IP Library Granted Patent US 10,905,775
Granted Patent B2
US 10,905,775 · App. 13/905,015 · Granted Feb 2, 2021

Particulate constructs for release of active agents

Inventors: Lawrence D. Mayer (North Vancouver, CA); Robert K. Prud'homme (Lawrenceville, NJ); Christine J. Allen (Toronto, CA); Walid S. Saad (Princeton, NJ)
Assignees: Celator Pharmaceuticals, Inc.; The Trustees of Princeton University
A61K47/6931A61K8/85A61K9/5153A61K45/06A61K47/22A61K47/54A61K47/543A61K47/545A61K47/55A61K47/551A61K47/552A61K47/58A61K47/59A61K47/593A61K47/60A61K47/6935A61Q17/04B82Y5/00A61K2800/57
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Quick Facts
Patent No.
US 10,905,775
App. No.
13/905,015
Granted
Feb 2, 2021
Kind
B2
Abstract

Particulate constructs stabilized by amphiphilic copolymers and comprising at least one active coupled to a hydrophobic moiety provide sustained release of the active in both in vitro and in vivo environments.

Claims (22)

1. A composition comprising particles obtained from fast mixing according to the Nano Precipitation process

a) an amphiphilic stabilizer,

b) a conjugate of the formula

(active−linker) n −hydrophobic moiety  (1)

wherein n is an integer of 1-100;

“active” refers to a first therapeutic agent;

“linker” is a divalent residue of an organic molecule which comprises a bond that is selectively cleavable by reduction or hydrolysis to control the rate of release of said active from the particles free of said hydrophobic moiety or portion thereof; and

“hydrophobic moiety” refers to the residue of an organic molecule that is insoluble in aqueous solution; and

c) a second therapeutic agent different from the first therapeutic agent to obtain said particles,

and wherein the hydrophobic moiety is a polymer having a molecular weight between 800 and 200,000 g/mole or is a natural product, and the amphiphilic stabilizer is a copolymer having a hydrophilic region and a hydrophobic region wherein said copolymer is a graft, block or random amphiphilic copolymer and has a molecular weight between 1,000 g/mole and 50,000 g/mole.

2. The composition of claim 1 wherein the hydrophobic moiety is a polymer of methyl acrylate, ethyl acrylate, propyl acrylate, n-butyl acrylate (BA), isobutyl acrylate, 2-ethyl acrylate, t-butyl acrylate, ethyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, an acrylonitrile, a methacrylonitrile, vinyl acetate, vinylversatate, vinylpropionate, vinylformamide, vinylacetamide, vinylpyridine, vinylimidazole; an aminoalkylacrylate, an aminoalkylmethacrylate, an aminoalkyl(meth)acrylamide, a styrene, cellulose acetate phthalate, cellulose acetate succinate, hydroxypropylmethylcellulose phthalate, or

is poly(D,L lactide), poly(D,L-lactide-co-glycolide), poly(glycolide), poly(hydroxybutyrate), poly(alkylcarbonate), a poly(orthoester), a polyester, poly(hydroxyvaleric acid), polydioxanone, poly(ethylene terephthalate), poly(malic acid), poly(tartronic acid), a polyanhydride, a polyphosphazene, a poly(amino acid) and copolymers, a poly(ethylene-vinyl acetate) (“EVA”) copolymer, silicone rubber, polyethylene, polypropylene, a polydiene, a maleic anhydride copolymer of vinyl-methylether and other vinyl ethers, a polyamide (nylon 6,6), a polyurethane, a poly(ester urethane), a poly(ether urethane), a poly(ester-urea), poly(valerolactone), a polyanhydride, a copolymer of poly(caprolactone) and poly(lactic acid), or

is a natural product which is vitamin E, vitamin K, vitamin A, beta carotene, astaxanthin, trans and cis retinal, retinoic acid, folic acid, dihydrofolate, retinyl acetate, retinyl palmitate), cholecalciferol, calcitriol, hydroxycholecalciferol, ergocalciferol, a-tocopherol, a-tocopherol acetate, a-tocopherol nicotinate, or estradiol.

3. The composition of claim 1 wherein the amphiphilic stabilizer is a copolymer of a hydrophilic block coupled with a hydrophobic block,

wherein the hydrophobic block is methyl acrylate, ethyl acrylate, propyl acrylate, n-butyl acrylate (BA), isobutyl acrylate, 2-ethyl acrylate, t-butyl acrylate, ethyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, an acrylonitrile; methacrylonitrile, vinyl acetate, vinylversatate, vinylpropionate, vinylformamide, vinylacetamide, vinylpyridine, vinylimidazole, an aminoalkylmethacrylate, an aminoalkyl(meth)acrylamide, styrene, cellulose acetate phthalate, cellulose acetate succinate, hydroxypropylmethylcellulose phthalate, poly(D,L lactide), poly (D,L-lactide-co-glycolide), poly(glycolide), poly(hydroxybutyrate), poly(alkylcarbonate), a poly(orthoester), a polyester, poly(hydroxyvaleric acid), polydioxanone, poly(ethylene terephthalate), poly(malic acid), poly(tartronic acid), a polyanhydride, a polyphosphazene, a poly(amino acid), a poly(ethylene-vinyl acetate) (“EVA”) copolymer, silicone rubber, polyethylene, polypropylene, a polydiene, a hydrogenated form of polydiene), maleic anhydride copolymers of vinyl methylether and other vinyl ethers, polyamides (nylon 6,6), polyurethane, poly(ester urethanes), poly(ether urethanes), poly(ester-urea), poly(ethylenevinyl acetate), poly(D,L-lactic acid), poly(L-lactic acid), poly(glycolic acid), a copolymer of lactic acid and glycolic acid, poly(caprolactone), poly(valerolactone), a polyanhydride, a copolymer of poly(caprolactone) and poly(lactic acid); and

the hydrophilic block is a carboxylic acid, a polyoxyethylene, a polyacrylamide, a copolymer of acrylamide with dimethylaminoethylmethacrylate, diallyldimethylammonium chloride, vinylbenzylthrimethylammonium chloride, acrylic acid, methacrylic acid, 2-acrylamido-2-methylpropane sulfonic acid, styrene sulfonate, polyvinyl pyrrolidone, starch, a starch derivative, dextran, a dextran derivative, a polypeptide, poly hyaluronic acid, an alginic acid, a polylactide, a polyethyleneimine, a polyionene, a polyacrylic acid, a polyiminocarboxylate, gelatin, or an unsaturated ethylenic mono or dicarboxylic acid.

4. The composition of claim 1 , wherein the hydrophobic moiety is vitamin E, vitamin A or vitamin K, or a retinol; or

wherein the hydrophobic moiety is polycaprolactone, polylactic acid, polystyrene, polybutadiene, polycaproic acid, polymethylbenzylate, poly(D,L-lactide), poly(D,L-lactide-co-glycolide), poly(glycolide), poly(hydroxybutyrate), poly(alkylcarbonate) poly(orthoesters), polyesters, poly(hydroxyvaleric acid), or copolymers thereof.

5. The composition of claim 1 , wherein the amphiphilic stabilizer is methoxypolyethylene glycol (mPEG)-polycaprolactone (PCL), mPEG-polystyrene, mPEG-polybutadiene, mPEG-polylactate, block copolymers of polyethylene oxide, and polypropylene oxide, or block copolymers of polyethylene oxide and polybutylene oxide.

6. The composition of claim 1 , wherein the particulate constructs comprise 10 3 -10 7 conjugates of formula (1).

7. The composition of claim 1 , wherein the particulate constructs have an average diameter less than 5 μ.

8. The composition of claim 1 wherein said first therapeutic agent is present in the form of formula (1) and the second therapeutic agent is in unbound form.

Assignments (8)
CORRECTIVE ASSIGNMENT TO CORRECT THE REMOVE 2 APPLICATION NUMBERS PREVIOUSLY RECORDED AT REEL: 07234 FRAME: 0137. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Oct 9, 2025
From: CELATOR PHARMACEUTICALS, INC.
To: JAZZ PHARMACEUTICALS THERAPEUTICS, INC.
Reel/Frame 073133/0142 →
CORRECTIVE ASSIGNMENT TO CORRECT THE REMOVAL OF 8 PROPERTY NUMBERS PREVIOUSLY RECORDED AT REEL: 072341 FRAME: 0137. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Oct 8, 2025
From: CELATOR PHARMACEUTICALS, INC.
To: JAZZ PHARMACEUTICALS THERAPEUTICS, INC.
Reel/Frame 073058/0985 →
CHANGE OF NAME Recorded Aug 7, 2025
From: CELATOR PHARMACEUTICALS, INC.
To: JAZZ PHARMACEUTICALS THERAPEUTICS, INC.
Reel/Frame 072341/0137 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2021
From: BANK OF AMERICA, N.A.
To: JAZZ PHARMACEUTICALS, INC.; JAZZ PHARMACEUTICALS IRELAND LIMITED; JAZZ PHARMACEUTICALS INTERNATIONAL LIMITED; JAZZ PHARMACEUTICALS INTERNATIONAL III LIMITED; CELATOR PHARMACEUTICALS, INC.; CAVION, INC.
Reel/Frame 056150/0708 →
SECURITY AGREEMENT Recorded May 5, 2021
From: CAVION, INC.; CELATOR PHARMACEUTICALS, INC.; JAZZ PHARMACEUTICALS IRELAND LIMITED; JAZZ PHARMACEUTICALS, INC.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 056151/0010 →
SECURITY AGREEMENT Recorded Jul 12, 2016
From: CELATOR PHARMACEUTICALS, INC.
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 039312/0397 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2013
From: PRUD'HOMME, ROBERT K.; SAAD, WALID S.
To: THE TRUSTEES OF PRINCETON UNIVERSITY
Reel/Frame 030858/0115 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2013
From: MAYER, LAWRENCE D.; ALLEN, CHRISTINE J.
To: CELATOR PHARMACEUTICALS, INC.
Reel/Frame 030858/0007 →