IP Library Granted Patent US 8,628,753
Granted Patent B2
US 8,628,753 · App. 12/892,379 · Granted Jan 14, 2014

Reduced dye probes for the detection of radical oxygen species

Inventors: Niren Murthy (Atlanta, GA); W. Robert Taylor (Stone Mountain, GA); Kousik Kundu (Atlanta, GA); Sarah F. Knight (Atlanta, GA); Sungmun Lee (Dunwoody, GA)
Assignees: Emory University; Georgia Tech Research Corporation
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Quick Facts
Patent No.
US 8,628,753
App. No.
12/892,379
Granted
Jan 14, 2014
Kind
B2
Abstract

Reduced dyes, such as hydrocyanines, deuterocyanines, and/or other deuterated dyes capable of detecting one or more reactive oxygen species are described herein. The reduced dyes exhibit little or no fluorescence due to the disrupted π conjugation. However, upon reaction with ROS, the reduced dyes are oxidized, regenerating the extended π conjugation and causing a substantial increase in fluorescence intensity. In many case, the oxidized dye is generally membrane impermeable. However, upon reduction, many of the reduced dyes are membrane permeable. Thus, reduced dyes can accumulate in cells and/or tissue to amplify the signal. Once inside the cell or tissue, the reduced dye is reoxidized upon reaction with ROS, and the oxidized dye again becomes membrane impermeable, trapping the dye within the cell. The reduced dyes can be used to image ROS, such as hydroxide radical and superoxide, in serum, cell cultures, tissue explants, and in vivo.

Claims (92)

1. A method of detecting reactive oxygen species, the method comprising contacting cells, cell cultures, tissues, organs, biological fluids, or combinations thereof, with an effective amount of one or more reduced dyes selected from the group consisting of hydrocyanines, deuterocyanines, and combinations thereof and determining if the reduced dye has been oxidized.

2. The method of claim 1 , wherein oxidation of the reduced dye is detected by fluorescence spectroscopy.

3. The method of claim 1 , wherein the oxidation of the reduced dye is detected by fluorescence microscopy.

4. The method of claim 3 , wherein the oxidation of the reduced dye is detected by confocal laser scanning microscopy.

5. The method of claim 3 , wherein the oxidation of the reduced dye is detected by total internal reflection fluorescence microscopy.

6. The method of claim 1 , wherein the reduced dye is a hydrocyanine.

7. The method of claim 6 , wherein the reduced dye is a deuterocyanine.

8. The method of claim 1 , wherein the hydrocyanine or deuterocyanine is selected from the group consisting of:

wherein X is hydrogen; halogen; C 1-20 alkyl; aryl; —OR, where R is C 1-20 alkyl or aryl; hydroxyl; —NR 5 R 6 , where R 5 and R 6 are independently hydrogen, C 1-20 alkyl or aryl; —CN, —SH; —NO 2 ; —S—C 1-20 alkyl; —S-aryl; aryl, —COOH;

—COH; —COR or —COOR, where R is defined above; or —CONR 13 R 14 , wherein R 13 and R 14 are independently hydrogen or R as defined above;

R 1 -R 4 are independently hydrogen, C 1-20 alkyl, C 1-20 alkyl sulfate, C 1-20 alkyl carboxylate; C 1-20 alkyl amino; aryl, benzyl, oligoethylene glycol, or polyethylene glycol;

R 5 and R 6 are independently hydrogen; hydroxyl; —OR 8 ; —NH 2 ; —NHR 9 ; —NR 10 R 11 , C 1-20 alkyl, C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; —COOH; —CO 2 − or —SO 3 − ; wherein R 8 -R 11 are the same as R; oligoethylene glycol, or polyethylene glycol;

n is an integer from 1-5;

R 12 is H or D; and

the benzene ring represented by dotted lines is optional;

wherein X is hydrogen; halogen; C 1-20 alkyl; aryl; —OR, where R is C 1-20 alkyl or aryl; hydroxyl; —NR 5 R 6 , where R 5 and R 6 are independently hydrogen, C 1-20 alkyl or aryl; —CN, —SH; —NO 2 ; —S—C 1-20 alkyl; —S-aryl; aryl, —COOH; —COH; —COR or —COOR, where R is defined above; or —CONR 12 R 13 , wherein R 12 and R 13 are independently hydrogen or R as defined above;

R 1 and R 2 are independently hydrogen, C 1-20 alkyl, C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; aryl, benzyl, oligoethylene glycol, or polyethylene glycol;

R 3 and R 4 are independently hydrogen; hydroxyl; —OR 7 ; —NH 2 ; —NHR 8 ; —NR 9 R 10 , C 1-20 alkyl, C 1-20 alkyl sulfate, C 1-20 alkyl carboxylate; C 1-20 alkyl amino; —COOH; —CO 2 − or —SO 3 − ; wherein R 7 -R 10 are the same as R; oligoethylene glycol, or polyethylene glycol;

n is an integer from 1-5;

R 11 is H or D, and

the benzene ring represented by dotted lines is optional;

wherein X is hydrogen; halogen; C 1-20 alkyl; aryl; —OR, where R is C 1-20 alkyl or aryl; hydroxyl; —NR 5 R 6 , where R 5 and R 6 are independently hydrogen, C 1-20 alkyl or aryl; —CN, —SH; —NO 2 ; —S—C 1-20 alkyl; —S-aryl; aryl, —COOH; —COH;

—COR or

—COOR, where R is defined above; or —CONR 12 R 13 , wherein R 12 and R 13 are independently hydrogen or R as defined above;

R 1 and R 2 are independently hydrogen, C 1-20 alkyl, C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; aryl, benzyl, oligoethylene glycol, or polyethylene glycol;

R 3 and R 4 are independently hydrogen; hydroxyl; —OR 7 ; —NH 2 ; —NHR 8 ; —NR 9 R 10 , C 1-20 alkyl, C 1-20 alkyl sulfate, C 1-20 alkyl carboxylate; C 1-20 alkyl amino; —COOH; —CO 2 − or —SO 3 − ; wherein R 7 -R 10 are the same as R; oligoethylene glycol, or polyethylene glycol;

n is an integer from 1-5;

R 11 is H or D; and

the benzene ring represented by dotted lines is optional

wherein X is hydrogen; halogen; C 1-20 alkyl; aryl; —OR, where R is C 1-20 alkyl or aryl; hydroxyl; —NR 5 R 6 , where R 5 and R 6 are independently hydrogen, C 1-20 alkyl or aryl; —CN, —SH; —NO 2 , —S—C 1-20 alkyl; —S-aryl; aryl, —COOH;

—COH; —COR or

—COOR, where R is defined above; or —CONR 17 R 18 , wherein R 17 and R 18 are independently hydrogen or R as defined above;

R 1 and R 2 are independently hydrogen, C 1-20 alkyl, C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; aryl, benzyl, oligoethylene glycol, or polyethylene glycol;

R 3 and R 4 are independently hydrogen; hydroxyl; —OR 12 ; —NHR 13 ;

—NR 14 R 15 , C 1-20 alkyl, C 1-20 alkyl sulfate, C 1-20 alkyl carboxylate; C 1-20 alkyl amino; —COOH; —CO 2 − or —SO 3 − ; wherein R 12 -R 15 are the same as R; oligoethylene glycol, or polyethylene glycol;

R 5 -R 8 are independently hydrogen or C 1-20 alkyl;

n is an integer from 1-5;

R 16 is H or D; and

the benzene ring represented by dotted lines is optional,

wherein if the benzene ring is not present, R 16 is D;

wherein X is hydrogen; halogen; C 1-20 alkyl; aryl; —OR, where R is C 1-20 alkyl or aryl; hydroxyl; —NR 5 R 6 , where R 5 and R 6 are independently hydrogen, C 1-20 alkyl or aryl; —CN, —SH; —NO 2 , —S—C 1-20 alkyl; —S-aryl; aryl, —COOH;

—COH; —COR or —COOR, where R is defined above; or —CONR 16 R 17 , wherein R 16 and R 17 are independently hydrogen or R as defined above;

R 1 and R 2 are independently hydrogen, C 1-20 alkyl, C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; aryl, benzyl, oligoethylene glycol, or polyethylene glycol;

R 3 and R 4 are independently hydrogen; hydroxyl; —OR 11 ; —NHR 12 ;

—NR 13 R 14 , C 1-20 alkyl, C 1-20 alkyl sulfate, C 1-20 alkyl carboxylate; C 1-20 alkyl amino; —COOH; —CO 2 − or —SO 3 − ; wherein R 11 -R 14 are the same as R; oligoethylene glycol, or polyethylene glycol;

R 5 -R 8 are independently hydrogen or C 1-20 alkyl;

R 15 is H or D; and

n is an integer from 1-5;

wherein X is hydrogen; halogen; C 1-20 alkyl; aryl; —OR, where R is C 1-20 alkyl or aryl; hydroxyl; —NR 5 R 6 , where R 5 and R 6 are independently hydrogen, C 1-20 alkyl or aryl; —CN, —SH; —NO 2 ; —S—C 1-20 alkyl; —S-aryl; aryl, —COOH;

—COH; —COR or —COOR, where R is defined above; or —CONR 12 R 13 , wherein R 12 and R 13 are independently hydrogen or R as defined above;

R 1 and R 2 are independently hydrogen, C 1-20 alkyl, C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; aryl, benzyl, oligoethylene glycol, or polyethylene glycol;

R 3 and R 4 are independently hydrogen; hydroxyl; —OR 7 ; —NHR 8 ;

—NR 9 R 10 , C 1-20 alkyl, C 1-20 alkyl sulfate, C 1-20 alkyl carboxylate; C 1-20 alkyl amino; oligoethylene glycol, or polyethylene glycol;

—COOH; —CO 2 − or —SO 3 − ; wherein R 7 -R 10 are the same as R;

R 11 is H or D; and

n is an integer from 1-5;

wherein X is hydrogen; halogen; C 1-20 alkyl; aryl; —OR, where R is C 1-20 alkyl or aryl; hydroxyl; —NR 5 R 6 , where R 5 and R 6 are independently hydrogen, C 1-20 alkyl or aryl; —CN, —SH; —NO 2 ; —S—C 1-20 alkyl; —S-aryl; aryl, —COOH; —COH; —COR or —COOR, where R is defined above; or —CONR 12 R 13 , wherein R 12 and R 13 are independently hydrogen or R as defined above;

R 1 and R 2 are independently hydrogen, C 1-20 alkyl, C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; aryl, benzyl, oligoethylene glycol, or polyethylene glycol; and

R 3 and R 4 are independently hydrogen; hydroxyl; —OR 7 ; —NHR 8 ;

—NR 9 R 10 , C 1-20 alkyl, C 1-20 alkyl sulfate, C 1-20 alkyl carboxylate; C 1-20 alkyl amino; —COOH; —CO 2 − or —SO 3 − ; wherein R 7 -R 10 are the same as R; oligoethylene glycol, or polyethylene glycol;

n is an integer from 1-5; and

q is 0, 1, or 2;

wherein X is hydrogen; halogen; C 1-20 alkyl; aryl; —OR, where R is C 1-20 alkyl or aryl; hydroxyl; —NR 5 R 6 , where R 5 and R 6 are independently hydrogen, C 1-20 alkyl or aryl; —CN, —SH; —NO 2 ; —S—C 1-20 alkyl; —S-aryl; aryl, —COOH;

—COH; —COR or —COOR, where R is defined above; or —CONR 12 R 13 , wherein R 12 and R 13 are independently hydrogen or R as defined above;

R 1 and R 2 are independently hydrogen, C 1-20 alkyl, C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; aryl, benzyl, oligoethylene glycol, or polyethylene glycol; and

R 3 and R 4 are independently hydrogen; hydroxyl; —OR 7 ; —NHR 8 ;

—NR 9 R 10 , C 1-20 alkyl, C 1-20 alkyl sulfate, C 1-20 alkyl carboxylate; C 1-20 alkyl amino; —COOH; —CO 2 − or —SO 3 −; wherein R 7 -R 10 are the same as R; oligoethylene glycol, or polyethylene glycol;

R 11 is D; and

n is an integer from 1-5;

wherein X is hydrogen; halogen; C 1-20 alkyl; aryl; —OR, where R is C 1-20 alkyl or aryl; hydroxyl; —NR 5 R 6 , where R 5 and R 6 are independently hydrogen, C 1-20 alkyl or aryl; —CN, —SH; —NO 2 ; —S—C 1-20 alkyl; —S-aryl; aryl, —COOH;

—COH; —COR or —COOR, where R is defined above; or —CONR 13 R 14 , wherein R 13 and R 14 are independently hydrogen or R as defined above;

R 1 -R 4 are independently hydrogen, C 1-20 alkyl; C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; aryl, benzyl, oligoethylene glycol, or polyethylene glycol;

R 5 and R 6 are independently hydrogen; hydroxyl; —OR 5 ; —NH 2 ; —NHR 6 ; —NR 7 R 8 , C 1-20 alkyl; C 1-20 alkyl sulfate; C 1-20 alkyl carboxylate; C 1-20 alkyl amino; —COOH; —CO 2 − ; or —SO 3 − ; wherein R 5 -R 8 are the same as R; oligoethylene glycol, or polyethylene glycol;

Y and Z are independently carbon, nitrogen or sulfur, wherein if Y and/or Z is carbon, the carbon is tetravalent having two substituents as defined above; if Y and/or Z is sulfur; the sulfur is divalent; and if Y and/or Z is nitrogen, the nitrogen is trivalent, having one substituent as defined above;

R 12 is H or D; and

the benzene ring represented by dotted lines is optional;

wherein X is hydrogen; halogen; C 1-20 alkyl; aryl; —OR, where R is C 1-20 alkyl or aryl; hydroxyl; —NR 5 R 6 , where R 5 and R 6 are independently hydrogen, C 1-20 alkyl or aryl; —CN, —SH; —NO 2 ; —S—C 1-20 alkyl; —S-aryl; —COOH; —COH;

—COR or —COOR, where R is defined above; or —CONR 13 R 14 , wherein R 13 and R 14 are independently hydrogen or R as defined above;

R 1 and R 2 are independently hydrogen, C 1-20 alkyl; C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; aryl, benzyl, oligoethylene glycol, or polyethylene glycol;

R 3 and R 4 are independently hydrogen; hydroxyl; —OR 5 ; —NH 2 ; —NHR 6 ; —NR 7 R 8 , C 1-20 alkyl; C 1-20 alkyl sulfonate, C 1-20 alkyl carboxylic acid or carboxylate; C 1-20 alkyl amino or quaternized amino; —COOH; —CO 2 − ; or —SO 3 − ; wherein R 5 -R 8 are independent selected from the group consisting of C 1-20 alkyl or aryl; oligoethylene glycol, or polyethylene glycol;

Z is carbon, nitrogen, sulfur, or oxygen, wherein if Y and/or Z is carbon, the carbon is tetravalent having two substituents as defined above; if Y and/or Z is sulfur and/or oxygen; the sulfur and/or oxygen is divalent; and if Y and/or Z is nitrogen, the nitrogen is trivalent, having one substituent as defined above;

R 12 is H or D; and

the benzene ring represented by dotted lines is optional.

9. The method of claim 8 , wherein the hydrocyanine or deuterocyanine is a compound of formula (d).

10. The method of claim 9 , wherein the benzene ring is absent.

11. The method of claim 10 , wherein X=H, R 1 and R 2 =methyl, ethyl, or (CH 2 ) 4 SO 3 Na, R 3 and R 4 =H, R 5 -R 8 =methyl, and R 16 =D or H.

12. The method of claim 9 , wherein the benzene ring is present.

13. The method of claim 12 , wherein X=H, R 1 and R 2 =methyl, ethyl, or (CH 2 ) 4 SO 3 Na, R 3 and R 4 =H, R 5 -R 8 =methyl, and R 16 =D or H.

14. The method of claim 8 , wherein the hydrocyanine or deuterocyanine is a compound of formula (g).

15. The method of claim 14 , wherein X=Cl, q=2, n=1, R 3 and R 4 =H, R 1 and R 2 =(CH 2 ) 4 SO 3 Na, and R 11 is hydrogen or deuterium.

16. The method of claim 1 , wherein the cells, tissue, biological fluids, or combinations thereof are contacted with the one or more reduced dyes in vitro.

17. The method of claim 1 , wherein the cells, tissue, biological fluids, or combinations thereof are contacted with the one or more reduced dyes in vivo.

Assignments (5)
CONFIRMATORY LICENSE Recorded Feb 6, 2015
From: EMORY UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 034915/0352 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2012
From: MURTHY, NIREN
To: GEORGIA TECH RESEARCH CORPORATION
Reel/Frame 028219/0687 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2012
From: KUNDU, KOUSIK; LEE, SUNGMUN
To: GEORGIA TECH RESEARCH CORPORATION
Reel/Frame 027553/0801 →
CONFIRMATORY LICENSE Recorded Apr 26, 2011
From: EMORY UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 026178/0981 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 3, 2011
From: TAYLOR, W. ROBERT; KNIGHT, SARAH F.
To: EMORY UNIVERSITY
Reel/Frame 025741/0198 →
Continuity (4)
Continuation In Part PCTUS2009038772 · Mar 30, 2009
Provisional Application 61040370 · Mar 28, 2008
Provisional Application 61100897 · Sep 29, 2008
Related Publication 20110070166A1 · Mar 24, 2011