US2017312295A1PendingUtilityA1

Ophthalmologic Irrigation Solutions and Method

Assignee: OMEROS CORPPriority: Jul 30, 2002Filed: Jan 25, 2017Published: Nov 2, 2017
Est. expiryJul 30, 2022(expired)· nominal 20-yr term from priority
A61P 39/06A61P 41/00A61P 43/00A61P 29/02A61P 27/04A61P 27/08A61P 27/12A61P 29/00A61P 25/04A61P 27/02A61P 25/02A61K 31/137A61K 31/573A61K 31/5377A61K 31/4164A61K 31/4409A61K 9/0048A61K 45/06A61P 23/02A61K 31/4174A61K 31/167A61K 31/445A61K 31/00A61P 23/00A61K 9/08A61K 31/192
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Claims

Abstract

Solutions for perioperative intraocular application by continuous irrigation during ophthalmologic procedures are provided. These solutions include multiple agents that act to inhibit inflammation, inhibit pain, effect mydriasis (dilation of the pupil), and/or decrease intraocular pressure, wherein the multiple agents are selected to target multiple molecular targets to achieve multiple differing physiologic functions, and are included in dilute concentrations in a balanced salt solution carrier.

Claims

exact text as granted — not AI-modified
The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows: 
     
         1 . A composition for use in promoting mydriasis during an intraocular ophthalmologic procedure, comprising a local anesthetic agent combined with a mydriatic agent that is an alpha-1 adrenergic receptor agonist in a physiologic carrier solution, wherein the alpha-1 adrenergic receptor agonist is included in the solution at a concentration of no more than 1,000,000 nanomolar and the local anesthetic agent is included in the solution at a concentration of no more than 100,000,000 nanomolar and wherein the agents are included in therapeutically effective amounts for mydriasis during the procedure when delivered intraocularly. 
     
     
         2 . The composition of  claim 1 , wherein the local anesthetic agent is selected from the group consisting of lidocaine, tetracaine, bupivacaine, and proparacaine. 
     
     
         3 . The composition of  claim 1 , wherein the alpha-1 adrenergic receptor agonist is selected from the group consisting of phenylephrine, epinephrine and oxymetazoline. 
     
     
         4 . The composition of  claim 1 , wherein the alpha-1 adrenergic receptor agonist is selected from the group consisting of phenylephrine and epinephrine. 
     
     
         5 . The composition of  claim 4 , wherein the local anesthetic agent is selected from the group consisting of lidocaine, tetracaine, bupivacaine, and proparacaine. 
     
     
         6 . The composition of  claim 1 , wherein the physiologic carrier solution comprises a liquid irrigation carrier. 
     
     
         7 . The composition of  claim 6 , wherein the liquid irrigation carrier comprises a balanced salt solution. 
     
     
         8 . The composition of  claim 1 , wherein the solution further comprises a non-steroidal anti-inflammatory drug (NSAID). 
     
     
         9 . The composition of  claim 8 , wherein the NSAID is selected from the group consisting of flurbiprofen, suprofen, diclofenac, ketoprofen and ketorolac. 
     
     
         10 . The composition of  claim 1 , wherein the alpha-1 adrenergic receptor agonist is included in the solution at a concentration of no more than 500,000 nanomolar and the local anesthetic agent is included in the solution at a concentration of no more than 1,200,000 nanomolar. 
     
     
         11 . A composition for use in promoting mydriasis during an intraocular ophthalmologic procedure, comprising a local anesthetic agent combined with a mydriatic agent that is an alpha-1 adrenergic receptor agonist in a physiologic carrier solution, wherein the local anesthetic agent and the alpha-1 adrenergic receptor agonist are included in therapeutically effective amounts to promote mydriasis during the procedure when delivered intraocularly and at concentrations less than that used for conventional topical or systemic delivery. 
     
     
         12 . The composition of  claim 11 , wherein the alpha-1 adrenergic receptor agonist is included in the solution at a concentration of no more than 500,000 nanomolar and the local anesthetic agent is included in the solution at a concentration of no more than 1,200,000 nanomolar.

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