IP Library Granted Patent US 9,682,075
Granted Patent B2
US 9,682,075 · App. 14/320,086 · Granted Jun 20, 2017

Tamper-resistant pharmaceutical compositions of opioids and other drugs

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Quick Facts
Patent No.
US 9,682,075
App. No.
14/320,086
Granted
Jun 20, 2017
Kind
B2
Abstract

Tamper-resistance pharmaceutical compositions have been developed to reduce the likelihood of improper administration of drugs, especially drugs such as opioids. The tamper-resistant compositions retard the release of drug, even if the physical integrity of the formulation is compromised (for example, by chopping with a blade or crushing) and the resulting material is placed in water, snorted, or swallowed. However, when administered as directed, the drug is slowly released from the composition as the composition is passes through the GI tract.

Claims (28)

1. A tamper resistant pharmaceutical composition comprising a plurality of solid particles each particle comprising:

(a) one or more drugs prone to abuse;

(b) one or more waxes, wax-like substances or mixtures thereof; and

(c) one or more fatty acids present at 42%-69% by weight of the particle

wherein the particles have a median particle size (D[0.5]) between about 200 microns and about 400 microns; and

wherein the drug is oxycodone or a pharmaceutically acceptable salt thereof and after oral administration as directed a therapeutically effective amount of drug is released over a period of 6-24 hours; and

the composition maintains a slow release of drug even if the particles are crushed with a mortar and pestle and swallowed.

2. The composition of claim 1 , wherein the particles are substantially spherical.

3. The composition of claim 1 , wherein the drug and the one or more fatty acids interact ionically.

4. The composition of claim 1 , wherein the fatty acids are selected from the group consisting of linoleic acid, octanoic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid.

5. The composition of claim 4 , wherein the fatty acid is myristic acid.

6. The composition of claim 1 , wherein the one or more wax or wax-like substances are selected from the group consisting of beeswax, glycowax, castor wax, carnauba wax, paraffins, microcrystalline wax, and candelilla wax.

7. The composition of claim 6 , wherein the wax or wax-like substances are beeswax and carnauba wax.

8. The composition of claim 7 , wherein the drug prone to abuse is oxycodone, the wax or wax-like substances are beeswax and carnauba wax, and the fatty acid is myristic acid.

9. A method of treating pain comprising administering to a human subject in need thereof, a therapeutically effective amount of a tamper resistant pharmaceutical composition comprising a plurality of particles, each particle comprising:

(a) one or more drugs prone to abuse;

(b) one or more waxes, wax-like substances or mixtures thereof; and

(c) one or more fatty acids present at 42%-69% by weight of the particle

wherein the drug is present as a solid dispersion or solid solution within the particles and

wherein the particles have a median particle size (D[0.5]) between about 200 microns and about 400 microns; and

wherein the drug is oxycodone or a pharmaceutically acceptable salt thereof and after oral administration as directed a therapeutically effective amount of drug is released over a period of 6-24 hours; and

the composition maintains a slow release of drug even if the particles are crushed with a mortar and pestle and swallowed.

10. A method of making the tamper resistant pharmaceutical composition of claim 1 , comprising:

(a) dispersing or dissolving a drug prone to abuse in a mixture comprising one or more waxes, wax-like substances or mixtures thereof; and

(b) forming a plurality of particles wherein the drug is present as a solid dispersion or solid solution within the particles and wherein the particles have a median particle size (D[0.5]) between about 200 microns and about 400 microns.

11. The method of claim 10 , wherein said process comprises a spinning disc atomization process.

12. The composition of claim 1 , wherein the particles have a median particle size (D[0.5]) between about 250 microns and about 400 microns.

13. The method of claim 9 , wherein the particles have a median particle size (D[0.5]) between about 250 microns and about 400 microns.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Dec 23, 2025
From: BIOPHARMA CREDIT PLC
To: COLLEGIUM PHARMACEUTICAL, INC.
Reel/Frame 073308/0335 →
RELEASE OF SECURITY INTEREST Recorded Dec 23, 2025
From: BIOPHARMA CREDIT PLC
To: COLLEGIUM PHARMACEUTICAL, INC.
Reel/Frame 073308/0342 →
AMENDED AND RESTATED PATENT SECURITY AGREEMENT Recorded Mar 22, 2022
From: COLLEGIUM PHARMACEUTICAL, INC.
To: BIOPHARMA CREDIT PLC
Reel/Frame 059474/0526 →
SECURITY INTEREST Recorded Feb 13, 2020
From: COLLEGIUM PHARMACEUTICAL, INC.
To: BIOPHARMA CREDIT PLC
Reel/Frame 051817/0583 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2014
From: RARIY, ROMAN V.; FLEMING, ALISON B.; HIRSH, JANE C.; SAIM, SAID; VARANASI, RAVI K.
To: COLLEGIUM PHARMACEUTICAL, INC.
Reel/Frame 033750/0847 →