IP Library Granted Patent US 9,758,625
Granted Patent B2
US 9,758,625 · App. 15/059,181 · Granted Sep 12, 2017

Polymeric BODIPY dyes and methods for using the same

Inventors: Glenn P. Bartholomew (Escondido, CA); Brent S. Gaylord (San Diego, CA); Lucy Zhao (San Diego, CA)
Assignee: Becton, Dickinson and Company
C08G79/08G01N33/582
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Quick Facts
Patent No.
US 9,758,625
App. No.
15/059,181
Granted
Sep 12, 2017
Kind
B2
Abstract

Polymeric BODIPY dyes including light harvesting BODIPY unit-comprising multichromophores are provided. In some embodiments, the dyes are polymeric tandem dyes that include a light harvesting BODIPY unit-comprising multichromophore and an acceptor chromophore covalently linked to the multichromophore in energy-receiving proximity therewith. The polymeric tandem dyes may be covalently linked to a specific binding member. Also provided are methods of evaluating a sample for the presence of a target analyte and methods of labelling a target molecule using compositions including the polymeric tandem dyes. Kits and systems for practicing the subject methods are also provided.

Claims (73)

1. A water soluble polymeric tandem dye comprising:

a light harvesting multichromophore that is a conjugated polymer comprising π conjugated BODIPY units; and

an acceptor chromophore covalently linked to the multichromophore in energy-receiving proximity therewith.

2. The dye according to claim 1 , wherein the multichromophore comprises a BODIPY-comprising conjugated segment described by formula (I):

wherein:

B is a BODIPY unit;

M is a π conjugated co-monomer;

each L is independently selected from the group consisting of a terminal group, a π conjugated segment, a linker and a linked specific binding member; and

n is an integer of 2 to 100,000.

3. The dye according to claim 2 , wherein the BODIPY unit is described by the structure:

wherein:

R 1 , R 2 , R 3 and R 4 are each independently selected from H, an alkyl and a substituted alkyl;

R 5 is selected from the group consisting of an alkyl, a substituted alkyl, an aryl, a substituted aryl, a heteroaryl, a substituted heteroaryl, wherein R 5 is optionally substituted with a water solubilizing group; and

each R is selected from the group consisting of F, OH, H, alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, substituted alkoxy, alkynyl and substituted alkynyl.

4. The dye according to claim 1 , wherein the multichromophore is described by the formula (II):

wherein:

B 1 and B 2 are each independently a BODIPY unit;

each M 1 and each M 2 are independently a π conjugated co-monomer;

a, b, c, d, e and f are each independently 0, 1 or 2, wherein b+e≧1;

n and m are independently 0 or an integer from 1 to 100,000, wherein n+m≧1;

p is an integer from 1 to 100,000; and

each L 2 is independently selected from the group consisting of a terminal group, a π conjugated segment, a linker and a linked specific binding member.

5. The dye according to claim 4 , wherein at least one of B 1 , B 2 , M 1 and M 2 comprises -L 1 -C 1 , wherein L 1 is an optional linker and C 1 is the acceptor chromophore.

6. The dye according to claim 4 , wherein the dye is described by the formula (III):

wherein each L 1 is an optional linker and each C 1 is an acceptor chromophore.

7. The dye according to claim 4 , wherein the dye is described by the formula (IV):

wherein each L 1 is an optional linker and each C 1 is an acceptor chromophore.

8. The dye according to claim 4 , wherein the dye is described by the formula (V):

wherein each L 2 is an optional linker and each C 1 is an acceptor chromophore.

9. The dye according to claim 4 , wherein the dye is described by the formula (VI):

wherein each L 1 is an optional linker and each C 1 is an acceptor chromophore.

10. The dye according to claim 4 , wherein B 1 and B 2 are each independently described by the following structure:

wherein R 6 is an aryl or a heteroaryl, optionally substituted with one or more water solubilizing groups.

11. The dye according to claim 4 , wherein at least one L 2 is -L 3 -Z where L 3 is a linker and Z is a specific binding member.

12. The dye according to claim 4 , wherein each M 1 and M 2 are each independently described by the following structure:

wherein:

each R 7 is independently selected from the group consisting of an alkyl, a substituted alkyl, an aralkyl, a substituted aralkyl, a PEG moiety and -L 1 -C 1 .

13. The dye according to claim 4 , wherein:

M 1 is described by the following structure:

wherein each R 8 is a substituted aralkyl that comprises a water solubilizing group; and

M 2 is described by the following structure:

wherein R 9 is a substituted alkyl that comprises a water solubilizing group, and R 19 is -L 1 -C 1 .

14. A labelled specific binding member, comprising:

a polymeric tandem dye comprising:

a water soluble light harvesting BODIPY unit-comprising multichromophore;

an acceptor chromophore covalently linked to the multichromophore in energy-receiving proximity therewith; and

a specific binding member covalently linked to the multichromophore.

15. The labelled specific binding member according to claim 14 , wherein the multichromophore comprises a BODIPY-comprising conjugated segment described by formula (I):

wherein:

B is a BODIPY unit;

M is a π conjugated co-monomer;

each L is independently selected from the group consisting of a terminal group, a π conjugated segment, a linker and a linked specific binding member; and

n is an integer of 1 to 100,000.

16. The labelled specific binding member according to claim 14 , wherein the BODIPY unit is described by the structure:

wherein:

R 1 , R 2 , R 3 and R 4 are each independently selected from H, an alkyl and a substituted alkyl;

R 5 is selected from the group consisting of an alkyl, a substituted alkyl, an aryl, a substituted aryl, a heteroaryl and a substituted heteroaryl, wherein R 5 is optionally substituted with a water solubilizing group; and

each R is selected from the group consisting of F, OH, H, alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkoxy, substituted alkoxy, alkynyl and substituted alkynyl.

17. The labelled specific binding member according to claim 14 , wherein the multichromophore is described by the formula (II):

wherein:

B 1 and B 2 are each independently a BODIPY unit;

each M 1 and each M 2 are independently a π conjugated co-monomer;

a, b, c, d, e and f are each independently 0, 1 or 2, wherein b+e≧1;

n and m are independently 0 to 100,000, wherein n+m≧1; and

one L 2 group is a terminal group (G 1 ) and the other L 2 group is a linked specific binding member.

18. The labelled specific binding member according to claim 17 , wherein at least one of B 1 , B 2 , M 1 and M 2 comprises -L 1 -C 1 , wherein L′ is an optional linker and C 1 is the acceptor chromophore.

19. The labelled specific binding member according to claim 14 , wherein the acceptor chromophore is selected from the group consisting of a cyanine dye, a xanthene dye, a coumarin dye, a thiazine dye and an acridine dye.

20. A method of evaluating a sample for the presence of a target analyte, the method comprising:

(a) contacting the sample with a polymeric tandem dye conjugate that specifically binds the target analyte to produce a labelling composition contacted sample, wherein the polymeric tandem dye conjugate comprises:

(i) a light harvesting BODIPY unit-comprising multichromophore;

(ii) an acceptor chromophore covalently linked to the multichromophore in energy-receiving proximity therewith; and

(iii) a specific binding member; and

(b) assaying the labelling composition contacted sample for the presence of a polymeric tandem dye conjugate-target analyte binding complex to evaluate whether the target analyte is present in the sample.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 17, 2017
From: ZHAO, LUCY
To: BECTON, DICKINSON AND COMPANY
Reel/Frame 040982/0605 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2016
From: BARTHOLOMEW, GLENN P.; GAYLORD, BRENT S.
To: BECTON, DICKINSON AND COMPANY
Reel/Frame 038291/0860 →
Continuity (2)
Provisional Application 62132446 · Mar 12, 2015
Related Publication 20160264737A1 · Sep 15, 2016