Multimeric peptidomimetic fibrosis specific dual-modality probes

1. A dual-modality probe having a formula selected from the group consisting of:

wherein

R is

L 1 , L 2 , L 3 , L 4 , L 5 and L 6 are linkers;

IRDye is a near infrared dye with wavelength in the range of 700-900 nm;

and

is a metal chelate independently selected from:

2. The dual-modality probe of claim 1 , wherein said linkers are selected from the group consisting of alkane, amino acid, —NHCO(CH 2 ) 5 —, polyethylene glycol, and polypropylene glycol.

3. The dual-modality probe of claim 1 , wherein said dual-modality probe is in a form of pharmaceutically acceptable salts, hydrates, and solvates.

4. The dual-modality probe of claim 1 , wherein M is selected from the group consisting of Cu, Fe, In, Mn, Tm, Yb, Y, Gd, Eu, and a lanthanide.

5. The dual-modality probe of claim 1 , wherein said near infrared dye is selected from the group consisting of IRDye 800CW, IRDye 78, IRDye 700DX, VivoTag-S 750, VivoTag 800, VivoTag-S 680, DY-750, DY-682, DY-675, Cypate, Cy7, Alexa Fluor 750, and Alexa Fluor 680.

6. The dual-modality probe of claim 1 , wherein said metal chelate and said IRDye are conjugated for concurrent magnetic resonance and near infrared optical imaging.

7. A method of making a dual-modality probe, said method comprising:

(a) providing an organic chelating ligand, wherein said organic chelating ligand selected from the group consisting of:

wherein

R is t-butyl ester, ester, or hydrogen;

and

R 1 is

(b) reacting said organic chelating ligand with a trifunctional linker moiety to result in a trifunctional linker moiety conjugated organic chelating ligand;

(c) deprotecting one or more functional group on said trifunctional linker moiety conjugated organic chelating ligand to yield one or more free functional group;

(d) chelating a metal ion on said one or more free functional group to result in a metal chelate;

(e) conjugating a near infrared fluorophore to result in a metal chelated near infrared conjugated carboxylic acid precursor;

(f) providing a multivalent scaffold, wherein said multivalent scaffold is selected from the group consisting of:

wherein

R 2 is Boc, Fmoc, Ac, Cbz, Bz, or Bn;

L 1 and L 2 are linkers;

and

R 1 is

(g) conjugating said multivalent scaffold with a targeting ligand to yield one or more targeting ligand conjugated multivalent scaffold; wherein said targeting ligand is

 wherein L 3 is independently selected from the group consisting of alkane, amino acid, polyethylene glycol, and polypropylene glycol

(h) deprotecting an amino protecting group on said one or more targeting ligand conjugated multivalent scaffold to obtain an amine containing targeting ligand conjugated multivalent scaffold; and

(i) reacting said amine containing targeting ligand conjugated multivalent scaffold with said metal chelated near infrared conjugated carboxylic acid precursor under a condition capable of forming an amide bond to results in said dual-modality probe.

8. The method of claim 7 , wherein said linkers are selected from the group consisting of alkane, amino acid, —NHCO(CH 2 ) 5 —, polyethylene glycol, and polypropylene glycol.

9. The method of claim 7 , wherein said dual-modality probe is in a form of pharmaceutically acceptable salts, hydrates, and solvates.

10. The method of claim 7 , wherein said metal ion is selected from the group consisting of Cu, Fe, In, Mn, Tm, Yb, Y, Gd, Eu, and a lanthanide.

11. The method of claim 7 , wherein said near infrared fluorophore is selected from the group consisting of IRDye 800CW, IRDye 78, IRDye 700DX, VivoTag-S 750, VivoTag 800, VivoTag-S 680, DY-750, DY-682, DY-675, Cypate, Cy7, Alexa Fluor 750, and Alexa Fluor 680.

12. The method of claim 7 , wherein said trifunctional linker moiety is amino acid, polymer, or dendrimer.

13. A method of making a dual-modality probe, said method comprising:

(a) providing a multivalent scaffold, wherein said multivalent scaffold is selected from the group consisting of:

wherein

R 2 is Boc, Fmoc, Ac, Cbz, Bz, or Bn;

L 1 and L a are linkers;

and

R 1 is

(b) conjugating said multivalent scaffold with a targeting ligand to yield one or more targeting ligand conjugated multivalent scaffold; wherein said targeting ligand is

 wherein L 3 is independently selected from the group consisting of alkane, amino acid, polyethylene glycol, and polypropylene glycol

(c) deprotecting an amino protecting group on said one or more targeting ligand conjugated multivalent scaffold to obtain an amine containing targeting ligand conjugated multivalent scaffold;

(d) reacting said amine containing targeting ligand conjugated multivalent scaffold with a trifunctional linker moiety to result in a trifunctional linker moiety containing targeting ligand conjugated multivalent scaffold;

(e) deprotecting one or more functional group on said trifunctional linker moiety containing targeting ligand conjugated multivalent scaffold to yield one or more free functional group;

(f) conjugating a near infrared fluorophore to result in a near infrared containing targeting ligand conjugated multivalent scaffold carboxylic acid precursor;

(g) providing a metal chelate, wherein said metal chelate selected from the group consisting of:

and

(h) reacting said metal chelate with said near infrared containing targeting ligand conjugated multivalent scaffold carboxylic acid precursor under a condition capable of forming an amide bond to results in said dual-modality probe.

14. The method of claim 13 , wherein said linkers are selected from the group consisting of alkane, amino acid, —NHCO(CH 2 ) 5 —, polyethylene glycol, and polypropylene glycol.

15. The method of claim 13 , wherein said dual-modality probe is in a form of pharmaceutically acceptable salts, hydrates, and solvates.

16. The method of claim 13 , wherein said near infrared fluorophore is selected from the group consisting of IRDye 800CW, IRDye 78, IRDye 700DX, VivoTag-S 750, VivoTag 800, VivoTag-S 680, DY-750, DY-682, DY-675, Cypate, Cy7, Alexa Fluor 750, and Alexa Fluor 680.

17. The method of claim 13 , wherein M is selected from the group consisting of Cu, Fe, In, Mn, Tm, Yb, Y, Gd, Eu, or a lanthanide.

18. The method of claim 13 , wherein said trifunctional linker moiety is amino acid, polymer, or dendrimer.