US2003100574A1PendingUtilityA1
Use and application of a pharmaceutical composition containing a mixture of natural-origin heterocyclical guanidine, for cosmetology, wound healing, focal dystonia and muscular spasm-related clinical pathologies
Priority: Nov 15, 2001Filed: Nov 14, 2002Published: May 29, 2003
Est. expiryNov 15, 2021(expired)· nominal 20-yr term from priority
Inventors:Nestor Antonio Lagos Wilson
A61P 29/00A61P 25/00A61P 27/02A61P 17/02A61P 13/10A61K 38/4886A61K 31/519A61K 31/40A61K 31/495A61K 31/52A61P 21/02A61P 17/00A61K 31/4168A61P 1/00A61P 21/00
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Claims
Abstract
Pharmaceutical compositions comprising tricyclic 3,4-propinoperhydropurines and uses thereof for blocking neuronal transmission are provided.
Claims
exact text as granted — not AI-modifiedWhat is claimed:
1 . A pharmaceutical composition for interfering with neuronal transmission, the composition comprising an effective amount of at least one compound represented by the following structure:
wherein R 1 and R 5 are independently H or OH; R 2 and R 3 are independently H or OSO 3 ; and R 4 is independently COONH 2 , OH, H, COONHSO 3 or COOCH 3 ; and a pharmacologically acceptable carrier.
2 . The composition of claim 1 , wherein the composition comprises a mixture of Gonyautoxin 2, Gonyautoxin 3 and Saxitoxin.
3 . The composition of claim 1 , wherein the composition comprises a mixture of Gonyautoxin 4, Gonyautoxin 1, Gonyautoxin 5, Gonyautoxin 3 and Gonyautoxin 2.
4 . The composition of claim 1 , wherein the composition comprises a mixture of Saxitoxin, neoSaxitoxin, Decarbamoyl-Saxitoxin, Gonyautoxin 3 and Gonyautoxin 2.
5 . The composition of claim 1 , further comprising Botulin A toxin.
6 . The composition of claim 1 , wherein the carrier is water.
7 . The composition of claim 1 , wherein the carrier is 0.09% Sodium Chloride.
8 . The composition of claim 1 , wherein the composition comprises about twenty to about forty units of the compound per milliliter of total solution.
9 . The composition of claim 8 , wherein the composition comprises forty units of the compound per milliliter of total solution.
10 . The composition of claim 1 , wherein the compound is diluted in a solution of acetic acid.
11 . A preparation for facial rejuvenation comprising an effective amount of the composition of claim 1 and a facial cream.
12 . The preparation of claim 11 , wherein said composition comprises about twenty to about forty units of the compound per milliliter of total solution.
13 . The preparation of claim 11 , wherein said composition comprises about forty units of the compound per milliliter of total solution.
14 . The preparation of claim 11 , wherein said carrier is water.
15 . The preparation of claim 11 , wherein said compound is diluted in a solution of acetic acid.
16 . The preparation of claim 11 , wherein the composition comprises a mixture of Gonyautoxin 2, Gonyautoxin 3 and Saxitoxin.
17 . The preparation of claim 11 , wherein the composition comprises a mixture of Saxitoxin, neoSaxitoxin, Decarbamoyl-Saxitoxin, Gonyautoxin 3 and Gonyautoxin 2.
18 . The preparation of claim 11 wherein the composition comprises a mixture of Gonyautoxin 4, Gonyautoxin 1, Gonyautoxin 5, Gonyautoxin 3 and Gonyautoxin 2.
19 . The preparation of claim 11 , further comprising Botulin A toxin.
20 . A method of interfering with neuronal transmission comprising contacting a neuron with an effective amount of the composition of claim 1 .
21 . The method of claim 20 , wherein the composition comprises a mixture of Gonyautoxin 2, Gonyautoxin 3 and Saxitoxin.
22 . The method of claim 20 , wherein the composition comprises a mixture of Saxitoxin, neoSaxitoxin, Decarbamoyl-Saxitoxin, Gonyautoxin 3 and Gonyautoxin 2.
23 . The method of claim 20 , wherein the composition comprises a mixture of Gonyautoxin 4, Gonyautoxin 1, Gonyautoxin 5, Gonyautoxin 3 and Gonyautoxin 2.
24 . The method of claim 20 , wherein the composition further comprises Botulin A toxin.
25 . The method of claim 20 , wherein about 100 to about 800 microliters of said composition is contacted with said neuron.
26 . The method of claim 20 , wherein less than one milliliter of said composition is contacted with said neuron.
27 . The method of claim 20 , wherein contacting an effective amount of the composition of claim 1 with a neuron comprises injecting the composition of claim 1 in an area proximate to the neuron.
28 . The method of claim 20 , wherein said composition comprises about forty units of the compound per milliliter of total solution.
29 . The method of claim 20 , wherein said composition comprises about 20 to about 40 units of the compound per milliliter of total solution.
30 . The method of claim 20 , wherein said compound is diluted in a solution of acetic acid.
31 . The method of claim 20 , wherein said neuron is in a muscle.
32 . The method of claim 31 , wherein said muscle is inside a human face.
33 . A method interfering with muscle contraction comprising contacting a muscle with an effective amount of the composition of claim 1 .
34 . The method of claim 33 , wherein the composition of claim 1 comprises a mixture of Gonyautoxin 2, Gonyautoxin 3 and Saxitoxin.
35 . The method of claim 33 , wherein the composition of claim 1 comprises a mixture of Saxitoxin, neoSaxitoxin, Decarbamoyl-Saxitoxin, Gonyautoxin 3 and Gonyautoxin 2.
36 . The method of claim 33 , wherein the composition of claim 1 comprises a mixture of Gonyautoxin 4, Gonyautoxin 1, Gonyautoxin 5, Gonyautoxin 3 and Gonyautoxin 2.
37 . The method of claim 33 , wherein the composition of claim 1 further comprises Botulin A toxin.
38 . The method of claim 33 , wherein the composition of claim 1 comprises about 20 to about 40 units of the compound per milliliter of the carrier.
39 . The method of claim 33 , wherein the carrier is acetic acid.
40 . The method of claim 33 , wherein the composition of claim 1 comprises about twenty to about forty units of the compound per milliliter of total solution.
41 . The method of claim 33 , wherein the composition of claim 1 comprises about forty units of the compound per milliliter of total solution.
42 . The method of claim 33 , wherein contacting an effective amount of the composition of claim 1 with a muscle comprises injecting the composition into an area proximate to the muscle.
43 . The method of claim 42 , wherein no more than one milliliter of the composition of claim 1 is injected into an area proximate to the muscle per injection point.
44 . The method of claim 42 , wherein about 100 to about 800 microliters of the composition of claim 1 is injected into an area proximate to the muscle per injection point.
45 . The method of claim 33 , wherein the muscle is inside a human face.
46 . The method of claim 33 , wherein the carrier is 0.09% sodium chloride.
47 . The method of claim 33 , wherein the compound is diluted in a solution of acetic acid.Join the waitlist — get patent alerts
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