IP Library Granted Patent US 7,112,318
Granted Patent B2
US 7,112,318 · App. 10/360,566 · Granted Sep 26, 2006

Non-invasive diagnostic imaging technology for mitochondria dysfunction using radiolabeled lipophilic salts

Assignee: The Johns Hopkins University
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Quick Facts
Patent No.
US 7,112,318
App. No.
10/360,566
Granted
Sep 26, 2006
Kind
B2
Abstract

The invention provides a series of lipophilic phosphonium cations (PhCs) labeled with 18 F for non-invasive assessment of ΔΨm, lipophilic ammonium cation analogs of the PhCs, and methods of using same for imaging and detection of mitochondrial-related pathologies in patients using PET or SPECT.

Claims (69)

1. A compound comprising at least one pharmaceutically acceptable anion and a cation represented by the following formula:

wherein

R 1 is alkyl, alkenyl, alkynyl, haloalkyl, cycloalkyl, or aralkyl, with R 1 being substituted by one or more groups comprising 18 F and optionally substituted by one or more additional groups;

R 2 , R 3 , and R 4 are independently selected at each occurrence of R 2 , R 3 , and R 4 from the group consisting of hydrogen, halogen, cyano, nitro, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted alkoxy, optionally substituted (cycloalkyl)alkyl, optionally substituted alkyithio, optionally substituted alkylsulfinyl, or optionally substituted alkylsulfonyl, and optionally substituted mono or dialkylcarboxamide; and

p, q, and r are independently selected numbers from zero to 5.

2. The compound of claim 1 wherein R 1 is aralkyl.

3. A compound comprising at least one pharmaceutically acceptable anion and a cation represented by the following formula:

wherein

Ar 1 , Ar 2 , and Ar 3 are independently selected from the group consisting of optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted aralkyl; and

m is an integer of to 1 to 5.

4. The compound of claim 3 wherein at least one of Ar 1 , Ar 2 , and Ar 3 is aryl.

5. The compound of claim 3 wherein at least one of Ar 1 , Ar 2 , and Ar 3 is phenyl.

6. The compound of claim 3 wherein each Ar 1 , Ar 2 , and Ar 3 is phenyl.

7. The compound of claim 3 wherein m is 1.

8. A compound which selected from the group consisting of:

18 F-4-fluorobenzyl-triphenylphosphonium;

18 F-2-fluorobenzyl-triphenylphosphonium; or

18 F-3-fluorobenzyl-triphenylphosphonium.

9. A compound selected from the group consisting of

18 F-2-fluoroethyl-triphenylphosphonium;

18 F-2-fluoroethyl-tri-ortho-tolylphosphonium;

18 F-2-fluoroethyl-tri-meta-tolylphosphonium;

18 F-2-fluoroethyl-tri-para-tolylphosphonium;

18 F-3-fluoropropyl-triphenylphosphonium;

18 F-3-fluoropropyl-tri-ortho-tolylphosphonium;

18 F-3-fluoropropyl-tri-meta-tolylphosphonium;

18 F-3-fluoropropyl-tri-para-tolylphosphonium;

18 F-4-fluorobutyl-triphenylphosphonium;

18 F-4-fluorobutyl-tri-ortho-tolylphosphonium;

18 F-4-fluorobutyl-tri-meta-tolylphosphonium;

18 F-4-fluorobutyl-tri-para-tolylphosphonium;

18 F-2-fluorobenzyl-tri-ortho-tolylphosphonium;

18 F-2-fluorobenzyl-tri-meta-tolylphosphonium;

18 F-2-fluorobenzyl-tri-para-tolylphosphonium;

18 F-3-fluorobenzyl-tri-ortho-tolylphosphonium;

18 F-3-fluorobenzyl-tri-meta-tolylphosphonium;

18 F-3-fluorobenzyl-tri-para-tolylphosphonium;

18 F-4-fluorobenzyl-tri-ortho-tolylphosphonium;

18 F-4-fluorobenzyl-tri-meta-tolylphosphonium;

18 F-4-fluorobenzyl-tri-para-tolylphosphonium;

18 F-3-fluoro-4-formyl-benzyl-triphenylphosphonium;

18 F-3-fluoro-4-formyl-benzyl-tri-ortho-tolylphosponium;

18 F-3-fluoro-4-formyl-benzyl-tri-meta-tolylphosphonium;

18 F-3-fluoro-4-formyl-benzyl-tri-para-tolylphosphonium;

( 18 F-4-fluorobenzyl)-(2-chloroethyl)-diphenylphosphonium;

( 18 F-4-fluorobenzyl)-(3-chloropropyl)-diphenylphosphonium;

( 18 F-4-fluorobenzyl)-(4-chlorobutyl)-diphenylphosphonium;

( 18 F-4-fluorobenzyl)-(6-chloropentyl)-diphenylphosphonium;

( 18 F-4-fluorobenzyl)-(5-chlorohexyl)-diphenylphosphonium;

18 F-2-fluoroethyl-tri(4-pyridyl)phosphonium;

18 F-3-fluoropropyl-tri(4-pyridyl)phosphonium;

18 F-4-fluorobutyl-tri(4-pyridyl)phosphonium;

18 F-2-fluorobenzyl-tri(4-pyridyl)phosphonium;

18 F-3-fluorobenzyl-tri(4-pyridyl)phosphonium;

18 F-4-fluorobenzyl-tri(4-pyridyl)phosphonium; or

18 F-3-fluoro-4-formyl-benzyl-tri(4-pyridyl)phosphonium.

10. An imaging method comprising:

contacting cells or tissues with a compound of any one of claims 1 – 9 ; and

making a radiographic image.

11. The method of claim 10 wherein a tumor is imaged.

12. The method of claim 10 wherein the compound preferentially accumulates in mitochondria of tumor cells.

13. The method of claim 11 wherein the tumor is neoplasm.

14. The method of claim 11 wherein the tumor is a lung tumor.

15. The method of claim 11 wherein the tumor is a breast tumor.

16. The method of claim 11 wherein the tumor is a prostate tumor.

17. The method of claim 11 wherein the tumor imaging method is capable of distinguishing between tissue inflammation and tumors.

18. The method of claim 10 wherein myocardial cells or tissue is imaged.

19. The method of claim 10 wherein the compound is detected by positron emission tomography.

20. The method of claim 10 wherein the subject is a human.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 7, 2017
From: JOHNS HOPKINS UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 044392/0119 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 2, 2003
From: MADAR, IGAL; RAVERT, HAYDEN T.; DANNELS, ROBERT; SCHEFFEL, URSULA A.; FROST, JAMES J.
To: JOHNS HOPKINS UNIVERSITY, THE
Reel/Frame 014576/0901 →
Continuity (2)
Provisional Application 6035456300 · Feb 6, 2002
Related Publication 20040033197A1 · Feb 19, 2004