ANTIMICROBIAL OPHTHALMIC TREATMENT SYSTEM AND METHOD

Information

  • Patent Application
  • 20070148127
  • Publication Number
    20070148127
  • Date Filed
    December 15, 2006
    17 years ago
  • Date Published
    June 28, 2007
    17 years ago
Abstract
An ophthalmic treatment system comprises an ophthalmic treatment solution and a biguanide antimicrobial agent in solid form and in contact with said treatment solution such as to inhibit bacterial and/or fungal growth in said solution. The biguanide is partially or wholly terminated with an amine compound.
Description
Claims
  • 1. An ophthalmic treatment system comprising an ophthalmic treatment solution and a biguanide antimicrobial agent in solid form and in contact with said treatment solution such as to inhibit bacterial and/or fungal growth in said solution, wherein said biguanide is partially or wholly terminated with an amine compound.
  • 2. The system of claim 1 wherein said biguanide antimicrobial agent is immobilized on a solid substrate.
  • 3. The system of claim 1 or claim 2 wherein said biguanide antimicrobial agent is substantially insoluble in said solution.
  • 4. The system of any preceding claim wherein said ophthalmic treatment solution is selected from an eye drop, a contact lens wetting solution, a contact lens cleaning solution, and a contact lens multi-purpose solution.
  • 5. The system of any preceding claim and including a container within which said ophthalmic treatment solution and said biguanide antimicrobial agent are accommodated.
  • 6. The system of claim 5 wherein said biguanide antimicrobial agent is incorporated in one or more elements contained within, but separate from, said container.
  • 7. The system of claim 5 wherein said biguanide antimicrobial agent is provided on the internal surface of the container.
  • 8. The system of any preceding claim wherein said biguanide is partially or wholly terminated at its cyanoguanidine end group by a primary or secondary monoamine containing about 2 to about 90 carbon atoms.
  • 9. The system of claim 8 wherein said monoamine is substituted with a functionality selected from the group consisting of fluoride, chloride, bromide, iodide, nitro, hydroxyl, ether, sulfide, disulfide, sulfoxide and sulfone.
  • 10. The system of claim 9 wherein said functionality is chloride.
  • 11. The system of any one of claims 8 to 10 wherein said monoamine includes octadecylamine.
  • 12. The system of any preceding claim wherein said biguanide is a polymeric biguanide having recurring units of the general formula:
  • 13. The system of claim 12 wherein at least one of X and Y is a C4 to C16 polymethylene radical.
  • 14. The system of any preceding claim wherein said biguanide is polyhexamethylene biguanide.
  • 15. A method of rendering an ophthalmic treatment solution resistant to bacterial and/or fungal growth comprising contacting the solution with a heterogeneous phase composition insoluble in said solution and comprising a biguanide antimicrobial agent wherein said biguanide is partially or wholly terminated with an amine compound.
  • 16. The method of claim 15 wherein said biguanide is partially or wholly terminated at its cyanoguanidine end group by a primary or secondary monoamine containing about 2 to about 90 carbon atoms.
  • 17. The method of claim 16 wherein said monoamine is substituted with a functionality selected from the group consisting of fluoride, chloride, bromide, iodide, nitro, hydroxyl, ether, sulfide, disulfide, sulfoxide and sulfone.
  • 18. The method of claim 17 wherein said functionality is chloride.
  • 19. The method of any one of claims 15 to 18 wherein said monoamine includes octadecylamine.
  • 20. The method of any one of claims 15 to 19 wherein said biguanide is a polymeric biguanide having recurring units of the general formula:
  • 21. The method of claim 20 wherein at least one of X and Y is a C4 to C16 polymethylene radical.
  • 22. The method of any one of claims 15 to 21 wherein said biguanide is polyhexamethylene biguanide.
Provisional Applications (1)
Number Date Country
60753020 Dec 2005 US