Orally bioavailable lipid-based constructs
The present invention is embodied by a composition capable of chaperoning a typically non-orally available therapeutic or diagnostic agent through the environment of the digestive tract such that the therapeutic or diagnostic agent is bioavailable. The composition may or may not be targeted to specific cellular receptors, such as hepatocytes. Therapeutic agents include, but are not limited to, insulin, calcitonin, serotonin, and other proteins. Targeting is accomplished with biotin or metal based targeting agents.
1. An orally bioavailable composition comprising constituents comprising
1,2-distearoyl-sn-glycero-3-phosphocholine;
cholesterol;
dihexadecyl phosphate;
and at least one additional lipid selected from the group consisting of MCC-PE (1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-[4-(p-maleimidomethyl)cyclohexane-carboxamide]) and MPB-PE (1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-[4-(p-maleimido) phenylbutyrate]);
wherein said 1,2-distearoyl-sn-glycero-3-phosphocholine, said dihexadecyl phosphate, and said cholesterol are present in said constituents in a ratio of 62 mole %:22 mole %:16 mole %;
wherein said composition further comprises at least one polypeptide therapeutic or diagnostic agent;
wherein said at least one therapeutic or diagnostic agent is covalently bound to said at least one additional lipid through a linker of formula —C(═O)—(CH 2 ) n S—, wherein n is an integer ranging from 1 to 10, wherein the carbonyl group of said linker is covalently bound to said at least one therapeutic or diagnostic agent, wherein the sulfur atom of said linker is covalently bound to said at least one additional lipid,
wherein a percentage ranging from 5% to 50% of said constituents exhibits an average diameter equal to or lower than 20 nm; and
wherein said composition is orally bioavailable in a mammal.
2. The composition of claim 1 , wherein said linker is derived from a linker precursor of formula succinimidyl-O—C(═O)—(CH 2 ) n SR, wherein R is a thiol-protecting group.
3. The composition of claim 1 , wherein said therapeutic agent is selected from the group consisting of insulin, interferon, erythropoietin, parathyroid hormone, calcitonin, rituximab, trastuzumab, uricase, tissue plasminogen activator, thymoglobin, a vaccine, antithrombin III, filgrastin, pramilitide acetate, exanatide, epifibatide, antivenins, IgG, IgM, HGH, GLP-1, blood clotting Factors VII and VIII, IX, X, and a monoclonal antibody.
4. The composition of claim 1 , wherein at least 25% of the cholesterol is thiocholesterol.
5. A method of preparing an orally bioavailable composition comprising constituents comprising 1,2-distearoyl-sn-glycero-3-phosphocholine; cholesterol; dihexadecyl phosphate; and at least one additional lipid selected from the group consisting of MCC-PE and MPB-PE;
the composition further comprising at least one polypeptide therapeutic or diagnostic agent; wherein said at least one therapeutic or diagnostic agent is covalently bound to said at least one additional lipid through a linker of formula —C(═O)—(CH 2 ) n S—, wherein n is an integer ranging from 1 to 10, wherein the carbonyl group of said linker is covalently bound to said at least one therapeutic or diagnostic agent, and wherein the sulfur atom of said linker is covalently bound to said at least one additional lipid, wherein a percentage ranging from 5% to 50% of said constituents exhibits an average diameter equal to or lower than 20 nm and wherein said composition is orally bioavailable in a mammal,
said method comprising:
mixing 1,2-distearoyl-sn-glycero-3-phosphocholine, cholesterol, dihexadecyl phosphate and said at least one additional lipid to form a mixture of lipid-based constituents,
wherein said 1,2-distearoyl-sn-glycero-3-phosphocholine, said dihexadecyl phosphate, and said cholesterol are present in said mixture in a ratio of 62 mole %:22 mole %:16 mole %;
reacting a therapeutic agent with a linker precursor of formula succinimidyl-O—C(═O)—(CH 2 ) n SR, wherein R is a thiol-protecting group and n is an integer ranging from 1 to 10, thus forming a therapeutic agent/linker conjugate wherein the carbonyl group of said linker precursor is covalently bound to said at least one therapeutic or diagnostic agent;
deprotecting said R group in said conjugate to form a deprotected conjugate comprising a thiol; and
contacting said deprotected conjugate comprising a thiol with said mixture of lipid-based constituents to form said composition.
6. The composition of claim 1 , further comprising a targeting agent selected from the group consisting of biotin-DHPE (2,3-diacetoxypropyl 2-(5-((3aS,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl) pentanamido)ethyl phosphate) and biotin-X-DHPE (2,3-diacetoxypropyl 2-(6-(5-((3aS,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)hexanamido)ethyl phosphate).
7. The composition of claim 1 , further comprising a reticuloendothelial system (RES) avoidance molecule.
8. The method of claim 5 , wherein the composition further comprises a targeting agent selected from the group consisting of biotin-DHPE (2,3-diacetoxypropyl 2-(5-((3aS,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)ethyl phosphate) and biotin-X-DHPE (2,3-diacetoxypropyl 2-(6-(5-((3aS,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)hexanamido)ethyl phosphate).
9. The method of claim 5 , wherein the composition further comprises a reticuloendothelial system (RES) avoidance molecule.