US2017028106A1PendingUtilityA1

Thromboresistant/bactericidal s-nitroso-n-acetylpenicillamine (snap)-doped nitric oxide release polymers with enhanced stability

Assignee: UNIV MICHIGAN REGENTSPriority: Feb 7, 2013Filed: Nov 5, 2014Published: Feb 2, 2017
Est. expiryFeb 7, 2033(~6.5 yrs left)· nominal 20-yr term from priority
A61P 7/00A61K 31/198C08J 2383/04A61L 2300/114A61K 31/197A61L 29/16C08J 7/065A61L 33/0082A61K 9/7007A61L 29/085C08J 5/18C08J 2375/04C08J 7/02A61L 33/04A61L 2300/404A61L 33/0088A61K 33/00A61K 9/70C08J 7/046
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Claims

Abstract

In an example of a method for making an NO-releasing polymeric composition, a discrete RSNO adduct is dissolved in a solvent to form a discrete RSNO adduct solution. A polymer material is soaked in the discrete RSNO adduct solution for a predetermined time to swell the polymer material and impregnate the polymer material with the discrete RSNO adduct.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for making an NO-releasing polymeric composition, comprising the steps of:
 dissolving a discrete RSNO adduct in a solvent to form a discrete RSNO adduct solution; and   soaking a polymer material in the discrete RSNO adduct solution for a predetermined time to swell the polymer material and impregnate the polymer material with the discrete RSNO adduct.   
     
     
         2 . The method as defined in  claim 1  wherein the polymer matrix is selected from the group consisting of a siloxane-based polyurethane elastomer, silicone rubber, and a thermoplastic silicone-polycarbonate-urethane, and wherein the discrete RSNO adduct is S-nitroso-N-acetylpenicillamine (SNAP). 
     
     
         3 . The method as defined in  claim 1  wherein the dissolving and the soaking are accomplished at room temperature ranging from about 17° C. to about 24° C. 
     
     
         4 . The method as defined in  claim 1  wherein dissolving is accomplished by:
 adding the S-nitroso-N-acetylpenicillamine (SNAP) to the solvent, wherein the solvent is selected from the group consisting of tetrahydrofuran, chloroform, methylene chloride, cyclohexanone, and combinations thereof; and 
 stirring the solution for a predetermined time. 
 
     
     
         5 . The method as defined in  claim 1 , further comprising completely immersing the polymer material in the discrete RSNO adduct solution prior to the soaking. 
     
     
         6 . The method as defined in  claim 1  wherein the predetermined time is about 24 hours, and wherein the soaking is accomplished in darkness. 
     
     
         7 . The method as defined in  claim 1  wherein after the soaking for the predetermined time, the method further comprises drying the impregnated polymer material in darkness.

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