IP Library Granted Patent US 8,888,674
Granted Patent B2
US 8,888,674 · App. 12/747,070 · Granted Nov 18, 2014

Methods and systems for magnetic focusing of therapeutic, diagnostic or prophylactic agents to deep targets

Inventors: Benjamin Shapiro (Washington, DC); Andreas Lüebbe (Paderborn, DE); Declan Diver (Glasgow, GB); Hugh Potts (Glasgow, GB); Roland Probst (Bobenheim-Roxheim, DE)
Assignees: University of Maryland College Park; University of Glasgow
A61M31/002A61N2/002A61B5/055A61B5/411
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,888,674
App. No.
12/747,070
Granted
Nov 18, 2014
Kind
B2
Abstract

Systems and methods are disclosed for trapping or focusing magnetizable particles comprising therapeutic agents at a distance using a dynamic magnetic field and feedback control, to enable the treatment of diseased areas deep inside a patient's body. The methods may be used to diagnose or treat diseased areas deep within a patient, for example tumors of the lungs, intestines, and liver, and is also useful in enhancing the permeability of solid tumors to chemotherapeutic agents.

Claims (38)

1. A method for treating a patient comprising the steps of:

(A) administering a ferrofluid comprising a plurality of magnetizable objects to a patient;

(B) applying a dynamic magnetic field to the patient using external magnets;

(C) sensing and monitoring over time locations of the plurality of magnetizable objects within the patient;

(D) shaping the applied dynamic magnetic field in three spatial dimensions over a period of time space and time using a feedback control algorithm that dictates actuation and strength of the external magnets in response to said sensing and monitoring; and

(E) directing and focusing a selected concentration of the plurality of magnetizable objects within the ferrofluid to a deep target area within the patient in response to said shaping the applied dynamic magnetic field.

2. The method of claim 1 , wherein said ferrofluid comprises a therapeutic, diagnostic, visualization or prophylactic agent.

3. The method of claim 1 , wherein said plurality of magnetizable objects are coupled to a therapeutic, diagnostic, visualization or prophylactic agent.

4. The method of claim 1 , wherein said deep target area is at least 5 centimeters inside the patient.

5. The method of claim 1 , wherein said magnetizable objects are between about 1 nm and 1 mm in diameter.

6. The method of claim 5 , wherein said magnetizable objects are between about 1 μm and 1 nm in diameter.

7. The method of claim 1 , wherein said administering step comprises injecting said plurality of magnetizable objects into the patient.

8. The method of claim 1 , wherein said magnetizable objects comprise a therapeutic, diagnostic, visualization or prophylactic agent.

9. The method of claim 1 , wherein said magnetizable objects comprise a detectable label.

10. The method of claim 9 , wherein said detectable label is a radioisotopic label, a paramagnetic label, a CARS (coherent anti-Stokes Raman Spectroscopy)-detectable label, a multiphoton fluorescence microscopy-detectable label, a harmonic microscopy-detectable label, an acoustic imaging-detectable label, an impedance spectroscopy-detectable label or a reflectance spectroscopy-detectable label.

11. The method of claim 1 , wherein said dynamic magnetic field has a rate of change of up to about 20 Tesla/second.

12. The method of claim 1 , wherein said deep target area is associated with a cancer, a disease of the vascular system, an infection, or non-cancerous disease material.

13. The method of claim 12 , wherein said deep target area is located at least 5 centimeters inside the patient.

14. The method of claim 1 , wherein said sensing and monitoring step comprises using magnetic resonance imaging.

15. The method of claim 1 , further comprising a feedback controller to control the dynamic magnetic field in response to said sensing and monitoring.

16. The method of claim 1 , wherein an effectiveness of said selected concentration of the plurality of magnetizable objects for treating the patient is measured over a period of time.

17. The method of claim 1 , wherein said shaping step comprises controlling the external magnets in time.

18. A method for treating a patient consisting essentially of the steps of:

(A) administering a ferrofluid comprising a plurality of magnetizable objects to a patient;

(B) applying a dynamic magnetic field to the patient using external magnets;

(C) sensing and monitoring over time locations of the plurality of magnetizable objects within the patient;

(D) shaping the applied dynamic magnetic field in three spatial dimensions over a period of time using a feedback control algorithm that dictates actuation and strength of the external magnets in response to said sensing and monitoring; and

(E) directing and focusing a selected concentration of the plurality of magnetizable objects within the ferrofluid to a deep target area within the patient in response to said shaping the applied dynamic magnetic field.

19. The method of claim 18 , wherein said ferrofluid comprises a therapeutic, diagnostic, visualization or prophylactic agent.

20. The method of claim 18 , wherein said plurality of magnetizable objects are coupled to a therapeutic, diagnostic, visualization or prophylactic agent.

21. The method of claim 18 , wherein said magnetizable objects comprise a therapeutic, diagnostic, visualization or prophylactic agent.

22. The method of claim 18 , wherein the deep target area is at least 5 centimeters inside the patient.

23. The method of claim 18 , wherein said magnetizable objects are between about 1 nm and 1 mm in diameter.

24. The method of claim 23 , wherein said magnetizable objects are between about 1 μm and 1 nm in diameter.

25. The method of claim 18 , wherein said magnetizable objects comprise a detectable label.

26. The method of claim 25 , wherein said detectable label is a radioisotopic label, a paramagnetic label, a CARS (coherent anti-Stokes Raman Spectroscopy)-detectable label, a multiphoton fluorescence microscopy-detectable label, a harmonic microscopy-detectable label, an acoustic imaging-detectable label, an impedance spectroscopy-detectable label or a reflectance spectroscopy-detectable label.

27. The method of claim 18 , wherein said dynamic magnetic field has a rate of change of up to about 20 Tesla/second.

28. The method of claim 18 , wherein said deep target area is associated with a cancer, a disease of the vascular system, an infection, or non-cancerous disease material.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 15, 2010
From: SHAPIRO, BENJAMIN; LUBBE, ANDREAS; PROBST, ROLAND
To: UNIVERSITY OF MARYLAND COLLEGE PARK
Reel/Frame 025361/0224 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 15, 2010
From: DIVER, DECLAN; POTTS, HUGH
To: UNIVERSITY OF GLASGOW
Reel/Frame 025361/0263 →
Continuity (2)
Provisional Application 60996931 · Dec 11, 2007
Related Publication 20110054237A1 · Mar 3, 2011