IP Library Granted Patent US 10,478,512
Granted Patent B2
US 10,478,512 · App. 15/903,783 · Granted Nov 19, 2019

Charge-balanced imaging agents

Inventors: John V. Frangioni (Wayland, MA); Maged M. Henary (Lawrenceville, GA)
Assignees: Beth Israel Deaconess Medical Center, Inc.; Georgia State University Research Foundation Inc.
A61K49/0032A61B6/00C07D209/02C07D209/42C07D255/02C09B23/0066C09B23/086C12Q1/02G01N33/582
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Quick Facts
Patent No.
US 10,478,512
App. No.
15/903,783
Granted
Nov 19, 2019
Kind
B2
Abstract

The present invention relates to compositions for and methods of optically imaging tissues or cells using imaging agents having desirable in vivo properties that result in improved signal-to-background ratio.

Claims (45)

1. A method of imaging tissue or cells, the method comprising:

(a) contacting the tissue or cells with an imaging agent comprising a dye;

(b) irradiating the tissue or cells at a wavelength absorbed by the dye;

(c) detecting an optical signal from the irradiated tissue or cells, wherein the signal-to-background ratio of the detected optical signal is at least about 1.1, thereby imaging the tissue or cells;

wherein the dye has the formula V:

wherein:

G is -L-TL, where TL is a targeting ligand comprising at least one binding moiety that binds to a biological target;

L has the formula:

E is absent or S;

Q is (CH2) q or a non-ionic oligomeric or polymeric solubilizing moiety;

J is C(O), C(O)O, or C(O)NH;

R 17 , R 18 , R 19 , and R 12 are independently selected from H, an ionic group, a non-ionic oligomeric or polymeric solubilizing group, halo, cyano, nitro, C 1-4 alkyl, C 1-4 alkoxy, and C 1-4 haloalkyl;

q is 0, 1, 2, 3, 4, 5, 6, 7, or 8;

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are independently selected from H, an ionic group, a non-ionic oligomeric or polymeric solubilizing group, halo, C 1-6 alkyl, aryl, and heteroaryl, wherein said alkyl, aryl, and heteroaryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups independently selected from halo, cyano, nitro, and C 1-4 haloalkyl;

or two adjacent R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 groups, together with the atoms to which they are attached, form a fused 5-7 membered aryl, heteroaryl, cycloalkyl, or heterocycloalkyl group, each optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from halo, cyano, nitro, and C 1-4 haloalkyl;

R 9 , and R 10 , are independently selected from an ionic group, a non-ionic oligomeric or polymeric solubilizing group, C 1-6 alkyl, aryl, and heteroaryl, wherein said alkyl, aryl, and heteroaryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups independently selected from halo, cyano, nitro, and C 1-4 haloalkyl;

R 11 and R 12 are independently selected from C 1-4 alkyl optionally substituted with 1, 2, or 3 halo;

R 13 and R 14 are independently selected from C 1-4 alkyl optionally substituted with 1, 2, or 3 halo;

R 15 and R 16 are independently selected from H and C 1-6 alkyl;

R 22 , R 23 , R 24 , R 25 , R 26 , and R 27 are independently selected from independently an ionic group, a non-ionic oligomeric or polymeric solubilizing group, halo, C 1-6 alkyl, aryl, and heteroaryl; and

v is 0, 1, 2, 3, 4, or 5,

wherein at least one of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 is an ionic group,

or an ester thereof, which permits covalent conjugation of the fluorophore to targeting ligands.

2. A dye, having the formula:

wherein:

G is -L-TL, where TL is a targeting ligand comprisiging at least one binding moiety that binds to a biological target;

L has the formula:

E is absent or S;

Q is (CH2) q or a non-ionic oligomeric or polymeric solubilizing moiety;

J is C(O), C(O)O, or C(O)NH;

R 17 , R 18 , R 19 , and R 12 are independently selected from H, an ionic group, a non-ionic oligomeric or polymeric solubilizing group, halo, cyano, nitro, C 1-4 alkyl, C 1-4 alkoxy, and C 1-4 haloalkyl;

q is 0, 1, 2, 3, 4, 5, 6, 7, or 8;

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are independently selected from H, an ionic group, a non-ionic oligomeric or polymeric solubilizing group, halo, C 1-6 alkyl, aryl, and heteroaryl, wherein said alkyl, aryl, and heteroaryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups independently selected from halo, cyano, nitro, and C 1-4 haloalkyl;

or two adjacent R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 groups, together with the atoms to which they are attached, form a fused 5-7 membered aryl, heteroaryl, cycloalkyl, or heterocycloalkyl group, each optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from halo, cyano, nitro, and C 1-4 haloalkyl;

R 9 , and R 10 , are independently selected from an ionic group, a non-ionic oligomeric or polymeric solubilizing group, C 1-6 alkyl, aryl, and heteroaryl, wherein said alkyl, aryl, and heteroaryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups independently selected from halo, cyano, nitro, and C 1-4 haloalkyl;

R 11 and R 12 are independently selected from C 1-4 alkyl optionally substituted with 1, 2, or 3 halo;

R 13 and R 14 are independently selected from C 1-4 alkyl optionally substituted with 1, 2, or 3 halo;

R 15 and R 16 are independently selected from H and C 1-6 alkyl;

R 22 , R 23 , R 24 , R 25 , R 26 , and R 27 are independently selected from independently an ionic group, a non-ionic oligomeric or polymeric solubilizing group, halo, C 1-6 alkyl, aryl, and heteroaryl; and

v is 0, 1, 2, 3, 4, or 5,

wherein at least one of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 is an ionic group,

or an ester thereof, which permits covalent conjugation of the fluorophore to targeting ligands.

3. The dye of claim 2 , wherein the ester is a N-hydroxysuccinimide ester.

4. The dye of claim 2 , isolated as a salt, acid, or combination thereof.

5. An imaging agent comprising the dye of claim 2 which is characterized as having detectable fluorescence with a signal-to-background ratio of at least about 1.1.

Continuity (5)
Continuation 15633233 · Jun 26, 2017
Continuation 14681068 · Apr 7, 2015
Continuation 13148137
Provisional Application 61150522 · Feb 6, 2009
Related Publication 20180177896A1 · Jun 28, 2018
Cited By (2)
US 12,545,641 US 12,559,476