STABILIZED MODIFIED RELEASE VITAMIN D FORMULATION AND METHOD OF ADMINISTERING SAME
A stabilized formulation for controlled release of a vitamin D compound is disclosed. The formulation can comprise one or both of 25-hydroxyvitamin D 2 and 25-hydroxyvitamin D 3 and a stabilizing compound. The stabilized formulations exhibit a stable dissolution profile following exposure to storage conditions and demonstrate improved pharmacokinetic parameters compared to unstabilized formulations.
1 . A pharmaceutical composition comprising a storage-stabilized formulation for sustained release of a vitamin D compound, wherein the storage-stabilized formulation comprises a mixture of: a vitamin D compound; and a stabilizing agent comprising selected from one or more of a cellulose ether, a poloxamer, a poly (ethylene oxide) polymer, a povidone polymer, and a fumed silica, in an amount of about 5 wt % to about 30 wt % of the storage-stabilized formulation, wherein the stabilizing agent maintains a difference of less than 30% between the amount of vitamin D compound released at any given time point after four hours during in vitro dissolution after two months exposure to storage conditions of 25° C. and 60% relative humidity and the amount released at the same dissolution time point during in vitro dissolution conducted prior to exposing the formulation to the storage conditions,
wherein the storage-stabilized formulation comprises a lipophilic matrix comprising the vitamin D compound.
2 . The pharmaceutical composition of claim 1 , wherein the lipophilic matrix comprises a wax.
3 . The pharmaceutical composition of claim 2 , wherein the lipophilic matrix comprises an emulsifier.
4 . The pharmaceutical composition of claim 3 , wherein the lipophilic matrix comprises a wax, an emulsifier, and an absorption enhancer.
5 . The pharmaceutical composition of claim 4 , wherein the wax comprises paraffin.
6 . The pharmaceutical composition of claim 1 , wherein the lipophilic matrix comprises a wax.
7 . The pharmaceutical composition of claim 1 , wherein the storage-stabilized formulation is an oral formulation for sustained release of the vitamin D compound in the gastrointestinal tract of a subject which ingests the formulation.
8 . The pharmaceutical composition of claim 1 , wherein the storage-stabilized formulation comprises a matrix that releasably binds and controllably releases the vitamin D compound.
9 . The pharmaceutical composition according to claim 1 , wherein the stabilizing agent comprises a poloxamer.
10 . The pharmaceutical composition according to claim 9 , wherein the poloxamer comprises polaxamer 407.
11 . The pharmaceutical composition according to claim 1 , wherein stabilizing agent comprises a poly (ethylene oxide) polymer.
12 . The pharmaceutical composition according to claim 1 , wherein the stabilizing agent comprises a povidone polymer.
13 . The pharmaceutical composition according to claim 1 , wherein the stabilizing agent comprises a fumed silica.
14 . The pharmaceutical composition according to claim 1 , wherein the vitamin D compound is one or more of vitamin D 3 (cholecalciferol), vitamin D 2 (ergocalciferol), 25-hydroxyvitamin D 3 , 25-hydroxyvitamin D 2 , 25-hydroxyvitamin D 4 , 25-hydroxyvitamin D 5 , 25-hydroxyvitamin D 7 , 1α,25-dihydroxyvitamin D 3 , 1α,25-dihydroxyvitamin D 2 , 1α,25-dihydroxyvitamin D 4 , 1,25-dihydroxy-19-nor-vitamin D 2 , and 1α-hydroxyvitamin D 3 .
15 . The pharmaceutical composition according to claim 14 , wherein the vitamin D compound comprises one or both of 25-hydroxyvitamin D 2 and 25-hydroxyvitamin D 3 .
16 . The pharmaceutical composition according to claim 1 , wherein the vitamin D compound comprises 25-hydroxyvitamin D 3 .
17 . The pharmaceutical composition of claim 1 , wherein the storage-stabilized formulation is in the form of a capsule, tablet, sachet, dragee, or suppository.
18 . The pharmaceutical composition of claim 17 , wherein the storage-stabilized formulation is in the form of a capsule.
19 . The pharmaceutical composition of claim 1 , wherein the formulation releases an amount of the vitamin D compound during in vitro dissolution after exposure to storage conditions for one month at 40° C. and 75% relative humidity that varies at any given dissolution time point after four hours compared to the amount released at the same dissolution time point during in vitro dissolution conducted prior to exposing the formulation to the storage conditions. by 30% or less.
20 . A method of vitamin D supplementation comprising administering to a subject the pharmaceutical composition of claim 1 .