US2004071770A1PendingUtilityA1
Method to reduce free radical-mediated tissue damage induced by caustic gas exposure using an antioxidant composition
Priority: Dec 11, 1992Filed: Sep 17, 2003Published: Apr 15, 2004
Est. expiryDec 11, 2012(expired)· nominal 20-yr term from priority
Inventors:Milton G. Smith
A61K 31/355A61K 2800/522A61K 33/06A61K 38/063A61K 8/23A61K 8/19A61K 8/675A61K 33/32A61K 8/31A61K 31/015A61Q 17/00A61K 45/06A61K 33/30A61K 8/14A61K 8/678A61K 33/34A61P 29/00A61K 31/375A61K 8/64A61K 9/127A61K 31/455A61K 8/27A61K 8/676A61K 33/24
46
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
A free radical quenching composition is disclosed comprising a liposome containing at least two antioxidants selected from the following group: beta-carotene, vitamin E, vitamin C, glutathione, niacin, and optionally at least one trace metal (Zn, Se, Cr, Cu, Mn). Also disclosed is a method for reducing the undesirable side effects of free radicals in a mammal by administering to a mammal in need of such antioxidants an effective amount of liposomes containing at least two antioxidants.
Claims
exact text as granted — not AI-modifiedWhat is claimed:
1 . A free radical quenching composition comprising a liposome containing at least two members selected from the group consisting of beta-carotene, vitamin E, vitamin C, glutathione, niacin, and optionally at least one trace metal.
2 . The composition according to claim 1 , wherein said composition comprises beta-carotene, vitamin E, vitamin C, glutathione, and niacin, and optionally at least one trace metal.
3 . The composition according to claim 1 , wherein said trace metal is Zn, Se, Cr, Cu, or Mn.
4 . A cream containing the composition according to claim 1 and a pharmaceutically acceptable carrier.
5 . A lotion containing the composition according to claim 1 and a pharmaceutically acceptable carrier.
6 . An injectable solution containing the composition according to claim 1 and a pharmaceutically acceptable carrier.
7 . A tablet containing the composition according to claim 1 and a pharmaceutically acceptable carrier.
8 . A method of delivering non-enzymatic antioxidants, comprising administering to a site in need thereof an effective amount of the composition according to claim 1 or 2 and optionally a pharmaceutically acceptable carrier.
9 . A method for reducing the undesirable side effects of free radicals in a mammal, comprising administering to a mammal in need thereof an effective amount of the composition according to claim 1 and optionally a pharmaceutically acceptable carrier.
10 . A method of treating inflammatory conditions in a mammal, comprising administering to a mammal in need thereof an effective amount of the composition according to claim 1 and optionally a pharmaceutically acceptable carrier.
11 . A method of increasing the level of antioxidants in mammalian cells, comprising administering to mammalian cells in need thereof an effective amount of the composition according to claim 1 and optionally a pharmaceutically acceptable carrier.
12 . A method of increasing the level of antioxidants in mammalian cells and/or organs which are ex situ awaiting transplantation, comprising administering to mammalian cells and/or organs in need thereof an effective amount of the composition according to claim 1 and optionally a pharmaceutically acceptable carrier.
13 . A method of treating inflammatory conditions in a mammal, comprising (a) diagnosing the clinical condition of said mammal, (b) administering to said mammal in need thereof an effective amount of the composition according to claim 1 and optionally a pharmaceutically acceptable carrier, and (c) monitoring the clinical condition of said mammal.Join the waitlist — get patent alerts
Track US2004071770A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.