High concentration local anesthetic formulations
A transdermal topical anesthetic formulation, which can be used to ameliorate or inhibit pain, has been developed. In the preferred embodiment, the topical anesthetic is a local anesthetic such as lidocaine, most preferably lidocaine free-base in a gel, and the dosage of the local anesthetic is effective in the painful area or immediately adjacent areas, to ameliorate or eliminate the pain. High concentration of local anesthetic in solution in the carrier is used to drive rapid release and uptake of the drug. Relief is typically obtained for a period of several hours.
1. A formulation in the form of a lotion, cream, or gel, comprising
a free base caine alkaloid local anesthetic, diglycol monoethyl ether, and propylene glycol in a lotion, cream, or gel, wherein the free base caine alkaloid local anesthetic is lidocaine free base which is present in an amount from greater than 20% by weight of the formulation, the formulation releases the largest dose of free base caine alkaloid local anesthetic from 0 to 8 hours after topical administration of the formulation to a patient, and the formulation also comprises isopropyl myristate and/or dimethyl isosorbide.
2. The formulation of claim 1 wherein the free base caine alkaloid local anesthetic is present in an amount between greater than 20% and 40% by weight.
3. The formulation of claim 1 wherein the free base caine alkaloid local anesthetic is present in an amount of approximately 40% by weight.
4. The formulation of claim 1 , wherein the formulation provides an initial burst release within two hours of administration.
5. The formulation of claim 1 , wherein the formulation provides an initial burst release within four hours of administration.
6. The formulation of claim 1 , wherein the formulation provides an initial burst release within six hours of administration.
7. The formulation of claim 1 wherein the concentration of the free base caine alkaloid local anesthetic is sufficiently high that release is governed by the Second Law of Thermodynamics, not simple diffusion.
8. The formulation of claim 1 wherein the formulation is a gel.
9. The formulation of claim 1 wherein the formulation is a non-aqueous gel.
10. The formulation of claim 8 wherein the free base caine alkaloid local anesthetic is present in an amount from greater than 20% to about 40% by weight of the formulation.
11. The formulation of claim 9 wherein the free base caine alkaloid local anesthetic is present in an amount from greater than 20% to about 40% by weight of the formulation.
12. The formulation of claim 8 wherein the free base caine alkaloid local anesthetic is present in an amount of about 40% by weight of the formulation.
13. The formulation of claim 9 wherein the free base caine alkaloid local anesthetic is present in an amount of about 40% by weight of the formulation.
14. The formulation of claim 8 wherein the formulation further comprises isopropyl myristate.
15. The formulation of claim 12 wherein the formulation further comprises isopropyl myristate.
16. The formulation of claim 8 wherein the formulation further comprises dimethyl isosorbide.
17. The formulation of claim 12 wherein the formulation further comprises dimethyl isosorbide.
18. The formulation of claim 12 wherein the formulation further comprises ethanol and hydroxypropyl cellulose.
19. The formulation of claim 15 wherein the formulation further comprises ethanol and hydroxypropyl cellulose.
20. The formulation of claim 17 wherein the formulation further comprises ethanol and hydroxypropyl cellulose.
21. The formulation of claim 1 wherein the formulation is a gel containing 40% w/w lidocaine free base, 20% w/w diglycol monoethyl ether, 10% w/w propylene glycol, and 10% w/w dimethyl isosorbide, and further comprising 18.80% w/w ethanol and 1.2% w/w hydroxypropyl cellulose.
22. The formulation of claim 1 wherein the formulation is a gel containing 40% w/w lidocaine free base, 10% w/w isopropyl myristate, 10% w/w diglycol monoethyl ether, and 20% w/w propylene glycol, and further comprising 18.80% w/w ethanol and 1.2% w/w hydroxypropyl cellulose.
23. The formulation of claim 12 wherein the formulation releases the largest dose of free base caine alkaloid local anesthetic from 0 to 6 hours after administration to the site.