IP Library Granted Patent US 11,020,375
Granted Patent B2
US 11,020,375 · App. 16/084,668 · Granted Jun 1, 2021

Edaravone dosage form

Inventors: Xinfu Zhou (Fuijian, CN); Ankit Parikh (Fujian, CN); Sanjay Garg (Fujian, CN)
Assignee: SUZHOU AUZONE BIOLOGICAL TECHNOLOGY CO., LTD.
A61K31/4152A61K9/08A61K9/10A61K9/107A61K47/02A61K47/14A61K47/22A61K47/34A61K47/44
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Quick Facts
Patent No.
US 11,020,375
App. No.
16/084,668
Granted
Jun 1, 2021
Kind
B2
Abstract

Disclosed is an Edaravone dosage form and a use thereof in preparing a drug used for treating diseases related to oxidative stress, the dosage form being selected from a lipid-based delivery system, a solid dispersion, micelles and a co-solvent based formulation.

Claims (10)

1. A solid phase dispersion formulation, comprising Edaravone as an active ingredient, and a polymer carrier selected from Soluplus, wherein the solid phase dispersion comprises Edaravone and Soluplus in a ratio of Edaravone:Soluplus of 1:1 to 1:16 by mass.

2. The solid phase dispersion formulation of claim 1 , further comprising a surfactant.

3. The solid phase dispersion formulation of claim 2 , wherein the surfactant includes an anionic, cationic, or amphoteric surfactant, selected from the group consisting of sodium dodecanesulfonate, sodium dodecyl sulfate (SDS), sodium lauryl sulfate (SLS), polyoxyethylene sorbitan long-chain fatty acid esters, Vitamin E-TPGS, bile salts, sodium deoxycholate, sodium glycocholate, polyoxyethylene polyoxypropylene glycols and combinations thereof.

4. The solid phase dispersion formulation of claim 2 , wherein the surfactant is TPGS 1000.

5. The solid phase dispersion formulation of claim 1 , comprising Edaravone, Soluplus and optionally TPGS 1000.

6. A method of preparing the solid phase dispersion formulation of claim 1 , comprising a step of:

dispersing Edaravone or a pharmaceutically acceptable salt thereof as an active ingredient in a polymer carrier and, optionally, a surfactant.

7. The method of claim 6 , further comprising a step selected from: melting ice bath agitation, thin film cooling, liquid nitrogen, spray congealing, hot-melt extrusion, Meltrex™, melt agglomeration or solvent evaporation, including oven drying, vacuum drying, rotary evaporation, heating on hot plate, spray drying, freeze drying, supercritical anti-solvent, co-precipitation, electrostatic spinning, spray freeze drying, ultra-rapid freezing or fluid-bed coating, and solvent melting.

8. The solid phase dispersion formulation of claim 1 , comprising Edaravone and Soluplus in a ratio of Edaravone:Soluplus of 1:5 by mass.

9. An oral pharmaceutical composition comprising Edaravone or a pharmaceutically acceptable salt thereof, and Soluplus in a ratio of Edaravone:Soluplus of 1:1 to 1:16 by mass.

Assignments (2)
CHANGE OF NAME Recorded Nov 15, 2024
From: SUZHOU AUZONE BIOLOGICAL TECHNOLOGY CO., LTD.
To: SHANGHAI AUZONE BIOLOGICAL TECHNOLOGY CO., LTD.
Reel/Frame 069277/0196 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2021
From: ZHOU, XINFU; PARIKH, ANKIT; GARG, SANJAY
To: SUZHOU AUZONE BIOLOGICAL TECHNOLOGY CO., LTD.
Reel/Frame 056084/0948 →
Priority Claims (1)
CN 201610149832.9 · Mar 16, 2016 · national
Continuity (1)
Related Publication 20190083463A1 · Mar 21, 2019