Compositions and methods for assessing eye vasculature

Patent metadata

Field	Value
Publication number	US-12303570-B2
Application number	US-202117492260-A
Country	US
Kind code	B2
Filing date	Oct 1, 2021
Priority date	May 12, 2015
Publication date	May 20, 2025
Grant date	May 20, 2025

Abstract

Compositions and methods for assessing blood vessels and organs of the body are disclosed herein, specifically methods for assessing the vasculature of the eye.

First claim

What is claimed is:

1. A method for assessing the eye vasculature in a subject in need thereof, comprising the steps of:
a. administering an effective amount of a compound of structural Formula I

or a salt thereof; wherein
X 1 and X 2 are independently chosen from —CO(AA), —CN, —CO 2 R 1 , —CONR 2 R 3 , —COR 4 , —NO 2 , —SOR 35 , —SO 2 R 6 , —SO 2 OR 7 and —PO 3 R 8 R 9 ; wherein at least one of X 1 and X 2 is —CO(AA);
Y 1 and Y 2 are independently chosen from —OR 10 , —SR 11 , —NR 12 R 13 , —N(R 14 )COR 15 , —CONH(PS); —P(R 16 ) 2 , —P(OR 17 ) 2 and

each Z 1 is independently chosen from a bond, —CR 18 R 19 —, —O—, —NR 20 —, —NCOR 21 —, —S—, —SO—, and —SO 2 —;
each R 1 to R 21 are independently chosen from hydrogen, C 1 -C 10 alkyl, C 1 -C 10 alkyl substituted with hydroxyl and carboxylic acid, C 3 -C 6 polyhydroxylated alkyl, C 5 -C 10 aryl, C 5 -C 10 heteroaryl, C 3 -C 5 heterocycloalkyl, C 3 -C 5 heterocycloalkyl substituted with C(O), —(CH 2 ) a CO 2 H, —(CH 2 ) a CO 2 H substituted with C 5 -C 10 heteroaryl, —(CH 2 ) a CONR 30 R 31 , —(CH 2 ) a NHSO 3 − , —(CH 2 ) a NHSO 3 H, —(CH 2 ) a OH, —(CH 2 ) a OPO 3 − , —(CH 2 ) a OPO 3 H 2 , —(CH 2 ) a OPO 3 H − , (CH 2 ) a OR 22 , —(CH 2 ) a OSO 3 − , —(CH 2 ) a OSO 3 H, —(CH 2 ) a PO 3 − , —(CH 2 ) a PO 3 H 2 , —(CH 2 ) a PO 3 H − , —(CH 2 ) a SO 3 − , —(CH 2 ) a SO 3 H, —(CH 2 ) d CO(CH 2 CH 2 O) c R 23 , —(CH 2 ) d (CH 2 CH 2 O) c R 24 , —(CHCO 2 H) a CO 2 H, —CH 2 (CHNH 2 ) a CH 2 NR 25 R 26 , —CH 2 (CHOH) a CO 2 H, —CH 2 (CHOH) a R 27 , —CH[(CH 2 ) b NH 2 ] a CH 2 OH, —CH[(CH 2 ) b NH 2 ] a CO 2 H, and —(CH 2 ) a NR 28 R 29 ;
each R 22 to R 31 are independently chosen from hydrogen, C 1 -C 10 alkyl, and C 1 -C 5 -dicarboxylic acid;
R 35 is chosen from C 1 -C 10 alkyl, C 1 -C 10 alkyl substituted with hydroxyl and carboxylic acid, C 3 -C 6 polyhydroxylated alkyl, C 5 -C 10 aryl, C 5 -C 10 heteroaryl, C 3 -C 5 heterocycloalkyl, C 3 -C 5 heterocycloalkyl substituted with C(O), —(CH 2 ) a CO 2 H, —(CH 2 ) a CO 2 H substituted with C 5 -C 10 heteroaryl, —(CH 2 ) a CONR 30 R 31 , —(CH 2 ) a NHSO 3 − , —(CH 2 ) a NHSO 3 H, —(CH 2 ) a OH, —(CH 2 ) a OPO 3 − , —(CH 2 ) a OPO 3 H 2 , —(CH 2 ) a OPO 3 H − , —(CH 2 ) a OR 21 , —(CH 2 ) a OSO 3 − , —(CH 2 ) a OSO 3 H, —(CH) a PO 3 − , —(CH 2 ) a PO 3 H 2 , —(CH 2 ) a PO 3 H − , —(CH 2 ) a SO 3 − , —(CH 2 ) a SO 3 H, —(CH 2 ) d CO(CH 2 CH 2 O) c R 23 , —(CH 2 ) d (CH 2 CH 2 O) c R 24 , —(CHCO 2 H) n CO 2 H, —CH 2 (CHNH 2 ) a CH 2 NR 25 R 26 , —CH 2 (CHOH) a CO 2 H, —CH 2 (CHOH) a R 27 , —CH[(CH 2 ) b NH 2 ] a CH 2 OH, —CH[(CH 2 ) b NH 2 ] a CO 2 H, and —(CH 2 ) a NR 28 R 29 ;
(AA) is a polypeptide chain comprising one or more natural or unnatural amino acids linked together by peptide bonds;
(PS) is a sulfated or non-sulfated polysaccharide chain comprising one or more monosaccharide units connected by glycosidic linkages; and
each ‘a’, ‘b’, and ‘d’ are independently chosen from 0 to 10, ‘c’ is chosen from 1 to 100 and each of ‘m’ and ‘n’ independently is an integer from 1 to 3; and

b. irradiating the subject's eye vasculature with non-ionizing radiation, wherein the radiation causes the compound to fluoresce;
c. detecting the fluorescence of the compound in the subject's eye vasculature; and
d. assessing the eye vasculature within the subject based on the detected fluorescence.

2. The method of claim 1 , wherein the compound is administered intravenously, subcutaneously or intraperitoneally.

3. The method of claim 1 , wherein the non-ionizing radiation has a wavelength of at least 350 nm.

4. The method of claim 1 , wherein the detected fluorescence of the compound in the subject's eye vasculature is measured over time.

5. The method of claim 1 , wherein the method further comprises assessing the subject's pulmonary and cardiac vasculature.

6. The method of claim 1 , wherein the method further comprises diagnosing the subject's renal function.

7. The method of claim 6 , wherein diagnosing the subject's renal function comprises:
exposing the compound to visible or near infrared light;
detecting spectral energy emanating from the compound after administering the compound to the subject; and
determining clearance of the compound from the body of the patient;
wherein the compound absorbs and emanates spectral energy in the visible and/or near infrared spectrum.

8. The method of claim 7 , further comprising comparing the subject's clearance of the compound to that of a normal clearance profile.

9. The method of claim 1 , wherein assessing the subject's eye vasculature comprises identifying ocular abnormalities.

10. The method of claim 9 , wherein the ocular abnormalities are selected from the group consisting of blood vessel architecture, ischemic spots, choroidal infarcts, Elschnig's spots, exudates, hemorrhages, and combinations thereof.

11. The method of claim 9 , wherein the ocular abnormalities are selected from the group consisting of vessel crossovers, vessel tortuosity, evidence of exudates, and combinations thereof.

12. The method of claim 1 , wherein assessing the subject's eye vasculature comprises comparing the detected fluorescence in the subject's eye to that of a normal eye under similar conditions.

13. The method of claim 1 wherein X 1 and X 2 are each —CO(AA) and Y 1 and Y 2 are each —NR 12 R 13 wherein one of R 12 and R 13 is hydrogen and the other of R 12 and R 13 is selected from the group consisting of hydrogen and C 1 -C 10 alkyl.

14. The method of claim 13 wherein each of R 12 and R 13 is hydrogen.

15. The method of claim 1 wherein the compound of structural formula I is

16. A method of assessing the location of a disease or an injury in a subject's eye vasculature, comprising the steps of:
a. administering an effective amount of a compound of structural Formula I

or a salt thereof; wherein
X 1 and X 2 are independently chosen from —CO(AA), —CN, —CO 2 R 1 , —CONR 2 R 3 , —COR 4 , —NO 2 , —SOR 35 , —SO 2 R 6 , —SO 2 OR 7 and —PO 3 R 8 R 9 ; wherein at least one of X 1 and X 2 is —CO(AA);
Y 1 and Y 2 are independently chosen from —OR 10 , —SR 11 , —NR 12R 13 , —N(R 14 )COR 15 , —CONH(PS); —P(R 16 ) 2 , —P(OR 17 ) 2 and

each Z 1 is independently chosen from a bond, —CR 18 R 19 —, —O—, —NR 20 —, —NCOR 21 —, —S, —SO—, and —SO 2 —;
each R 1 to R 21 are independently chosen from hydrogen, C 1 -C 10 alkyl, C 1 -C 10 alkyl substituted with hydroxyl and carboxylic acid, C 3 -C 6 polyhydroxylated alkyl, C 5 -C 10 aryl, C 5 -C 10 heteroaryl, C 3 -C 5 heterocycloalkyl, C 3 -C 5 heterocycloalkyl substituted with C(O), —(CH 2 ) a CO 2 H, —(CH 2 ) a CO 2 H substituted with C 5 -C 10 heteroaryl, —(CH 2 ) a CONR 30 R 31 , —(CH 2 ) a NHSO 3 − , —(CH 2 ) a NHSO 3 H, —(CH 2 ) a OH, —(CH 2 ) a OPO 3 − , —(CH 2 ) a OPO 3 H 2 , —(CH 2 ) a OPO 3 H − , (CH 2 ) a OR 22 , —(CH 2 ) a OSO 3

Assignees

• Medibeacon Inc

Inventors

• Dorshow Richard B
• Rogers Thomas E

Classifications

• A61B5/0261

  using optical means, e.g. infrared light · CPC title

• A61B5/0082

  adapted for particular medical purposes · CPC title

• A61B5/0071

  by measuring fluorescence emission · CPC title

• A61B1/042

  characterised by a proximal camera, e.g. a CCD camera · CPC title

• C07K5/06139

  with the first amino acid being heterocyclic · CPC title