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Tamper resistant dosage forms

a technology of dosage forms and tamper-resistant materials, applied in the direction of powder delivery, drug compositions, textiles and paper, etc., can solve the problems of patient receiving the dose more quickly than the patient, and the abuse of pharmaceutical products

Inactive Publication Date: 2013-09-26
PURDUE PHARMA LP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent text is referring to a group of tablets that are moving together in a way that prevents them from sticking to each other. This is called a bed of free flowing tablets and it can be created by setting a coating pan at a certain speed or using a fluidized bed of tablets. The technical effect of this invention is that it helps to prevent sticking of tablets during processing, making them easier to handle and work with.

Problems solved by technology

Pharmaceutical products are sometimes the subject of abuse.
Controlled release opioid agonist dosage forms which can liberate a portion of the opioid upon exposure to ethanol, can also result in a patient receiving the dose more rapidly than intended if a patient disregards instructions for use and concomitantly uses alcohol with the dosage form.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

[0387]In Example 1 a 200 mg tablet including 10 mg of oxycodone HCl was prepared using high molecular weight polyethylene oxide in combination with hydroxypropyl cellulose.

Composition:

[0388]

Ingredientmg / unit%Oxycodone HCl105Polyethylene Oxide16080(MW: approximately4,000,000;Polyox ™ WSR-301)Hydroxypropyl3015Cellulose(Klucel ™ HXF)Total200100

Process of Manufacture:

[0389]The processing steps to manufacture tablets were as follows:[0390]1. Oxycodone HCl, Polyethylene Oxide and hydroxypropyl cellulose was dry mixed in a low / high shear Black & Decker Handy Chopper dual blade mixer with a 1.5 cup capacity.[0391]2. Step 1 blend was compressed to target weight on a single station tablet Manesty Type F 3 press[0392]3. Step 2 tablets were spread onto a tray and placed in a Hotpack model 435304 oven at 70° C. for approximately 14.5 hours to cure the tablets.

[0393]In vitro testing including testing tamper resistance (hammer and breaking strength test) and resistance to alcohol extraction was pe...

example 2

[0398]In Example 2 three different 100 mg tablets including 10 and 20 mg of Oxycodone HCl were prepared using high molecular weight polyethylene oxide and optionally hydroxypropyl cellulose.

Compositions:

[0399]

Example 2.1Example 2.2Example 2.3Ingredientmg / unitmg / unitmg / unitOxycodone HCl102010Polyethylene Oxide908085(MW: approximately4,000,000;Polyox ™ WSR301)Hydroxypropyl005Cellulose(Klucel ™ HXF)Total100100100

Process of Manufacture:

[0400]The processing steps to manufacture tablets were as follows:[0401]1. Oxycodone HCl, Polyethylene Oxide and Hydroxypropyl Cellulose were dry mixed in a low / high shear Black & Decker Handy Chopper dual blade mixer with a 1.5 cup capacity.[0402]2. Step 1 blend was compressed to target weight on a single station tablet Manesty Type F 3 press.[0403]3. Step 2 tablets were spread onto a tray placed in a Hotpack model 435304 oven at 70-75° C. for approximately 6 to 9 hours to cure the tablets.

[0404]In vitro testing including testing for tamper resistance (b...

example 3

[0407]In Example 3a 200 mg tablet prepared including 10 mg oxycodone HCl and high molecular weight polyethylene oxide were prepared.

Composition:

[0408]

Ingredientmg / unit%Oxycodone HCl105Polyethylene Oxide18894(MW: approximately4,000,000;Polyox ™ WSR301)Magnesium Stearate21Total200100

Process of Manufacture:

[0409]The processing steps to manufacture tablets were as follows:[0410]1. Oxycodone HCl, Polyethylene Oxide and Magnesium Stearate were dry mixed in a low / high shear Black & Decker Handy Chopper dual blade mixer with a 1.5 cup capacity.[0411]2. Step 1 blend was compressed to target weight on a single station tablet Manesty Type F 3 press.[0412]3. Step 2 tablets were placed onto a tray placed in a Hotpack model 435304 oven at 70° C. for 1 to 14 hours to cure the tablets.

[0413]In vitro testing including testing for tamper resistance (breaking strength test) was performed as follows:

[0414]The tablets were tested in vitro using USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gas...

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Abstract

The present invention relates to pharmaceutical dosage forms, for example to a tamper resistant dosage form including an opioid analgesic, and processes of manufacture, uses, and methods of treatment thereof.

Description

[0001]This application claims priority from U.S. Provisional Application Ser. No. 60 / 840,244, filed Aug. 25, 2006, the disclosure of which is hereby incorporated by reference.TECHNICAL FIELD OF THE INVENTION[0002]The present invention relates to pharmaceutical dosage forms, for example to a tamper resistant dosage form including an opioid analgesic, and processes of manufacture, uses, and methods of treatment thereof.BACKGROUND OF THE INVENTION[0003]Pharmaceutical products are sometimes the subject of abuse. For example, a particular dose of opioid agonist may be more potent when administered parenterally as compared to the same dose administered orally. Some formulations can be tampered with to provide the opioid agonist contained therein for illicit use. Controlled release opioid agonist formulations are sometimes crushed, or subject to extraction with solvents (e.g., ethanol) by drug abusers to provide the opioid contained therein for immediate release upon oral or parenteral adm...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K9/00A61J3/06
CPCA61K9/1641B29C43/003A61K9/2072A61K9/2095A61K9/2866A61K9/209A61K45/06A61J3/06A61K9/0002A61K9/2853A61K31/485A61K47/34A61K47/10A61K9/2077A61J3/10A61K9/2031A61K9/2013A61K9/2054A61P25/00A61P25/04A61P29/00A61P29/02A61K9/16A61K9/2086A61K9/28A61K9/2018A61K9/2893A61J3/005B29C37/0025B29C43/52B29K2071/02A61K9/0053B29B7/88B29C35/045B29C2035/046B29K2105/0035B29B7/02B29C35/16B29C43/02B29C71/009B29C2035/1658B29L2031/753A61K9/284A61K9/2027B29K2105/251B29C71/00B29K2995/0088
Inventor MCKENNA, WILLIAM H.MANNION, RICHARD O.O'DONNELL, EDWARD P.HUANG, HAIYONG H.
Owner PURDUE PHARMA LP
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