Polymorphic forms of ivabradine hydrochloride

Patent metadata

Field	Value
Publication number	US-9382209-B2
Application number	US-201514818236-A
Country	US
Kind code	B2
Filing date	Aug 4, 2015
Priority date	Nov 14, 2011
Publication date	Jul 5, 2016
Grant date	Jul 5, 2016

Abstract

Stable crystalline Form II and stable crystalline Form III of ivabradine hydrochloride and processes for their preparation are disclosed.

First claim

We claim:

1. A storage stable crystalline Form II of ivabradine hydrochloride having characteristic X-ray powder diffraction peaks at about 15.50°, 18.02°, 19.00°, 19.80°, 22.42°, 24.16°, and 25.46°±0.2° (2θ); comprising a packaging which includes placing crystalline ivabradine hydrochloride under nitrogen atmosphere in a non-permeable bag or placing crystalline ivabradine hydrochloride in polyethylene bag, optionally containing oxygen busters and sealing it or placing crystalline ivabradine hydrochloride in a triple laminated bag, optionally containing oxygen busters and sealing it or placing crystalline ivabradine hydrochloride in triple laminated bag inside a high density polyethylene (HDPE) container.

2. A storage stable crystalline Form II of ivabradine hydrochloride having characteristic X-ray powder diffraction peaks at about 15.50°, 18.02°, 19.00°, 19.80°, 22.42°, 24.16°, and 25.46°±0.2° (2θ) and has no detectable quantity of crystalline β, δ, γ, or amorphous forms after storage for 6 months at 40° C. and a relative humidity of 75% or at 25° C. and a relative humidity of 60%.

3. A storage stable crystalline Form II of ivabradine hydrochloride which is characterized by X-ray powder diffraction peaks at about 8.05°, 8.69°, 12.11°, 15.50°, 16.18°, 18.02°, 19.00°, 19.80°, 21.72°, 22.42°, 24.16°, 25.46° and 27.36°±0.2° (2θ).

4. A crystalline Form II of ivabradine hydrochloride having characteristic X-ray powder diffraction peaks at about 15.50°, 18.02°, 19.00°, 19.80°, 22.42°, 24.16°, and 25.46°±0.2° (2θ) comprising a process of packaging which includes:
(a) placing crystalline ivabradine hydrochloride under nitrogen atmosphere in a non-permeable bag and tying with a thread;
(b) placing the bag of step (a) inside a black color polyethylene bag, optionally containing oxygen busters and sealing it;
(c) placing the bag of step (b) inside a triple laminated bag, optionally containing oxygen busters and sealing it; and
(d) placing the sealed triple laminated bag inside a high density polyethylene (HDPE) container and sealing it.

5. The storage stable crystalline Form II of ivabradine hydrochloride according to claim 3 , which is further characterized by a differential scanning calorimetry (DSC) endothermic peak in the range of 197° C.-199° C.

6. The storage stable crystalline Form II of ivabradine hydrochloride according to claim 3 , which is prepared by the process comprising:
(a) providing a solution of ivabradine hydrochloride in one or more solvents by heating at about 30° C. to about 120° C.;
(b) obtaining the crystalline Form II of ivabradine hydrochloride by the removal of the solvents; and
(c) drying the crystalline Form II of ivabradine hydrochloride at about 40° C. to about 70° C., wherein the solvent is at least one member selected from the group consisting of methanol, ethanol, isopropanol, butanol, dimethylformamide, dimethylacetamide, dimethylsulfoxide, N-methylpyrrolidone, methyl ethyl ketone, acetone, methyl isobutyl ketone, ethyl acetate, butyl acetate, isopropyl acetate, acetonitrile, tetrahydrofuran, 2-methyltetrahydrofuran, 1,4-dioxane, water and mixtures thereof.

7. The process according to claim 6 , wherein the removal of the solvent comprises one or more of filtration, filtration under vacuum, decantation, centrifugation, distillation and distillation under vacuum.

8. The storage stable crystalline Form II of ivabradine hydrochloride according to claim 3 , which is prepared by the process comprising:
(a) contacting ivabradine base with hydrogen chloride in one or more first solvents to obtain ivabradine hydrochloride;
(b) obtaining a solution of ivabradine hydrochloride in one or more second solvents;
(c) optionally adding water to the solution, heating the solution and cooling to obtain the ivabradine hydrochloride wet-cake; and
(d) treating the wet-cake with one or more of first solvents to obtain the crystalline Form II of ivabradine hydrochloride.

9. The process according to claim 8 , wherein the first is at least one member selected from the group consisting of methanol, ethanol, isopropanol, butanol, dimethylformamide, dimethyl acetamide, dimethylsulfoxide, N-methylpyrrolidone, methyl ethyl ketone, acetone, methyl isobutyl ketone, ethyl acetate, butyl acetate, isopropyl acetate, acetonitrile, tetrahydrofuran, 2-methyl tetrahydrofuran, 1,4-dioxane, water, or mixtures thereof.

10. The process according to claim 8 , wherein the second solvent comprises one or more of dimethylformamide, dimethylacetamide, dimethylsulfoxide, N-methylpyrrolidone, acetonitrile, tetrahydrofuran, 2-methyltetrahydrofuran, 1,4-dioxane, water, or mixtures thereof.

11. A pharmaceutical composition comprising a therapeutically effective amount of crystalline Form II of ivabradine hydrochloride according to claim 3 together with one or more pharmaceutically acceptable carriers, excipients, or diluents.

12. The storage stable crystalline Form II of ivabradine hydrochloride according to claim 3 , having particle size distributions wherein the 10th volume percentile particle size (D10) is less than about 50 μm, the 50th volume percentile particle size (D50) is less than about 200 μm, or the 90th volume percentile particle size (D90) is less than about 400 μm, or any combination thereof.

13. The storage stable crystalline Form II of ivabradine hydrochloride according to claim 3 is stable after exposure to a relative humidity of 75% at 40° C. or 60% at 25° C. for a period of at least six months and is substantially free from known crystalline forms or an amorphous form.

Assignees

• Cadila Healthcare Ltd

Inventors

• Dwivedi Shriprakash Dhar
• Prasad Ashok
• Sharma Mukul Hariprasad
• Sharma Piyush Rajendra
• Parihar Jayprakash Ajitsingh

Classifications

• C07D223/16 Primary

  Benzazepines; Hydrogenated benzazepines · CPC title

• B65D31/04

  with multiple walls (B65D81/3881 takes precedence; for shock absorbing purposes B65D81/03) · CPC title

• Y10T428/2982

  Particulate matter [e.g., sphere, flake, etc.] · CPC title

• C07B2200/13

  Crystalline forms, e.g. polymorphs · CPC title

• C30B7/02

  by evaporation of the solvent · CPC title