US2011152231A1PendingUtilityA1
Methylsulfonylmethane (msm) for treatment of drug resistant microorganisms
Est. expiryOct 30, 2029(~3.3 yrs left)· nominal 20-yr term from priority
A61P 31/10A61P 31/00A61P 43/00A61P 31/16A61P 31/04C12N 1/38A61K 45/06C12P 7/06A61K 31/437A61K 9/0014A61K 31/10C12P 7/56A01N 41/10C12N 1/20A61K 31/43C12N 1/18A61K 31/431Y02E50/10Y02A50/30Y02E50/30
48
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Embodiments of the invention relate generally to the use of compositions comprising methylsulfonylmethane (MSM), and one or more therapeutic agents, for the treatment of drug-sensitive and drug resistant microorganisms. In several embodiments, such compositions are effective in treating drug resistant infectious diseases, for example, MRSA.
Claims
exact text as granted — not AI-modified1 . A method of inhibiting a drug resistant bacterial pathogen, comprising:
selecting a drug resistant bacterial pathogen; and contacting the bacterial pathogen with a composition comprising a therapeutically effective amount of MSM and a therapeutically effective amount of an agent that inhibits the drug-sensitive form of the drug resistant bacterial pathogen, thereby inhibiting a drug resistant bacterial pathogen.
2 . The method of claim 1 , wherein the bacterial pathogen is MRSA.
3 . The method of claim 1 , wherein the agent is a Beta-lactam antibiotic.
4 . The method of claim 3 , wherein the agent comprises penicillin derivatives, cephalosporins, penems, monobactams, carbapenems, Beta-lactamase inhibitors or a combination of two or more thereof.
5 . The method of claim 3 , wherein the agent comprises methicillin, oxacillin or penicillin.
6 . The method of claim 1 , wherein the effective amount of MSM is about 5-20% MSM, about 5-16% MSM, about 5-10% MSM, about 5-8% MSM, about 9-16% MSM or about 10-15% MSM.
7 . The method of claim 1 , wherein the effective amount of MSM is about 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or 16% MSM.
8 . The method of claim 1 , wherein the effective amount of MSM is about 10-16% MSM.
9 . The method of claim 1 , wherein the bacterial pathogen is on a surface.
10 . The method of claim 1 , wherein the bacterial pathogen is in a subject.
11 . The method of claim 1 , wherein the composition is administered topically.
12 . The method of claim 1 , wherein the composition is administered with an inhalant device.
13 . The method of claim 1 , wherein the bacterial pathogen is contacted with the composition for about 24, 36, 48, 60, 72, 84, 96, 108 or 120 hours.
14 . The method of claim 1 , wherein the composition comprises 0-5% sodium chloride.
15 . A method of sensitizing a drug resistant bacterial pathogen to a drug the bacterial pathogen is resistant to, comprising
selecting a drug resistant bacterial pathogen; and contacting the bacterial pathogen with a composition comprising a therapeutically effective amount of MSM, thereby sensitizing the drug resistant bacterial pathogen to the drug the bacterial pathogen is resistant to.
16 . The method of claim 15 , wherein the bacterial pathogen is MRSA.
17 . The method of claim 15 , wherein the agent is a Beta-lactam antibiotic.
18 . The method of claim 17 , wherein the agent comprises penicillin derivatives, cephalosporins, penems, monobactams, carbapenems, Beta-lactamase inhibitors or a combination of two or more thereof.
19 . The method of claim 17 , wherein the agent comprises methicillin, oxacillin or penicillin.
20 . The method of claim 15 , wherein the effective amount of MSM is about 5-20% MSM, about 5-16% MSM, about 5-10% MSM, about 5-8% MSM, about 9-16% MSM or about 10-15% MSM.
21 . The method of claim 15 , wherein the effective amount of MSM is about 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or 16% MSM.
22 . The method of claim 15 , wherein the effective amount of MSM is about 10-16% MSM.
23 . The method of claim 15 , wherein the bacterial pathogen is on a surface.
24 . The method of claim 15 , wherein the bacterial pathogen is in a subject.
25 . The method of claim 15 , wherein the composition is administered topically.
26 . The method of claim 15 , wherein the composition is administered with an inhalant device.
27 . The method of claim 15 , wherein the bacterial pathogen is contacted with the composition for about 24, 36, 48, 60, 72, 84, 96, 108 or 120 hours.
28 . The method of claim 15 , wherein the composition comprises 0-5% sodium chloride.
29 . A method of inhibiting a drug-sensitive bacterial pathogen from developing drug resistance, comprising:
selecting a drug sensitive bacterial pathogen; and contacting the drug-sensitive bacterial pathogen with a composition comprising a therapeutically effective amount of MSM and a therapeutically effective amount of an agent that inhibits the drug-sensitive bacterial pathogen, thereby inhibiting the drug-sensitive bacterial pathogen from developing drug resistance.
30 . The method of claim 29 , wherein the bacterial pathogen is Staphylococcus aureus.
31 . The method of claim 29 , wherein the agent is a Beta-lactam antibiotic.
32 . The method of claim 31 , wherein the agent comprises penicillin derivatives, cephalosporins, penems, monobactams, carbapenems, Beta-lactamase inhibitors or a combination of two or more thereof.
33 . The method of claim 31 , wherein the agent comprises methicillin, oxacillin or penicillin.
34 . The method of claim 29 , wherein the effective amount of MSM is about 5-20% MSM, about 5-16% MSM, about 5-10% MSM, about 5-8% MSM, about 9-16% MSM or about 10-15% MSM.
35 . The method of claim 29 , wherein the effective amount of MSM is about 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or 16% MSM.
36 . The method of claim 29 , wherein the effective amount of MSM is about 10-16% MSM.
37 . The method of claim 29 , wherein the bacterial pathogen is on a surface.
38 . The method of claim 29 , wherein the bacterial pathogen is in a subject.
39 . The method of claim 29 , wherein the composition is administered topically.
40 . The method of claim 29 , wherein the composition is administered with an inhalant device.
41 . The method of claim 29 , wherein the bacterial pathogen is contacted with the composition for about 24, 36, 48, 60, 72, 84, 96, 108 or 120 hours.
42 . The method of claim 29 , wherein the composition comprises 0-5% sodium chloride.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.