Claims
- 1) A method for the treatment of bacterial infections, comprising:
administering parenterally an effective amount of a therapeutic agent, said therapeutic agent comprising at least one lytic enzyme produced by a bacteria infected with a bacteriophage specific for said bacteria and a carrier for delivering said lytic enzyme to the site of the infection.
- 2) The method according to claim 1, wherein the at least one lytic enzyme is for the treatment of Pseudomonas.
- 3) The method according to claim 1, wherein the at least one lytic enzyme is for the treatment of Streptococcus
- 4) The method according to claim 1, wherein the at least one lytic enzyme is for the treatment of Staphylococcus.
- 5) The method according to claim 1, wherein the at least one lytic enzyme is for the treatment of Clostridium.
- 6) The method according to claim 1, wherein said composition further comprises a buffer that maintains pH of the composition at a range between about 4.0 and about 9.0.
- 7) The method according to claim 6, wherein the buffer maintains the pH of the composition at the range between about 5.5 and about 7.5.
- 8) The method according to claim 6, wherein said buffer comprises a reducing reagent.
- 9) The method according to claim 8, wherein said reducing reagent is dithiothreitol.
- 10) The method according to claim 6, wherein said buffer comprises a metal chelating reagent.
- 11) The method according to claim 10, wherein said metal chelating reagent is ethylenediaminetetracetic disodium salt.
- 12) The method according to claim 6, wherein said buffer is a citrate-phosphate buffer.
- 13) The method according to claim 1, further comprising a bactericidal or bacteriostatic agent as a preservative.
- 14) The method according to claim 1, wherein said at least one lytic enzyme is lyophilized.
- 15) The method according claim 1, further comprising administering a concentration of about 100 to about 500,000 active enzyme units per milliliter of fluid in the wet environment of the nasal or oral passages.
- 16) The method according to claim 15, further comprising administering the concentration of about 100 to about 10,000 active enzyme units per milliliter of fluid in the wet environment of the nasal or oral passages.
- 17) The method according to claim 1, wherein said therapeutic agent is administered intravenously.
- 18) The method according to claim 1, wherein said therapeutic agent is administered intramuscularly.
- 19) The method according to claim 1, wherein said therapeutic agent is administered subcutaneously.
- 20) The method according to claim 1, wherein the therapeutic agent further comprises at least one complementary agent which potentiates the bactericidal activity of the lysine enzyme, said complementary agent being selected from the group consisting of penicillin, synthetic penicillins bacitracin, methicillin, cephalosporin, polymyxin, cefaclor. Cefadroxil, cefamandole nafate, cefazolin, cefixime, cefmetazole, cefonioid, cefoperazone, ceforanide, cefotanme, cefotaxime, cefotetan, cefoxitin, cefpodoxime proxetil, ceftazidime, ceftizoxime, ceftriaxone, cefriaxone moxalactam, cefuroxime, cephalexin, cephalosporin C, cephalosporin C sodium salt, cephalothin, cephalothin sodium salt, cephapirin, cephradine, cefuroximeaxetil, dihydratecephalothin, moxalactam, loracarbef. mafate and chelating agents in an amount effective to synergistically enhance the therapeutic effect of the lysin enzyme.
- 21) The method according to claim 1, wherein said carrier comprises of distilled water, a saline solution, albumin, a serum, and any combinations thereof.
- 22) The method according to claim 1, wherein said carrier further comprises preservatives.
- 23) The method according to claim 22, wherein said preservatives comprise p-hydroxybenzoates.
- 24) The method according to claim 1, wherein said carrier comprises an isotonic solution for an injection, said isotonic solution comprising a compound selected from group consisting of sodium chloride, dextrose, mannitol, sorbitol, lactose, phosphate buffered saline, gelatin, albumin, a vasoconstriction agent and combinations
- 25) The method according to claim 24, wherein said further carrier further comprises DMSO.
- 26) A composition for the treatment of bacterial infections, comprising:
a therapeutic agent comprising an effective amount of at least one lytic enzyme produced by a bacteria infected with a bacteriophage specific for said bacteria and a carrier for the PARENTERAL delivery of said lytic enzyme to the site of the infection.
- 27) The composition according to claim 26, wherein the at least one lytic enzyme is for the treatment of Pseudomonas.
- 28) The composition according to claim 26, wherein the at least one lytic enzyme is for the treatment of Streptococcus
- 29) The composition according to claim 26, wherein the at least one lytic enzyme is for the treatment of Staphylococcus.
- 30) The composition according to claim 26, wherein the at least one lytic enzyme is for the treatment of Clostridium.
- 31) The composition according to claim 26, wherein said composition further comprises a buffer that maintains pH of the composition at a range between about 4.0 and about 9.0.
- 32) The composition according to claim 31, wherein the buffer maintains the pH of the composition at the range between about 5.5 and about 7.5.
- 33) The composition according to claim 31, wherein said buffer comprises a reducing reagent.
- 34) The composition according to claim 33, wherein said reducing reagent is dithiothreitol.
- 35) The composition according to claim 31, wherein said buffer comprises a metal chelating reagent.
- 36) The composition according to claim 35, wherein said metal chelating reagent is ethylenediaminetetracetic disodium salt.
- 37) The composition according to claim 31, wherein said buffer is a citrate-phosphate buffer.
- 38) The composition according to claim 26, further comprising a bactericidal or bacteriostatic agent as a preservative.
- 39) The composition according to claim 26, wherein said at least one lytic enzyme is lyophilized.
- 40) The composition according claim 26, further comprising administering a concentration of about 100 to about 500,000 active enzyme units per milliliter of fluid in the wet environment of the nasal or oral passages.
- 41) The composition according to claim 40, further comprising administering the concentration of about 1000 to about 100,000 active enzyme units per milliliter of fluid in the wet environment of the nasal or oral passages.
- 42) The composition according to claim 26, wherein said therapeutic agent is administered intravenously.
- 43) The composition according to claim 26, wherein said therapeutic agent is administered intramuscularly.
- 44) The method according to claim 26, wherein said therapeutic agent is administered subcutaneously.
- 45) The composition according to claim 26, wherein the therapeutic agent further comprises at least one complementary agent which potentiates the bactericidal activity of the lysine enzyme, said complementary agent being selected from the group consisting of penicillin, synthetic penicillins bacitracin, methicillin, cephalosporin, polymyxin, cefaclor. Cefadroxil, cefamandole nafate, cefazolin, cefixime, cefmetazole, cefonioid, cefoperazone, ceforanide, cefotanme, cefotaxime, cefotetan, cefoxitin, cefpodoxime proxetil, ceftazidime, ceftizoxime, ceftriaxone, cefriaxone moxalactam, cefuroxime, cephalexin, cephalosporin C, cephalosporin C sodium salt, cephalothin, cephalothin sodium salt, cephapirin, cephradine, cefuroximeaxetil, dihydratecephalothin, moxalactam, loracarbef. mafate and chelating agents in an amount effective to synergistically enhance the therapeutic effect of the lysin enzyme.
- 46) The composition according to claim 26, wherein said carrier comprises of distilled water, a saline solution, albumin, a serum, and any combinations thereof.
- 47) The composition according to claim 26, wherein said carrier further comprises preservatives.
- 48) The composition according to claim 47, wherein said preservatives comprise p-hydroxybenzoates.
- 49) The composition according to claim 26, wherein said carrier comprises an isotonic solution for an injection, said isotonic solution comprising a compound selected from group consisting of sodium chloride, dextrose, mannitol, sorbitol, lactose, phosphate buffered saline, gelatin, albumin, a vasoconstriction agent and combinations
- 50) The composition according to claim 26, wherein said carrier further comprises DMSO.
Parent Case Info
[0001] The following application is a continuation of Ser. No. 09/482,992, filed Jan. 14, 2000 which is a continuation in part of U.S. patent application Ser. No. 09/395,636, filed Sep. 14, 1999.
Continuations (1)
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Number |
Date |
Country |
Parent |
09482992 |
Jan 2000 |
US |
Child |
09908737 |
Jul 2001 |
US |
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
09395636 |
Sep 1999 |
US |
Child |
09482992 |
Jan 2000 |
US |