Methods for tissue analysis

US9282931B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9282931-B2
Application numberUS-201113251594-A
CountryUS
Kind codeB2
Filing dateOct 3, 2011
Priority dateOct 30, 2000
Publication dateMar 15, 2016
Grant dateMar 15, 2016

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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The invention relates to methods and systems to optically analyze samples such as tissue based on speckle patterns of microscopic motion, such as Brownian motion.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of analyzing a tissue structure, comprising: illuminating the tissue structure with at least one of a coherent light or a partially coherent light from a light source onto the tissue structure; receiving a further light reflected from the tissue structure and forming a series of speckle patterns based on the further light; and obtaining speckle pattern data from the series of speckle patterns at time intervals sufficient to measure a microscopic motion within the tissue structure or within a tissue adjacent to the structure; and assessing the tissue structure by analyzing spatial characteristics of the speckle pattern data, and determining at least one of structural characteristics or biomechanical characteristics of the tissue structure which is in vivo tissue based on the assessment of the tissue structure. 2. The method of claim 1 , wherein the microscopic motion is at least one of a Brownian motion or a motion of cells or cellular organelles. 3. The method of claim 1 , further comprising providing a device which includes the light source in direct contact with the tissue structure. 4. The method of claim 1 , further comprising providing a detector which is configured to detect a far field speckle from the further light, and which is located farther than one wavelength of light from the tissue structure. 5. The method of claim 1 , wherein further comprising providing a detector which is configured to detect a near field speckle from the further light, and which is located within one wavelength of light from the tissue structure. 6. The method of claim 1 , wherein the assessing procedure comprises comparing each of the speckle patterns to a series of reference speckle patterns, and quantifying temporal correlation differences between the speckle patterns and the reference patterns. 7. The method of claim 6 , wherein the assessing procedure further comprises digitizing each of the speckle patterns, and the quantifying subprocedure comprises evaluating a cross-correlation between the speckle patterns and the reference patterns. 8. The method of claim 7 , wherein the assessing procedure further comprises determining a decorrelation rate for the speckle patterns. 9. The method of claim 6 , wherein the assessing procedure further comprises digitizing each of the speckle patterns, and the quantifying substep comprises evaluating a maximum cross-correlation between the speckle patterns and the reference patterns. 10. The method of claim 1 , wherein the assessing procedure further comprises analyzing spatial characteristics of the speckle patterns to determine structural characteristics of the tissue structure. 11. The method of claim 10 , wherein the illuminating procedure comprises illuminating multiple locations of the tissue structure in succession, the receiving procedure comprises forming a separate series of speckle patterns for each respective location of the tissue structure, and the analyzing procedure comprises analyzing each separate series of the speckle patterns and comparing the separate series to determine structural differences between the respective locations of the tissue structure. 12. The method of claim 1 , wherein the assessing of the tissue is performed by a computer structural arrangement that analyzes the changes in the speckle patterns at time intervals sufficient to measure the changes caused by the microscopic motion of the objects. 13. The method of claim 1 , wherein the assessing step includes assessing the tissue structure that is plaque. 14. The method of claim 1 , wherein the assessing step includes assessing the tissue structure that is a blood vessel. 15. The method of claim 1 , wherein the assessing step includes assessing the tissue structure that is a coronary artery. 16. The method of claim 1 , the assessing of the tissue is performed by a computer structural arrangement that receives data associated with heart beats. 17. A method for analyzing tissue, comprising: illuminating the tissue with at least one of a coherent light or a partially coherent light from a light source onto the tissue; receiving a further light reflected from the tissue and form a series of speckle patterns based on the further light; and analyzing changes in the speckle patterns at time intervals sufficient to measure changes caused by a microscopic motion of objects within the tissue which is in vivo tissue.

Assignees

Inventors

Classifications

  • Evaluating blood vessel condition, e.g. elasticity, compliance · CPC title

  • Optical coherence imaging · CPC title

  • for radial illumination · CPC title

  • Confocal scanning · CPC title

  • of noise induced by motion artifacts · CPC title

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Frequently asked questions

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What does patent US9282931B2 cover?
The invention relates to methods and systems to optically analyze samples such as tissue based on speckle patterns of microscopic motion, such as Brownian motion.
Who is the assignee on this patent?
Tearney Guillermo J, Bouma Brett E, Gen Hospital Corp
What technology area does this patent fall under?
Primary CPC classification A61B5/6885. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Mar 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).