Orally disintegrating tablet containing asenapine
The present invention relates to an orally disintegrating tablet (ODT) containing asenapine maleate and to a process for preparing the ODT. In a first aspect, the present invention relates to an ODT containing asenapine maleate and low substituted hydroxypropylcellulose. In a second aspect, the present invention relates to an ODT containing crystalline asenapine maleate and the ODT is prepared using conventional tabletting techniques as direct compression and granulation. In a third aspect, the present invention relates to an ODT containing asenapine maleate and a carboxylic acid, and to the use of a carboxylic acid for enhancing storage stability of an asenapine maleate containing ODT.
1. An orally disintegrating tablet comprising
a) a granular component comprising asenapine maleate and low substituted hydroxypropylcellulose (L-HPC),
b) and a pharmaceutical excipient.
2. The orally disintegrating tablet according to claim 1 , wherein the tablet is prepared by dry granulation.
3. The orally disintegrating tablet according to claim 1 , wherein the weight ratio of asenapine maleate to L-HPC is from 0.5 to 1.5.
4. The orally disintegrating tablet according to claim 1 , wherein the tablet is prepared by wet granulation.
5. The orally disintegrating tablet according to claim 1 , further comprising a carboxylic acid.
6. The orally disintegrating tablet according to claim 5 , wherein the carboxylic acid is selected from monocarboxylic acid, dicarboxylic acid, tricarboxylic acid, and mixtures thereof.
7. The orally disintegrating tablet according to claim 5 , wherein the carboxylic acid is a C 2-6 carboxylic acid, which is optionally substituted with at least one of hydroxy, amino and mercapto.
8. The orally disintegrating tablet according to claim 1 , wherein the asenapine maleate is crystalline asenapine maleate.
9. A process for preparing an orally disintegrating tablet according to claim 1 comprising the method steps of:
i) preparing a mixture containing asenapine maleate and L-HPC,
ii) compacting the mixture obtained in step (i) to form a comprimate,
iii) converting the comprimate obtained in step (ii) into a granulate,
iv) optionally mixing the granulate obtained in step (iii) with a pharmaceutical excipient, and
v) subjecting the granulate obtained in step (iii) or the mixture obtained in step (iv) to compression to obtain the tablet.
10. A process for preparing an orally disintegrating tablet according to claim 1 comprising the method steps of:
i) preparing a mixture containing asenapine maleate and L-HPC,
ii) granulating the mixture obtained in step (i) with a granulation liquid to form a wet granulate,
iii) drying the wet granulate obtained in step (ii) to form a dry granulate,
iv) optionally mixing the granulate obtained in step (iii) with a pharmaceutical excipient, and
v) subjecting the granulate obtained in step (iii) or the mixture obtained in step (iv) to compression to obtain the tablet.
11. The process according to claim 10 , wherein method step (ii) is carried out using a granulation liquid consisting of isopropyl alcohol containing povidone.
12. The process according to claim 9 , wherein the mixture in step (i) consists of asenapine maleate and L-HPC, and wherein the granulate obtained in step (iii) is mixed with a pharmaceutical excipient.
13. The orally disintegrating tablet according to claim 2 , wherein the weight ratio of asenapine maleate to L-HPC is from 0.5 to 1.5.
14. The orally disintegrating tablet according to claim 4 , wherein the weight ratio of asenapine maleate to L-HPC is from 0.5 to 3.5.
15. The orally disintegrating tablet according to claim 8 , wherein crystalline asenapine maleate is monoclinic asenapine maleate (form H).
16. The orally disintegrating tablet according to claim 2 , wherein the weight ratio of asenapine maleate to L-HPC is from 0.7 to 1.2.
17. The orally disintegrating tablet according to claim 4 , wherein the weight ratio of asenapine maleate to L-HPC is from 1.5 to 3.5.