IP Library › Granted Patent US 10,532,104
Granted Patent B2
US 10,532,104 · App. 15/601,170 · Granted Jan 14, 2020

Biotin complexes for treatment and diagnosis of Alzheimer'S disease

Inventor: David R. Elmaleh (Newton, MA)
Assignee: The General Hospital Corporation
A61K47/551A61K31/4188A61K31/713A61K47/549A61K49/085A61K51/0497C12N15/111C12N15/113C12N2310/14C12N2310/3517
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Quick Facts
Patent No.
US 10,532,104
App. No.
15/601,170
Granted
Jan 14, 2020
Kind
B2
Abstract

Described herein are compositions and methods for treating or imaging Alzheimer's disease (AD). The compositions comprise a biotin moiety and a siRNA moiety, without the need for a targeting agent such as an antibody, avidin, or streptavidin. In certain embodiments, the compositions further comprise a diagnostic agent.

Claims (14)

1. A composition comprising a biotin moiety and a siRNA moiety, wherein the siRNA moiety comprises a nucleotide of SEQ ID NO: 2 or a nucleic acid that has at least 95% sequence homology with SEQ ID NO: 2.

2. The composition of claim 1 , wherein the composition further comprises a linker between the siRNA and the biotin.

3. The composition of claim 1 , wherein the composition does not comprise an antibody, an antigen, avidin, or streptavidin.

4. The composition of claim 1 , wherein the composition further comprises a diagnostic agent.

5. The composition of claim 4 , wherein the diagnostic agent is selected from the group consisting of a fluorophore, a chromophore, a chemoluminescing agent, a radionuclide, an unpair spin atom, a free radical, and a contrast agent.

6. The composition of claim 1 , wherein the composition is able to transfect cells in vivo.

7. The composition of claim 1 , wherein the composition partially, substantially, or completely deletes, silences, inactivates, interferes with, or down-regulates a gene that encodes selenoprotein P.

8. The composition of claim 1 , wherein the siRNA moiety comprises a guanosine at the 5′-end.

9. The composition of claim 1 , wherein the sense or the antisense strand of the siRNA moiety is equal to or less than 30 nucleotides in length.

10. A pharmaceutically acceptable formulation, wherein the pharmaceutically acceptable formulation comprises a therapeutically-effective amount of a composition of claim 1 and a pharmaceutically acceptable carrier or diluent.

11. A method generating an image of a subject, comprising the steps of:

administering to a subject in need of imaging a detectable amount of a composition of claim 4 , and

generating an image.

12. The method of claim 11 , wherein said subject is a human.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 25, 2017
From: ELMALEH, DAVID R.
To: THE GENERAL HOSPITAL CORPORATION
Reel/Frame 043086/0626 →
Continuity (3)
Division 14421022
Provisional Application 61695487 · Aug 31, 2012
Related Publication 20170326244A1 · Nov 16, 2017
Cited By (3)
US 12,227,567 US 12,281,166 US 12,497,458