US2005042274A1PendingUtilityA1
Compounds and compositions for delivering active agents
Priority: Dec 16, 1999Filed: Dec 31, 2003Published: Feb 24, 2005
Est. expiryDec 16, 2019(expired)· nominal 20-yr term from priority
C07C 235/64C07C 235/60C07C 235/84C07C 237/42
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Claims
Abstract
Compounds and compositions for the delivery of active agents are provided. Methods of administration and preparation are provided as well.
Claims
exact text as granted — not AI-modified1 . A compound selected from the group consisting of compounds:
and salts thereof.
2 . A composition comprising:
(A) an active agent; and (B) the compound of claim 1 , and mixtures thereof.
3 . The composition of claim 2 , wherein the active agent is selected from the group consisting of a biologically active agent, a chemically active agent, and a combination thereof.
4 . The composition of claim 3 , wherein the biologically active agent comprises at least one protein, polypeptide, peptide, hormome, polysaccharide, mucopolysaccharide, carbohydrate, or lipid.
5 . The composition of claim 3 , wherein the biologically active agent is selected from the group consisting of: growth hormones, human growth hormones recombinant human growth hormones (rhGH), bovine growth hormones, porcine growth hormones, growth hormone releasing hormones, growth hormone releasing factor, interferons, α-interferon, β-interferon, γ-interferon, interleukin-1, interleukin-2, insulin, porcine insulin, bovine insulin, human insulin, human recombinant insulin, insulin-like growth factor (IGF), IGF-1, heparin, unfractionated heparin, heparinoids, dermatans, chondroitins, low molecular weight heparin, very low molecular weight heparin, ultra low molecular weight heparin, calcitonin, salmon calcitonin, eel calcitonin, human calcitonin; erythropoietin (EPO), atrial naturetic factor, antigens, monoclonal antibodies, somatostatin, protease inhibitors, adrenocorticotropin, gonadotropin releasing hormone, oxytocin, leutinizing-hormone-releasing-hormone, follicle stimulating hormone, glucocerebrosidase, thrombopoeitin, filgrastim. postaglandins, cyclosporin, vasopressin, cromolym sodium, sodium chromoglycate, disodium chromoglycate, vancomycin, desferrioxamine (DFO), parathyroid hormone (PTH), fragments of PTH, antimicrobials, anti-fungal agents, vitamins; analogs, fragments, mimetics and polyethylene glycol (PEG)-modified derivatives of these compounds; and any combination thereof.
6 . The composition of claim 3 , wherein the biologically active agent comprises insulin, heparin, calcitonin, parathyroid hormone, erythropoietin, growth hormones or combinations thereof.
7 . The composition of claim 3 , wherein the biologically active agent comprises recombinant human growth hormones.
8 . The composition of claim 3 , wherein the biologically active agent comprises parathyroid hormone.
9 . The composition of claim 3 , wherein the biologically active agent comprises insulin.
10 . The composition of claim 3 , wherein the biologically active agent comprises heparin.
11 . The composition of claim 3 , wherein the biologically active agent comprises calcitonin.
12 . The composition of claim 3 , wherein the biologically active agent comprises interferon.
13 . A composition comprising:
(A) an active agent; and (B) a poly(amino acid) comprising a compound having a formula selected from the group consisting of the compounds of claim 1 , salts thereof and mixtures thereof.
14 . The composition of claim 13 wherein the poly (amino acid) is a polypeptide.
15 . A dosage unit form comprising:
(A) the composition of claim 2; and (B) (a) an excipient
(b) a dilutent
(c) a disintegrant,
(d) a lubricant,
(e) a plasticizer,
(f) a colorant,
(g) a dosing vehicle, or
(h) any combination thereof.
16 . The dosage unit form of claim 15 , wherein the active agent is selected from the group consisting of a biologically active agent, a chemically active agent, and a combination thereof.
17 . The dosage unit form of claim 16 , wherein the biologically active agent comprises at least one protein, polypeptide, peptide, hormone, polysaccharide, mucopolysaccharide, carbohydrate, or lipid.
18 . The dosage unit form of claim 16 , wherein the biologically active agent is selected from the group consisting of:
growth hormones, human growth hormones (hGH), recombinant human growth hormones (rhGH), bovine growth hormones, porcine growth hormones, growth hormone releasing hormones, growth hormone releasing factor, interferons, α-interferon, β-interferon, γ-interferon, interleukin-1, interleukin-2, insulin, porcine insulin, bovine insulin, human insulin, human recombinant insulin, insulin-like growth factor, insulin-like growth factor-1, heparin, unfractionated heparin, heparinoids, dermatans, chondroitins, low molecular weight heparin, very low molecular weight heparin, ultra low molecular weight heparin, calcitonin, salmon calcitonin, eel calcitonin, human calcitonin; erythropoietin, atrial naturetic factor, antigens, monoclonal antibodies, somatostatin, protease inhibitors, adrenocorticotropin, gonadotropin releasing hormone, oxytocin, leutinizing-hormone-releasing-hormone, follicle stimulating hormone, glucocerebrosidase, thrombopoeitin, filgrastim. postaglandins, cyclosporin, vasopressin, cromolym sodium, sodium chromoglycate, disodium chromoglycate, vancomycin, desferrioxamine, parathyroid hormone, fragments of PTH, antimicrobials, anti-fungal agents, vitamins; analogs, fragments, mimetics and polyethylene glycol-modified derivatives of these compounds; and any combination thereof.
19 . The dosage unit form of claim 16 , wherein the biologically active agent comprises insulin, heparin, calcitonin, parathyroid hormone, erythropoietin, human growth hormones or combinations thereof.
20 . The dosage unit form of claim 15 , wherein the active agent comprises recombinant human growth hormone.
21 . The dosage unit form of claim 15 , wherein the active agent comprises parathyroid hormone.
22 . The dosage unit form of claim 15 , wherein the active agent comprises insulin.
23 . The dosage unit form of claim 15 , wherein the active agent comprises heparin.
24 . The dosage unit form of claim 15 , wherein the active agent comprises calcitonin.
25 . The dosage unit form of claim 15 , wherein the active agent comprises interferon.
26 . The dosage unit form of claim 15 , wherein the dosage unit form comprises a dosing vehicle comprising a tablet, a capsule, a powder, or a liquid.
27 . The dosage unit form of claim 15 , wherein the dosing vehicle is liquid selected from the group consisting or water, 1,2-propane diol, ethanol, and any combination
28 . A method for administering a biologically-active agent to an animal in need of the agent, the method comprising administering orally to the animal the composition of claim 3 .
29 . A method for preparing a composition comprising mixing:
(A) at least one active agent; (B) the compound of claim 1; and (C) optionally, a dosing vehicle.Join the waitlist — get patent alerts
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