IP Library Granted Patent US 10,254,227
Granted Patent B2
US 10,254,227 · App. 15/352,427 · Granted Apr 9, 2019

Fluorescence biopsy specimen imager and methods

Inventor: Han-Wei Wang (Lincoln, NE)
Assignee: LI-COR, Inc.
G01N21/6458G01N21/6428G01N21/6456G02B21/367G06T7/0012G06T7/55G06T11/60G06T15/205G06T17/20H04N5/2256H04N5/332H04N7/181G01N2021/1787G01N2021/6439G01N2201/06113G01N2201/12G06T2207/10024G06T2207/10048G06T2207/10056G06T2207/10064G06T2207/30024G06T2207/30096G06T2207/30196
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Quick Facts
Patent No.
US 10,254,227
App. No.
15/352,427
Granted
Apr 9, 2019
Kind
B2
Abstract

Biopsy imaging devices with an imaging stage configured to rotate and tilt a biological sample, as well as a method for using it, are described. The stage can use rotating bearings or extendible, telescoping arms. The device has a white light for taking normal pictures and a near-infrared laser light for causing a fluorescence-biomolecule probed sample to fluoresce for fluorescence images in a light-tight housing. A set of both types of pictures are taken from angles around, above, and below the biopsy sample with one or more cameras to generate a 3-D model in a computer of the biopsy with fluorescence markings. The 3-D model can then be rendered and viewed on a display by a surgeon to determine if sufficient margins were removed from the patient.

Claims (51)

1. A method for imaging a biological sample from a subject, the method comprising:

illuminating the biological sample on an imaging stage with visible light, wherein the imaging stage is mechanically connected to a first rotary bearing having a first rotational axis configured to project through the imaging stage, wherein the imaging stage is mechanically connected to a second rotary bearing having a second rotational axis configured to project through the imaging stage, and wherein the second rotational axis is orthogonal to the first rotational axis;

imaging, using a first camera, a plurality of two-dimensional (2-D) reflected light images of the biological sample;

rotating the imaging stage around angles of the first or second rotational axis between imaging at least two of the plurality of 2-D reflected light images;

irradiating the biological sample on the imaging stage with near infrared light;

recording, using a second camera, a plurality of 2-D fluorescence images of the biological sample;

turning the imaging stage around angles of the first or second rotational axis between recording at least two of the plurality of 2-D fluorescence images; and

rendering an image produced from the reflected light images and the fluorescence images.

2. The method of claim 1 , further comprising:

constructing a three-dimensional (3-D) model of the biological sample based upon the plurality of 2-D reflected light images; and

adding fluorescence information to the 3-D model of the biological sample based upon the plurality of 2-D fluorescence images.

3. The method of claim 2 , wherein the 3-D model is a first 3-D model, the method further comprising:

producing a second 3-D model of the biological sample based upon the plurality of 2-D fluorescence images; and

projecting the second 3-D model onto the first 3-D model by interposing points of the second 3-D model into the first 3-D model to add fluorescence information to the 3-D model.

4. The method of claim 1 , wherein the first camera and the second camera are the same camera.

5. The method of claim 1 , wherein the imaging stage has a transparent portion, and wherein the imaging stage is configured to hold at least a portion of the biological sample within an imaging volume.

6. The method of claim 5 , wherein at least one of the plurality of 2-D reflected light images is imaged through the transparent portion of the imaging stage, and at least one of the plurality of 2-D fluorescence images is recorded through the transparent portion of the imaging stage.

7. The method of claim 1 , further comprising:

overlaying a 2-D reflected light image imaged with the imaging stage at an angle, with a 2-D fluorescence image recorded with the imaging stage at the same angle, to render a rendered image.

8. The method of claim 7 , further comprising:

normalizing a contrast of the 2-D reflected light image with a contrast of the 2-D fluorescence image such that the contrasts are relatively equal.

9. The method of claim 1 , wherein at each angle a 2-D reflected light image is imaged and a 2-D fluorescence image is recorded before rotating and turning the imaging stage to another angle.

10. The method of claim 5 , wherein the imaging stage is transparent.

11. The method of claim 1 , wherein the method further comprises:

moving, using a translational bearing, the imaging stage horizontally in at least one direction.

12. The method of claim 11 , wherein the moving of the imaging stage includes moving the imaging stage into and out of an imaging volume.

13. The method of claim 1 , further comprising:

conveying, using a conveyor system, the biological sample onto or off of the imaging stage.

14. The method of claim 1 , further comprising:

applying a probe molecule having a binding affinity to a subset of cells of the biological sample.

15. The method of claim 14 , further comprising:

excising the biological sample from a subject, wherein the applying of the probe molecule is performed prior to the excising.

16. The method of claim 14 , further comprising:

excising the biological sample from a subject, wherein the applying of the probe molecule is performed subsequent to the excising.

17. The method of claim 14 , wherein the probe biomolecule is an antibody that binds an antigen.

18. The method of claim 17 , wherein the antigen is selected from the group consisting of a lung cancer cell surface antigen, a brain tumor cell surface antigen, a glioma cell surface antigen, a breast cancer cell surface antigen, an esophageal cancer cell surface antigen, a common epithelial cancer cell surface antigen, a common sarcoma cell surface antigen, and an osteosarcoma cell surface antigen.

19. The method of claim 1 , wherein the irradiating is with near-infrared light having a wavelength of about 650 nm to about 1400 nm.

20. A method for imaging a biological sample from a subject, the method comprising:

moving, using a translational bearing, an imaging stage horizontally in at least one direction into and out of an imaging volume;

illuminating the biological sample on the imaging stage with visible light;

imaging, using a first camera, a plurality of two-dimensional (2-D) reflected light images of the biological sample;

irradiating the biological sample on the imaging stage with near infrared light;

recording, using a second camera, a plurality of 2-D fluorescence images of the biological sample; and

rendering an image produced from the reflected light images and the fluorescence images.

21. A method for imaging a biological sample from a subject, the method comprising:

applying a probe molecule having a binding affinity to a subset of cells of the biological sample;

illuminating the biological sample on an imaging stage with visible light;

imaging, using a first camera, a plurality of two-dimensional (2-D) reflected light images of the biological sample;

irradiating the biological sample on the imaging stage with near infrared light;

recording, using a second camera, a plurality of 2-D fluorescence images of the biological sample; and

rendering an image produced from the reflected light images and the fluorescence images.

Assignments (2)
SECURITY INTEREST Recorded Dec 1, 2021
From: LI-COR, INC.
To: MIDCAP FINANCIAL TRUST
Reel/Frame 058293/0889 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 16, 2016
From: WANG, HAN-WEI
To: LI-COR, INC.
Reel/Frame 040347/0264 →
Continuity (4)
Continuation 15049970 · Feb 22, 2016
Provisional Application 62185407 · Jun 26, 2015
Provisional Application 62119660 · Feb 23, 2015
Related Publication 20170059487A1 · Mar 2, 2017
Cited By (1)
US 12,557,989