Methods and compositions to treat myocardial conditions
Methods, devices, kits and compositions to treat a myocardial infarction. In one embodiment, the method includes the prevention of remodeling of the infarct zone of the ventricle. In other embodiments, the method includes the introduction of structurally reinforcing agents. In other embodiments, agents are introduced into a ventricle to increase compliance of the ventricle. In an alternative embodiment, the prevention of remodeling includes the prevention of thinning of the ventricular infarct zone. In another embodiment, the prevention of remodeling and thinning of the infarct zone involves the cross-linking of collagen and prevention of collagen slipping. In other embodiments, the structurally reinforcing agent may be accompanied by other therapeutic agents. These agents may include, but are not, limited to pro-fibroblastic and angiogenic agents.
1. A method to treat a myocardial condition, comprising:
identifying an infarct region within a ventricle of a subject; and
delivering a dispersible solution into the infarct region comprising (i) a structurally reinforcing agent having synthetic microparticles dispersed throughout, and (ii) a treatment agent,
wherein the structurally reinforcing agent is a single component capable of forming a bioerodible gel reinforcement at the infarct region,
wherein the synthetic microparticles have a smooth surface capable of inducing collagen deposition and are selected from the group consisting of polymethyl methacrylate microparticles, polymethyl methacrylate-co butyl methacrylate microparticles, carbon microparticles, polystyrene microparticles, cross-linked acrylic hydrogel microparticles and poly(lactic-co-glycolic acid) microparticles, and
wherein delivering further comprises administering multiple dosages of the solution having a predetermined volume so as to disperse solution over the infarct region.
2. The method of claim 1 wherein the structurally reinforcing agent, once delivered, increases the modulus of elasticity of the infarct region.
3. The method of claim 1 wherein delivering the structurally reinforcing agent prevents thinning of the ventricle.
4. The method of claim 1 wherein delivery of the structurally reinforcing agent occurs within 2 weeks of a myocardial infarction (MI).
5. The method of claim 1 wherein at least 20 percent of the ventricular myocardium of the subject is akinetic or dyskinetic.
6. The method of claim 5 wherein the structurally reinforcing agent, once delivered, enhances the modulus of elasticity of the infarct region.
7. The method of claim 6 wherein the structurally reinforcing agent is one of hyaluronic acid, bovine collagen, high molecular weight ultra-pure polyacrylamide in water, dispersed bovine collagen or high molecular weight poly vinyl pyrrolidone (PVP).
8. The method of claim 1 wherein the structurally reinforcing agent comprises:
a material which is delivered to the infarct region in a liquid phase and which transitions to a solid phase in the infarct region in the presence of an endogenous material.
9. The method of claim 8 , wherein the structurally reinforcing agent consists of at least one of the group consisting of tropoelastin, and octyl cyanoacrylate.
10. The method of claim 1 , further comprising delivering at least one matrix metalloproteinase inhibitor (MMPI) to the infarct region of the ventricle.
11. The method of claim 1 wherein delivering the structurally reinforcing agent comprises introducing the structurally reinforcing agent to the ventricle through a procedure.
12. The method of claim 11 wherein the procedure to the ventricle region comprises accessing the ventricle through at least one of a sub-xiphoid procedure, a percutaneous transluminal procedure or an open-chest procedure in conjunction with Coronary Bypass Graft (CABG).
13. The method of claim 12 wherein the percutaneous transluminal access procedure for introduction of the structurally reinforcing agent into the ventricle comprises at least one of the following modes consisting of intracoronary infusion, intraventricular catheter, intravenous pressure perfusion, transvascular needle catheter, and retrograde venous perfusion.
14. The method of claim 1 wherein the at least one structurally reinforcing agent is suspended in a solution.
15. The method of claim 1 wherein delivery of the structurally reinforcing agent comprises delivering a sufficient amount of the structurally reinforcing agent such that, once delivered, the stiffness of the ventricle is increased.
16. The method of claim 1 wherein the predetermined volume is from 1 microliter to 100 microliters.
17. A method as in claim 1 wherein the at least one structurally reinforcing agent releases a recruiting agent which recruits cells to the infarct region.
18. The method of claim 1 wherein each dosage is administered to a different site within the infarct region.
19. The method of claim 1 wherein the predetermined volume is from 1 microliter to 100 microliters and the structurally reinforcing agent, once delivered, is bioerodible, and wherein each dosage is administered to a different site within the infarct region.
20. The method of claim 1 wherein multiple dosages is greater than two.
21. A method to treat a myocardial condition, comprising:
identifying an infarct region within a ventricle of a subject; and
delivering into a border zone of the infarct region a solution comprising (i) a structurally reinforcing agent having synthetic microparticles dispersed throughout, and (ii) a treatment agent,
wherein the structurally reinforcing agent is a single component capable of forming a bioerodible gel reinforcement at the infarct region,
wherein the synthetic microparticles have a smooth surface capable of inducing collagen deposition and are selected from the group consisting of polymethyl methacrylate microparticles, polymethyl methacrylate-co butyl methacrylate microparticles, carbon microparticles, polystyrene microparticles, cross-linked acrylic hydrogel microparticles and poly(lactic-co-glycolic acid) microparticles, and
wherein delivering further comprises administering multiple dosages of the solution having a predetermined volume so as to disperse the solution over the infarct border zone region.
22. The method of claim 21 wherein the structurally reinforcing agent, once delivered, increases the modulus of elasticity of the infarct region.
23. The method of claim 21 wherein delivery of the structurally reinforcing agent occurs within 2 weeks of a myocardial infarction (MI).
24. The method of claim 21 wherein at least 20 percent of the ventricular myocardium of the subject is akinetic or dyskinetic.
25. The method of claim 21 wherein the predetermined volume is from 1 microliter to 100 microliters.
26. The method of claim 21 wherein multiple dosages is greater than two.