US2004146590A1PendingUtilityA1
Molecular neurochirurgie for pain control administering locally capsaicin or resinferatoxin
Priority: Mar 22, 2001Filed: Mar 22, 2001Published: Jul 29, 2004
Est. expiryMar 22, 2021(expired)· nominal 20-yr term from priority
A61K 31/165A61P 29/00A61K 31/357A61K 31/167A61K 31/16
53
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present invention provides methods and kits for the selective ablation of pain-sensing neurons. The methods comprise administration of a vanilloid receptor agonist to a ganglion in an amount that causes death of vanilloid receptor-bearing neurons. Accordingly, the present invention provides methods of controlling pain and inflammatory disorders that involve activation of vanilloid receptor-bearing neurons.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of selectively ablating pain-sensing neurons from a ganglion, said method comprising intraganglionic administration of a vanilloid receptor 1 agonist to a ganglion selected from the group consisting of a dorsal root ganglion, a trigeminal ganglion, or an autonomic ganglion in an amount sufficient to ablate the neurons.
2 . The method of claim 1 , wherein the vanilloid receptor 1 agonist is administered to a patient suffering from chronic pain.
3 . The method of claim 1 , wherein the vanilloid receptor 1 agonist is administered to a patient suffering from post-herpetic neuralgia.
4 . The method of claim 1 , wherein the ganglion is a dorsal root ganglion.
5 . The method of claim 1 , wherein the ganglion is a trigeminal ganglion.
6 . The method of claim 1 , wherein the ganglion is an autonomic ganglion.
7 . The method of claim 1 , wherein the vanilloid receptor 1 agonist is selected from the group consisting of a resiniferatoxin or a capsaicin.
8 . A method of claim 7 , wherein the vanilloid receptor agonist is a resiniferatoxin.
9 . A method of claim 1 , wherein the amount is from 50 nanograms to 50 micrograms.
10 . A method of claim 9 , wherein the amount is from about 500 nanograms to about 50 micrograms.
11 . A method of claim 1 , wherein intraganglionic administration comprises direct injection into the ganglion.
12 . A method of claim 1 , wherein intraganglionic administration comprises injection into a nerve root.
13 . A method of claim 1 , further comprising administration of a local anesthetic.
14 . The method of claim 13 , wherein the local anesthetic is lidocaine, bupivicaine, tetracaine, or ropivicaine.
15 . A method of selectively ablating pain-sensing neurons from a ganglion, said method comprising intrathecal administration of a vanilloid receptor agonist to a dorsal root ganglion.
16 . The method of claim 15 , wherein the vanilloid receptor agonist is administered to a patient suffering from chronic pain.
17 . The method of claim 15 , wherein the vanilloid receptor agonist is selected from the group consisting of a resiniferatoxin or a capsaicin.
18 . The method of claim 15 , wherein the vanilloid receptor agonist is a resiniferatoxin.
19 . The method of claim 15 , wherein the amount is from 100 nanograms to 500 micrograms.
20 . The method of claim 15 , wherein the amount is from about 500 nanograms to about 500 micrograms.
21 . The method of claim 15 , further comprising administration of a local anesthetic.
22 . The method of claim 15 , wherein the local anesthetic is tetracaine, ropivicaine, or bupivicaine.
23 . A kit for selectively ablating pain sensing neurons from a ganglion selected from the group consisting of a dorsal root ganglion, a trigeminal ganglion, or an autonomic ganglion, said kit comprising a compartment containing a vanilloid receptor agonist in an amount sufficient to ablate the neurons and instructional materials describing how to use the kit.
24 . The kit of claim 23 , wherein the vanilloid receptor agonist is a resiniferatoxin.
25 . The kit of claim 23 , wherein the vanilloid receptor agonist is a capsaicin.
26 . The kit of claim 23 , further comprising a local anesthetic.
27 . The kit of claim 26 , wherein the local anesthetic is lidocaine or bupivicaine.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.