IP Library Granted Patent US 11,173,119
Granted Patent B2
US 11,173,119 · App. 16/711,591 · Granted Nov 16, 2021

Nanolipogel vehicles for controlled delivery of different pharmaceutical agents

Inventors: Tarek M. Fahmy (New Haven, CT); Eric Stern (Jamaica Plain, MA); Richard A. Flavell (Guillford, CT); Jason Park (New York, NY); Alyssa Siefert (Naugatuck, CT); Stephen H. Wrzesinski (Slingerlands, NY)
Assignee: Yale University
A61K9/127A61K9/0019A61K9/1271A61K9/1273A61K9/1277A61K9/5153A61K31/343A61K38/1841A61K38/2013A61K47/24A61K47/40A61K47/58A61K47/6849A61K47/6937A61K47/6951B82Y5/00C07K16/2812
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 11,173,119
App. No.
16/711,591
Granted
Nov 16, 2021
Kind
B2
Abstract

A “nanolipogel” is a delivery vehicle including one or more lipid layer surrounding a hydrogel core, which may include an absorbent such as a cyclodextrin or ion-exchange resin. Nanolipogels can be constructed so as to incorporate a variety of different chemical entities that can subsequently be released in a controlled fashion. These different incorporated chemical entities can differ dramatically with respect to size and composition. Nanolipogels have been constructed to contain co-encapsulated proteins as well as small hydrophobic drugs within the interior of the lipid bilayer. Agents incorporated within nanolipogels can be released into the milieu in a controlled fashion, for example, nanolipogels provide a means of achieving simultaneous sustained release of agents that differ widely in chemical composition and molecular weight. Additionally, nanolipogels can favorably modulate biodistribution.

Claims (16)

1. A nanolipogel comprising

a polymeric matrix core comprising a host molecule that can bind a therapeutic, diagnostic or prophylactic agent to be delivered, releasing the agent under in vivo conditions, and

a lipid shell.

2. The nanolipogel of claim 1 wherein the polymeric matrix, the lipid shell, or both are crosslinked.

3. The nanolipogel of claim 1 comprising an agent complexed to the host molecules, dispersed within the polymeric matrix, dispersed in or bound to the lipid shell, or combinations thereof.

4. The nanolipogel of claim 1 wherein the polymeric matrix comprises polymer selected from the group consisting of polylactic acid), poly(glycolic acid), poly(lactic acid-co-glycolic acids), polyhydroxyalkanoates; polycaprolactones; poly(orthoesters); polyanhydrides; poly(phosphazenes); poly(lactide-co-caprolactones); poly(glycolide-co-caprolactones); polycarbonates; polyamides, polypeptides, and poly(amino acids); polyesteramides; other biocompatible polyesters; poly(dioxanones); poly(alkylene alkylates); hydrophilic polyethers; polyurethanes; polyetheresters; polyacetals; polycyanoacrylates; polysiloxanes; poly(oxyethylene)poly(oxypropylene) copolymers; polyketals; polyphosphates; polyhydroxyvalerates; polyalkylene oxalates; polyalkylene succinates; poly(maleic acids), polyvinyl alcohols, polyvinylpyrrolidone; poly(alkylene oxides); celluloses, polyacrylic acids, albumin, collagen, gelatin, prolamines, polysaccharides, derivatives, copolymers, and blends thereof.

5. The nanolipogel of claim 3 wherein the agent is selected from the group of therapeutic, prophylactic, diagnostic, and nutraceutical agents consisting of small molecule active agents, proteins, polypeptides, polysaccharide, and nucleic acids.

6. The nanolipogel of claim 5 wherein the agent is selected from the group consisting of antibiotics, antivirals, anti-parasitics, cytokines, growth factors, growth inhibitors, hormones, hormone antagonists, antibodies and bioactive fragments thereof, antigen and vaccine formulations, anti-inflammatories, immunomodulators, and oligonucleotide drugs, paramagnetic molecules, fluorescent compounds, magnetic molecules, and radionuclides, x-ray imaging agents, and contrast agents.

7. The nanolipogel of claim 6 wherein the agent is selected from the group consisting of alkylating agents, antimetabolite, antimitotics, anthracyclines, cytotoxic antibiotics, topoisomerase inhibitors, antibodies to vascular endothelial growth factor; thalidomide; endostatin; angiostatin; receptor tyrosine kinase (RTK) inhibitors); tyrosine kinase inhibitors; transforming growth factor-α or transforming growth factor-β inhibitors, and antibodies to the epidermal growth factor receptor.

8. The nanolipogel of claim 1 comprising a liposomal shell composed of one or more concentric lipid layers, optionally crosslinked, wherein the lipids can be neutral, anionic or cationic lipids at physiologic pH.

9. The nanolipogel of claim 8 wherein the lipid is selected from the group consisting of cholesterol, phospholipids, lysolipids, lysophospholipids, and sphingolipids, and derivatives thereof.

10. The nanolipogel of claim 8 comprising lipid selected from the group consisting of phosphatidylcholine; phosphatidylserine, phosphatidylglycerol, phosphatidylinositol; glycolipids; sphingomyelin, ceramide galactopyranoside, gangliosides, cerebrosides; fatty acids, sterols; 1,2-diacyl-sn-glycero-3-phosphoethanolamines, 1,2-dihexadecylphosphoethanolamine, 1,2-distearoylphosphatidylcholine, 1,2-dipalmitoylphosphatidylcholine, 1,2-dimyristoylphosphatidylcholine, N-[1-(2,3-dioleoyloxy) propyl]-N,N,N-trimethyl ammonium salts, dimethyldioctadecyl ammonium bromide, 1,2-diacyloxy-3-trimethylammonium propanes, N[1-(2,3-dioloyloxy)propyl]-N,N-dimethyl amine, 1,2-diacyloxy-3-dimethylammonium propanes, N[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride, 1,2-dialkyloxy-3-dimethylammonium propanes, dioctadecylamidoglycylspermine, 3-[N-(N′,N-dimethylamino-ethane)carbamoyl]cholesterol (DC-Chol); 2,3-dioleoyloxy-N-(2-(sperminecarboxamido)-ethyl)-N,N-dimethyl-1-propanaminium trifluoro-acetate (DOSPA), β-alanyl cholesterol, cetyltrimethylammonium bromide (CTAB), diC 14 -amidine, N-tert-butyl-N′-tetradecyl-3-tetradecylamino-propionamidine, N-(alpha-trimethylammonioacetyl)didodecyl-D-glutamate chloride (TMAG), ditetradecanoyl-N-(trimethylammonio-acetyl) diethanolamine chloride, 1,3-dioleoyloxy-2-(6-carboxy-spermyl)-propylamide (DOSPER), and N,N,N′,N′-tetramethyl-, N′-bis(2-hydroxylethyl)-2,3-dioleoyloxy-1, 4-butanediammonium iodide, 1-[2-(acyloxy)ethyl]2-alkyl(alkenyl)-3-(2-hydroxyethyl)-imidazolinium chloride derivatives, and 2,3-dialkyloxypropyl quaternary ammonium derivatives containing a hydroxyalkyl moiety on the quaternary amine.

11. The nanolipogel of claim 1 wherein the lipid is a PEGylated derivative of a neutral, anionic, or cationic lipid.

12. The nanolipogel of claim 10 , wherein the 1-[2-(acyloxy)ethyl]2-alkyl(alkenyl)-3-(2-hydroxyethyl)-imidazolinium chloride derivatives are selected from the group consisting of 1-[2-(9(Z)-octadecenoyloxy) ethyl]-2-(8(Z)-heptadecenyl-3-(2-hydroxyethyl)imidazolinium chloride (DOTIM) and 1-[ 2 -(hexadecanoyloxy)ethyl]-2-pentadecyl-3-(2-hydroxyethyl)imidazolinium chloride (DPTIM).

13. The nanolipogel of claim 10 , wherein the 2,3-dialkyloxypropyl quaternary ammonium derivatives containing a hydroxyalkyl moiety on the quaternary amine are selected from 1,2-dioleoyl-3-dimethyl[1]hydroxyethyl ammonium bromide (DORI), 1,2-dioleyloxypropyl-3-dimethyl-hydroxyethyl ammonium bromide (DORIE), 1,2-dioleyloxypropyl-3-dimetyl-hydroxypropyl ammonium bromide (DORIE-HP), 1,2-dioleyl-oxy-propyl-3-dimethyl-hydroxybutyl ammonium bromide (DORIE-HB), 1,2-dioleyloxypropyl-3-dimethyl-hydroxypentyl ammonium bromide (DORIE[1]Hpe), 1,2-dimyristyloxypropyl-3-dimethyl-hydroxylethyl ammonium bromide (DMRIE), 1,2-dipalmityloxypropyl-3-dimethyl-hydroxyethyl ammonium bromide (DPRIE), and 1,2-disteryloxypropyl-3-dimethyl-hydroxyethyl ammonium bromide (DSRIE).

14. The nanolipogel of claim 4 , wherein the polyhydroxyalkanoates are selected from the group consisting of poly3-hydroxybutyrate and poly4-hydroxybutyrate.

Assignments (3)
CONFIRMATORY LICENSE Recorded Mar 28, 2025
From: YALE UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 070672/0781 →
LICENSE Recorded May 7, 2020
From: YALE UNIVERSITY
To: MODULATE THERAPEUTICS INC
Reel/Frame 052598/0264 →
LICENSE Recorded May 7, 2020
From: YALE UNIVERSITY
To: IMMUNOVA LLC
Reel/Frame 052598/0330 →
Continuity (7)
Continuation 15923139 · Mar 16, 2018
Continuation 15155055 · May 15, 2016
Continuation In Part 14394161
Provisional Application 61623486 · Apr 12, 2012
Provisional Application 61747624 · Dec 31, 2012
Provisional Application 61747614 · Dec 31, 2012
Related Publication 20200179283A1 · Jun 11, 2020