes the KA methods 70 seconds and the ET method 50 minutes to solve the problem, indicating that the KA as approximately 40 times faster than the ET meth...

example 2

The Errors of the KA Due to Shadowing Effect

[0084] So-called shadowing effect appears when certain surface areas are blocked from the source by the geometry of the interface. Since the KA only considers first order reflections at the interface, errors appear in the proximities of the shadow regions of a source. Furthermore, since these shadow areas are not taken into account in the KA, it predicts higher values of the intensity for these areas.

[0085] Referring to FIGS. 5 (a)-(d), the shadow effect is demonstration of for the KA method and for the infinite case for a cylinder of R=2.5 cm with a sine profile in the boundary of amplitude 0.5 cm, and period π / 4. The error is plotted as a percentage of the absolute photon field strength at each point. Error committed for different source locations using the KA are shown in (a) and (c) and using the homogeneous Green's function in (b) and (d). The following source locations were considered: (ρ=2.3 cm, θ=0) for (a) and (b), and (ρ=1.5 cm...

example 3

The Errors of the KA When Imaging Small Volumes with Weak Absorption

[0087] A comparison of the intensity generated by a point source in a cylindrical geometry using the KA versus the exact solution, (ET) with different several radius and optical properties is shown in FIG. 6. Error in the KA were plotted against absorption coefficient for different radii and scattering coefficients for a case of a smooth cylinder (i.e., no shadowing effect).

[0088] The smaller the dimensions of the geometry and the smaller the absorption coefficient the larger the error committed by the KA method. As seen in this figure, the error increases as the volume of the medium or the absorption decreases. From FIG. 6(a), it can be concluded that in order to make practical use of the KA (assuming a minimum of 5% accuracy), either large volumes and therefore small curvatures need to be present (R>2.5 cm), or very large absorption coefficients are needed (μa>0.1 l / cm).

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Abstract

A method for tomographic imaging of diffuse medium includes directing waves into a diffusive medium, solving a surface-bounded inversion problem by forward field calculations through decomposition of contributions from the multiple reflections from an arbitrary surface within the diffusive medium or outside the diffusive medium into a sum of different orders of reflection up to an arbitrary order, and using contact or non-contact measurements of waves outside said diffusive medium to generate a tomographic image.

Description

RELATED APPLICATIONS [0001] This application is a continuation of International Application No. PCT / US03 / 17558, which designated the United States and was filed on Jun. 4, 2003, published in English, which claims the benefit of U.S. Provisional Application No. 60 / 385,931, filed on Jun. 4, 2002. The entire teachings of the above applications are incorporated herein by reference.BACKGROUND OF THE INVENTION [0002] Optical imaging is an evolving clinical imaging modality that uses penetrating lights rays to create images of both intrinsic and extrinsic biological scatterers. Light offers unique contrast mechanisms that can be based on absorption, e.g., probing of hemoglobin concentration or blood saturation, and / or fluorescence, e.g., probing for weak auto-fluorescence, or exogenously administered fluorescent probes (Neri et al., Nat. Biotech. 15:1271-1275, 1997; Ballou et al., Cancer Immunol. Immunother. 41:257-63, 1995; and Weissleder, et al., Nat. Biotech. 17:375-178, 1999). Preferab...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61B5/00A61B5/05G01N21/47
CPCA61B5/0059A61B5/0073A61B5/415A61B5/418A61B5/4887A61B5/4528G01N21/4795G01N33/49A61B5/0071A61B5/4504
Inventor RIPOLL, JORGENTZIACHRISTOS, VASILISMADDEN, KAREN N.
Owner VISEN MEDICAL INC
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