Nanoparticulate and controlled release compositions comprising nilvadipine
The present invention provides a composition comprising nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, useful in the treatment and prevention of hypertension or related cardiovascular disorders. In one embodiment, the composition comprises nanoparticulate particles comprising nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, and at least one surface stabilizer. The nanoparticulate particles have an effective average particle size of less than about 2000 nm. In another embodiment, the composition comprises a modified release composition that, upon administration to a patient, delivers nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, in a bimodal, multimodal or continuous manner. The invention also relates to dosage forms containing such compositions, and to methods for the treatment and prevention of hypertension or related cardiovascular disorders.
1 . A stable nanoparticulate composition comprising: (A) particles comprising nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, said particles having an effective average particle size of less than about 2000 nm in diameter; and (B) at least one surface stabilizer.
2 . The composition of claim 1 , wherein said particles are in a crystalline phase, an amorphous phase, a semi-crystalline phase, a semi amorphous phase, or a mixture thereof.
3 . The composition of claim 1 further comprising one or more pharmaceutically acceptable excipients, carriers, or a combination thereof.
4 . The composition of claim 1 , wherein the surface stabilizer is selected from the group consisting of a non-ionic surface stabilizer, an anionic surface stabilizer, a cationic surface stabilizer, a zwitterionic surface stabilizer, and an ionic surface stabilizer.
5 . The composition of claim 1 , wherein the composition comprises:
(a) about 50 to about 500 g/kg nilvadipine;
(b) about 10 to about 70 g/kg hypromellose;
(c) about 1 to about 10 g/kg docusate sodium;
(d) about 100 to about 500 g/kg sucrose;
(e) about 1 to about 40 g/kg sodium lauryl sulfate;
(f) about 50 to about 400 g/kg lactose monohydrate;
(g) about 50 to about 300 g/kg silicified microcrystalline cellulose;
(h) about 20 to about 300 g/kg crospovidone; and
(i) about 0.5 to about 5 g/kg magnesium stearate.
6 . The composition of claim 5 , further comprising a coating agent.
7 . The composition of claim 1 , wherein the composition comprises:
(a) about 100 to about 300 g/kg nilvadipine;
(b) about 30 to about 50 g/kg hypromellose;
(c) about 0.5 to about 10 g/kg docusate sodium;
(d) about 100 to about 300 g/kg sucrose;
(e) about 1 to about 30 g/kg sodium lauryl sulfate;
(f) about 100 to about 300 g/kg lactose monohydrate;
(g) about 50 to about 200 g/kg silicified microcrystalline cellulose;
(h) about 50 to about 200 g/kg crospovidone; and
(i) about 0.5 to about 5 g/kg magnesium stearate.
8 . The composition of claim 7 , further comprising a coating agent.
9 . The composition of claim 1 , additionally comprising one or more active compounds useful for the prevention and treatment of hypertension or a related cardiovascular disorder.
10 . The composition of claim 1 wherein said particles contain a reservoir which contains nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, said reservoir being enclosed by a semi-permeable membrane which allows for water to be imbibed into said particles, thus generating pressure which forces said nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, out of said particles.
11 . The composition of claim 10 wherein said reservoir comprises also an osmotic agent.
12 . A method of preparing the composition of claim 1 comprising contacting particles comprising said nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, with at least one surface stabilizer for a period of time and under conditions sufficient to provide a nanoparticulate composition comprising nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, having an effective average particle size of less than about 2000 nm in diameter.
13 . A method of preventing and/or treating hypertension and/or a related cardiovascular disorder comprising administering a composition according to claim 1 .
14 . A pharmaceutical composition comprising a first component of active ingredient-containing particles and at least one subsequent component of active ingredient-containing particles, wherein at least one of said components comprises particles wherein nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, is the active ingredient and at least one of said components further comprises a modified release coating, a modified release matrix material, or both, such that the composition, following oral delivery to a subject, delivers the active ingredient in a continuous, bimodal or multimodal manner.
15 . The composition of claim 14 wherein said particles comprising nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, comprise nanoparticles which comprise nilvadipine, or a salt, derivative, prodrug, or polymorph thereof.
16 . The composition of claim 14 wherein said particles comprising nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, are nanoparticles which comprise nilvadipine, or a salt, derivative, prodrug, or polymorph thereof.
17 . The composition of claim 14 wherein each component comprises particles in which nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, is the active ingredient.
18 . The composition of claim 14 , wherein the first component comprises an immediate release component and at least one subsequent component comprises a modified release component.
19 . The composition of claim 14 , wherein the active ingredient-containing particles are erodable.
20 . The composition of claim 14 wherein said composition further comprises an enhancer.
21 . A dosage form comprising the composition of claim 14 .
22 . The dosage form of claim 21 comprising a blend of active ingredient-containing particles contained within a hard gelatin or soft gelatin capsule.
23 . The dosage form of claim 21 , wherein the active ingredient-containing particles are in the form of mini-tablets and the capsule contains a mixture of said mini-tablets.
24 . The dosage form of claim 21 in the form of tablet.
25 . The dosage form of claim 21 wherein the particles containing nilvadipine, or a salt, derivative, prodrug, or polymorph thereof, are provided in a rapidly dissolving dosage form.
26 . The dosage form of claim 24 wherein the tablet is a fast-melt tablet.
27 . A method for preventing and/or treating hypertension or a related cardiovascular disorder comprising the step of administering a therapeutically effective amount of the composition of claim 14 .
28 . The composition of claim 14 wherein the modified-release coating comprises a pH-dependent polymer coating for releasing a pulse of the active ingredient in said patient following a time delay of about 6 to about 12 hours after administration of said composition to said patient.