IP Library Granted Patent US 11,364,299
Granted Patent B2
US 11,364,299 · App. 14/762,573 · Granted Jun 21, 2022

Non-addictive analgesic sustained-release drug delivery system and preparation method thereof

Inventors: Tao Chen (Shaanxi, CN); Wudang Lu (Shaanxi, CN); Weiping Yu (Shaanxi, CN); Jianli Gao (Shaanxi, CN); Danfeng Kong (Shaanxi, CN); Qingchuan Zhao (Shaanxi, CN); Weijiao Wang (Shaanxi, CN); Qinyuan Wu (Shaanxi, CN)
Assignee: LIPONT PHARMACEUTICALS INC.
A61K47/10A61K9/0019A61K9/08A61K31/135A61K31/245A61K31/381A61K31/42A61K31/445A61K31/47A61K47/14A61K47/44B65B3/003B65B7/161B65B31/003
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 11,364,299
App. No.
14/762,573
Granted
Jun 21, 2022
Kind
B2
Abstract

A non-addictive analgesic sustained-release drug delivery system, comprising: (1) a narcotic analgesic drug having a concentration of 1 mg/ml-160 mg/ml, the drug being selected from a group consisting of: a local analgesic drug, and the combination of the local analgesic drug and a nonsteroidal analgesic drug and/or an opioid analgesic drug; (2) a drug menstruum in a proportion of 1%-75% (v/v), the menstruum being selected from a group consisting of benzyl alcohol, ethanol, benzyl benzoate, ethyl lactate, and tetrahydrofurfuryl polyethylene glycol ether; and (3) a drug sustained-release formulation having a proportion of 25%-99% (v/v), the sustained-release formulation being selected from a group consisting of natural vegetable oil, synthetic lipid, artificially improved half-natural lipid and derivative thereof. Also disclosed are a preparation process and use of the sustained-release drug delivery system.

Claims (7)

1. A non-addictive sustained-release drug delivery system comprising:

i) 12-50 mg/ml (w/v) of an anesthetic analgesic comprising a local anesthetic or a combination of a local anesthetic and at least one of parecoxib or dezocine;

ii) 10%-40% (v/v) of a drug menstruum comprising benzyl alcohol and/or benzyl benzoate, or a combination of ethanol together with benzyl alcohol and/or benzyl benzoate; and

iii) 60%-90% (v/v) of a drug sustained-release agent comprising soybean oil and/or castor oil,

wherein the local anesthetic is selected from the group consisting of ropivacaine free base or a methanesulfonate, hydrochloride, citrate, sulfate, lactate, succinate, fumarate, glutamate, ethylsulfonate, benzenesulfonate, salicylate, or maleate salt thereof, and

wherein the non-addictive sustained-release drug delivery system is oily, homogenous, and configured for injection.

2. The non-addictive sustained-release drug delivery system of claim 1 , wherein the anesthetic analgesic is ropivacaine free base.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 31, 2015
From: CHEN, TAO; LU, WUDANG; YU, WEIPING; GAO, JIANLI; KONG, DANFENG; ZHAO, QINGCHUAN; WANG, WEIJIAO; WU, QINYUAN
To: LIPONT PHARMACEUTICALS INC.
Reel/Frame 036458/0393 →
Priority Claims (1)
CN 201310022657.3 · Jan 22, 2013 · national
Continuity (1)
Related Publication 20150359891A1 · Dec 17, 2015