US2008219927A1PendingUtilityA1

Adenosine derivative formulations for medical imaging

Assignee: THAKUR AJIT BPriority: Jan 18, 2007Filed: Jan 16, 2008Published: Sep 11, 2008
Est. expiryJan 18, 2027(~0.5 yrs left)· nominal 20-yr term from priority
A61K 49/0002B82Y 5/00A61P 9/08A61K 47/6951
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Claims

Abstract

A stable composition useful for myocardial perfusion imaging contains one or more 2-alkynyladenosine derivatives; and a solvent which is made up of water and hydroxypropyl-β-cyclodextrin.

Claims

exact text as granted — not AI-modified
1 . A stable composition useful for myocardial perfusion imaging, comprising:
 (a) an adenosine derivative, which is methyl trans-4-[3-[6-amino-9-(N-ethyl-β-D-ribofuranosyluronamide)-9H-purin-2-yl]prop-2-ynyl]cyclohexane carboxylate or a pharmaceutically acceptable salt thereof; and,   (b) a solvent consisting essentially of water and hydroxypropyl-β-cyclodextrin.   
     
     
         2 . The composition of  claim 1 , further comprising a buffer. 
     
     
         3 . The composition of  claim 2 , wherein the buffer comprises: sodium citrate and citric acid. 
     
     
         4 . The composition of  claim 1 , wherein the concentration of hydroxypropyl-β-cyclodextrin is about 0.1-10% w/v. 
     
     
         5 . The composition of  claim 4 , wherein the concentration of hydroxypropyl-β-cyclodextrin is about 0.5-2% w/v. 
     
     
         6 . The composition of  claim 1 , wherein the molar ratio of the adenosine derivative to hydroxypropyl-β-cyclodextrin is about 1:30 to 1:150. 
     
     
         7 . The composition of  claim 1 , wherein hydroxyethyl-β-cyclodextrin is absent from the composition. 
     
     
         8 . The composition of  claim 1 , wherein any other β-cyclodextrin is absent from the composition. 
     
     
         9 . The composition of  claim 1 , wherein any other solvent is absent from the composition. 
     
     
         10 . The composition of  claim 1 , wherein the composition is storage stable for at least about 3 months. 
     
     
         11 . A method of inducing cardiovascular stress, which comprises administering to a patient a pharmacologic vasodilation formulation, comprising:
 (a) an adenosine derivative, which is methyl trans-4-[ 3 -[6-amino-9-(N-ethyl-β-D-ribofuranosyluronamide)-9H-purin-2-yl]prop-2-ynyl]cyclohexane carboxylate or a pharmaceutically acceptable salt thereof,   (b) a solvent consisting essentially of water and hydroxypropyl-β-cyclodextrin; and,   (c) buffer.   
     
     
         12 . The method of  claim 11 , wherein the composition is administered intravenously. 
     
     
         13 . The method of  claim 11 , wherein the adenosine derivative is administered at a dose not exceeding about 5 mcg/kg of body weight. 
     
     
         14 . The method of  claim 13 , wherein the adenosine derivative is administered at a dose not exceeding about 2 mcg/kg of body weight. 
     
     
         15 . The method of  claim 11 , wherein the adenosine derivative is administered at a dose within the range of about 0.5-5 mcg/kg. 
     
     
         16 . The method of  claim 11 , wherein the adenosine derivative is administered via an intracoronary route to the human in a dose of about 0.05-0.5 mcg thereof sufficient to provide coronary artery dilation. 
     
     
         17 . A cardiovascular stress testing kit, comprising:
 (a) an adenosine derivative, which is methyl trans-4-[3-[6-amino-9-(N-ethyl-β-D-ribofuranosyluronamide)-9H-purin-2-yl]prop-2-ynyl]cyclohexane carboxylate or a pharmaceutically acceptable salt thereof; and,   (b) a solvent consisting essentially of water and hydroxypropyl-β-cyclodextrin.   
     
     
         18 . The kit of  claim 17 , wherein hydroxyethyl-β-cyclodextrin is absent from the solvent.

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