Particulate constructs for release of active agents
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.
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.