Method and apparatus for combining injury-mediated therapy and drug delivery

• US 6,199,554 B1
• Filed: 03/27/1998
• Issued: 03/13/2001
• Est. Priority Date: 03/27/1998
• Status: Expired due to Fees

• Current Assignee: Brigham and Women's Hospital Incorporated
• Original Assignee: Brigham and Women's Hospital Incorporated
• Inventors: Dzau, Victor, Cohn, Lawrence H., Sayeed-Shah, Umer, Mann, Michael J.
• Primary Examiner(s): Nguyen, Dinh X.
• Application Number:
  US09/049,882
• Time in Patent Office: 1,082 Days
• Field of Search: 128/898, 604/20, 604/890.1, 604/46, 604/48, 604/49, 606/15, 606/7, 606/2, 607/88, 607/89
• US Class Current: 128/898
• CPC Class Codes: A61B 18/00 Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body eye surgery A61F9/007; ear surgery A61F11/00
• CPC Class Codes: A61B 18/20 using laser
• CPC Class Codes: A61B 2017/00247 Making holes in the wall of the heart, e.g. laser Myocardial revascularization
• CPC Class Codes: A61B 2017/22082 after introduction of a substance
• CPC Class Codes: A61B 2017/320069 for ablating tissue
• CPC Class Codes: A61B 2018/00392 Transmyocardial revascularisation
• CPC Class Codes: A61K 38/18 Growth factors; Growth regulators
• CPC Class Codes: A61K 38/30 Insulin-like growth factors, i.e. somatomedins, e.g. IGF-1, IGF-2 insulin-like growth factor binding protein A61K38/1754
• CPC Class Codes: A61K 48/00 Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: A61P 9/00 Drugs for disorders of the cardiovascular system

Abstract

A method of enhancing injury-induced revascularization of a tissue as treatment of a disease, such as coronary artery disease, is described. The method involves (i) creating injury in a tissue (e.g., muscle, such as cardiac muscle) by, for example, use of a laser, an ultrasonic device, or a Thermal probe, and (ii) injecting into the tissue a revascularization-promoting molecule or a nucleic acid molecule encoding a revascularization-promoting molecules Also described is an apparatus that can be used to practice this method.

Claims

1. A method of enhancing injury-induced revascularization of a tissue as treatment of a disease, said method comprising the steps of:

i) creating a track to tissue injury in said tissue, and

ii) injecting into said tissue a revascularization-promoting molecule or a nucleic acid molecule encoding a revascularization-promoting molecule, wherein the track of the injection is in a predetermined direction relative to but not within, said tack of tissue injury,

said method resulting in improvement of a condition of said disease to a greater degree than results from injury-induced revascularization treatment alone.

2. The method of claim 1, wherein said track of tissue injury is made with a laser.

3. The method of claim 2, wherein said laser is a carbon dioxide laser.

4. The method of claim 1, wherein time between creating said track of tissue injury and making said injection is less than 5.0 seconds.

5. The method of claim 4, wherein said time is less than 1.0 second.

6. The method of claim 4, wherein said time is less than 0.1 second.

7. The method of claim 1, wherein said revascularization-promoting molecule is a pro-angiogenic factor.

8. The method of claim 7, wherein said pro-angiogenic factor is vascular endothelial growth factor, fibroblast growth factor, platelet derived growth factor, insulin-like growth factor, epidermal growth factor, transforming growth factor, hepatocyte growth factor, proliferin, angiotropin, or angiopoietin.

9. The method of claim 1, wherein said nucleic acid molecule is naked DNA.

10. The method of claim 1, wherein cellular entry of said nucleic acid molecule is facilitated by non-live viral mediated transfer.

11. The method of claim 1, wherein said nucleic acid molecule is mixed with a lipid polyamine admixture.

12. The method of claim 1, wherein said nucleic acid molecule is operably linked to a promoter in a recombinant viral vector.

13. The method of claim 12, wherein said viral vector is a retrovirus, adenovirus, adeno-associated virus, or lentivirus.

14. The method of claim 1, wherein said tissue is muscle.

15. The method of claim 14, wherein said muscle is cardiac muscle.

16. The method of claim 1, wherein said condition improves as a result of increased vascularization of tissue affected by said disease.

17. The method of claim 1, wherein said disease is coronary artery disease.

18. The method of claim 1, wherein said condition of said disease is abnormal left ventricular wall motion or abnormal myocardial function.

19. The method of claim 1, wherein the number of said injections is equal IQ or greater than the number of said tracks of tissue injury in the treated tissue.

20. The method of claim 1, wherein said injection track is less than 4 mm from said track of tissue injury.

21. The method of claim 1, wherein said molecule undergoes sustained release.

22. A method of increasing expression of a gene in a tissue, said method comprising the steps of;

i) creating a track tissue injury in said tissue, and

ii) injecting into said tissue a nucleic acid molecule comprising said gene, wherein the track of the injection is in a predetermined direction relative to buy within said track of tissue injury,

said method resulting in increased expression of said gene compared to expression that results firm injection of said nucleic acid molecule alone.

23. The method of claim 22, when the track of said injection parallels said of tissue injury.

24. The method of claim 22, said nucleic acid molecule is naked DNA.

25. The method of claim 22, wherein cellular entry of said nucleic acid molecule is facilitated by non-live viral mediated transfer.

26. The method of claim 22, wherein said nucleic acid molecule is mixed with a lipid polyamine admixture.

27. The method of claim 22, wherein said nucleic acid molecule is operably linked to a promoter in a recombinant viral vector.

28. The method of claim 22, wherein said viral vector is a retrovirus, adenovirus, adeno-associated virus, or lentivirus.