Crystalline rotigotine base and preparation process therefor
View Patent ↗An isolated and pure crystalline rotigotine base of polymorph Form I, and processes for producing the crystalline rotigotine base are disclosed. Also disclosed is a transdermal patch for the delivery of rotigotine base using the disclosed isolated and pure form of rotigotine base, which can be used in treatment of Parkinson's Disease and other disorders ameliorated or treated by rotigotine, including restless leg syndrome.
1. A method of preparing the crystalline rotigotine base having an X-ray powder diffraction pattern comprising peaks at 14.6, 15.2, 15.6, 16.6, 17.0, 19.7, 20.2, 22.6 and 27.8 degrees 2θ, the method comprising:
(a) dissolving or partially dissolving rotigotine hydrochloride in a first organic solvent and water;
(b) adding a base to the mixture of (a) to form rotigotine base;
(c) removing the water and the first organic solvent of (b) to form a residue;
(d) adding water and a second organic solvent to the residue;
(e) removing the water and the second organic solvent from the mixture of step (d) to obtain crude rotigotine base; and
(f) crystallizing the crude rotigotine base from a third organic solvent selected from n-pentane, n-hexane, cyclohexane, n-heptane, petroleum ether, and mixtures thereof, to form crystalline rotigotine base.
2. The method of claim 1 further comprising (g) one or more of collecting, washing, and drying the crystalline rotigotine base.
3. The method of claim 2 , wherein the washing comprises washing with a fourth solvent selected from n-pentane, n-hexane, cyclohexane, n-heptane, petroleum ether, and mixtures thereof.
4. The method of claim 2 , wherein the fourth solvent comprises n-hexane.
5. The method of claim 1 , wherein the first organic solvent comprises dichloromethane.
6. The method of claim 1 , wherein the second organic solvent comprises diethyl ether.
7. The method of claim 1 , wherein the third organic solvent is n hexane.
8. The method of claim 1 , wherein the rotigotine base in the solution or partial solution has a concentration of up to about 0.5 mg/mL.
9. The method of claim 1 , wherein the base is selected from sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, and combinations thereof.
10. A method of purifying impure rotigotine base comprising:
(a) admixing the impure rotigotine base with an organic solvent selected from n-pentane, n-hexane, cyclohexane, n-heptane, petroleum ether, and mixtures thereof;
(b) precipitating purified crystalline rotigotine base from the mixture of (a); and
(c) isolating, washing, drying, and optionally milling the crystalline rotigotine base.
11. The method of claim 10 , wherein the organic solvent of step (a) comprises n-hexane.