Blood Glucose Monitoring System And Method

• US 20080214912A1
• Filed: 01/10/2008
• Published: 09/04/2008
• Est. Priority Date: 01/10/2007
• Status: Abandoned Application

• Current Assignee: Vytrace Corporation
• Original Assignee: Glucose Sensing Technologies, LLC
• Inventors: Cano, Gerald G.
• Application Number:
  US11/972,190
• Publication Number:
  US 20080214912A1
• Time in Patent Office: Days
• US Class Current: 600/316
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1459 invasive, e.g. introduced into the body by a catheter A61B5/1464 takes precedence

Abstract

An optrode for insertion into a blood vessel can include at least one fiber optic, a sheath enclosing at least part of the fiber optic and sensor material in optical communication with one end of the fiber optic. The sensor material is operative for diffracting electromagnetic waves received from the fiber optic and is responsive to changes in an amount of glucose in contact therewith for changing a diffraction of the electromagnetic waves as a function thereof. A membrane covering a distal end of the sheath passes to the sensor material glucose from blood in contact with the side of the membrane opposite the sensor material. Electromagnetic waves input into the fiber optic cable are diffracted by the sensor material. A concentration of glucose in the blood can be estimated from the amount of diffraction of the electromagnetic waves. A signal can be output related to the estimated glucose concentration.

Claims

1. A blood glucose monitoring system comprising:

at least one fiber optic cable;

a biocompatible sheath enclosing at least part of the at least one fiber optic cable;

sensor material supported at one end of the sheath in optical communication with one end of the at least one fiber optic cable, the sensor material operative for diffracting electromagnetic waves received from the at least one fiber optic cable, the sensor material responsive to changes in an amount of glucose in contact therewith for changing a diffraction of the electromagnetic waves as a function thereof; and

a biocompatible membrane covering the one end of the sheath, the biocompatible membrane in contact with the sensor material and operative for passing to the sensor material glucose from blood in contact with the side of the membrane opposite the sensor material while avoiding the passage of one or more blood proteins to the sensor material.

2. The system of claim 1, further including means for determining a concentration glucose in the blood, said means responsive to the diffracted electromagnetic waves for determining as a function thereof the concentration of glucose in the blood and for outputting a signal related thereto.

3. The system of claim 2, further including another fiber optic cable enclosed at least in part by the sheath, wherein one fiber optic cable is operative for delivering the electromagnetic waves to the sensor material and the other fiber optic cable is operative for delivering the diffracted electromagnetic waves to the means for determining.

4. The system of claim 2, wherein the at least one fiber optic cable delivers the electromagnetic waves to the sensor material and delivers the diffracted electromagnetic waves to the means for determining.

5. The system of claim 1, wherein the electromagnetic waves comprise visible light.

6. The system of claim 1, wherein:

the sensor material is comprised of either polymerized crystalline colloidal array (PCCA) material or holographic material; and

the PCCA material and the holographic material are each comprised of a hydrogel, means for diffraction and a molecular recognition agent that expands and contracts the sensor material as a function of the amount of glucose in contact therewith.

7. The system of claim 6, wherein:

the hydrogel of the PCCA material is one of the following;

an acrylamide;

purified agarose;

N-vinylpyrolidone;

methacrylate or hydroxy-ethyl-methacrylate; and

the hydrogel of the holographic material is one of the following;

polyvinyl alcohol;

polyvinylpyrrolidone;

polyhydroxyethyl acrylate;

polyhydroxyethyl methacrylate;

polyacrylamides;

polymethacrylamides;

homopolymers, or copolymers, of polymerisable derivatives of crown ethers;

or esters of, or co- or terpolymers of, polyhydroxyethylacrylate, polyhydroxyethylmethacrylate, polymethacrylamide or polyacrylamide.

8. The system of claim 6, wherein the PCCA material is either acrylamide or hydroxy-ethyl-methacrylate.

9. The system of claim 6, wherein:

the means for diffraction of the PCCA material is one of the following;

self organized colloidal particles or charged colloidal particles selected from the group consisting of colloidal polystyrene, polymethylmethacrylate, silicon dioxide, aluminum oxide, polytetrafluoroethylene and poly N-isopropylacrylamide; and

the means for diffraction of the holographic material is silver halide.

10. The system of claim 6, wherein:

the molecular recognition agent of the PCCA material is one of the following;

glucose oxidase;

dihydroxides of boron, barium, calcium, magnesium, and strontium;

boronic acid;

phenylboronic acid;

p-nitrophenylboronic acid;

4-methoxyphenylboronic acid;

alpha-naphthylboronic acid;

4-aminomethyl-2-N,N′

-dimethylaminomethylphenylboronic acid;

3-fluoro-4-aminophenylboronic acid;

2-fluoro-5-aminophenylboronic acid, or boronic acid derivatives having a pK_a value less than 7; and

the molecular recognition agent of the holographic material is one of the following boronic acids;

2-(((4-(acrylamidomethyl)phenylamino)methyl)phenylboronic acid;

2-((3-methacrylamidopropylamino)methyl)phenylboronic acid;

acrylamido-phenylboronic acid;

2-acrylamido-phenylboronic acid;

3-acrylamido-phenylboronic acid;

3-acrylamido-6-fluoro-phenylboronic acid;

amino-fluoro-phenylboronic acid;

4-amino 3-fluoro-phenylboronic acid;

or

5-amino 2-fluoro-phenylboronic acid.

11. The system of claim 1, wherein the means for determining is operative for periodically determining a concentration of glucose in the blood.

12. The system of claim 1, wherein the sheath is made from a polymer having a coating that avoids the growth of microorganisms.

13. A method of measuring blood glucose concentration comprising:

(a) inserting a vascular access catheter percutaneously into a blood vessel;

(b) inserting through the lumen of the catheter and into a flow of blood in the blood vessel at least the distal end of an optrode comprised of at least one fiber optic cable, a biocompatible sheath enclosing at least part of the at least one fiber optic cable, sensor material supported at the distal end of the sheath in optical communication with one end of the at least one fiber optic cable, the sensor material operative for diffracting electromagnetic waves received from the at least one fiber optic cable, the sensor material responsive to changes in an amount of glucose in contact therewith for changing a diffraction of the electromagnetic waves as a function thereof, and a biocompatible membrane covering the distal end of the sheath, the biocompatible membrane in contact with the sensor material and operative for passing to the sensor material glucose from blood in contact with the side of the membrane opposite the sensor material while avoiding the passage of one or more blood proteins to the sensor material;

(c) inputting electromagnetic waves into the at least one fiber optic cable;

(d) estimating from the diffraction of the electromagnetic waves input in step (c) a concentration of glucose in the blood; and

(e) outputting a signal related to the estimate in step (d).

14. The method of claim 13, wherein steps (c) and (e) are repeated substantially continuously.

15. The method of claim 13, wherein the electromagnetic waves of step (c) comprise visible white light.

16. The method of claim 13, wherein the optrode includes another fiber optic cable enclosed at least in part by the sheath, wherein one fiber optic cable is operative for delivering the electromagnetic waves to the sensor material and the other fiber optic cable is operative for delivering the diffracted electromagnetic waves from the sensor material.

17. The method of claim 13, wherein:

the sensor material is comprised of either polymerized crystalline colloidal array (PCCA) material or holographic material; and

the PCCA material and the holographic material are each comprised of a hydrogel, means for diffraction and a molecular recognition agent that expands and contracts the sensor material as a function of the amount of glucose in contact therewith.