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Abuse-proofed dosage form

a dosage form and dosage technology, applied in the field of abuse-proofed dosage forms, can solve the problems of preventing subsequent abuse, pulverizing the dosage form considerably more difficult using conventional means, and preventing the subsequent abuse, so as to prevent parenteral, nasal and/or oral abus

Inactive Publication Date: 2007-03-01
GRUNENTHAL GMBH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0016] The breaking strength of at least 500 N (measured as stated in the specification) means that pulverization of the dosage form is considerably more difficult using conventional means, so considerably complicating or preventing the subsequent abuse.
[0019] The dosage form according to the invention is thus suitable for preventing parenteral, nasal and / or oral abuse of active ingredients, preferably of pharmaceutical active ingredients, with abuse potential.

Problems solved by technology

The breaking strength of at least 500 N (measured as stated in the specification) means that pulverization of the dosage form is considerably more difficult using conventional means, so considerably complicating or preventing the subsequent abuse.
If comminution is inadequate, parenteral, in particular intravenous, administration cannot be performed safely or extraction of the active ingredient therefrom takes too long for the abuser or there is no “kick” when taken orally, as release is not instantaneous.

Method used

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  • Abuse-proofed dosage form
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Examples

Experimental program
Comparison scheme
Effect test

example 1

[0202]

ComponentsPer tabletPer batchTramadol HCl100.0mg1495.0gPolyethylene oxide, NF, MW 7 000 000167.8mg2508.6g(Polyox WSR 303, Dow Chemicals)Hydroxypropylmethylcellulose33.5mg500.8g100 000 mPa · sPolyethylene glycol (PEG 6000)33.5mg500.8gButylhydroxytoluene (BHT)0.2mg3.0gTotal weight335.0mg5008.2g

[0203] The stated quantity of BHT was dissolved in ethanol (96%), such that a 7.7% (mass / mass) ethanolic solution was obtained. This was mixed initially with 150 g of polyethylene oxide in a high speed mixer for 30 minutes and then the remaining quantity of polyethylene oxide was added and stirring continued for a further 30 minutes. The composition was dried for 12 h at 40° C. All the further components were added and mixed for 15 min in a free-fall mixer. The powder mixture was apportioned into an extruder. Extrusion was performed using a model Micro 27 GL 40 D double screw extruder with a spindle diameter of 18 mm manufactured by Leistritz (Nürnberg). Screws with blunt ends were used, t...

example 2

[0207]

ComponentsPer TabletPer batchOxycodon HCl20.0mg410.1g13.7%Polyethylene oxide 7 000 000107.2mg2199.3g73.2%(Polyox WSR 303, DOW Chemicals)Polyethylene glycol (PEG 6000)15.0mg307.8g10.3%Hypromellose (Metholose 90 SH3.8mg76.8g 2.6%100 000 cP, ShinEtsu)α-Tocopherol0.2mg3.0g 0.1%Aerosil (highly disperse SiO2)0.2mg3.0g 0.1%146.4mg3000.0g 100%

[0208] 50 g of the polyethylene oxide, 3 g α-tocopherol and 3 g Aerosil were mixed to a homogeneous mixture by means of a mortar. All the further components were added and mixed for 15 minutes in a free-fall mixer.

[0209] Extrusion was performed using a model Micro 27 PH 40 D twin screw extruder manufactured by Leistritz (Nürnberg). Screws having eccentric ends were used. The die used is a heatable round die having a diameter of 9 mm.

[0210] The following parameters were selected for extrusion:

Screw speed:100rpmThroughput:4kg / hProduct temperature:134°C.Casing temperature:heating zones 1 to 10:100°C.heating zone 11 (die):120°C.

[0211] The extruda...

example 3

[0215]

ComponentsPer TabletPer batch%Oxycodon HCl20.0mg333.3g11.1Polyethylene oxide 7 000 000122.6mg2060.7g68.7(Polyox WSR 303, DOW Chemicals)Polyethylene glycol (PEG 6000)18.0mg300.0g10.0Hypromellose (Metholose 90 SH18.0mg300.0g10.0100 000 cP, ShinEtsu)α-Tocopherol0.2mg3.0g0.1Aerosil (highly disperse SiO2)0.2mg3.0g0.1180mg3000.0g100%

[0216] 50 g of the polyethylene oxide, 3 g α-tocopherol and 3 g Aerosil were mixed to a homogeneous mixture by means of a mortar. All the further components were added and mixed for 15 minutes in a free-fall mixer.

[0217] Extrusion was performed using a model Micro 27 PH 40 D twin screw extruder manufactured by Leistritz (Nürnberg). Screws having eccentric ends were used. The die used is a heatable round die having a diameter of 9 mm.

[0218] The following parameters were selected for extrusion:

Screw speed:100rpmThroughput:4kg / hProduct temperature:134°C.Casing temperature:heating zones 1 to 10:100°C.heating zone 11 (die):120°C.

[0219] The extrudate, whic...

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Abstract

The invention relates to a dosage form that is thermoformed without discoloration and is safeguarded from abuse, comprising at least one synthetic or natural polymer having a breaking strength of at least 500 N in addition to one or more active substances that could be subject to abuse. The invention also relates to a corresponding method for producing said dosage form.

Description

CROSS REFERENCE TO RELATED APPLICATIONS [0001] This application is a Continuation-in-Part-Application of pending U.S. patent application Ser. No. 11 / 349,544 filed on Feb. 6, 2006, a Continuation-in-Part-Application of pending U.S. patent application Ser. No. 11 / 348,295 filed on Feb. 6, 2006, a Continuation-in-Part-Application of pending U.S. patent application Ser. No. 10 / 718,112 filed on Nov. 20, 2003 and claims priority of German Patent Application No. 10 2005 005446.3 filed on Feb. 4, 2005 and German Patent Application No. 10 336 400.5 filed on Aug. 6, 2003.BACKGROUND OF THE INVENTION [0002] The present invention relates to an abuse-proofed dosage form thermoformed by extrusion without discoloration and containing, in addition to one or more active ingredients with abuse potential (A) optionally together with physiologically acceptable auxiliary substances (B), at least one synthetic or natural polymer (C) and optionally at least one wax (D), wherein the dosage form exhibits a br...

Claims

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Application Information

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IPC IPC(8): A61K49/00A61K31/485
CPCA61K9/2027A61K9/2031A61K9/2054A61K9/2095A61K31/135A61J3/07A61K9/0092A61K9/2072A61K31/485A61K9/2004A61K9/2009A61K9/2013A61K9/2068A61K9/2086
Inventor ARKENAU-MARIC, ELISABETHBARTHOLOMAUS, JOHANNESKUGELMANN, HEINRICH
Owner GRUNENTHAL GMBH
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