Measurement of capillary flow using nuclear magnetic resonance

• US 4,788,500 A
• Filed: 10/01/1987
• Issued: 11/29/1988
• Est. Priority Date: 08/14/1985
• Status: Expired due to Fees

• Current Assignee: Brigham and Women's Hospital Incorporated
• Original Assignee: Brigham and Women's Hospital Incorporated
• Inventors: Hawkes, Robert C., Patz, H. Samuel
• Primary Examiner(s): Levy, Stewart J.
• Assistant Examiner(s): NOT, DEFINED
• Application Number:
  US07/103,467
• Time in Patent Office: 425 Days
• Field of Search: 128/653, 324/306, 324/307, 324/309, 324/311, 324/312
• US Class Current: 324/309
• CPC Class Codes: G01F 1/716 using electron paramagnetic resonance [EPR] or nuclear magnetic resonance [NMR]
• CPC Class Codes: G01R 33/563 of moving material, e.g. flow contrast angiography

Abstract

An improved method for measuring very slow flow rates using nuclear magnetic resonance techniques is disclosed. The basic technique is that of steady state free precession, in which a sequence of radio frequency pulses are applied to nuclei in a magnetic field having a substantial gradient, so that a driven equilibrium state is obtained and which is characterized by a spatial periodicity in the magnetization response of the nuclei. Two images are generated. The two images may be generated using different time intervals between the application of the radio frequency pulses. Alternatively, the two images may be generated using different effective gradients. The spatial periodicity, and the NMR response of flowing nuclei to the spatial periodicity, is thus different during the two image formations. One image is subtracted from the other, which cancels signals from static nuclei in the signal, while relatively fast flowing nuclei, namely in the larger blood vessels or the like, never reach the equilibrium state. The subtraction difference is therefore proportional only to nuclei which are part of relatively slowly flowing liquids, such as in capillary blood flow in organs.

Claims

1. A method for providing an image of a sample, wherein individual elements of said image have intensities corresponding to the quantity of slowly flowing fluids contained in said sample, said method comprising the steps of:

(a) generating a first image using an imaging technique wherein;

a first magnetization spatial periodicity is established;

a detected NMR signal from slowly flowing fluids is dependent on the value of said first magnetization spatial periodicity, and a detected NMR signal from stationary material is not substantially dependent on said first magnetization spatial periodicity; and

fast flowing fluids to not substantially contribute to the intensities of first image elements;

(b) adjusting a magnetization spatial periodicity control parameter comprising an interpulse interval;

(c) generating a second image using an imaging technique wherein;

a second magnetization spatial periodicity is established;

a detected NMR signal from slowly flowing fluids is dependent on the value of said second magnetization spatial periodicity, and a detected NMR signal from stationary material is not substantially dependent on said second magnetization spatial periodicity; and

fast flowing fluids do not substantially contribute to the intensities of second image elements; and

(d) mathematically manipulating said first and second images to produce a third image the intensity of whose elements are determined substantially solely by the nuclear magnetic resonance of nuclei in slowly flowing fluids in said sample.

2. A method for providing an image of a sample, wherein individual elements of said image have intensities corresponding to the quantity of slowly flowing fluids contained in said sample, said method comprising the steps of:

(a) generating a first image using an imaging technique wherein;

a first magnetization spatial periodicity is established;

a detected NMR signal from slowly flowing fluids is dependent on the value of said first magnetization spatial periodicity, and a detected NMR signal from stationary material is not substantially dependent on said first magnetization spatial periodicity; and

fast flowing fluids do not substantially contribute to the intensities of first image elements;

(b) adjusting a magnetization spatial periodicity control parameter comprising an effective gradient;

(c) generating a second image using an imaging technique wherein;

a second magnetization spatial periodicity is established;

a detected NMR signal from slowly flowing fluids is dependent on the value of said second magnetization spatial periodicity, and a detected NMR signal from stationary material is not substantially dependent on said second magnetization spatial periodicity; and

fast flowing fluids do not substantially contribute to the intensities of second image elements; and

(d) mathematically manipulating said first and second images to produce a third image the intensity of whose elements are determined substantially solely by the nuclear magnetic resonance of nuclei in slowly flowing fluids in said sample.

3. A method for providing an image of a sample, wherein individual elements of said image have intensities corresponding to the quantity of slowly flowing fluids contained in said sample, said method comprising the steps of:

(a) generating a first image using an imaging technique wherein;

a first magnetization spatial periodicity is established;

a detected NMR signal from slowly flowing fluids is dependent on the value of said first magnetization spatial periodicity, and a detected NMR signal from stationary material is not substantially dependent on said first magnetization spatial periodicity; and

fast flowing fluids to not substantially contribute to the intensities of first image elements;

(b) adjusting a magnetization spatial periodicity control parameter;

(c) generating a second image using an imaging technique wherein;

a second magnetization spatial periodicity is established;

a detected NMR signal from slowly flowing fluids is dependent on the value of said second magnetization spatial periodicity, and a detected NMR signal from stationary material is not substantially dependent on said second magnetization spatial periodicity; and

fast flowing fluids do not substantially contribute to the intensities of second image elements; and

(d) mathematically manipulating said first and second images to produce a third image the intensity of whose elements are determined substantially solely by the nuclear magnetic resonance of nuclei in slowly flowing fluids in said sample.

4. The method according to claim 3 wherein said image generation steps comprise:

using an SSFP imaging technique.

5. The method according to claim 4, wherein said step of using said SSFP imaging technique comprises:

applying a gradient of magnitude small enough to be produced by standard clinical NMR equipment.

6. The method according to claim 5, wherein said step of using said SSFP imaging technique comprises:

applying a gradient of a magnitude which does not exceed 1.0 Gauss/cm.

7. The method according to claim 5, wherein said step of using said SSFP imaging technique comprises:

applying a gradient of a magnitude which does not exceed 0.25 Gauss/cm.

8. The method according to claim 3, wherein said generating steps comprise:

applying a gradient of magnitude small enough to be produced by standard clinical NMR equipment.

9. The method according to claim 8, wherein said generating steps comprise:

applying a gradient of a magnitude which does not exceed 1.0 Gauss/cm.

10. The method according to claim 8, wherein said generating steps comprise:

applying a gradient of a magnitude which does not exceed 0.25 Gauss/cm.

11. The method according to claim 3, wherein said adjusting step comprises:

changing an interpulse interval of periodic radio frequency pulses which are used in said imaging technique.

12. The method of claim 11, further comprising:

reversing said gradient for a portion of each interpulse interval.

13. The method according to claim 3, wherein the nuclei in said slowly flowing fluid have a zero mean velocity.

14. The method according to claim 3, wherein the nuclei in said solely flowing fluid have a non-zero mean velocity.

15. The method according to claim 3, wherein

said sample comprises living biological tissue;

and

said slowly flowing fluid comprises blood flowing through capillaries.

16. The method according to claim 3, wherein said step of mathematically manipulating comprises:

subtracting said second image from said first image to substantially eliminate contributions to the intensities of the third image'"'"'s elements from stationary nuclei in said sample.

17. The method according to claim 3, wherein said adjusting step comprises:

changing an effective gradient.

18. The method according to claim 17, wherein said image generation steps comprise:

applying periodic radio frequency pulses to define interpulse intervals; and

maintaining positions of spin echoes in said interpulse intervals to be identical in said two image generation steps.

19. The method according to claim 17, wherein said image generation steps comprise:

maintaining a read gradient applied when acquiring information from spin echoes to be identical in each of said two image generation steps.

20. The method according to claim 17, wherein said image generation steps comprise:

restricting an effective gradient to values such that there are an integral number of half-wavelengths of spatially periodic magnetization along at least one voxel linear dimension.

21. The method according to claim 17, wherein said image generation steps comprise:

applying periodic radio frequency pulses to define interpulse intervals;

maintaining positions of spin echoes in said interpulse intervals to be identical in said two image generation steps;

maintaining a read gradient applied when acquiring information from spin echoes to be identical in each of said two image generation steps; and

restricting an effective gradient to values such that there are an integral number of half-wavelengths of spatially periodic magnetization along at least one voxel linear dimension.

22. An apparatus for providing an image of a sample, wherein individual elements of said image have intensities corresponding to the quantity of slowly flowing fluids contained within said sample, said apparatus comprising:

imaging means for generating images in which substantially no contribution is made to the image element intensities by fast flowing fluids;

means for adjusting a magnetization spatial periodicity control parameter comprising an interpulse interval, for allowing said imaging means to generate two images using an imaging technique wherein;

respectively different magnetization spatial periodicities are established during the generation of said two images;

a detected NMR signal from slowly flowing fluids is dependent on the value of said magnetization spatial periodicity; and

a detected NMR signal from stationary material is not substantially dependent on the value of said magnetization spatial periodicity; and

means for mathematically manipulating said two images to produce a third image whose image element intensities are determined substantially solely by the nuclear magnetic resonance of nuclei in slowly flowing fluids in said sample.

23. An apparatus for providing an image of a sample, wherein individual elements of said image have intensities corresponding to the quantity of slowly flowing fluids contained within said sample, said apparatus comprising:

imaging means for generating images in which substantially no contribution is made to the image element intensities by fast flowing fluids;

means for adjusting a magnetization spatial periodicity control parameter comprising an effective gradient, for allowing said imaging means to generate two images using an imaging technique wherein;

respectively different magnetization spatial periodicities are established during the generation of said two images;

a detected NMR signal from slowly flowing fluids is dependent on the values of said magnetization spatial periodicity; and

a detected NMR signal from stationary material is not substantially dependent on the value of said magnetization spatial periodicity; and

means for mathematically manipulating said two images to produce a thrd image whose image element intensities are determined substantially solely by the nuclear magnetic resonance of nuclei in slowly flowing fluids in said sample.

24. An apparatus for providing an image of a sample, wherein individual elements of said image have intensities corresponding to the quantity of slowly flowing fluids contained within said sample, said apparatus comprising:

imaging means for generating images in which substantially no contribution is made to the image element intensities by fast flowing fluids;

means for adjusting a magnetization spatial periodicity control parameter for allowing said imaging means to generate two images using an imaging technique wherein;

respectively different magnetization spatial periodicities are established during the generation of said two images;

a detected NMR signal from slowly flowing fluids is dependent on the value of said magnetization spatial periodicity; and

a detected NMR signal from stationary material is not substantially dependent on the value of said magnetization spatial periodicity; and

means for mathematically manipulating said two images to produce a third image whose image element intensities are determined substantially solely by the nuclear magnetic resonance of nuclei in slowly flowing fluids in said sample.

25. The apparatus according to claim 24, wherein said imaging means comprises:

SSFP imaging means.

26. The apparatus according to claim 25, wherein said SSFP imaging means comprises:

gradient generation means for applying a gradient of magnitude small enough to be produced by standard clinical NMR equipment.

27. The apparatus according to claim 26, wherein said SSFP imaging means comprises:

gradient generation means for applying a gradient of magnitude which does not exceed 1.0 Gauss/cm.

28. The apparatus according to claim 26, wherein said SSFP imaging means comprises:

gradient generation means for applying a gradient of magnitude which does not exceed 0.25 Gauss/cm.

29. The apparatus according to claim 24, wherein said imaging means comprises:

gradient generation means for applying a gradient of magnitude small enough to be produced by standard clinical NMR equipment.

30. The apparatus according to claim 29, wherein said imaging means comprises:

gradient generation means for applying a gradient of magnitude which does not exceed 1.0 Gauss/cm.

31. The apparatus accordin to claim 29, wherein said imaging means comprises:

gradient generation means for applying a gradient of magnitude which does not exceed 0.25 Gauss/cm.

32. The apparatus of claim 24, wherein said means for adjusting comprises:

means for changing an interpulse interval of periodic radio frequency pulses used in said imaging means.

33. The apparatus of claim 32 further comprising:

means for varying said gradient field during the interpulse intervals, whereby an additional peak of the detected signal is formed, displaced in time from said radio frequency pulses.

34. The apparatus according to claim 24, wherein the nuclei in said slowly flowing fluid have a zero mean velocity.

35. The apparatus according to claim 24, wherein the nuclei in said slowly flowing fluid have a non-zero mean velocity.

36. The apparatus according to claim 24, wherein:

said sample comprises living biological tissue; and

said slowly flowing fluid comprises blood flowing through capillaries.

37. The apparatus according to claim 24, wherein said means for mathematically manipulating comprises:

means for subtracting images for substantially eliminating contributions to the intensities of the third image'"'"'s elements from stationary nuclei in said sample.

38. The apparatus of claim 24, wherein said means for adjusting comprises:

means for changing an effective gradient in said imaging means.

39. The apparatus according to claim 38, wherein said imaging means comprises:

means for applying periodic radio frequency pulses to define interpulse intervals; and

means for positioning spin echoes in said interpulse intervals identically in the generation of said two images.

40. The apparatus according to claim 38, wherein said imaging means comprises:

gradient means for maintaining a read gradient applied when acquiring information from spin echoes to be identical in said generation of said two images.

41. The apparatus according to claim 38, wherein said imaging means comprises:

gradient means for restricting an effective gradient to values such that there are an integral number of half-wavelengths of spatially periodic magnetization along at least one voxel linear dimension.

42. The apparatus according to claim 38, wherein said imaging comprises comprises:

means for applying periodic radio frequency pulses to define interpulse intervals;

means for positioning spin echoes in said interpulse intervals identically in the generation of said two images;

gradient means for maintaining a read gradient applied when acquiring information from spin echoes to be identical in said generation of said two images, an for restricting an effective gradient to values such that there are an integral number of spatially periodic magnetization half-wavelengths along at least one voxel linear dimension.