Killing antibiotic-resistant bacteria with a formulation that is safe for oral administration
Abstract
The teachings provided herein generally relate to binding systems that kill antibiotic-resistant bacteria, wherein the binding systems are safe for oral administration. More particularly, the systems taught herein include methods of treating a subject having an antibiotic-resistant bacterial infection, comprising administering an effective amount of a binding system to a subject having an antibiotic-resistant bacterial infection. The binding system can be administered orally in a formulation having, for example, a tannin having a gallic acid ester and hydrogen peroxide in a pharmaceutically acceptable carrier.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A method of killing an antibiotic-resistant bacteria, comprising:
contacting an effective amount of a binding system to a subject having an antibiotic-resistant bacteria, the binding system comprising a combination of: a tannin having a gallic acid ester and a molecular weight ranging from about 500 Daltons to about 4000 Daltons; and, hydrogen peroxide;
wherein,
the hydrogen peroxide is combined with the tannin at a weight ratio that ranges from about 1:1000 to about 10:1 of the tannin to the hydrogen peroxide; and,
the combination is effective at killing the antibiotic-resistant bacteria.
2 . The method of claim 1 , wherein the binding system further comprises an ellagitannin.
3 . The method of claim 1 , wherein the binding system further comprises a gallotannin.
4 . The method of claim 1 , wherein the binding system further comprises a punicalagin.
5 . The method of claim 1 , wherein the binding system further comprises a catechin.
6 . The method of claim 1 , wherein the antibiotic-resistant bacteria is a methicillin resistant staphylococcus aureus (MRSA).
7 . The method of claim 1 , wherein the antibiotic-resistant bacteria is an antibiotic-resistant Klebsiella pneumonia.
8 . The method of claim 1 , wherein the antibiotic-resistant bacteria is an antibiotic-resistant bacteria selected from the group consisting of Escherichia coli, Salmonella enterica serotype typhimurium, Staphylococcus aureus , a methicillin resistant staphylococcus aureus (MRSA), Pseudomonas aeruginosa, Listeria monocytogenes, Pasteurella multocida, Proteus vulgaris, Klebsiella pneumonia, Bacillus cereus, Bordetella bronchiseptica.
9 . The method of claim 1 , wherein the antibiotic-resistant bacteria is an antibiotic-resistant Salmonella enterica serotype typhimurium.
10 . The method of claim 1 , wherein the antibiotic-resistant bacteria is an antiobiotic-resistant Pseudomonas aeruginosa.
11 . A formulation for killing antibiotic-resistant bacteria, comprising a combination of:
a tannin having a gallic acid ester and a molecular weight ranging from about 500 Daltons to about 4000 Daltons; hydrogen peroxide; and, a pharmaceutically acceptable carrier; wherein, the binding system formulation is created by combining the hydrogen peroxide with the tannin at a weight ratio that ranges from about 1:1000 to about 10:1 of the tannin to the hydrogen peroxide.
12 . The formulation of claim 11 , wherein the binding system further comprises an ellagitannin.
13 . The formulation of claim 11 , wherein the binding system further comprises a gallotannin.
14 . The formulation of claim 11 , wherein the binding system further comprises a punicalagin.
15 . The formulation of claim 11 , wherein the binding system further comprises a catechin.
16 . A method of treating a subject having an antibiotic-resistant bacterial infection, comprising:
administering an effective amount of a binding system to a subject having an antibiotic-resistant bacterial infection, the binding system comprising a combination of:
a tannin having a gallic acid ester and a molecular weight ranging from about 500 Daltons to about 4000 Daltons; and,
hydrogen peroxide;
wherein,
the hydrogen peroxide is combined with the ellagitannin at a weight ratio that ranges from about 1:1000 to about 10:1 of the an extract to the hydrogen peroxide; and,
the administering is effective at killing the antibiotic-resistant bacteria.
17 . The method of claim 16 , wherein the binding system further comprises an ellagitannin.
18 . The method of claim 16 , wherein the binding system further comprises a gallotannin.
19 . The method of claim 16 , wherein the binding system further comprises a punicalagin.
20 . The method of claim 16 , wherein the binding system further comprises a catechin.
21 . The method of claim 16 , wherein the antibiotic-resistant bacteria is a methicillin resistant staphylococcus aureus (MRSA).
22 . The method of claim 16 , wherein the antibiotic-resistant bacteria is an antibiotic-resistant Klebsiella pneumonia.
23 . The method of claim 16 , wherein the antibiotic-resistant bacteria is an antibiotic-resistant bacteria selected from the group consisting of Escherichia coli, Salmonella enterica serotype typhimurium, Staphylococcus aureus , a methicillin resistant staphylococcus aureus (MRSA), Pseudomonas aeruginosa, Listeria monocytogenes, Pasteurella multocida, Proteus vulgaris, Klebsiella pneumonia, Bacillus cereus, Bordetella bronchiseptica.
24 . The method of claim 16 , wherein the antibiotic-resistant bacteria is an antibiotic-resistant Salmonella enterica serotype typhimurium.
25 . The method of claim 16 , wherein the antibiotic-resistant bacteria is an antiobiotic-resistant Pseudomonas aeruginosa.Join the waitlist — get patent alerts
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