US2006240119A1PendingUtilityA1
Pharmacologically active strong acid solutions
Est. expiryApr 6, 2021(expired)· nominal 20-yr term from priority
Inventors:David Martucci
A61P 9/12A61K 31/185A61K 33/42A61K 33/14A61P 31/10A61K 45/06A61P 31/04A61P 31/00A61K 31/191A61K 31/14A61P 35/00A61P 25/00A61K 33/18A61K 31/42A61P 31/12Y02A50/30
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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 pharmaceutical composition comprising a mixture of three strong acids and three weak acids.
2 . The composition of claim 1 wherein at least one (1) of the weak acids is hydrofluoric acid.
3 . The composition of claim 1 wherein the acids are selected from the group consisting of sulfuric, hydrochloric, oxalic, phosphoric, citric and hydrofluoric acids.
4 . The composition 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 composition of claim 1 further comprising glycerin.
8 . The composition of claim one wherein the composition has a pH of below 1.
9 . A method of treating a patient suffering from at least on of the following conditions selected from the group of: cancer related pain, cancer, high blood pressure, and infectious disease; comprising the internal administration of a composition comprising a mixture of HCl, H 2 SO 4 , H 2 C 2 O 4 , H 3 PO 4 , H 8 C 6 O 7 , and HF.
10 . The method of claim 9 wherein the patient is premedicated with a pharmaceutical product selected from the group consisting of: H 2 blockers, proton pump inhibitors, anti-inflammatories, antiemetics, and combinations thereof.
11 . The method of claim 9 wherein the cancer is selected from the group consisting of: endocrine, brain, ovarian, breast, venereal, prostate, skin, bone, lung, liver, stomach, colon, head and neck, blood or lymph, bone marrow, digestive tract, combinations thereof, chemotherapy resistant cancer and radiation resistant cancer.
12 . The method of claim 11 wherein the cancer is injected with the composition.
13 . The method of claim 9 in which cancer cells are selectively destroyed.
14 . The method of claim 9 wherein tumor markers are reduced.
15 . The method of claim 9 wherein the chromatin is destroyed in the cancer cells.
16 . The method of claim 9 wherein the infectious disease is selected from the group consisting of: bacteria, viruses and fungi.
17 . The method of claim 9 wherein the composition has a pH of below 1.
18 . The method of claim 9 wherein the composition is administered through a method selected from the group consisting of: orally, intravenously, intramuscularly, intraperitoneally sub-cutaneously, rectally, intra-urethrally, topically, intravesically, intravaginally, and combinations thereof.
19 . A method of treating cancer comprising the administration, to a patient in need thereof, an effective amount of a an acid buffer comprising:
HCl
5-15%
H 2 C 2 O 4
0.15-2%
H 3 PO 4
2-7%
HF
2-7%
wherein the pH is of the undiluted buffer is below 1.
20 . The method of claim 19 wherein the buffer is diluted in a pharmacologically acceptable solvent.Join the waitlist — get patent alerts
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