IP Library Granted Patent US 10,532,026
Granted Patent B2
US 10,532,026 · App. 16/110,056 · Granted Jan 14, 2020

Thermo-responsive gelling artificial lacrima

Inventors: Takeshi Yamamura (Tokyo, JP); Ayaka Yamamuro (Tokyo, JP); Emi Izukura (Tokyo, JP); Moto Kimura (Tokyo, JP); Tomohiro Otsuka (Tokyo, JP)
Assignee: WAKAMOTO PHARMACEUTICAL CO., LTD.
A61K9/0048A61K9/06A61K31/194A61K31/5383A61K47/10A61K47/12A61K47/32A61K47/38A61P27/02A61P27/04
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Quick Facts
Patent No.
US 10,532,026
App. No.
16/110,056
Granted
Jan 14, 2020
Kind
B2
Abstract

The present invention is an aqueous solution which contains two types of methyl celluloses, polyethylene glycol, polyvinylpyrrolidone, and citric acid or a pharmaceutically acceptable salt thereof. The composition of the present invention maintains a low viscosity around room temperature, but the composition is suddenly increased in the viscosity due to heat around the body temperature and has thixotropy even after gelation.

Claims (14)

1. An ophthalmic aqueous composition comprising:

(A) methyl cellulose having a label viscosity of 4 and methyl cellulose having a label viscosity of 15 in a total amount having a mass ratio of 1:4 to 4:1 and combined total concentration of 0.2 to 5 w/v %;

(B) polyethylene glycol having a weight average molecular weight of 4000 or 8000 at 0.5 to 4.0 w/v %;

(C) polyvinylpyrrolidone K25 at 0.5 to 4.0 w/v %; and

(D) citric acid or sodium salts thereof at 1.0 to 4.0 w/v %,

wherein all w/v % are based on the total amount of the composition, and

wherein the ophthalmic aqueous composition has a gelling property.

2. A method for protecting cornea, mitigating a corneal epithelial disorder, or recovery from a corneal disorder, comprising administrating to a subject in need thereof a composition which comprises:

(A) methyl cellulose having a label viscosity of 4 and methyl cellulose having a label viscosity of 15 in a total amount having a mass ratio of 1:4 to 4:1 and a combined total concentration of 0.2 to 5 w/v %;

(B) polyethylene glycol having a weight average molecular weight of 4000 or 8000 at 0.5 to 4.0 w/v %;

(C) polyvinylpyrrolidone K25 at 0.5 to 4.0 w/v %; and

(D) citric acid or sodium salts thereof at 1.0 to 4.0 w/v %,

wherein all w/v % are based on the total amount of the composition, and

wherein the ophthalmic aqueous composition has a gelling property.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 31, 2018
From: YAMAMURA, TAKESHI; YAMAMURO, AYAKA; IZUKURA, EMI; KIMURA, MOTO; OTSUKA, TOMOHIRO
To: WAKAMOTO PHARMACEUTICAL CO., LTD.
Reel/Frame 046770/0206 →
Priority Claims (2)
JP 2017-086512 · Apr 25, 2017 · national
JP 2017-249891 · Dec 26, 2017 · national
Continuity (2)
Continuation PCTJP2018016854 · Apr 25, 2018
Related Publication 20180360746A1 · Dec 20, 2018