US2015320690A1PendingUtilityA1

Tamper resistant immediate release capsule formulation comprising tapentadol

Assignee: GRUENENTHAL GMBHPriority: May 12, 2014Filed: May 11, 2015Published: Nov 12, 2015
Est. expiryMay 12, 2034(~7.8 yrs left)· nominal 20-yr term from priority
A61K 31/137A61K 9/485A61K 9/4808A61K 9/4858A61K 9/4866A61K 9/0053A61P 25/36A61P 29/00A61P 25/04
43
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Claims

Abstract

The invention is directed to an immediate release capsule which mitigates the abuse of Tapentadol or physiologically acceptable salt thereof by direct intravenous injection. The capsule comprises a tamper resistant formulation which when mixed with water and heated, results in a turbid, bubbling mixture that is not injectable with a standard insulin syringe.

Claims

exact text as granted — not AI-modified
1 . A tamper resistant pharmaceutical capsule comprising a capsule filling and a capsule shell, wherein said capsule filling is encapsulated by said capsule shell and comprises:
 (a) Tapentadol or a physiologically acceptable salt thereof in an amount within the range of from 10 mg to 400 mg, as equivalent weight relative to Tapentadol free base; and   (b) a liquid excipient blend comprising a solvent, a surfactant, and a viscosity enhancer;   wherein the capsule provides immediate release of Tapentadol or the physiologically acceptable salt thereof upon oral administration.   
     
     
         2 . The capsule according to  claim 1 , wherein a mixture of 250 milligrams of the liquid excipient blend with 5 milliliters of water at the mixture's boiling point forms a viscous phase which cannot pass through a 25 millimeter needle having an inner diameter of 0.60 millimeters. 
     
     
         3 . The capsule according to  claim 1 , wherein the viscosity enhancer comprises colloidal anhydrous silica and/or a gum. 
     
     
         4 . The capsule according to  claim 3 , wherein the gum is selected from the group consisting of  acacia , agar, tragacanth, guar gum, xanthan gum, locust bean gum, tara gum, karaya, gellan gum, welan gum, and rhamsan gum. 
     
     
         5 . The capsule according to  claim 1 , wherein the total content of viscosity enhancer is within the range of from 0.1 to 10 wt.-%, relative to the total weight of the capsule filling. 
     
     
         6 . The capsule according to  claim 1 , wherein the total content of solvent is within the range of from 10 to 90 wt.-%, relative to the total weight of the capsule filling. 
     
     
         7 . The capsule according to  claim 1 , wherein the liquid excipient blend comprises an ion exchange resin. 
     
     
         8 . The capsule according to  claim 7 , wherein the ion exchange resin is anionic. 
     
     
         9 . The capsule according to  claim 1 , wherein the total content of ion exchange resin is within the range of from 0.1 to 25 wt.-%, relative to the total weight of the capsule filling. 
     
     
         10 . The capsule according to  claim 1 , wherein the surfactant is nonionic. 
     
     
         11 . The capsule according to  claim 10 , wherein the nonionic surfactant is selected from the group consisting of glycerol monoesters with C 6-18 -fatty acids, glycerol diesters with identical or different C 6-18 -fatty acids, glycerol triesters with identical or different C 6-18 -fatty acids, polyethylene glycol monoesters with C 6-18 -fatty acids, polyethylene glycol diesters with identical or different C 6-18 -fatty acids, and mixtures of any of the foregoing. 
     
     
         12 . The capsule according to  claim 1 , wherein the total content of surfactant is within the range of from 0.1 to 35 wt.-%, relative to the total weight of the capsule filling. 
     
     
         13 . The capsule according to  claim 1 , wherein the total content of Tapentadol or physiologically acceptable salt thereof, as equivalent weight relative to Tapentadol free base, is within the range of from 0.1 to 25 wt.-%, relative to the total weight of the capsule filling. 
     
     
         14 . A method for treating pain in a patient in need of such treatment, said method comprising administering to said patient at least one capsule according to  claim 1 . 
     
     
         15 . A method for preventing parenteral abuse of Tapentadol or a physiologically acceptable salt thereof, said method comprising providing the Tapentadol or a physiologically acceptable salt thereof in the form of a capsule according to  claim 1 .

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