IP Library › Granted Patent US 11,759,428
Granted Patent B2
US 11,759,428 · App. 16/965,726 · Granted Sep 19, 2023

Pharmaceutical formulation comprising esomeprazole and sodium bicarbonate

Inventors: Jong Seo Choi (Yongin-Si, KR); Min Soo Kim (Yongin-Si, KR); Shin Jung Park (Yongin-Si, KR); Jong Lae Lim (Yongin-Si, KR)
Assignee: CHONG KUN DANG PHARMACEUTICAL CORP.
A61K9/2886A61K9/2095A61K9/284A61K9/2893A61K31/4439A61K33/10
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Quick Facts
Patent No.
US 11,759,428
App. No.
16/965,726
Granted
Sep 19, 2023
Kind
B2
Abstract

The present invention relates to a stable pharmaceutical formulation comprising omeprazole, its enantiomer, or its pharmaceutically acceptable salt, and sodium bicarbonate, and a method for preparing the same. Specifically, the present invention provides a stable formulation by preventing omeprazole, its enantiomer, or its pharmaceutically acceptable salt, from coming in direct contact with sodium bicarbonate, to reduce the production of impurities.

Claims (20)

1. A pharmaceutical formulation comprising a first layer, a second layer, a third layer, and a fourth layer;

the first layer comprising omeprazole, its enantiomer, or its pharmaceutically acceptable salt;

the second layer comprising a coating agent, wherein the coating agent is polyvinyl alcohol;

the third layer comprising an antacid, wherein the antacid is sodium bicarbonate; and

the fourth layer comprising a coating agent, wherein the coating agent is polyvinyl alcohol;

wherein the second layer separates the first layer from the third layer.

2. The pharmaceutical formulation according to claim 1 , wherein the ratio of the coating agent in the second and fourth layers to the omeprazole, its enantiomer, or its pharmaceutically acceptable salt, is from 0.1:1 to 7:1 by weight.

3. The pharmaceutical formulation according to claim 2 , wherein the ratio of the coating agent in the second and fourth layers to the omeprazole, its enantiomer, or its pharmaceutically acceptable salt, is from 1.5:1 to 5:1 by weight.

4. The pharmaceutical formulation according to claim 1 , wherein the omeprazole, its enantiomer, or its pharmaceutically acceptable salt is esomeprazole.

5. The pharmaceutical formulation according to claim 1 , wherein the omeprazole, its enantiomer, or its pharmaceutically acceptable salt is a magnesium salt of esomeprazole.

6. A method for preparing a pharmaceutical formulation comprising omeprazole, its enantiomer, or its pharmaceutically acceptable salt; and sodium bicarbonate, the method comprising the steps:

coating a core with a coating solution comprising omeprazole, its enantiomer, or its pharmaceutically acceptable salt to prepare a first coated material;

coating the first coated material with a second coating solution comprising polyvinyl alcohol to prepare a second coated material;

tableting the second coated material with sodium bicarbonate to prepare a core tablet; and

coating the core tablet with a third coating solution comprising polyvinyl alcohol.

7. A method for preparing a pharmaceutical formulation comprising 20 mg or 40 mg of esomeprazole magnesium trihydrate based on the weight of esomeprazole, and 800 mg of sodium bicarbonate, the method comprising the steps:

coating a core with a coating solution comprising esomeprazole magnesium trihydrate to prepare a first coated material;

coating the first coated material with a second coating solution comprising polyvinyl alcohol to prepare a second coated material;

tableting the second coated material with sodium bicarbonate to prepare a core tablet; and

coating the core tablet with a third coating solution comprising polyvinyl alcohol.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2020
From: CHOI, JONG SEO; KIM, MIN SOO; PARK, SHIN JUNG; LIM, JONG LAE
To: CHONG KUN DANG PHARMACEUTICAL CORP.
Reel/Frame 053343/0668 →
Priority Claims (1)
KR 10-2018-0010987 · Jan 29, 2018 · national
Continuity (1)
Related Publication 20210030687A1 · Feb 4, 2021
Cited By (1)
US 12,251,375