US2017100412A1PendingUtilityA1

Ophthalmologic irrigation solutions and method

Assignee: OMEROS CORPPriority: Jul 30, 2002Filed: Jun 30, 2016Published: Apr 13, 2017
Est. expiryJul 30, 2022(expired)· nominal 20-yr term from priority
A61P 39/06A61P 43/00A61P 41/00A61P 25/04A61P 27/02A61P 27/08A61P 29/02A61P 27/12A61P 27/04A61P 25/02A61P 29/00A61K 31/5377A61K 31/137A61P 23/00A61K 31/167A61K 31/445A61K 31/4174A61K 31/4409A61K 45/06A61K 31/4164A61K 9/0048A61P 23/02A61K 31/573A61K 31/00A61K 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 perioperatively inhibiting ocular inflammation and maintaining mydriasis during an intraocular ophthalmologic procedure, comprising an anti-inflammatory agent and a mydriatic agent in a physiologic irrigation solution for intraocular delivery, wherein the anti-inflammatory agent comprises a non-steroidal anti-inflammatory drug (NSAID) and the mydriatic agent comprises an alpha-1 adrenergic receptor agonist, wherein the NSAID and the alpha-1 adrenergic receptor agonist are included at concentrations less than that used for conventional topical or systemic delivery and in a therapeutically effective amount for the maintenance of mydriasis during the procedure and the reduction of postoperative pain when delivered intraocularly during the intraocular ophthalmologic procedure. 
     
     
         2 . The composition of  claim 1 , wherein the NSAID is selected from the group consisting of flurbiprofen, suprofen, diclofenac, ketoprofen, ketorolac, indomethacin, naproxen, ibuprofen. 
     
     
         3 . The composition of  claim 1 , wherein the NSAID is selected from the group consisting of flurbiprofen, suprofen, diclofenac, ketoprofen and ketorolac. 
     
     
         4 . The composition of  claim 2 , wherein the alpha-1 adrenergic receptor agonist is selected from the group consisting of phenylephrine, epinephrine, and oxymetazoline. 
     
     
         5 . The composition of  claim 1 , wherein the alpha-1 adrenergic receptor agonist is selected from the group consisting of phenylephrine, epinephrine, and oxymetazoline. 
     
     
         6 . The composition of  claim 1 , wherein the alpha-1 adrenergic receptor agonist is selected from the group consisting of phenylephrine and epinephrine. 
     
     
         7 . The composition of  claim 1 , wherein the NSAID is included in the solution at a concentration of no more than 100,000 nanomolar and the alpha-1 adrenergic receptor agonist is included in the solution at a concentration of no more than 500,000 nanomolar. 
     
     
         8 . The composition of  claim 1 , wherein the physiologic solution comprises a balanced salt solution liquid irrigation. 
     
     
         9 . The composition of  claim 8 , wherein the balanced salt solution liquid irrigation carrier further comprises an adjuvant selected from a cellular energy source, a buffering agent, a free-radical scavenger and mixtures thereof. 
     
     
         10 . The composition of  claim 1 , wherein the solution further comprises an analgesic agent selected from the group consisting of local anesthetics and opioids. 
     
     
         11 . The composition of  claim 10 , wherein: the local anesthetic, if selected, is selected from the group consisting of lidocaine, tetracaine, bupivacaine, and proparacaine; and the opioid, if selected, is selected from the group consisting of morphine, fentanyl and hydromorphone. 
     
     
         12 . A composition for use in perioperatively inhibiting ocular inflammation and maintaining mydriasis during an intraocular ophthalmologic procedure, comprising an anti-inflammatory agent and a mydriatic agent in a physiologic irrigation solution for intraocular delivery, wherein the anti-inflammatory agent comprises a non-steroidal anti-inflammatory drug (NSAID) and the mydriatic agent comprises an alpha-1 adrenergic receptor agonist, wherein the NSAID and the alpha-1 adrenergic receptor agonist are included at concentrations less than that used for conventional topical or systemic delivery and in a therapeutically effective amount for the maintenance of pupil dilation and inhibition of miosis during the procedure and the reduction of postoperative pain when delivered intraocularly during the intraocular ophthalmologic procedure.

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