Sterilized liquid compositions of cyanoacrylate monomer mixtures
Cyanoacrylate adhesive compositions comprise a mixture of two cyanoacrylate monomers, including 2-octyl cyanoacrylate and n-butyl cyanoacrylate. The monomers are stabilized and sterilized by irradiation, and do not substantially increase in viscosity after sterilization or after two years of shelf storage. These compositions have anti-microbial properties, and may be used to close wounds as well as secure catheters inserted into the body in place.
1. A method for inhibiting bacterial infection of the skin, comprising applying a cyanoacrylate adhesive composition to the skin and allowing the composition to cure on the skin, thereby reducing bacteria colonization on the skin, wherein the composition comprises a mixture of about 78% to about 82% by weight of monomeric 2-octyl cyanoacrylate, about 22% to about 18% by weight of monomeric n-butyl cyanoacrylate, about 2000 ppm to about 14,000 ppm of butylated hydroxyl anisole, and about 10 ppm to about 200 ppm of sulfur dioxide or about 5 ppm to about 50 ppm of an acid stabilizer selected from the group consisting of sulfuric acid, phosphoric acid, and perchloric acid, wherein the composition is sterilized by electron beam (E-beam) irradiation, wherein the viscosity of the sterilized composition increases by no more than about 300% over a period of at least two years of shelf storage, and wherein the composition does not contain any plasticizer.
2. The method of claim 1 , wherein the composition comprises a mixture of about 79% to about 81% by weight of monomeric 2-octyl cyanoacrylate, about 21% to about 19% by weight of monomeric n-butyl cyanoacrylate, about 2000 ppm to about 14,000 ppm of butylated hydroxyl anisole, and about 10 ppm to about 200 ppm of sulfur dioxide.
3. The method of claim 1 , wherein the composition comprises a mixture of about 79% to about 81% by weight of monomeric 2-octyl cyanoacrylate, about 21% to about 19% by weight of monomeric n-butyl cyanoacrylate, about 2000 ppm to about 8000 ppm of butylated hydroxyl anisole, and about 10 ppm to about 200 ppm of sulfur dioxide.
4. The method of claim 1 , wherein the composition comprises a mixture of about 80% by weight of monomeric 2-octyl cyanoacrylate, about 20% by weight of monomeric n-butyl cyanoacrylate, about 2000 ppm to about 14,000 ppm of butylated hydroxyl anisole, and about 10 ppm to about 200 ppm of sulfur dioxide.
5. The method of claim 1 , further comprising re-applying the cyanoacrylate adhesive composition to the skin after a period of time, and allowing the re-applied composition to cure on the skin.
6. The method of claim 1 , wherein the composition further comprises about 10 ppm to about 150 ppm of a polymerization accelerator.
7. The method of claim 6 , wherein the polymerization accelerator is a crown ether.
8. The method of claim 1 , wherein viscosity of the composition increases no more than about 200% after sterilization.
9. The method of claim 1 , wherein the viscosity of the sterilized composition increases no more than about 300% after about two years of shelf storage.
10. The method of claim 1 , wherein the viscosity of the sterilized composition increases no more than about 250% after about two years of shelf storage.
11. The method of claim 1 , wherein the viscosity of the sterilized composition increases no more than about 200% after about two years of shelf storage.
12. A method for inhibiting bacterial infection of the skin, comprising applying a cyanoacrylate adhesive composition to the skin and allowing the composition to cure on the skin, thereby reducing bacteria colonization on the skin, wherein the composition comprises a mixture of about 78% to about 82% by weight of monomeric 2-octyl cyanoacrylate, about 22% to about 18% by weight of monomeric n-butyl cyanoacrylate, about 2000 ppm to about 14,000 ppm of butylated hydroxyl anisole, and about 10 ppm to about 200 ppm of sulfur dioxide or about 5 ppm to about 50 ppm of an acid stabilizer selected from the group consisting of sulfuric acid, phosphoric acid, and perchloric acid, wherein the composition is sterilized by gamma irradiation, wherein the viscosity of the sterilized composition increases by no more than about 600% over a period of at least two years of shelf storage, and wherein the composition does not contain any plasticizer.
13. The method of claim 12 , wherein the composition comprises a mixture of about 79% to about 81% by weight of monomeric 2-octyl cyanoacrylate, about 21% to about 19% by weight of monomeric n-butyl cyanoacrylate, about 2000 ppm to about 14,000 ppm of butylated hydroxyl anisole, and about 10 ppm to about 200 ppm of sulfur dioxide.
14. The method of claim 12 , wherein the composition comprises a mixture of about 79% to about 81% by weight of monomeric 2-octyl cyanoacrylate, about 21% to about 19% by weight of monomeric n-butyl cyanoacrylate, about 2000 ppm to about 8000 ppm of butylated hydroxyl anisole, and about 10 ppm to about 200 ppm of sulfur dioxide.
15. The method of claim 12 , wherein the composition comprises a mixture of about 80% by weight of monomeric 2-octyl cyanoacrylate, about 20% by weight of monomeric n-butyl cyanoacrylate, about 2000 ppm to about 14,000 ppm of butylated hydroxyl anisole, and about 10 ppm to about 200 ppm of sulfur dioxide.
16. The method of claim 12 , wherein the composition further comprises about 10 ppm to about 150 ppm of a polymerization accelerator.
17. The method of claim 12 , further comprising re-applying the cyanoacrylate adhesive composition to the skin after a period of time, and allowing the re-applied composition to cure on the skin.
18. A method for inhibiting bacterial infection of the skin, comprising applying a cyanoacrylate adhesive composition to the skin and allowing the composition to cure on the skin, thereby reducing bacteria colonization on the skin, wherein the composition comprises a mixture of about 80% by weight of monomeric 2-octyl cyanoacrylate, about 20% by weight of monomeric n-butyl cyanoacrylate, about 2000 ppm to about 8000 ppm of butylated hydroxyl anisole, and about 10 ppm to about 200 ppm of sulfur dioxide or about 5 ppm to about 50 ppm of an acid stabilizer selected from the group consisting of sulfuric acid, phosphoric acid, and perchloric acid, wherein the composition is sterilized by ethylene oxide exposure or irradiation, the viscosity of the composition increases no more than 200% after sterilization, and wherein the sterilized composition has at least two years of shelf stability as measured by an American Society for Testing and Materials (ASTM) accelerated aging standard, and wherein the composition does not contain any plasticizer or antimicrobial agent.