3D imaging of live cells with ultraviolet radiation

• US 8,143,600 B2
• Filed: 02/18/2008
• Issued: 03/27/2012
• Est. Priority Date: 02/18/2008
• Status: Expired due to Fees

• Current Assignee: VisionGate, Inc.
• Original Assignee: VisionGate, Inc.
• Inventors: Seibel, Eric J., Nelson, Alan C., Fauver, Mark E., Rahn, J. Richard
• Primary Examiner(s): Kim, Kiho
• Application Number:
  US12/032,959
• Publication Number:
  US 20090208072A1
• Time in Patent Office: 1,499 Days
• Field of Search: 250/458.1, 250/459.1, 250/461.1, 250/461.2
• US Class Current: 250/461.2
• CPC Class Codes: G01N 15/1436 the optical arrangement forming an integrated apparatus with the sample container, e.g. a flow cell
• CPC Class Codes: G01N 2015/1445 Three-dimensional imaging, imaging in different image planes, e.g. under different angles or at different depths, e.g. by a relative motion of sample and detector, for instance by tomography
• CPC Class Codes: G01N 2021/1787 Tomographic, i.e. computerised reconstruction from projective measurements
• CPC Class Codes: G01N 21/4795 spatially resolved investigating of object in scattering medium in vivo A61B
• CPC Class Codes: G06T 11/006 Inverse problem, transformation from projection-space into object-space, e.g. transform methods, back-projection, algebraic methods

Abstract

A method for 3D imaging of cells in an optical tomography system includes moving a biological object relatively to a microscope objective to present varying angles of view. The biological object is illuminated with radiation having a spectral bandwidth limited to wavelengths between 150 nm and 390 nm. Radiation transmitted through the biological object and the microscope objective is sensed with a camera from a plurality of differing view angles. A plurality of pseudoprojections of the biological object from the sensed radiation is formed and the plurality of pseudoprojections is reconstructed to form a 3D image of the cell.

Claims

1. A system for 3D imaging of live cells in an optical tomography system comprising:

a microfluidics cartridge including a tube positioned relative to a microscope objective, a conduit loop having a first port coupled to an entrance valve, a second port coupled to an exit valve, a semi-permeable membrane portion, a rotating portion and an imaging window;

where the rotating portion is mounted between a first fitting and a second fitting, where the first fitting couples the rotating portion to the entrance valve and the second fitting couples the rotating portion to the exit valve;

a rotation mechanism attached to the rotating portion;

a microscope objective located to view objects through the imaging window;

an axial translation mechanism coupled to the microscope objective;

a second conduit interfacing with the semi-permeable membrane, where the second conduit carries nutrients into the conduit loop and waste products out of the conduit loop;

at least one radiation source positioned to illuminate the imaging window including a biological object held therein, where the at least one radiation source generates radiation having a spectral bandwidth limited to wavelengths between 150 nm and 390 nm;

at least one sensor positioned to sense radiation transmitted through the biological object and the microscope objective;

an image processor coupled to receive data from the sensor; and

a reconstruction module coupled to the image processor, where the reconstruction module processes the data to form a 3D image of the biological object.

2. The system of claim 1 wherein the nutrients include oxygen and a buffer.

3. The system of claim 1 wherein the axial translation mechanism comprises a piezoelectric transducer.

4. The system of claim 1 wherein the at least one radiation source comprises a computer-controlled light source and condenser lens assembly.

5. The system of claim 1 wherein a computer is linked to control the piezoelectric transducer, where the piezoelectric transducer axially moves the objective lens so as to extend the depth of field of the objective lens.

6. The system of claim 1 wherein the spectral bandwidth has wavelengths further limited to between 240 nm and 300 nm.

7. The system of claim 1 wherein the spectral bandwidth has wavelengths further limited to between 260 nm and 265 nm.

8. The system of claim 1 wherein the spectral bandwidth has wavelengths further limited to between 280 nm and 285 nm.

9. The system of claim 1, wherein the radiation stimulates native fluorescence from the live cell, further comprising measuring the stimulated fluorescence.

10. The system of claim 1, wherein a size of a voxel in the reconstructed 3D image is known, the reconstruction means further comprising a means for measuring a concentration of molecules absorbing the radiation by measuring the absorbance per voxel.

11. The system of claim 1 wherein the biological object includes a live cell.

12. The system of claim 1 wherein the microfluidics cartridge is contained in a temperature-controlled aqueous environment.

13. The system of claim 12 wherein the aqueous environment comprises physiological buffered saline.

14. The system of claim 1 wherein the sensed radiation includes imaging signals emanating from DNA.

15. The system of claim 1 wherein the sensed radiation includes imaging signals emanating from protein.

16. The method of claim 1 wherein the sensed radiation includes imaging signals emanating from hydrophilic surfaces.

17. The system of claim 1 wherein the generated radiation comprises multiple wavelengths.

18. The system of claim 1 wherein the reconstruction module processes the data using ratio imaging.

19. The system of claim 18 wherein the ratio imaging includes images formed from wavelengths ranging from 260 nm to 280 nm.

20. The system of claim 1 wherein the at least one radiation source comprises multiple sources for generating at least first and second selected wavelengths selected to enhance natural radiation absorbance by DNA.

21. The system of claim 1 wherein the spectral bandwidth is limited to wavelengths selected to enhance natural radiation absorbance by protein.

22. The system of claim 1 wherein the at least one radiation source comprises multiple sources transmitting at least two selected wavelengths that are pulsed in time series.

23. The system of claim 1 wherein the at least one radiation source comprises multiple sources transmitting at least two selected wavelengths.

24. The system of claim 1 wherein the sensor is an ultraviolet pixel array detector.

25. The system of claim 1 comprising a beamsplitter positioned to split radiation into at least two selected wavelengths.

26. The system of claim 25 wherein the beamsplitter is selected from the group consisting of a polarizing beam splitter, a Wollaston prism, a birefringent element, a half-silvered mirror, a 50/50 intensity beamsplitter, a dielectric optically coated mirror, a pellicle film and a dichroic mirrored prism.

27. The system of claim 1 wherein the at least one sensor comprises:

a first light detector positioned to receive light having a first wavelength; and

a second light detector sensitive to a second wavelength, the second light detector positioned to receive light having the second wavelength.

28. The system of claim 27 wherein the first light detector is sensitive to radiation having a wavelength matching the natural absorbance of human DNA.

29. The system of claim 27 wherein the second light detector is sensitive to radiation having a wavelength matching the natural absorbance of protein.

30. The system of claim 27 wherein the first light detector is sensitive to radiation having a wavelength that includes imaging signals emanating from hydrophilic surfaces.

31. The system of claim 1 further comprising at least one filter interposed between the at least one sensor and the transmitted radiation.

32. The system of claim 1 wherein the microfluidics cartridge and second conduit are enclosed in a temperature-controlled environment.

33. An optical tomography method including separate imaging stages along the same pathway comprising:

transporting a plurality of biological objects along a pathway to a first stage;

illuminating at least one object of the plurality of objects with visible light at the first stage to produce a diffraction pattern;

sensing the diffraction pattern;

analyzing the diffraction pattern to produce a diffraction analysis;

illuminating the at least one object with visible light at a second stage;

sensing visible light emanating from the at least one object to produce a first plurality of pseudoprojection images;

illuminating the at least one object with DUV light at a first wavelength at a third stage;

sensing the DUV light at a first wavelength emanating from the at least one object to produce a second plurality of pseudoprojection images;

illuminating the at least one object with DUV light at a second wavelength at a fourth stage;

sensing the DUV light at a second wavelength emanating from the at least one object to produce a third plurality of pseudoprojection images;

sorting the at least one object responsively to the first, second and third pluralities of pseudoprojection images and the diffraction analysis.

34. The method of claim 33 further comprising counting the biological objects.

35. The method of claim 33 wherein the plurality of biological objects comprise live cells.

36. The method of claim 33 wherein the DUV light at a first wavelength is in the range of 255 nm-265 nm.

37. The method of claim 33 wherein the DUV light at a second wavelength is in the range of 275 nm-285 nm.

38. The method of claim 33 wherein the diffraction pattern further comprises a dark-field imaging pattern.