IP Library Granted Patent US 9,554,996
Granted Patent B2
US 9,554,996 · App. 13/741,915 · Granted Jan 31, 2017

Compositions and methods for delivery of poorly soluble drugs

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,554,996
App. No.
13/741,915
Granted
Jan 31, 2017
Kind
B2
Abstract

Described herein are compositions comprising particles of poorly soluble drugs encapsulated by stabilizers. Further described are pharmaceutical compositions comprising such encapsulated compositions. Also described are methods of making such encapsulated particle compositions, and methods of making the corresponding pharmaceutical compositions. The encapsulated particle compositions described herein allow poorly soluble drugs to be administered with good bioavailability by routes that are non-invasive to patients, such as by oral administration.

Claims (15)

1. A particle delivery system (PDS) comprising dry particles having an average diameter of less than about 2 mm, wherein the dry particles comprise a poorly soluble drug and a stabilizer comprising polyethylene glycol (PEG), wherein

the amount of the poorly soluble drug present in the dry particles ranges from about 0.2% to about 4% by mass of the dry particles,

the poorly soluble drug is encapsulated by the stabilizer,

the poorly soluble drug comprises at least one drug selected from codeine, fentanyl, hydrocodone, hydromorphone, morphine, methylnaltrexone, nalbuphine, nalmefene, oxymorphone, oxycodone, pethidine, tramadol, and combinations or mixtures thereof,

and wherein the stabilizer is water soluble.

2. The composition of claim 1 , wherein the PEG has an average molecular weight ranging from about 100 Daltons to about 100,000 Daltons.

3. The PDS of claim 2 , wherein the PEG is PEG 3350.

4. The PDS of claim 1 , further comprising a surfactant.

5. The PDS of claim 4 , wherein the surfactant is a nonionic surfactant.

6. A pharmaceutical composition comprising the PDS of claim 1 and at least one second compound.

7. The pharmaceutical composition of claim 6 , wherein the composition is formulated for oral administration.

8. The pharmaceutical composition of claim 6 , wherein the at least one second compound is a drug chosen from opioid receptor antagonists, anti-inflammatory drugs, analgesics, and combinations or mixtures thereof.

9. The pharmaceutical composition of claim 8 , wherein the drug comprises an opioid receptor antagonist.

10. The pharmaceutical composition of claim 9 , wherein the drug comprises naloxone or a pharmaceutically acceptable salt thereof.

11. The pharmaceutical composition of claim 10 , wherein the naloxone salt is naloxone HCl.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2018
From: NANOTHERAPEUTICS INC
To: NANOSHIFT, LLC
Reel/Frame 046656/0784 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2017
From: TALTON, JAMES D
To: NANOTHERAPEUTICS, INC.
Reel/Frame 040954/0786 →
RELEASE OF SECURITY INTEREST Recorded May 19, 2016
From: WHITE OAK GLOBAL ADVISORS, LLC AS AGENT
To: NANOTHERAPEUTICS, INC.
Reel/Frame 038651/0947 →
SECURITY INTEREST Recorded Mar 20, 2015
From: NANOTHERAPEUTICS, INC.
To: WHITE OAK GLOBAL ADVISORS, LLC
Reel/Frame 035236/0932 →