US2011087004A1PendingUtilityA1
Enhanced oral transcompartmental delivery of therapeutic or diagnostic agents
Est. expiryFeb 8, 2021(expired)· nominal 20-yr term from priority
Inventors:Srinivasan RamanathanStanley SteinMichael LeibowitzPatrick J. SinkoTamara MinkoGregory WilliamsGoubao ZhangXiaoping ZhangShahrair PooyanSeong Hee ParkBo-Xing QiuPankaj Paranjpe
A61K 47/665A61K 47/60A61K 47/62B82Y 5/00A61K 38/08
48
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Claims
Abstract
The invention is directed to pharmaceutical compositions and methods for delivery of a therapeutic or diagnostic agent from one bodily compartment to one or more other bodily compartment by administering one of the following conjugates: a polymer having multiple functional groups at least one of which is covalently bound to a therapeutic or diagnostic agent, and at least one cell uptake promoter covalently bound to the therapeutic or diagnostic agent; or a polymer and at least one cell uptake promoter bound thereto; the polymer further comprising multiple functional groups at least one of which is covalently bound a therapeutic or diagnostic agent.
Claims
exact text as granted — not AI-modified1 - 27 . (canceled)
28 . A transcompartmental delivery promoting composition comprising:
a) a polymer having multiple functional groups, at least one of which is covalently bound to a peptide independently selected from the group consisting of SEQ ID NOS: 1-8, and at least one cell uptake promoter covalently bound to said peptide selected from the group consisting of SEQ ID NOS: 1-8; or b) a polymer and at least one cell uptake promoter bound thereto; the polymer further comprising multiple functional groups at least one of which is covalently bound to at least one peptide selected independently from the group consisting of SEQ ID NOS: 1-8; wherein said polymer of (a) or (b) is selected from the group consisting of carboxymethylcellulose, dextran, polyvinyl alcohol, polyvinyl pyrrolidone, poly-1,3-dioxolane, poly-1,3,6-trioxane, an amino acid homopolymer, polypropylene oxide, a copolymer of ethylene glycol/propylene glycol, an ethylene/maleic anhydride copolymer, an amino acid copolymer, a copolymer of polyethylene glycol and an amino acid, a polypropylene oxide/ethylene oxide copolymer, and a polyethylene glycol/thiomalic acid copolymer; and any combination thereof, and wherein further each cell uptake promoter of (a) or (b) is independently selected from the group consisting of biotin, folate, pantothenate, B-6, B-12, glucose, N-acetyl glucosamine, RANTES, IL-2, Tat, penetratin, VEGF, RI TAT, gp41, VEGF, myristic acid, stearic acid, aptamers containing 5-(1-pentyl)-2′-deoxyuridine neuramimidase, CD4, CD44, influenza virus hemagglutinin, estrogen, progesterone, LHRH, ACTH, growth hormone, lectins, ICAM and analogues thereof.
29 - 35 . (canceled)
36 . The composition of claim 28 , wherein said functional group comprises a ketone, an ester, a carboxylic acid, an aldehyde, an alcohol, a thiol, or an amine.
37 . The composition of claim 36 , wherein said functional group is a thiol.
38 . The composition of claim 28 , wherein said multiple functional groups are derived from a thiol compound bound to said polymer.
39 . The composition of claim 38 , wherein said thiol compound is cysteamine, 1-amino-2-methyl-2-propanethiol, or 1-amino-2-propanethiol.
40 - 68 . (canceled)
69 . The composition of claim 28 , wherein the polymer has at least 3 arms comprising a functional group.
70 . The composition of claim 28 , wherein the polymer has at least 4 arms comprising a functional group.
71 . The composition of claim 28 , wherein the polymer has at least 8 arms comprising a functional group.
72 . The composition of claim 71 , wherein the polymer has at least 8 arms comprising a functional group, and the same or different cell uptake promoter is attached to at least two of the arms.
73 . The composition of claim 72 , wherein the polymer has at least 8 arms comprising a functional group, and the same or different cell uptake promoter is attached to four of the arms.
74 . The composition of claim 28 , wherein at least two same or different peptides selected from the group consisting of SEQ ID NOS: 1-8 are independently bound to a functional group on an arm of the polymer.
75 . The composition of claim 28 , consisting of (A) a polymer having 8 arms, (B) at least two same or different cell uptake promoter moieties each independently covalently bound to a functional group on an arm of said polymer, and (C) a peptide selected from the group consisting of SEQ ID NOS: 1-8 covalently bound to afunctional groups on an arm of said polymer.
76 . The composition of claim 28 , consisting of (A) a polymer having 8 arms, (B) at least four same or different cell uptake promoter moieties each independently covalently bound to a functional group on a polymer arm, and (C) at least one of the peptides selected from the group consisting of SEQ ID NOS: 1-8, each independently covalently bound to a functional group on an arm of said polymer.
77 . The composition of claim 28 , wherein four peptides independently selected from the group consisting of SEQ ID NOS: 1-8 are each covalently bound to a functional group on an arm of said polymer.
78 . The composition of claim 28 , wherein the polymer size is about 20 kDa.Cited by (0)
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