Compositions and methods for treatment of neurological disorders
Described herein are compositions comprising, and methods for using, biocompatible cold slurries and methods of administering the same to provide reversible inhibition of peripheral nerves in a subject in need thereof.
1. A method comprising:
accessing tissue comprising one or more peripheral nerves; and
injecting a biocompatible ice slurry around the one or more peripheral nerves, wherein:
the biocompatible ice slurry is configured to cool the one or more peripheral nerves for a duration sufficient to inhibit the one or more peripheral nerves in the subject; and
said inhibition is reversible.
2. The method of claim 1 , wherein injecting the biocompatible ice slurry around the one or more peripheral nerves comprises providing the biocompatible ice slurry along a perineural sheath of the one or more peripheral nerves.
3. The method of claim 1 , wherein the one or more peripheral nerves are at least one of subcutaneous nerves, autonomic nerves, or somatic nerves.
4. The method of claim 1 , wherein the biocompatible ice slurry is configured to cool the one or more peripheral nerves to a temperature sufficient to crystallize a plurality of lipids of a myelin sheath of the one or more peripheral nerves.
5. The method of claim 1 , wherein the biocompatible ice slurry is configured to cool the one or more peripheral nerves to a temperature of between about 5° C. and about −40° C.
6. The method of claim 1 , wherein the biocompatible ice slurry is configured to have a first equilibration temperature of between about 4° C. and about −30° C.
7. The method of claim 6 , wherein the biocompatible ice slurry is configured to have a second equilibration temperature of between about 2° C. and about −30° C.
8. The method of claim 1 , wherein the duration sufficient to inhibit the one or more peripheral nerves in the subject is at least about 5 minutes.
9. The method of claim 1 , wherein the biocompatible ice slurry comprises a plurality of ice crystals.
10. The method of claim 9 , wherein the biocompatible ice slurry is configured to cool the one or more peripheral nerves by tissue cooling, wherein the tissue cooling comprises a first heat exchange stage, a second heat exchange stage, and a third heat exchange stage, wherein:
(i) the first heat exchange stage comprises reaching a local equilibrium temperature by rapid equilibration between the biocompatible ice slurry and the tissue, wherein at least some of the ice of the biocompatible ice slurry melts;
(ii) the second heat exchange stage comprises maintaining the local equilibrium temperature, wherein the remaining ice of the biocompatible ice slurry melts; and
(iii) the third heat exchange stage comprises gradually warming the tissue.
11. The method of claim 1 , wherein the biocompatible ice slurry is configured to cool the one or more peripheral nerves by tissue cooling, wherein the tissue cooling comprises:
(i) exchanging heat stored by a heat capacity of the biocompatible ice slurry and the tissue;
(ii) exchanging heat released by crystallization of one or more lipids of the tissue or one or more lipids of a myelin sheath of the one or more peripheral nerves; and
(iii) exchanging heat absorbed by melting of the biocompatible ice slurry.
12. A method comprising:
accessing tissue comprising one or more peripheral nerves; and
administering a biocompatible ice slurry around the one or more peripheral nerves, wherein:
the biocompatible ice slurry is configured to cool the one or more peripheral nerves for a duration sufficient to inhibit the one or more peripheral nerves in the subject; and
said inhibition is reversible.
13. The method of claim 12 , wherein administering the biocompatible ice slurry around the one or more peripheral nerves comprises injecting the biocompatible ice slurry into a tissue having the one or more peripheral nerves.
14. The method of claim 12 , wherein administering the biocompatible ice slurry around the one or more peripheral nerves comprises providing the biocompatible ice slurry along a perineural sheath of the one or more peripheral nerves.
15. The method of claim 12 , wherein the biocompatible ice slurry is configured to cool the one or more peripheral nerves to a temperature sufficient to crystallize a plurality of lipids of a myelin sheath of the one or more peripheral nerves.
16. The method of claim 12 , wherein the biocompatible ice slurry is configured to cool the one or more peripheral nerves to a temperature of between about 5° C. and about −40° C.
17. The method of claim 12 , wherein the biocompatible ice slurry has a first equilibration temperature of between about 4° C. and about −30° C.
18. The method of claim 17 , wherein the biocompatible ice slurry has a second equilibration temperature of between about 2° C. and about −30° C.
19. The method of claim 12 , wherein the duration sufficient to inhibit the one or more peripheral nerves in the subject is at least about 5 minutes.
20. The method of claim 12 , wherein the biocompatible ice slurry comprises a plurality of ice crystals.
21. The method of claim 20 , wherein the biocompatible ice slurry is configured to cool the one or more peripheral nerves by tissue cooling, wherein the tissue cooling comprises a first heat exchange stage, a second heat exchange stage, and a third heat exchange stage, wherein:
(i) the first heat exchange stage comprises reaching a local equilibrium temperature by rapid equilibration between the biocompatible ice slurry and the tissue, wherein at least some of the ice of the biocompatible ice slurry melts;
(ii) the second heat exchange stage comprises maintaining the local equilibrium temperature, wherein the remaining ice of the biocompatible ice slurry melts; and
(iii) the third heat exchange stage comprises gradually warming the tissue.
22. The method of claim 12 , wherein the biocompatible ice slurry is configured to cool the one or more peripheral nerves by tissue cooling, wherein the tissue cooling comprises:
(i) exchanging heat stored by a heat capacity of the biocompatible ice slurry and the tissue;
(ii) exchanging heat released by crystallization of one or more lipids of the tissue or one or more lipids of a myelin sheath of the one or more peripheral nerves; and
(iii) exchanging heat absorbed by melting of the biocompatible ice slurry.