Transdermal venous access locking solutions
Microbial growth inhibiting solutions and methods of employing the microbial growth inhibiting solutions in flushing and coating medical devices are disclosed. In alternative embodiments, the microbial growth inhibiting solutions include combinations of a chelating agent with a C 4 -C 9 carboxylate antimicrobial agent, for example, such as n-octanoic acid. Methods of using these microbial growth inhibiting solutions for coating a medical device and for inhibiting catheter infection are also disclosed.
1. A microbial growth inhibiting solution comprising caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent and an agent that is a chelator and a buffer, wherein the said carboxylate antimicrobial agent is present in an amount ranging from about 0.05 mg/mL to about 5 mg/mL, wherein the agent that is a chelator and a buffer is citrate and is present in an amount ranging from about 1 mg/mL to about 200 mg/mL, and wherein the solution has a pH of 5.2 or less.
2. The microbial growth inhibiting solution of claim 1 further comprising an additional chelating agent selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
3. The microbial growth inhibiting solution of claim 2 , wherein the additional chelating agent chelates Ca, Mg, Mn, Fe or Zn.
4. The microbial growth inhibiting solution of claim 2 , wherein the additional chelating agent is present in an amount ranging from about 0.1 mg/mL to about 2 mg/mL.
5. The microbial growth inhibiting solution of claim 2 , wherein the additional chelating agent is present in an amount ranging from about 0.25 mg/mL to about 0.5 mg/mL.
6. The microbial growth inhibiting solution of claim 1 , wherein the solution comprises saline, Ringer's solution, or water.
7. The microbial growth inhibiting solution of claim 1 further comprising an additional chelating agent present in an amount ranging from about 0.1 mg/mL to about 2 mg/mL wherein the antimicrobial agent is present in an amount ranging from about 0.071 mg/mL to about 1.15 mg/mL.
8. The microbial growth inhibiting solution of claim 7 , wherein the antimicrobial agent comprises sodium caprylate, and the additional chelating agent comprises disodium ethylenediaminetetraacetic acid.
9. A method of disinfecting an implanted catheter from bacteria and fungi, the method comprising:
introducing to a lumen of a catheter a microbial growth inhibiting solution comprising a caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent a citrate buffer and a chelating agent, wherein the said antimicrobial agent is present in an amount ranging from about 0.05 mg/mL to about 5 mg/mL the citrate is present in an amount ranging from about 1 mg/ml to about 200 mg/ml, and the chelating agent is present in an amount ranging from about 0.01 mg/mL to about 2 mg/mL, and wherein the composition has a pH of 5.2 or less.
10. The method of claim 9 , wherein at least a portion of the catheter is sufficiently porous to permit diffusion of the solution outwardly from the lumen to the outer surface of the catheter and into tissues or the bloodstream surrounding the catheter to inhibit infection.
11. The method of claim 9 , wherein the chelating agent is present in an amount ranging from about 0.1 mg/mL to about 1 mg/mL and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
12. The method of claim 9 , wherein the chelating agent is present in an amount ranging from about 0.25 mg/mL to about 0.5 mg/mL and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
13. The method of claim 9 , wherein the microbial growth inhibiting solution comprises the citrate buffer is present in an amount ranging from about 1.5 to about 24 mM, wherein caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent is present in an amount ranging from about 0.071 mg/mL to about 1.15 mg/mL, and the chelating agent is present in an amount ranging from about 0.0625 mg/mL to about 1 mg/mL.
14. The method of claim 13 , wherein the C 4 -C 9 carboxylate antimicrobial agent comprises sodium caprylate, the buffer comprises citrate, and the chelating agent comprises disodium ethylenediaminetetraacetic acid.
15. A method for coating a medical device, the method comprising:
exposing the medical device to a microbial growth inhibiting solution for a sufficient amount of time to provide a coating on the exposed surface of the device, wherein the microbial growth inhibiting solution comprises caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent a citrate buffer and a chelating agent, wherein the said antimicrobial agent is present in an amount ranging from about 0.05 mg/mL to about 5 mg/mL, the citrate is present in an amount ranging from about 1 mg/ml to about 200 mg/ml, and the chelating agent is present in an amount ranging from about 0.01 mg/mL to about 2 mg/mL, and wherein the composition has a pH of 5.2 or less.
16. The method of claim 15 further comprising treating the device with a surfactant before exposing the device to the microbial growth inhibiting solution.
17. The method of claim 16 , wherein the surfactant is selected from the group of surfactant consisting of tridodecylmethyl ammonium chloride, benzalkonium chloride and combinations thereof.
18. The method of claim 15 , wherein the chelating agent is present in an amount ranging from about 0.1 mg/mL to about 1 mg/mL and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
19. The method of claim 15 , wherein the chelating agent is present in an amount ranging from about 0.25 mg/mL to about 0.5 mg/mL and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
20. The method of claim 15 , wherein the microbial growth inhibiting solution comprises the citrate present in an amount ranging from about 1.5 to about 24 mM, wherein caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent is present in an amount ranging from about 0.071 mg/mL to about 1.15 mg/mL, and the chelating agent is present in an amount ranging from about 0.0625 mg/mL to about 1 mg/mL.
21. The method of claim 20 , wherein the C 4 -C 9 carboxylate antimicrobial agent comprises sodium caprylate, the buffer comprises citrate, and the chelating agent comprises disodium ethylenediaminetetraacetic acid.
22. A medical device coated with a microbial growth inhibiting solution comprising caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent and a chelating agent, wherein the said antimicrobial agent is present in an amount ranging from about 0.05 mg/mL to about 5 mg/mL the citrate is present in an amount ranging from about 1 mg/ml to about 200 mg/ml, and the chelating agent is present in an amount ranging from about 0.01 mg/mL to about 2 mg/mL, and wherein the composition has a pH of 5.2 or less.
23. The medical device of claim 22 , wherein the medical device is selected from the group of devices consisting of a central venous catheter, a peripheral intravenous catheter, an arterial catheter, a Swant-Ganz catheter, a hemodialysis catheter, an umbilical catheter, a percutaneous nontunneled silicone catheter, a cuffed tunneled central venous catheter and a subcutaneous central venous pert.
24. The medical device of claim 22 , wherein the chelating agent is present in an amount ranging from about 0.1 mg/mL to about 1 mg/mL and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
25. The medical device of claim 22 , wherein the chelating agent is present in an amount ranging from about 0.25 mg/mL to about 0.5 mg/mL and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
26. The medical device of claim 22 , wherein the microbial growth inhibiting solution comprises the citrate present in an amount ranging from about 1.5 to about 24 mM, wherein caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent is present in an amount ranging from about 0.071 mg/mL to about 1.15 mg/mL, and the chelating agent is present in an amount ranging from about 0.0625 mg/mL to about 1 mg/mL.
27. The medical device of claim 26 , wherein the C 4 -C 9 carboxylate antimicrobial agent comprises sodium caprylate, the buffer comprises citrate, and the chelating agent comprises disodium ethylenediaminetetraacetic acid.
28. A method for locking and/or flushing an implanted catheter, the method comprising:
filling a lumen of an implanted catheter open to a body lumen with a microbial growth inhibiting solution comprising caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent a citrate buffer and a chelating agent, wherein the said antimicrobial agent is present in an amount ranging from about 0.05 mg/mL to about 5 mg/mL the citrate is present in an amount ranging from about 1 mg/ml to about 200 mg/ml, and the chelating agent is present in an amount ranging from about 0.01 mg/mL to about 2 mg/mL, and wherein the composition has a pH of 5.2 or less.
29. The method of claim 28 , wherein the chelating agent is present in an amount ranging from about 0.1 mg/mL to about 1 mg/mL and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
30. The method of claim 28 , wherein the chelating agent is present in an amount ranging from about 0.25 mg/mL to about 0.5 mg/mL and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
31. The method of claim 28 , wherein the microbial growth inhibiting solution comprises the citrate present in an amount ranging from about 1.5 to about 24 mM, wherein caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent is present in an amount ranging from about 0.071 mg/mL to about 1.15 mg/mL, and the chelating agent is present in an amount ranging from about 0.0625 mg/mL to about 1 mg/mL.
32. The method of claim 31 , wherein the C 4 -C 9 carboxylate antimicrobial agent comprises sodium caprylate, the buffer comprises citrate, and the chelating agent comprises disodium ethylenediaminetetraacetic acid.
33. A kit for locking and/or flushing an implanted catheter, the kit comprising:
a container holding a volume of a microbial growth inhibiting solution comprising caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent a citrate buffer and a chelating agent, wherein the said antimicrobial agent is present in an amount ranging from about 0.05 mg/mL to about 5 mg/mL the citrate is present in an amount ranging from about 1 mg/ml to about 200 mg/ml, and the chelating agent is present in an amount ranging from about 0.01 mg/mL to about 2 mg/mL, and wherein the composition has a pH of 5.2 or less; and
an implantable catheter lumen that receives the microbial growth inhibiting solution.
34. The kit of claim 33 , wherein the container comprises a syringe.
35. The kit of claim 33 , wherein the chelating agent is present in an amount ranging from about 0.1 mg/mL to about 1 mg/mL and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochioride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
36. The kit of claim 33 , wherein the chelating agent is present in an amount ranging from about 0.25 mg/mL to about 0.5 mg/mL and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetria mine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
37. The kit of claim 33 , wherein the microbial growth inhibiting solution comprises the citrate present in an amount ranging from about 1.5 to about 24 mM, wherein caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent is present in an amount ranging from about 0.5 mM to about 8 mM, and the chelating agent is present in an amount ranging from about 0.0625 mg/mL to about 1 mg/mL.
38. The kit of claim 37 , wherein the C 4 -C 9 carboxylate antimicrobial agent comprises sodium caprylate, the buffer comprises citrate, and the chelating agent comprises disodium ethylenediaminetetraacetic acid.
39. A kit for locking and/or flushing an implanted catheter, the kit comprising:
a container having a first compartment holding caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent a citrate buffer and a chelating agent in powder form and a second compartment holding a pharmacologically acceptable carrier solution, wherein the said carboxylate antimicrobial agent is present in an amount ranging from about 0.05 mg/mL to about 5 mg/mL the citrate is present in an amount ranging from about 1 mg/ml to about 200 mg/ml, and the chelating agent is present in an amount ranging from about 0.01 mg/mL to about 2 mg/mL, and wherein the composition has a pH of 5.2 or less when mixed with the pharmacologically acceptable carrier solution.
40. The kit of claim 39 , wherein the container comprises an implantable catheter lumen.
41. The kit of claim 39 , wherein the container comprises a syringe.
42. The kit of claim 39 , wherein the chelating agent is present in an amount ranging from about 0.1 mg/mL to about 1 mg/mL when mixed with the pharmacologically acceptable carrier solution and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
43. The kit of claim 39 , wherein the chelating agent is present in an amount ranging from about 0.25 mg/mL to about 0.5 mg/mL when mixed with the pharmacologically acceptable carrier solution and is selected from the group consisting of ethylenediaminetetraacetic acid, diethylenetriamine pentaacetic acid, ethylene glycol tetraacetic acid, etidronate, dimercaptosuccinic acid, deferoxamine, dimercaprol, triethylene tetramine dihydrochloride, zinc citrate, combination of bismuth and citrate, penicillamine, pharmaceutically acceptable salts thereof and combinations thereof.
44. The kit of claim 39 , wherein first compartment or the second compartment comprises the citrate present in an amount ranging from about 1.5 to about 24 mM, wherein caprylic acid or a pharmaceutically acceptable salt thereof antimicrobial agent is present in an amount ranging from about 0.071 mg/mL to about 1.15 mg/mL, and the chelating agent is present in an amount ranging from about 0.0625 mg/mL to about 1 mg/mL when mixed with the pharmacologically acceptable carrier solution.
45. The kit of claim 44 , wherein the C 4 -C 9 carboxylate antimicrobial agent comprises sodium caprylate, the buffer comprises citrate, and the chelating agent comprises disodium ethylenediaminetetraacetic acid.