Claims for Patent: 11,202,772

Summary for Patent: 11,202,772

Title:	Duloxetine sprinkles
Abstract:	The present invention relates in part a to multiparticulate sprinkle dosage form comprising duloxetine or a pharmaceutically acceptable salt thereof, having higher acid resistance as compared to commercially available delayed release formulations. It further relates to various methods of administering the said multiparticulate sprinkle dosage forms.
Inventor(s):	Agarwal; Ravindra (Udaipur, IN), Singhal; Tarun (Bharatpur, IN), Kochhar; Ravi (Haryana, IN)
Assignee:	Sun Pharmaceutical Industries Limited (Mumbai, IN)
Application Number:	17/129,173
Patent Claims:	1. A multi-particulate sprinkle dosage form comprising a plurality of discrete units, wherein each unit comprises: (a) a drug core comprising duloxetine or a pharmaceutically acceptable salt thereof; and (b) an enteric coating layer surrounding the drug core; wherein not more than 15% of 1-naphthol impurity is released from the dosage form after 6 hours when placed in 0.1 N HCl dissolution media. 2. The multi-particulate sprinkle dosage form of claim 1, wherein not more than 5% of 1-naphthol impurity is released from the dosage form after 6 hours when placed in a 0.1 N HCl dissolution media. 3. A multi-particulate sprinkle dosage form comprising a plurality of discrete units, wherein each unit comprises: (a) a drug core comprising duloxetine or a pharmaceutically acceptable salt thereof; and (b) an enteric coating layer surrounding the drug core; wherein not more than 90% of duloxetine is released from the dosage form after 1 or 2 hours when placed in a 40% ethanol dissolution media. 4. A multi-particulate sprinkle dosage form comprising a plurality of discrete units, wherein each unit comprises: (a) a drug core comprising duloxetine or a pharmaceutically acceptable salt thereof; and (b) an enteric coating layer surrounding the drug core; wherein the sprinkle dosage form exhibits dissolution of not more than 75% of duloxetine within 75 minutes, when placed in a dissolution media comprising 0.1 N HCl and 20% alcohol. 5. A multi-particulate sprinkle dosage form comprising a plurality of discrete units, wherein each unit comprises: an inert core, and a drug layer surrounding the inert core; wherein the drug layer comprises duloxetine or a pharmaceutically acceptable salt thereof; an enteric coating layer surrounding the drug core; wherein not more than 90% of duloxetine is released from the dosage form after 1 or 2 hours when placed in 40% ethanol dissolution media. 6. The multi-particulate sprinkle dosage form of claim 5, wherein not more than 5% of 1-naphthol impurity is released after 4 hours from the dosage form when placed in 0.1 N HCl dissolution media. 7. The multi-particulate sprinkle dosage form of claim 1, wherein the enteric coating layer comprises a polymer selected from methacrylic acid copolymers, cellulose acetate phthalate, cellulose acetate succinate, polymethacrylic acid, hydroxypropyl methyl cellulose, hydroxypropyl methylcellulose phthalate, polyvinyl acetate phthalate, hydroxyethyl ethyl cellulose phthalate, cellulose acetate tetrahydrophthalate, acrylic resin, and mixtures thereof. 8. The multi-particulate sprinkle dosage form according to claim 7, wherein the polymer is present in an amount of about 75% to about 99% by weight based on the weight of the enteric coating. 9. The multi-particulate sprinkle dosage form of claim 1, wherein the dosage form further comprises a finishing layer containing a cushioning agent selected from the group consisting of polyethylene glycols, polyoxyethylenes, colloidal and/or amorphous silicon dioxide, microcrystalline cellulose, polyvinyl acetate, waxes, fats, lipids, gums, and mixtures thereof, surrounding the enteric coating. 10. The multi-particulate sprinkle dosage form according to claim 9, wherein the cushioning agent is present in an amount of about 2% to about 20% based on the total weight of the dosage form. 11. The multi-particulate sprinkle dosage form of claim 1, wherein the dosage form contains duloxetine or pharmaceutically acceptable salts thereof in an amount of about 20% by weight of the dosage form. 12. The multi-particulate sprinkle dosage form of claim 1, wherein the discrete units are pellets, beads, particles, granules, or minitablets. 13. The multi-particulate sprinkle dosage form of claim 3, wherein the enteric coating layer comprises a polymer selected from methacrylic acid copolymers, cellulose acetate phthalate, cellulose acetate succinate, polymethacrylic acid, hydroxypropyl methyl cellulose, hydroxypropyl methylcellulose phthalate, polyvinyl acetate phthalate, hydroxyethyl ethyl cellulose phthalate, cellulose acetate tetrahydrophthalate, acrylic resin, and mixtures thereof. 14. The multi-particulate sprinkle dosage form according to claim 13, wherein the polymer is present in an amount of about 75% to about 99% by weight based on the weight of the enteric coating. 15. The multi-particulate sprinkle dosage form of claim 3, wherein the dosage form further comprises a finishing layer containing a cushioning agent selected from the group consisting of polyethylene glycols, polyoxyethylenes, colloidal and/or amorphous silicon dioxide, microcrystalline cellulose, polyvinyl acetate, waxes, fats, lipids, gums, and mixtures thereof, surrounding the enteric coating. 16. The multi-particulate sprinkle dosage form according to claim 15, wherein the cushioning agent is present in an amount of about 2% to about 20% based on the total weight of the dosage form. 17. The multi-particulate sprinkle dosage form of claim 5, wherein the enteric coating layer comprises a polymer selected from methacrylic acid copolymers, cellulose acetate phthalate, cellulose acetate succinate, polymethacrylic acid, hydroxypropyl methyl cellulose, hydroxypropyl methylcellulose phthalate, polyvinyl acetate phthalate, hydroxyethyl ethyl cellulose phthalate, cellulose acetate tetrahydrophthalate, acrylic resin, and mixtures thereof. 18. The multi-particulate sprinkle dosage form according to claim 17, wherein the polymer is present in an amount of about 75% to about 99% by weight based on the weight of the enteric coating. 19. The multi-particulate sprinkle dosage form of claim 5, wherein the dosage form further comprises a finishing layer containing a cushioning agent selected from the group consisting of polyethylene glycols, polyoxyethylenes, colloidal and/or amorphous silicon dioxide, microcrystalline cellulose, polyvinyl acetate, waxes, fats, lipids, gums, and mixtures thereof, surrounding the enteric coating. 20. The multi-particulate sprinkle dosage form according to claim 19, wherein the cushioning agent is present in an amount of about 2% to about 20% based on the total weight of the dosage form.