Targeted Conjugates Encapsulated in Particles and Formulations Thereof
Particles, including nanoparticles and microparticles, and pharmaceutical formulations thereof, containing conjugates of an active agent such as a therapeutic, prophylactic, or diagnostic agent attached to a targeting moiety via a linker have been designed which can provide improved temporospatial delivery of the active agent and/or improved biodistribution. Methods of making the conjugates, the particles, and the formulations thereof are provided. Methods of administering the formulations to a subject in need thereof are provided, for example, to treat or prevent cancer or infectious diseases.
1 . A particle encapsulating conjugate comprising an active agent coupled to a targeting moiety by a linker.
2 . The particle of claim 1 , wherein the conjugate comprises a formula selected from the group X-Y-Z, X-Y-Z-Y-X, X-(Y-Z) n , (X-Y) n -Z, X-Y-Z n , and (X-Y-Z-Y) n -Z;
wherein X is a targeting moiety,
Y is a linker,
Z is an active agent, and
n is an integer between 2 and 1,000.
3 . The particle of claim 1 , wherein the conjugate comprises the formula X-Y-Z;
wherein X is a targeting moiety,
Y is a linker, and
Z is an active agent.
4 . The particle of any one of claims 1 - 3 , wherein each linker is independently selected from the group consisting of substituted and unsubstituted C 1 -C 30 alkyl, substituted and unsubstituted C 2 -C 30 alkenyl, substituted and unsubstituted C 2 -C 30 alkynyl, substituted and unsubstituted C 3 -C 30 cycloalkyl, substituted and unsubstituted C 1 -C 30 heterocycloalkyl, substituted and unsubstituted C 3 -C 30 cycloalkenyl, substituted and unsubstituted C 1 -C 30 heterocycloalkenyl, substituted and unsubstituted aryl, and substituted and unsubstituted heteroaryl.
5 . The particle of claim 4 , wherein each linker is independently selected from the group consisting of C 2 -C 30 carboxylic acids, C 2 -C 30 di-carboxylic acids, and derivatives thereof.
6 . The particle of claim 5 , wherein the linker is a derivative of a C 2 -C 30 carboxylic acids or a C 2 -C 30 di-carboxylic acid comprising an atom or group of atoms selected from the group consisting of —O—, —C(═O)—, —NR, —O—C(═O)—NR—, —S—, and —S—S—, wherein R is a linear or branched alkyl or heteroalkyl group.
7 . The particle of claim 4 , wherein the linker is selected from the group consisting of C 2 -C 30 carboxylic acids and di-carboxylic acids containing a dithio (—S—S—) group in the backbone.
8 . The particle of claim 4 , wherein the linker is not polymeric.
9 . The particle of any one of claims 1 - 3 , wherein the active agent is selected from the group consisting of therapeutic, prophylactic, nutraceutical, and diagnostic agents.
10 . The particle of claim 9 wherein the active agent is selected from chemotherapeutic agents, anti-infective agents, and combinations thereof.
11 . The particle of claim 9 wherein the active agent is a protein, peptide, lipid, carbohydrate, sugar, nucleic acid, or combination thereof.
12 . The particle of claim 9 , wherein the active agent is an organometallic compound.
13 . The particle of claim 12 , wherein the active agent is a platinum compound.
14 . The particle of claim 13 , wherein the active agent is cabazitaxel.
15 . The particle of any one of claims 1 - 14 , wherein the targeting moiety is selected from the group consisting of peptides and polypeptides, antibody mimetics, nucleic acids, glycoproteins, small molecules, carbohydrate, and lipids.
16 . The particle of claim 15 , wherein the targeting moiety targets cancer cells.
17 . The particle of claim 15 , wherein the targeting moiety targets a marker selected from the group consisting of CD19, CD70, CD56, PSMA, alpha integrin, CD22, CD138, EphA2, AGS-5, Nectin-4, HER2, GPMNB, CD74, and Le.
18 . The particle of claim 15 , wherein the targeting moiety is selected from the group consisting of RGD, Cy5.5, and PSMA.
19 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
20 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
21 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
22 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
23 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
24 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
25 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
26 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
27 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
28 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
29 . The particle of claim 3 , wherein the particle comprises a conjugate having the formula
30 . The particle of claim 1 , wherein the polymeric matrix comprises one or more polymers selected from the group consisting of hydrophobic polymers, hydrophilic polymers, and copolymers thereof.
31 . The particle of claim 19 , wherein the hydrophobic polymers are selected from the group consisting of polyhydroxyacids, polyhydroxyalkanoates, polycaprolactones, poly(orthoesters), polyanhydrides, poly(phosphazenes), poly(lactide-co-caprolactones), polycarbonates, polyesteramides, polyesters, and copolymers thereof.
32 . The particle of claim 19 , wherein the hydrophilic polymers are selected from the group consisting of polyalkylene glycols, polyalkylene oxides, poly(oxyethylated polyol), poly(olefinic alcohol), polyvinylpyrrolidone), poly(hydroxyalkylmethacrylamide), poly(hydroxyalkylmethacrylate), poly(saccharides), poly(hydroxy acids), poly(vinyl alcohol), and copolymers thereof.
33 . The particle of claim 1 , wherein the polymeric matrix comprises one or more polymers selected from the group consisting of poly(lactic acid), poly(glycolic acid), poly(lactic-co-glycolic acid), poly(ethylene oxide), poly(ethylene glycol), poly(propylene glycol), and copolymers thereof.
34 . The particle of claim 1 , wherein the particle has a diameter between 10 nm and 300 nm or 50 and 120 nm.
35 . The particle of claim 1 , wherein the particle has a diameter between 500 nm and 1.5 microns or between 300 and 500 nm.
36 . The particle of claim 1 , wherein the polymeric matrix comprises two or more different polymers.
37 . The particle of claim 1 , wherein the conjugate is present in an amount between 0.1% and 10% (w/w) based upon the weight of the particle.
38 . A pharmaceutical formulation comprising the particle of claim 1 and a pharmaceutically acceptable excipient.
39 . A method of making the particle of claim 1 comprising the steps of
forming a conjugate comprising an active agent connected to a targeting moiety by a linker, and
forming a particle comprising a polymeric matrix encapsulating the conjugate.
40 . The method of claim 39 , wherein the conjugate is formed from a linker precursor selected from the group consisting of C 2 -C 30 carboxylic acids and substituted carboxylic acids, C 2 -C 30 di-carboxylic acids and substituted di-carboxylic acids, and acid anhydrides, acid esters, and acid halides thereof.
41 . A method of treating a subject in need thereof comprising administering a therapeutically effective amount of the formulation of claim 38 .