US2015320690A1PendingUtilityA1
Tamper resistant immediate release capsule formulation comprising tapentadol
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-modified1 . 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 .Join the waitlist — get patent alerts
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