IP Library Granted Patent US 8,029,765
Granted Patent B2
US 8,029,765 · App. 10/584,821 · Granted Oct 4, 2011

SMMR (small molecule metabolite reporters) for use as in vivo glucose biosensors

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Quick Facts
Patent No.
US 8,029,765
App. No.
10/584,821
Granted
Oct 4, 2011
Kind
B2
Abstract

Small Molecule Metabolite Reporters (SMMRs) for use as in vivo glucose biosensors, sensor compositions, and methods of use, are described. The SMMRs include boronic acid-containing xanthene, coumarin, carbostyril and phenalene-based small molecules which are used for monitoring glucose in vivo, advantageously on the skin.

Claims (32)

1. A method of measuring a compound or metabolite thereof, comprising contacting a reporter compound of the following formula:

wherein

D is a heteroatom (O or N);

R 10 is H or CH 3 ;

R 12 is

wherein L is an amino-containing linking moiety; and

at least one boronic acid moiety is present; and salts thereof, which reporter compound is sensitive to the presence of said compound or metabolite thereof, with an area of the body where said metabolites may be found, and detecting a photometric change in said reporter compound indicative of said compound or metabolite thereof.

2. The method of claim 1 , wherein said area of the body is skin.

3. The method of claim 1 , wherein said area of the body is the layer of the skin known as stratum corneum.

4. The method of claim 1 , wherein said area of the body is the layer of the skin known as epidermis.

5. The method of claim 1 , wherein said area of the body is the layer of the skin known as dermis.

6. The method of claim 1 , wherein said compound is glucose.

7. A method of measuring a compound or metabolite thereof, comprising:

contacting a reporter compound or a salt thereof with a sample of a biological fluid containing an amount of the compound or metabolite thereof; and

detecting a photometric change in the reporter compound that is indicative of the compound or metabolite thereof;

wherein the reporter compound has a structure represented by the following formula:

Wherein:

D is a heteroatom (O or N);

R 10 is H or CH 3 ;

R 12 is

wherein L is an amino-containing linking moiety; and

at least one boronic acid moiety is present.

8. The method of claim 7 , wherein the compound or metabolite thereof is glucose.

9. A compound having a structure represented by the following formula:

wherein:

D is a heteroatom (O or N);

R 10 is H or CH 3 ;

R 12 is

wherein L is an amino-containing linking moiety; and

at least one boronic acid moiety is present.

10. The compound of claim 9 , wherein the amino-containing linking moiety is selected from the group consisting of an unsubstituted amino group, a substituted amino group, an amido group, and a sulfamido group.

11. A reagent strip comprising the compound of claim 9 .

Assignments (2)
CHANGE OF NAME Recorded May 22, 2012
From: MASIMO LABORATORIES, INC.
To: CERCACOR LABORATORIES, INC.
Reel/Frame 028252/0427 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2007
From: BELLOTT, EMILE M.; BU, DONGSHENG; CHIDS, DR. JAMES J.; LAMBERT, CHRISTOPHER; NIENABER, HUBERT A.; SHI, SHIRLEY J.; WANG, ZHAOLIN; WORKMAN, JEROME J.; ZELENCHUK, ALEX R.
To: MASIMO LABORATORIES, INC.
Reel/Frame 020026/0650 →