US2018071334A1PendingUtilityA1
Reducing the proliferation of carcinoma cells by administration of a poly-oxygenated metal hydroxide
Est. expiryMar 30, 2036(~9.7 yrs left)· nominal 20-yr term from priority
A61P 7/08A61K 33/08A61K 47/6823A61K 47/60A61K 33/06A61K 47/02A61K 9/08A61K 9/0026A61K 47/6923A61K 47/6921A61K 47/48861A61K 47/48215
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Claims
Abstract
A colloid or crystalline solution with the addition of poly-oxygenated metal hydroxide particles. The solution is configured to treat a condition of a mammal, including a human individual and an animal, including a depletion of hemoglobin and hemorrhagic shock. The solution can be intravenously administered. In some embodiments, the poly-oxygenated metal hydroxide is an aluminum poly-oxygenated hydroxide, such as O×66™. The poly-oxygenated metal hydroxide may have particles having a diameter of less than or equal to 1 um, and specifically having a diameter of less than or equal to 100 nm.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . An oxygen enabled solution, comprising:
a fluid; and a quantity of a poly-oxygenated metal hydroxide material disposed in the fluid and forming a colloid or crystalline solution.
2 . The oxygen enabled solution as specified in claim 1 wherein the poly-oxygenated metal hydroxide material is configured to provide bioavailable oxygen molecules to a mammal when administered to the mammal.
3 . The oxygen enabled solution as specified in claim 2 wherein the solution is a 75-90% colloid or crystalline solution with 10-25% addition of the poly-oxygenated metal hydroxide material.
4 . The oxygen enabled solution as specified in claim 3 wherein the solution is a 75-90% colloid with 10-25% addition of the poly-oxygenated metal hydroxide material.
5 . The oxygen enabled solution as specified in claim 3 wherein the fluid is phosphate buffered saline (PBS).
6 . The oxygen enabled solution as specified in claim 5 wherein the fluid is a lactated Ringers solution (LRS).
7 . The oxygen enabled solution as specified in claim 3 wherein the solution is a 75-90% crystalline solution with 10-25% addition of the poly-oxygenated metal hydroxide material.
8 . The oxygen enabled solution as specified in claim 8 wherein the fluid is phosphate buffered saline (PBS).
9 . The oxygen enabled solution as specified in claim 3 wherein the solution has a concentration range of 0.1 mg/l to 1000 mg/l.
10 . The oxygen enabled solution as specified in claim 1 wherein the poly-oxygenated metal hydroxide material comprises particles that are surface modified.
11 . The oxygen enabled solution as specified in claim 10 wherein the poly-oxygenated metal hydroxide material comprises nano-sized particles surface modified with polyethylene glycol (PEG).
12 . The oxygen enabled solution as specified in claim 11 wherein the solution is configured to resuscitate a mammal having a depletion of hemoglobin.
13 . The oxygen enabled solution as specified in claim 1 wherein the solution is configured to resuscitate a mammal in hemorrhagic shock.
14 . The oxygen enabled solution as specified in claim 12 wherein the solution comprises an oxygen resuscitative fluid configured to increase tissue interstitial fluid (ISF) oxygen, tension (PO 2 ) in a mammal when administered to the mammal.
15 . The oxygen enabled solution as specified in claim 13 wherein the solution comprises an oxygen resuscitative fluid configured to increase tissue interstitial fluid (ISF) oxygen tension (PO 2 ) in a mammal when administered to the mammal.
16 . The oxygen enabled solution as specified in claim 1 wherein the poly-oxygenated metal hydroxide material comprises a poly-oxygenated aluminum hydroxide.
17 . The oxygen enabled solution as specified in claim 1 wherein the poly-oxygenated metal hydroxide material comp s particles having a diameter of less than or equal to 100 um.
18 . The oxygen enabled solution as specified in claim 1 wherein the poly-oxygenated metal hydroxide material comprises particles having a diameter of less than or equal to 10 um.
19 . The oxygen enabled solution as specified in claim 1 wherein the solution is configured to be administered to a mammal intravenously.
20 . The oxygen enabled solution as specified in claim 1 wherein the mammal is a human individual.Join the waitlist — get patent alerts
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