High penetration composition and uses thereof
The present invention relates to compositions and uses of novel high penetration compositions or high penetration prodrugs (HPP), in particular HPPs for 4-aminophenol derivatives, which are capable of crossing biological barriers with high penetration efficiency. The HPPs herein are capable of being converted to parent active drugs or drug metabolites after crossing the biological barrier and thus can render treatments for the conditions that the parent drugs or metabolites can. Additionally, due to the ability of penetrating biological barriers, the HPPs herein are capable of reaching areas that parent drugs may not be able to access or to render a sufficient concentration at the target areas and therefore render novel treatments. The HPPs herein can be administered to a subject through various administration routes. For example, the HPPs can be locally delivered to an action site of a condition with a high concentration due to their ability of penetrating biological barriers and thus obviate the need for a systematic administration. For another example, the HPPs herein can be systematically administer to a biological subject and enter the general circulation with a faster rate.
1. A compound having the structure:
2. A composition comprising a compound according to Structure 1a:
wherein R 1 and R 2 are each ethyl;
R 3 is H;
A − is Cl − ; and
n is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.
3. The composition according to claim 2 , further comprising a pharmaceutically acceptable carrier.
4. The composition according to claim 3 , wherein the pharmaceutically acceptable carrier is polar.
5. The composition according to claim 3 , wherein the pharmaceutically acceptable carrier is selected from the group consisiting of alcohol, acetone, ester, buffer, water, isotonic saline and Ringers solution.
6. The composition according to claim 2 , further comprising a pharmaceutically acceptable auxiliary agent selected from the group consisting of pH adjusting agents, buffering agents, and toxicity adjusting agents.
7. The composition according to claim 2 , wherein the concentration of the compound is from 5 weight percent to 20 weight percent.
8. The composition according to claim 2 , wherein the composition is formulated for transdermal administration.
9. The composition according to claim 8 , wherein the composition is formulated as a transdermal patch.
10. The composition according to claim 2 , wherein the composition is formulated as a solution, a spray, a lotion, an ointment, an emulsion or a gel.
11. The composition according to claim 10 , wherein the composition is formulated as a spray.
12. The composition according to claim 11 , wherein the spray is administered orally or nasally.