IP Library Granted Patent US 9,808,538
Granted Patent B2
US 9,808,538 · App. 14/937,169 · Granted Nov 7, 2017

PSMA-targeted NIR dyes and their uses

Inventors: Sumith A. Kularatne (West Lafayette, IN); Philip S. Low (West Lafayette, IN); Pravin Gagare (West Lafayette, IN); Carrie Myers (Chesterfield, MO)
Assignee: On Target Laboratories, LLC
A61K49/0052A61K49/0032A61K49/0056C07D209/20C07K5/0606C07K5/06026C07K5/06078C07K5/06095C07K5/06121C07K5/06147C07K5/06156C07K5/0806C07K5/0812C07K5/0817C07K5/1019C07K7/06G01N21/6428G01N33/57492A61K49/16C12Y304/17021G01N2021/6439G01N2333/948
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Quick Facts
Patent No.
US 9,808,538
App. No.
14/937,169
Granted
Nov 7, 2017
Kind
B2
Abstract

The present disclosure relates to prostate specific membrane antigen (PSMA) targeted compounds conjugated to near-infra red (NIR) dyes and methods for their therapeutic and diagnostic use. More specifically, this disclosure provides compounds and methods for diagnosing and treating diseases associated with cells and/or vasculature expressing prostate specific membrane antigen (PSMA), such as prostate cancer and related diseases. The disclosure further describes methods and compositions for making and using the compounds, methods incorporating the compounds, and kits incorporating the compounds.

Claims (38)

1. A method of optical imaging of a biological tissue that expresses PSMA, the method comprising:

(a) contacting the biological tissue with a composition a compound having the formula: B—X—Y—Z, wherein

B comprises a compound capable of binding to prostate specific membrane antigen (PSMA),

X, is selected from the group consisting of polyethylene glycol (PEG), N-amino-dPEG2-acid and polyethylene amine (PEA),

Y comprises at least one amino acid, or derivative thereof, and

Z comprises a near-infra red (NIR) dye,

(b) allowing time for the compound in the composition to distribute within the biological target;

(c) illuminating the tissue with an excitation light of a wavelength absorbable by the compound; and

(d) detecting the optical signal emitted by the compound.

2. The method of claim 1 , wherein the signal emitted by the compound is used to construct an image.

3. The method of claim 1 , wherein the biological tissue is selected from the group consisting of prostate cells, prostate cancer cells, bladder cancer cells, pancreatic cancer cells, liver cancer cells, lung cancer cells, kidney cancer cells, sarcoma cells, breast cancer cells, brain cancer cells, neuroendocrine carcinoma cells, colon cancer cells, testicular cancer cells and melanoma cells.

4. A method of optical imaging of a biological tissue that expresses PSMA, the method comprising:

(a) contacting the biological tissue with a composition a compound having the structural formula:

or a pharmaceutically acceptable salt thereof, or isotopes thereof, wherein:

R 1 represents a hydrogen or SO 3 H;

R 2 represents a hydrogen, or CH 3 , or C 3 H 6 SO 3 − , or C 3 H 6 SO 3 H or C 4 H 8 SO 3 − , or C 4 H 8 SO 3 H or C 3 H 6 N + (CH 3 ) 3 ;

R 3 , and R 5 each represents a carbon, optionally one or more sharing bonds, or oxygen, or sulfur, or nitrogen

R 4 represents a carbon with optionally one or more sharing bonds;

R 6 represents nitrogen, oxygen, or sulfur or no atom (direct C—C bond between aromatic ring and vinyl ring);

R 7 is optional and when present represents electron donating aromatic substitution group;

R 8 is optional and when present represents linkers with aromatic amino acids such as Phe, Trp, His, Tyr, or derivative of them, and/or cationic amino acids such Arg, Lys, or derivative of them, and/or anionic amino acids such as Asp, Glu or derivative of them, and/or unnatural amino acids of aromatic/cationic/anionic acids or derivative;

R 9 represents a PEG, N-amino-dPEG2-acid, PEA, or derivative of them;

R 10 represents a CO 2 H, PO 3 H 2 , SO 3 H, CH 2 SO 3 H, CH 2 CONHCH 2 SO 3 H, CH 2 CONHCH 2 CH 2 SO 3 H;

R 11 represents CO 2 H, SO 3 H, CH 2 CONHCH 2 SO 3 H, CH 2 CONHCH 2 CH 2 SO 3 H; and

R 12 represents independently represents a hydrogen, a methyl group, CH 2 COOH, a CH 2 and may optionally represent each a CH 2 sharing a bond,

(b) allowing time for the compound in the composition to distribute within the biological target;

(c) illuminating the tissue with an excitation light of a wavelength absorbable by the compound; and

(d) detecting the optical signal emitted by the compound.

5. The method of claim 4 , wherein the signal emitted by the compound is used to construct an image.

6. The method of claim 4 , wherein the biological tissue is selected from the group consisting of prostate cells, prostate cancer cells, bladder cancer cells, pancreatic cancer cells, liver cancer cells, lung cancer cells, kidney cancer cells, sarcoma cells, breast cancer cells, brain cancer cells, neuroendocrine carcinoma cells, colon cancer cells, testicular cancer cells and melanoma cells.

7. A method of identifying a target cell type in a biological sample comprising:

a) contacting the biological sample with a compound having the formula: B—X—Y—Z, wherein

B comprises a compound capable of binding to prostate specific membrane antigen (PSMA),

X, is selected from the group consisting of polyethylene glycol (PEG), N-amino-dPEG2-acid and polyethylene amine (PEA),

Y comprises at least one amino acid, or derivative thereof, and

Z comprises a near-infra red (NIR) dye,

b) for a time and under conditions that allow for binding of the compound to at least one cell of the target cell type or vasculature of the target tissue; and

c) optically detecting the presence or absence of the compound of in the biological sample, wherein presence of the compound in detecting step b) indicates that the target cell type is present in the biological sample.

Assignments (3)
CHANGE OF NAME Recorded May 15, 2024
From: ON TARGET LABORATORIES, LLC
To: ON TARGET LABORATORIES, INC.
Reel/Frame 067419/0833 →
JOINT RESEARCH AGREEMENT Recorded Jan 25, 2024
From: ON TARGET LABORATORIES, INC.
To: PURDUE RESEARCH FOUNDATION; ON TARGET LABORATORIES, LLC
Reel/Frame 067202/0093 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2016
From: KULARATNE, SUMITH A; LOW, PHILIP S; GAGARE, PRAVIN; MYERS, CARRIE
To: ON TARGET LABORATORIES
Reel/Frame 038285/0578 →
Continuity (2)
Provisional Application 62216157 · Sep 9, 2015
Related Publication 20170065729A1 · Mar 9, 2017