US2010278910A1PendingUtilityA1
Rare earth metal compounds, methods of making, and methods of using the same
Assignee: SPECTRUM PHARMACEUTICALS INCPriority: May 24, 2002Filed: Jun 14, 2010Published: Nov 4, 2010
Est. expiryMay 24, 2022(expired)· nominal 20-yr term from priority
A61P 7/08A61P 43/00A61P 3/12A61P 3/00A61P 1/00C01F 17/247C01F 17/271B01J 20/28057C02F 1/281B01J 20/0207C09C 1/3661B01J 20/06C01P 2002/60C01P 2006/12C02F 2103/026B01J 20/3234C02F 1/001C01P 2006/90C02F 2101/105B01J 20/0288C02F 2101/20C01P 2006/14B01J 20/3078C01P 2004/61Y10T428/2982C01P 2004/03B01J 20/3236C01P 2004/80C01P 2002/72C02F 2101/103B01J 20/0277A61K 9/20A61K 9/10C07F 5/003A61K 9/48A61K 31/28A61K 9/0053A61K 9/08A61K 33/244A61K 33/24
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Claims
Abstract
Rare earth metal compounds, particularly lanthanum, cerium, and yttrium, are formed as porous particles and are effective in binding metals, metal ions, and phosphate. A method of making the particles and a method of using the particles is disclosed. The particles may be used in the gastrointestinal tract or the bloodstream to remove phosphate or to treat hyperphosphatemia in mammals. The particles may also be used to remove metals from fluids such as water.
Claims
exact text as granted — not AI-modified1 . A pharmaceutical composition comprising a La 2 O 2 CO 3 compound and a pharmaceutically acceptable vehicle or diluent.
2 . The pharmaceutical composition of claim 1 , wherein the La 2 O 2 CO 3 compound has a phosphate binding capacity of at least 45 mg phosphate per gram of compound.
3 . The pharmaceutical composition of claim 2 , wherein the La 2 O 2 CO 3 compound has a phosphate binding capacity of at least 50 mg phosphate per gram of compound.
4 . The pharmaceutical composition of claim 3 , wherein the La 2 O 2 CO 3 compound has a phosphate binding capacity of at least 75 mg phosphate per gram of compound.
5 . The pharmaceutical composition of claim 4 , wherein the La 2 O 2 CO 3 compound has a phosphate binding capacity of at least 100 mg phosphate per gram of compound.
6 . The pharmaceutical composition of claim 2 , wherein the La 2 O 2 CO 3 compound has a BET surface area of at least about 10 m 2 /g.
7 . The pharmaceutical composition of claim 6 , wherein the La 2 O 2 CO 3 compound has a BET surface area of at least about 20 m 2 /g.
8 . The pharmaceutical composition of claim 7 , wherein the La 2 O 2 CO 3 compound has a BET surface area of at least 35 m 2 /g.
9 . The pharmaceutical composition of claim 3 , wherein the La 2 O 2 CO 3 compound is made according to the following steps:
a) providing a lanthanum acetate or lanthanum chloride solution; b) mixing a carbonate solution with the lanthanum acetate or lanthanum chloride solution to form a precipitate comprising La 2 O 2 CO 3 ; c) filtering the precipitate to form a filter cake; and, d) drying the filter cake to provide the La 2 O 2 CO 3 compound.
10 . The pharmaceutical composition according to claim 9 , wherein the carbonate solution is mixed with the lanthanum acetate or lanthanum chloride solution at a temperature between about 30° C. and about 90° C.
11 . The pharmaceutical composition according to claim 10 , wherein the carbonate solution is mixed with the lanthanum acetate or lanthanum chloride solution at a temperature of 80° C.
12 . The pharmaceutical composition according to claim 10 , wherein the filter cake is dried at a temperature between about 400° C. and about 700° C.
13 . The pharmaceutical composition according to claim 1 , wherein the La 2 O 2 CO 3 compound and the vehicle or diluent are formulated to provide an orally ingestible form.
14 . The pharmaceutical composition according to claim 13 , wherein the orally ingestible form is selected from the group consisting of liquid solution, liquid suspension, tablet, capsule, and gelcap.
15 . The pharmaceutical composition of claim 1 , wherein the pharmaceutically acceptable vehicle or diluent is cellulose or carboxymethyl cellulose.Cited by (0)
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