US2006240118A1PendingUtilityA1
Pharmacologically active strong acid solutions
Est. expiryApr 6, 2021(expired)· nominal 20-yr term from priority
Inventors:David Martucci
A61P 9/12A61K 33/18A61P 35/00A61K 31/191A61K 31/42A61P 31/12A61K 45/06A61P 31/10A61K 31/185A61K 33/42A61P 31/04A61K 31/14A61P 31/00A61K 33/14A61P 25/00Y02A50/30
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Claims
Abstract
A composition and therapeutic methods therefore for pharmacologically strong acid solutions comprising a mixture of strong and weak acids.
Claims
exact text as granted — not AI-modified1 . A method of disinfecting comprising the administration or application of a composition comprising a mixture of three strong acids and three weak acids.
2 . The method of claim 1 wherein at least one (1) of the weak acids is hydrofluoric acid.
3 . The method of claim 1 wherein the acids are selected from the group consisting of sulfuric, hydrochloric, oxalic, phosphoric, citric and hydrofluoric acids.
4 . The method of claim 1 wherein the acids are present in the following concentrations by weight:
HCl
3-25%
H 2 C 2 O 4
0.1-10%
H 3 PO 4
3-10%
HF
1-30%
5 . The composition of claim 1 wherein the acids are present in the following concentrations by weight:
HCl
5-15%
H 2 C 2 O 4
0.15-2%
H 3 PO 4
2-7%
HF
2-7%
6 . The composition of claim 1 wherein the acids are present in the following approximate concentrations by weight:
HCl
11%
H 2 C 2 O 4
0.3%
H 3 PO 4
6%
H 2 SO 4
16%
HF
5%
H 8 C 6 O 7
0.3%
7 . The method of claim 1 wherein the acid composition further comprises glycerin.
8 . The composition of claim one wherein the composition has a pH of below 1 before dilution.
9 . The method of claim 1 wherein infection is reduced or prevented in a circulatory access port.
10 . The method of claim 9 wherein the acid composition is administered by means of the circulatory access port.
11 . The method of claim 9 wherein the acid composition is administered intravenously.
12 . The method of claim 9 wherein the circulatory access port is selected from the group consisting of: stents, peripheral catheters and central catheters.
13 . The method of claim 9 wherein the circulatory access port is a subclavian catheter.
14 . A method of treating infection in a patient in need thereof comprising the administration of an effective amount of a strong acid buffer comprising a mixture of three strong acids and three weak acids.
15 . The method of claim 14 wherein at least one (1) of the weak acids is hydrofluoric acid.
16 . The method of claim 14 wherein the acids are selected from the group consisting of sulfuric, hydrochloric, oxalic, phosphoric, citric and hydrofluoric acids.
17 . The method of claim 14 wherein the acids are present in the following concentrations by weight prior to dilution:
HCl
3-25%
H 2 C 2 O 4
0.1-10%
H 3 PO 4
3-10%
HF
1-30%
18 . The method of claim 14 wherein the acids are present in the following concentrations by weight prior to dilution:
HCl
>5-15%
H 2 C 2 O 4
0.15-2%
H 3 PO 4
2-7%
HF
2-7%
19 . A method of preventing growth of microorganisms in a substance comprising the addition of the composition of claim 1 to the substance.
20 . The method of claim 19 , wherein the substance comprises a tissue culture.Join the waitlist — get patent alerts
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