Controlled release compositions comprising a combination of isosorbide dinitrate and hydralazine hydrochloride
The invention relates to a controlled release composition comprising a combination of isosorbide dinitrate and hydralazine, such as hydralazine hydrochloride, that in operation delivers the drug in a pulsed or multi-modal manner for the treatment of angina, ischaemic heart disease, arterial hypertension and related disease conditions. Preferably, the isosorbide dinitrate and hydralazine hydrochloride can be released from the dosage form in an erodable, diffusion and/or osmotic-controlled release profile.
1. A hard gelatin capsule comprising:
a population of isosorbide dinitrate immediate-release beads comprising: isosorbide dinitrate in an amount from about 2.5 mg to about 30 mg, mannitol, povidone, silicon dioxide, and sugar spheres;
a population of isosorbide dinitrate sustained-release beads comprising: isosorbide dinitrate in an amount from about 2.5 mg to about 30 mg, mannitol, povidone, silicon dioxide, sugar spheres, triethyl citrate, an ammonio methacrylate copolymer, and a methacrylic acid copolymer;
a population of hydralazine immediate-release beads comprising: hydralazine, or a salt thereof, in an amount from about 0.5 mg to about 60 mg, povidone, silicon dioxide, sugar spheres, and citric acid; and
a population of hydralazine sustained-release beads comprising: hydralazine, or a salt thereof, in an amount from about 2.5 mg to about 30 mg, povidone, silicon dioxide, sugar spheres, citric acid, an ammonio methacrylate copolymer, a methacrylic acid copolymer, and triethyl citrate.
2. The capsule of claim 1 wherein the hydralazine is hydralazine hydrochloride.
3. A method for the treatment of a patient having angina, ischaemic heart disease, or arterial hypertension comprising orally administering to the patient a therapeutically effective amount of the capsule of claim 1 .
4. A method for the treatment of a patient having angina, ischaemic heart disease, or arterial hypertension comprising orally administering to the patient a therapeutically effective amount of the capsule of claim 2 .
5. The capsule of claim 1 , wherein the populations of isosorbide dinitrate immediate-release beads and hydralazine immediate-release beads comprise about 10% to about 60% of the total population of beads.
6. The capsule of claim 1 , wherein the populations of isosorbide dinitrate sustained-release beads and hydralazine sustained-release beads comprise about 30% to about 90% of the total population of beads.