IP Library Granted Patent US 9,603,872
Granted Patent B2
US 9,603,872 · App. 12/598,287 · Granted Mar 28, 2017

Methods and compositions for mitochondrial replacement therapy

Inventors: Anne M. Cataldo (Sutton, MA); Bruce M. Cohen (Lexington, MA)
Assignee: The McLeon Hospital Corporation
A61K35/12A01K67/0271A01K67/0276C12N9/1252G01N33/6896A01K2207/15A01K2217/00A01K2217/05A01K2217/075A01K2227/105A01K2267/0356A61K35/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,603,872
App. No.
12/598,287
Granted
Mar 28, 2017
Kind
B2
Abstract

The invention features methods, kits, and compositions for mitochondrial replacement in the treatment of disorders arising from mitochondrial dysfunction. The invention also features methods of diagnosing neuropsychiatric (e.g., bipolar disorder) and neurodegenerative disorders based on mitochondrial structural abnormalities.

Claims (11)

1. A method for delivering mitochondria in vivo into a brain cell of a subject, said method comprising:

(i) providing a composition comprising a suspension of liposome packaged isolated and substantially pure mitochondria isolated from cells and separated from non-mitochondrial cellular constituents, wherein the combined mass of the non-mitochondrial cellular constituents are less than 5% of the mass of the mitochondria in the composition; and

(ii) intramuscularly or intravenously administering to said subject said composition, thereby delivering mitochondria into the brain cell.

2. The method of claim 1 , wherein said mitochondria are syngeneic mitochondria.

3. The method of claim 1 , wherein said mitochondria are allogeneic mitochondria.

4. The method of claim 1 , wherein said mitochondria are xenogeneic mitochondria.

5. The method of claim 1 , wherein said cells are progenitor cells.

6. The method of claim 1 , further comprising administering to said subject a second agent selected from vitamin A, vitamin C, vitamin D, vitamin E, vitamin K, folic acid, choline, vitamin B 1 , vitamin B 2 , vitamin B 5 , vitamin B 6 , vitamin B 12 , biotin, nicotinamide, betacarotene, coenzyme Q, selenium, superoxide dismutase, glutathione peroxide, uridine, creatine succinate, pyruvate, dihydroxyacetone, acetyl-L-carnitine, alpha-lipoic acid, cardiolipin, omega fatty acid, lithium carbonate, lithium citrate, calcium, and mixtures thereof.

7. The method of claim 1 , wherein said composition is administered intravenously.

8. The method of claim 1 , wherein said liposome is a lipid micelle.

9. The method of claim 8 , wherein said lipid micelle is formed from 2,3-dioleyloxy-N-[2-(sperminecarboxamido)ethyl]-N,N-dimethyl-1-propanaminium trifluoroacetate (DOSPA) and dioleoyl phosphatidylethanolamine (DOPE).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 18, 2016
From: CATALDO, ANNE M.; COHEN, BRUCE M.
To: THE MCLEAN HOSPITAL CORPORATION
Reel/Frame 039473/0117 →
Continuity (2)
Provisional Application 60927240 · May 2, 2007
Related Publication 20110008310A1 · Jan 13, 2011