US2015064285A1PendingUtilityA1

Slow release magnesium composition and uses thereof

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Assignee: MAGCEUTICS INCPriority: Jul 1, 2009Filed: Mar 21, 2014Published: Mar 5, 2015
Est. expiryJul 1, 2029(~3 yrs left)· nominal 20-yr term from priority
A61K 9/20A61K 33/14A61K 31/194A61K 31/191A61K 31/195A61K 9/284A61P 3/02A61K 9/2027A61K 31/28A61K 33/06A61K 31/198A61P 25/28
67
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Claims

Abstract

The present invention provides compositions that contain magnesium and threonate, or a threonate precursor molecule, formulated for extended or modified release to provide physiological concentrations over a desired time period. The extended release or modified release form is particularly useful in providing Mg to a subject while avoiding adverse side effects such as diarrhea.

Claims

exact text as granted — not AI-modified
1 . An oral dosage form comprising magnesium (Mg) and threonate (T) in a controlled release formulation, wherein the magnesium of said controlled release formulation has an in vitro dissolution profile in a dissolution medium, and wherein said dissolution profile ranges between less than or equal to 35% in 1 hour, and greater than or equal to 70% in 4 to 12 hours as measured using a USP type II (paddle) dissolution system at 75 rpm, at a temperature of 37° C. 
     
     
         2 . The oral dosage form of  claim 1 , wherein said magnesium and threonate in said oral dose form is encapsulated in a tablet. 
     
     
         3 . The oral dosage form of  claim 1 , wherein at least a portion of said magnesium (Mg) and threonate (T) are complexed in a salt form of MgT 2 . 
     
     
         4 . The oral dosage form of  claim 1 , wherein at least a portion of said magnesium (Mg) and threonate (T) are complexed in a salt form of MgT 2  present in an amount equal to at least about 20 mg of Mg by weight. 
     
     
         5 . The oral dosage form of  claim 1 , wherein said oral dosage form comprises at least 10 mg of elemental magnesium. 
     
     
         6 . The oral dosage form of  claim 1 , wherein said oral dosage form comprises at least 20 mg of elemental magnesium. 
     
     
         7 . The oral dosage form of  claim 1 , wherein said magnesium (Mg) is present in an amount greater than about 1% by weight. 
     
     
         8 . The oral dosage form of  claim 1 , wherein said magnesium (Mg) is present in an amount greater than about 5% by weight. 
     
     
         9 . (canceled) 
     
     
         10 . (canceled) 
     
     
         11 . (canceled) 
     
     
         12 . The oral dosage form of  claim 1  further comprising one or more antioxidant selected from the group consisting of resveratrol, ellagic acid, quercetin, lipoic acid and vitamin C. 
     
     
         13 . (canceled) 
     
     
         14 . The oral dosage form of  claim 1 , wherein said oral dose form further comprises magnesium and threonate in an immediate release formulation that releases at least 80% of the magnesium from said immediate release formulation within 1 hour as measured in a dissolution medium using a USP type II (paddle) dissolution system at 75 rpm, at a temperature of 37° C. 
     
     
         15 . (canceled) 
     
     
         16 . (canceled) 
     
     
         17 . (canceled) 
     
     
         18 . (canceled) 
     
     
         19 . (canceled) 
     
     
         20 . (canceled) 
     
     
         21 . (canceled) 
     
     
         22 . (canceled) 
     
     
         23 . The oral dosage form of  claim 1 , wherein upon administering said oral dosage form to a Sprague-Dawley rat at a dosage of equal to or less than 75 mg/kg/day yields an incidence of diarrhea of less than 20%. 
     
     
         24 . (canceled) 
     
     
         25 . The oral dosage form of  claim 1 , wherein the magnesium of said controlled release formulation has a dissolution rate of magnesium of about 40-80% within about 6 to 10 hours. 
     
     
         26 . The oral dosage form of  claim 23 , wherein said oral dosage form provides for an incidence of diarrhea of less than 50% when administered at a dosage of equal to or less than about 130 mg/kg/day. 
     
     
         27 . (canceled) 
     
     
         28 . (canceled) 
     
     
         29 . (canceled) 
     
     
         30 . (canceled) 
     
     
         31 . (canceled) 
     
     
         32 . (canceled) 
     
     
         33 . The oral dosage form of  claim 1 , wherein upon administering said oral dosage form to a subject at least about 50% of said administered magnesium is absorbed in said subject, or at least 30% of the magnesium administered to the subject is retained over a period of at least two days when said oral dosage form is administered at a dose of 20 mg/kg/day or higher. 
     
     
         34 . (canceled) 
     
     
         35 . (canceled) 
     
     
         36 . (canceled) 
     
     
         37 . (canceled) 
     
     
         38 . (canceled) 
     
     
         39 . A method of treating a condition related to magnesium deficiency comprising administering to a subject in need thereof an oral dosage form of  claim 1 . 
     
     
         40 . (canceled) 
     
     
         41 . (canceled) 
     
     
         42 . (canceled) 
     
     
         43 . (canceled) 
     
     
         44 . (canceled) 
     
     
         45 . (canceled) 
     
     
         46 . (canceled)

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