초록 ▼

Chemical permeation enhancers (CPEs) improve access of local anesthetics to the nerve, thereby improving their performance. Surfactants, representing three CPE sub-groups: anionic, cationic, and nonionic surfactants, were co-injected with tetrodotoxin (TTX) or bupivacaine at the sciatic nerve of Spr

Chemical permeation enhancers (CPEs) improve access of local anesthetics to the nerve, thereby improving their performance. Surfactants, representing three CPE sub-groups: anionic, cationic, and nonionic surfactants, were co-injected with tetrodotoxin (TTX) or bupivacaine at the sciatic nerve of Sprague-Dawley rats. All enhancers produced marked concentration-dependent improvements in the frequency and duration of block with TTX but not bupivacaine. An in vitro toxicity assay showed a wide range of CPE myotoxicity, but in vivo histological assessment showed no signs of muscle or nerve damage at concentrations of CPEs that produced a half-maximal increase in the duration of block of TTX. There was no systematic relationship between the enhancers' charge or hydrophobicity and their enhancement of block duration or potency. Thus, CPEs can provide marked prolongation of nerve blockade from TTX, without apparent local tissue toxicity, and therefore enhance the clinical applicability of TTX for prolonged-duration local anesthesia.

대표청구항 ▼

1. A method for enhancing nerve blockade comprising administering an effective amount of a site I sodium channel local anesthetic selected from the group consisting of tetrodotoxin (TTX), saxitoxin (STX), decarbamoyl saxitoxin, neosaxitoxin, and gonyautoxins in combination with an effective amount o

1. A method for enhancing nerve blockade comprising administering an effective amount of a site I sodium channel local anesthetic selected from the group consisting of tetrodotoxin (TTX), saxitoxin (STX), decarbamoyl saxitoxin, neosaxitoxin, and gonyautoxins in combination with an effective amount of a chemical penetration enhancer selected from the group consisting of sodium octyl sulfate, sodium dodecyl sulfate, octyl-trimethyl-ammonium bromide, and dodecyl-trimethyl-ammonium bromide to increase duration of sensory nerve blockade more than the additive effect of the local anesthetic and chemical permeation enhancer. 2. The method of claim 1 wherein the local anesthetic is neosaxitoxin. 3. The method of claim 1 further comprising administering a vasoconstrictor. 4. The method of claim 1 further comprising a charged local anesthetic selected from the group consisting of amino-amide or amino-ester local anesthetics or derivatives thereof, at least partly amphiphilic local anesthetics, local anesthetics that act not on the surface of the ceil, and at least partly charged local anesthetics. 5. The method of claim 1 comprising providing a kit comprising a vial having the local anesthetic therein and a second vial containing a diluent therein. 6. The method of claim 1 comprising administering the anesthetic as a bolus dosage unit. 7. The method of claim 1 comprising administering the anesthetic in a continuous or sustained release formulation. 8. The method of claim 1 comprising administering the anesthetic in a topical or aerosol formulation. 9. An anesthetic composition for enhancing nerve blockade comprising an effective amount of a site I sodium channel local anesthetic selected from the group consisting of tetrodotoxin (TTX), saxitoxin (STX), decarbamoyl saxitoxin, neosaxitoxin, and gonyautoxins in combination with an effective amount of a chemical penetration enhancer selected from the group consisting of sodium octyl sulfate, sodium dodecyl sulfate, octyl-trimethyl-ammonium bromide, and dodecyl-trimethyl-ammonium bromide, to increase duration of sensory blockade more than the additive effect of the local anesthetic and chemical permeation enhancer. 10. The composition of claim 9 wherein the local anesthetic is neosaxitoxin. 11. The composition of claim 9 further comprising a vasoconstrictor. 12. The composition of claim 9 further comprising a charged local anesthetic selected from the group consisting of amino-amide or ambo-ester local anesthetics or derivatives thereof, at least partly amphiphilic local anesthetics, local anesthetics that act not on the surface of the cell, and at least partly charged local anesthetics. 13. The composition of claim 9 in a kit comprising a vial comprising the local anesthetic therein and a second vial comprising a diluent therein. 14. The composition of claim 9 comprising the anesthetic as a bolus dosage unit. 15. The composition of claim 9 comprising the anesthetic in a continuous or sustained release formulation. 16. The composition of claim 9 comprising the anesthetic in a topical or aerosol formulation. 17. The composition of claim 9 comprising a site I sodium channel local anesthetic selected from the group consisting of tetrodotoxin (TTX) in a concentration of between 10 and 120 micromolar, saxitoxin (STX) in a concentration of between 5 and 60 micromolar, decarbamoyl saxitoxin in a concentration between 30 and 480 micromolar, and neosaxitoxin in a concentration between 3 and 40 micromolar. 18. The composition of claim 9 comprising chemical penetration enhancer is selected from the group consisting of sodium octyl sulfate in a concentration of between 10 and 100 mM, sodium dodecyl sulfate in a concentration between one and 40 mM, octyl-trimethyl-ammonium bromide in a concentration of between 20 and 120 mM, and dodecyl-trimethyl-ammonium bromide in a concentration of between 0.5 and 10 mM. 19. The composition of claim 17 comprising chemical penetration enhancer is selected from the group consisting of sodium octyl sulfate in a concentration of between 10 and 100 mM, sodium dodecyl sulfate in a concentration between one and 40 mM, octyl-trimethyl-ammonium bromide in a concentration of between 20 and 120 mM, and dodecyl-trimethyl-ammonium bromide in a concentration of between 0.5 and 10 mM. 20. The composition of claim 12 wherein the local anesthetics has Formula I or Formula II: where R1-R5 are independently selected from hydrogen; linear, branched, or cyclic alkyl and aryl groups. 21. The composition of claim 20 wherein the local anesthetic is selected from the group consisting of QX-314 ((N-(2,6)dimethylphenylcarbamoylmethyl triethylammonium bromide); QX-222 (2-((2,6-dimethylphenyl)amino)-N,N,N-trimethyl-2-oxoethanaminium); QX-572 (N,N-bis(phenylcarbamoylmethyl)-dimethylammonium chloride), tonicaine, bupivacaine, charged tetracine derivatives, and charged derivatives of flecainide. 22. The composition of claim 9 wherein the effective amount of local anesthetic and effective amount of chemical penetration enhancer do not increase cytotoxicity. 23. The method of claim 1 wherein the effective amount of local anesthetic and effective amount of chemical penetration enhancer do not increase cytotoxicity.