IP Library › Granted Patent US 8,227,634
Granted Patent B2
US 8,227,634 · App. 12/154,445 · Granted Jul 24, 2012

Imaging agents and methods of imaging NAALADase or PSMA

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Quick Facts
Patent No.
US 8,227,634
App. No.
12/154,445
Granted
Jul 24, 2012
Kind
B2
Abstract

The present invention relates to compounds particularly asymmetric urea compounds which are labeled with one or more radioisotopes and which are suitable for imaging or therapeutic treatment of tissues, organs, or tumors which express NAALADase and/or PSMA. In another embodiment, the invention relates to methods of imaging tissues, organs, or tumors using radiolabeled compounds of the invention, particularly tissues, organs, or tumors which express NAALADase and/or PSMA to which the compounds of the invention have an affinity.

Claims (23)

1. An imaging method comprising the steps of:

providing a radiolabeled compound according to the formula:

wherein

R is selected from the group consisting of fluoroalkyl, aryl, benzyl, thiol, and alkylthiol, each of which is optionally substituted with an optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted alkanoyl, or optionally substituted aralky, optionally substituted alkoxy, optionally substituted aralkyloxy, or optionally substituted phenoxy, and the R group comprises one or more isotopes selected from 11 C, 18 F, 99 Tc, 123 I or any combination thereof;

Q is hydrogen, optionally substituted alkyl, optionally substituted benzyl or optionally substituted phenyl; and

Z is Q or a tetrazole; or a pharmaceutically acceptable salt thereof;

contacting cells or tissues with the radiolabeled compound; and

making a radiographic image.

2. The method of claim 1 , wherein the imaging method is suitable for use in imaging glutamateric neurotransmission.

3. The method of claim 1 , wherein the imaging method is suitable for use in imaging presynaptic glutamatergic neurotransmission.

4. The method of claim 1 , wherein the imaging method is suitable for imaging of cancer which expresses at least one of NAALADase or PSMA.

5. The method of claim 1 , wherein the imaging method is suitable for imaging of prostate cancer.

6. The method of claim 5 , wherein the imaging method is suitable for imaging prostate cancer including metastases.

7. The method of claim 1 , wherein the imaging method is suitable for imaging angiogenesis.

8. The method of claim 7 , wherein the angiogenesis is associated with tumors, collagen vascular disease, cancer, stroke, vascular malformations, retinopathy, and normal tissue development.

9. The method of claim 1 , wherein the radiolabeled compound exhibits a target to non-target ratio of at least about 5:1.

10. The method of claim 1 , wherein the radiolabeled compound is stable in vivo.

11. The method of claim 1 , wherein the radiolabeled compound substantially localizes to a site or sites expressing at least one of NAALADase or PSMA, within about 120 minutes after administration.

12. The method of claim 1 , wherein the radiolabeled compound substantially localizes to a site or sites expressing at least one of NAALADase or PSMA, within about 60 minutes after administration.

13. The method of claim 1 , wherein the radiolabeled compound substantially localizes to a site or sites expressing at least one of NAALADase or PSMA, within about 30 minutes after administration.

14. The method of claim 1 , wherein the radiolabeled compound is detected by a gamma camera, positron emission tomography (PET) or single photon emission tomography (SPECT).

15. The method of claim 1 , wherein the subject is a human, rat, mouse, cat, dog, horse, sheep, cow, monkey, avian, or amphibian.

16. The method of claim 1 wherein the radiographic image is made using the radiolabeled compound.

Continuity (2)
Continuation 10340864 · Jan 10, 2003
Related Publication 20090117042A1 · May 7, 2009