METHODS FOR TREATING BACTERIAL INFECTION
This invention relates to methods for treating bacterial infection, which methods find utility in the treatment of, for example, infected ulcers, optionally infected diabetic ulcers. In particular, this invention relates to treating bacterial infection, for example, infected diabetic ulcers by topical administration of at least one aminoglycoside antibiotic at the site of infection, in combination with at least one antibacterial agent, which antibacterial agent is administered remote from the site of infection, preferably administered systemically. In a particular embodiment, the present invention relates to a composition for use in treating bacterial infection, the composition comprising gentamicin sulphate (a water-soluble broad-spectrum aminoglycoside antibiotic) uniformly dispersed in a type-I collagen matrix; incombination with at least one systemically-administered antibacterial agent. The present invention provides bactericidal activity against most strains of aerobic gram-negative and gram-positive and facultative anaerobic gram-negative pathogens, including methicillin-resistant Staphylococcus aureus.
1 . (canceled)
2 . A method of treating bacterial infection at a site of infection, the method comprising the step of topically administering at least one aminoglycoside antibiotic at the site of infection; and administering at least one antibacterial agent, which at least one antibacterial agent is administered remote from the site of infection.
3 . The method according to claim 2 , wherein the at least one aminoglycoside antibiotic is gentamicin, or a salt thereof.
4 . The method according to claim 2 , wherein the at least one aminoglycoside antibiotic is gentamicin sulphate.
5 . The method according to claim 4 , wherein the gentamicin sulphate is administered in an equivalent amount of 32.5-130.0 mg of gentamicin.
6 . The method according to claim 2 , wherein the at least one aminoglycoside antibiotic is administered topically as a composition comprising at least one aminoglycoside antibiotic and a polymeric matrix comprising collagen.
7 . The method according to claim 2 , wherein the topical administering step comprises the step of topically applying the composition comprising the at least one aminoglycoside antibiotic and the polymeric matrix comprising collagen to the site of infection.
8 . The method according to claim 6 , wherein the at least one aminoglycoside antibiotic is uniformly, or homogenously, dispersed throughout the polymeric matrix comprising collagen.
9 . (canceled)
10 . The method according to claim 6 ; wherein the polymeric matrix comprises Type-I collagen.
11 . The method according to claim 6 ; wherein the at least one aminoglycoside antibiotic is uniformly (or homogenously) dispersed throughout the polymeric matrix in an amount of 0.1-10.0 mg/cm 2 of polymeric matrix.
12 . The method according to claim 11 ; wherein the at least one aminoglycoside antibiotic is gentamicin sulphate and is uniformly, or homogenously, dispersed throughout the polymeric matrix in an amount equivalent to gentamicin of 1.3 mg/cm 2 of polymeric matrix.
13 . The method according to claim 11 ; wherein the at least one aminoglycoside antibiotic is gentamicin sulphate and is uniformly, or homogenously, dispersed throughout the polymeric matrix in an amount equivalent to gentamicin of 5.2 mg/cm 2 of polymeric matrix.
14 . The method according to claim 6 ; wherein the polymeric matrix has a two-dimensional surface area of 6.25-100 cm 2 .
15 . The method according to claim 2 ; wherein the at least one aminoglycoside antibiotic is gentamicin, or a salt thereof, and is administered at least once daily in an amount equivalent to gentamicin of 32.5-130.0 mg.
16 . The method according to claim 2 ; wherein the at least one aminoglycoside antibiotic is gentamicin, or a salt thereof, and is administered at least once weekly in an amount equivalent to gentamicin of 32.5-130.0 mg.
17 . (canceled)
18 . The method according to claim 2 ; wherein the at least one antibacterial agent is administered by a route selected from oral and parenteral administration.
19 . (canceled)
20 . The method according to claim 2 ; wherein the at least one antibacterial agent is selected from nitroimidazole compounds, lincosamides, sulfonamide compounds, dihydrofolate reductase inhibitors, lipopeptide molecules, tetracycline compounds, compounds comprising a beta-lactam moiety, glycopeptides, oxazolidinones, and quinolones.
21 . The method according to claim 20 ; wherein the at least one antibacterial agent is a fluoroquinolone.
22 . The method according to claim 21 ; wherein the fluoroquinolone is ciprofloxacin, moxifloxacin, ofloxacin, balofloxacin, grepafloxacin, levofloxacin, pazufloxacin, sparfloxacin, temafloxacin, or tosulfloxacin.
22 . The method according to claim 2 , wherein the at least one aminoglycoside antibiotic is co-administered in combination with the at least one antibacterial agent.
24 . The method according to claim 2 , wherein the at least one antibacterial agent is administered prior to, and is co-administered in combination with the at least one aminoglycoside antibiotic.
25 . The method according to claim 2 ; wherein the bacterial infection is by an aerobic gram-negative bacteria, an aerobic gram-positive bacteria, or an anaerobic gram-negative bacteria.
26 . (canceled)
27 . A method of treating infected ulcers, the method comprising the step of topically administering at least one aminoglycoside antibiotic at the site of infection; and administering at least one antibacterial agent, which at least one antibacterial agent is administered remote from the site of infection.
28 . The method according to claim 27 , wherein the diabetic ulcer is a diabetic lower limb ulcer.
29 - 31 . (canceled)
32 . The method according to claim 16 , wherein the gram-positive bacteria is a Streptococcus , a Staphylococcus , an Enterococcus , a Gram positive cocci, or a Peptostreptococcus ; and the gran-negative bacteria is an Acubetibacter , an Aocaligenes , a Bacteroides , a Burkholderia , an Enterobacter , a Klebsiella , a Morganella , an Ochrobactrum , a Proteus , a Providencia , a Pseudomonas , or a Serratia.