COMPOSITIONS AND METHODS FOR TREATING METABOLIC DISORDERS
Compositions and methods for improving the pharmacokinetics and reducing the risk of adverse events resulting from biguanide compound administration are provided, comprising administering delayed release formulations of such compounds having a lag phase release.
1 - 33 . (canceled)
34 . A delayed-release oral dosage form having
a core comprising a biguanide compound, or a salt thereof, and
an enteric coating surrounding the core that delays release of the biguanide compound after ingestion until reaching one or more regions of the intestine downstream of the duodenum,
wherein the oral dosage form releases less than 5%, 2%, or 1% of the biguanide compound in vitro in an aqueous medium of 0.1 N HCl for 120 minutes.
35 . The oral dosage form of claim 34 , wherein the oral dosage form releases less than 15%, 10%, 5%, 3%, 2%, or 1% of the biguanide compound in vitro after the dosage form contacts the aqueous medium of 0.1 N HCl for two hours and is subsequently transferred to an aqueous medium at a pH of about 6.8 for a lag phase of at least ten minutes, fifteen minutes, or twenty minutes.
36 . The oral dosage form of claim 34 , wherein the oral dosage form releases less than 5%, 2%, or 1% of the biguanide compound when transferred to an aqueous medium at pH 5.5 for at least one hour.
37 . The oral dosage form of claim 34 , wherein less than 25%, 20%, 15%, 10%, or 5% of the biguanide compound is released during a lag phase of at least ten or fifteen minutes at pH 6.8 after
two hours in an aqueous medium of 0.1 N HCl, and
30 minutes in an aqueous medium at pH 5.5.
38 . The oral dosage form of claim 34 , wherein less than 15%, 10%, or 5% of the biguanide compound is released after
two hours in an aqueous medium of 0.1 N HCl,
30 minutes in an aqueous medium at pH 5.5, and
a lag phase of at least ten or fifteen minutes at pH 6.8.
and at least 60% of the biguanide compound is released after the lag phase and within 60 minutes at pH 6.8,
and at least 90% of the biguanide compound is released within 90 to 120 minutes at pH 6.8.
39 . A delayed-release oral dosage form having
a core comprising a biguanide compound, or a salt thereof, and
an enteric coating surrounding the core that delays release of the biguanide compound after ingestion until reaching one or more regions of the intestine downstream of the duodenum,
wherein the oral dosage form releases less than 15% of the biguanide compound during a lag phase after the dosage form is contacted with an aqueous medium at a pH of about 6.8
and releases greater than 90% of the biguanide compound after contacting an aqueous medium at a pH of 6.8 for a total of 120 minutes,
wherein the lag phase is at least ten minutes.
40 . The oral dosage form of claim 39 , wherein the oral dosage form releases less than 5% of the biguanide compound during the lag phase after the dosage form is contacted with the aqueous medium at the pH of about 6.8.
41 . The oral dosage form of claim 40 , wherein the oral dosage form releases less than 2% of the biguanide compound during the lag phase after the dosage form is contacted with the aqueous medium at the pH of about 6.8.
42 . The oral dosage form of claim 39 , wherein the oral dosage form releases greater than 95% of the biguanide compound after contacting the aqueous medium at the pH of 6.8 for the total of 120 minutes.
43 . The oral dosage form of claim 42 , wherein the oral dosage form releases greater than 98% of the biguanide compound after contacting the aqueous medium at the pH of 6.8 for the total of 120 minutes.
44 . The oral dosage form of claim 39 , wherein the lag phase is at least 15 minutes.
45 . A delayed-release oral dosage form having
a core comprising a biguanide compound, or a salt thereof, and
an enteric coating surrounding the core that delays release of the biguanide compound after ingestion until reaching one or more regions of the intestine downstream of the duodenum,
wherein the enteric coating comprises a first polymer and a second polymer.
46 . The delayed-release oral dosage of claim 45 , wherein the second polymer dissolves at a lower pH than the first polymer.
47 . The delayed-release oral dosage form of claim 45 , wherein the first polymer is Eudragit FS.
48 . The delayed-release oral dosage form of claim 45 , wherein the second polymer is Eudragit L.
49 . The delayed-release oral dosage form of claim 45 , wherein the enteric coating comprises Eudragit FS and Eudragit L in about a 6:4 to about a 4:6 ratio.
50 . The delayed-release oral dosage form of claim 45 , wherein the enteric coating comprises about 40% Eudragit FS and about 60% Eudragit L.
51 . The delayed-release oral dosage form of claim 34 , wherein the biguanide compound or salt thereof is metformin or metformin hydrochloride.
52 . The delayed-release oral dosage form of claim 34 , wherein the oral dosage form is an enterically coated tablet or capsule.
53 . The delayed-release oral dosage form of claim 52 , wherein the oral dosage form is an enterically coated tablet.