Cyanoacrylate-based liquid microbial sealant drape
The invention relates to methods of using compositions for forming microbial sealant drapes. In particular, the invention relates to the use of compositions of combinations of cyanoacrylates for the in situ formation of drapes that can be used in surgery to protect patients from surgical site infections.
1. A microbial sealant drape composition, comprising 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.
2. The microbial sealant drape composition of claim 1 , wherein the composition, when applied to a surgical site, reduces microbial colonization of the surgical site by at least 99.9% within 15 minutes of being applied to the surgical site.
3. The microbial sealant drape composition of claim 1 , wherein the composition, when applied to a surgical site, polymerizes into a film resistant to passage of viruses.
4. The microbial sealant drape composition of claim 1 , wherein the composition, when applied to a surgical site, polymerizes into film having a thickness of about 50 to 60 μm.
5. The microbial sealant drape composition of claim 1 , wherein the composition is compatible with skin preparation products, surgical incise drapes, and wound closure products.
6. The microbial sealant drape composition of claim 1 , wherein the composition is compatible with lasers, defibrillators, and electrocautery equipment.
7. The microbial sealant drape composition of claim 1 , wherein the composition is sterilized by Electron-beam (E-beam) irradiation.
8. The microbial sealant drape composition of claim 1 , wherein the composition provides a surface coverage greater than 200 inch 2 .
9. A method for reducing microbial colonization of a surgical site, comprising applying the microbial sealant drape composition of claim 1 to the surgical site.
10. The microbial sealant drape composition of claim 1 , wherein the composition, when applied to a surgical site, does not increase the temperature of the skin at the surgical site to which the composition has been applied more than about 0.25° C.
11. The microbial sealant drape composition of claim 1 , wherein the flashpoint of the microbial sealant drape composition is greater than 240° F.
12. The microbial sealant drape composition of claim 1 , wherein the composition is bactericidal.
13. The microbial sealant drape composition of claim 1 , wherein the composition is sterilized by irradiation.
14. The microbial sealant drape composition of claim 1 , wherein the composition does not contain any plasticizer.
15. The microbial sealant drape composition of claim 1 , wherein the ASTM accelerated aging standard is the ASTM F1980-02 standard.