US2014212460A1PendingUtilityA1
Cyclooxygenase Inhibitor and Calcium Channel Antagonist Compositions and Methods for Use in Urological Procedures
Est. expiryMay 20, 2025(expired)· nominal 20-yr term from priority
A61P 25/08A61P 25/04A61P 25/00A61P 29/00A61P 13/10A61L 2300/402A61K 31/21A61K 31/4422A61K 9/0034A61L 2300/432A61L 2300/41A61K 31/455A61P 13/06A61P 13/00A61K 31/40A61K 31/00A61L 31/16A61K 9/08A61P 13/02A61K 31/44A61P 13/12A61K 31/192A61P 41/00A61K 47/12A61K 47/10A61K 47/14A61K 47/02A61K 9/0014
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Claims
Abstract
Compositions of a cyclooxygenase inhibitor and a calcium channel antagonist in a liquid carrier. The composition may be administered the urinary tract during urological diagnostic, interventional, surgical and other medical procedures. One disclosed composition comprises ketoprofen and nifedipine in a liquid irrigation carrier, and includes a solubilizing agent, stabilizing agents and a buffering agent.
Claims
exact text as granted — not AI-modified1 . A locally deliverable composition for inhibiting pain/inflammation and spasm, comprising a combination of ketoprofen and a calcium channel antagonist in a carrier, each of the ketoprofen and the calcium channel antagonist included in a therapeutically effective amount such that the combination inhibits pain/inflammation and spasm at a site of local delivery.
2 . The composition of claim 1 , wherein the calcium channel antagonist comprises an L-type calcium channel antagonist.
3 . The method of claim 2 , wherein the L-type calcium channel antagonist is selected from the group consisting of verapamil, diltiazem, bepridil, mibefradil, nifedipine, nicardipine, isradipine, amlodipine, felodipine, nisoldipine and nimodipine.
4 . The method of claim wherein the L-type calcium channel antagonist comprises a dihydropyridine.
5 . The composition of claim 4 , wherein the L-type calcium channel antagonist is selected from the group consisting of nifedipine, nicardipine, isradipine, amlodipine, felodipine, nisoldipine and nimodipine.
6 . The method of claim 5 , wherein the L-type calcium channel antagonist comprises nifedipine.
7 . The composition of claim 5 , wherein the L-type calcium channel antagonist has an onset of action of less than or equal to 10 minutes.
8 . The composition of claim 1 , wherein the calcium channel antagonist comprises nifedipine.
9 . The composition of claim 8 , wherein ketoprofen and nifedipine are included in the composition in a ketoprofen:nifedipine molar ratio of from 10:1 to 1:10.
10 . The composition of claim 9 , wherein ketoprofen and nifedipine are included in the composition in a ketoprofen:nifedipine molar ratio of from 4:1 to 1:1.
11 . The composition of claim 10 , wherein ketoprofen and nifedipine are included in the composition in a ketoprofen:nifedipine molar ratio of 3:1.
12 . The composition of claim 8 , wherein ketoprofen is included in the composition at a concentration of no more than 500,000 nanomolar and nifedipine is included in the composition at a concentration of no more than 200,000 nanomolar.
13 . The composition of claim 12 , wherein ketoprofen is included in the composition at a concentration of no more than 300,000 nanomolar and nifedipine is included in the composition at a concentration of no more than 100,000 nanomolar.
14 . The composition of claim 13 , wherein ketoprofen is included in the composition at a concentration of no more than 50,000 nanomolar and nifedipine is included in the composition at a concentration of no more than 25,000 nanomolar.
15 . The composition of claim 1 , wherein ketoprofen is included in the composition at a concentration of no more than 500,000 nanomolar and the calcium channel antagonist is included in the composition at a concentration of no more than 200,000 nanomolar.
16 . The composition of claim 15 , wherein ketoprofen is included in the composition at a concentration of no more than 300,000 nanomolar and the calcium channel antagonist is included in the composition at a concentration of no more than 100,000 nanomolar.
17 . The composition of claim 16 , wherein ketoprofen is included in the composition at a concentration of no more than 50,000 nanomolar and the calcium channel antagonist is included in the composition at a concentration of no more than 25,000 nanomolar.
18 . The composition of claim 1 , wherein ketoprofen comprises the S-(+)-enantiomer, dexketoprofen.
19 . The composition of claim 1 , wherein the composition is coated onto an implantable device or medical instrument.
20 . The composition of claim 1 , wherein the composition is impregnated into an implantable device or medical instrument.
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