System and method for monitoring nitric oxide levels using a non-invasive, multi-band biosensor

1. A biosensor for monitoring nitric oxide (NO) of a patient in vivo, comprising:

a PPG circuit configured to:

obtain a first spectral response for light reflected at a first wavelength from skin tissue of the patient, wherein the first wavelength has a high absorption coefficient for nitric oxide in arterial blood flow; and

obtain a second spectral response for light reflected at a second wavelength from skin tissue of the patient, wherein the second wavelength has a low absorption coefficient for nitric oxide in arterial blood flow; and

a processing circuit configured to:

determine an NO measurement value for nitric oxide using the first spectral response and the second spectral response;

determine a measurement value for at least a first species of hemoglobin; and

obtain an adjusted measurement value of nitric oxide by compensating the NO measurement value for nitric oxide using the measurement value of the first species of hemoglobin.

2. The biosensor of claim 1 , wherein the first wavelength has a high absorption coefficient for nitric oxide in arterial blood flow and is in a range of approximately 370 nm to 410 nm.

3. The biosensor of claim 1 , wherein the processing circuit is configured to obtain the adjusted measurement value of nitric oxide by compensating the NO measurement value for nitric oxide using the measurement value of the first species of hemoglobin by:

obtain a value Lλ1 using the first spectral response, wherein the value Lλ1 isolates the first spectral response due to pulsating arterial blood flow;

obtain a value Lλ2 using the second spectral response, wherein the value Lλ2 isolates the second spectral response due to pulsating arterial blood flow;

obtain the NO measurement value R λ1, λ2 from a ratio of the value Lλ1 and the value Lλ2; and

lessen the NO measurement value R λ1, λ2 using the measurement value for at least the first species of hemoglobin to obtain the adjusted measurement value of nitric oxide.

4. The biosensor of claim 1 , wherein the processing circuit is further configured to:

access a calibration database that includes a correlations of the adjusted measurement value of nitric oxide to a concentration level of nitric oxide (NO); and

obtain the concentration level of nitric oxide using the calibration database.

5. The biosensor of claim 4 , wherein the calibration database includes a range of the adjusted measurement value of nitric oxide and correlated concentration levels of nitric oxide and wherein the calibration database is generated using nitric oxide level measurements obtained from a large sample population.

6. The biosensor of claim 5 , wherein the calibration database includes different correlations between the range of the adjusted measurement values of nitric oxide and the concentration levels of nitric oxide depending on the underlying skin tissue.

7. The biosensor of claim 1 , wherein the processing circuit is further configured to determine the measurement value for at least the first species of hemoglobin by:

process a third spectral response for light at a third wavelength reflected from skin tissue of the patient, wherein the third wavelength has a high absorption coefficient for at least the first species of hemoglobin; and

determine the measurement value for at least the first species of hemoglobin using the third spectral response.

8. The biosensor of claim 7 , wherein the processing circuit is further configured to:

process a fourth spectral response for light at a fourth wavelength reflected from skin tissue of the patient, wherein the fourth wavelength has a high absorption coefficient for at least a second species of hemoglobin; and

determine a measurement value for the second species of hemoglobin using a Beer-Lambert matrix equation and the fourth spectral response for at least the second species of hemoglobin.

9. The biosensor of claim 8 , wherein the processing circuit is further configured to:

obtain the adjusted measurement value of nitric oxide by compensating the NO measurement value using the measurement value for the first species of hemoglobin and the measurement value for the second species of hemoglobin.

10. A method for monitoring nitric oxide (NO) of a patient in vivo, comprising:

obtaining a first spectral response for light reflected a first wavelength from skin tissue of the patient, wherein the first wavelength has a high absorption coefficient for nitric oxide in arterial blood flow;

obtaining a second spectral response for light reflected a second wavelength from skin tissue of the patient, wherein the second wavelength has a low absorption coefficient for nitric oxide in arterial blood flow;

determining an NO measurement value for nitric oxide using the first spectral response and the second spectral response;

determining a concentration level for at least a first species of hemoglobin; and

obtaining an adjusted measurement value of nitric oxide by compensating the NO measurement value using the concentration level for at least the first species of hemoglobin.

11. The method of claim 10 , wherein the first wavelength has a high absorption coefficient for nitric oxide in arterial blood flow and is in a range of approximately 370 nm to 410 nm.

12. The method of claim 10 , further comprising:

obtaining a value Lλ1 using the first spectral response, wherein the value L λ1 isolates the first spectral response due to pulsating arterial blood flow;

obtaining a value Lλ2 using the second spectral response, wherein the value L λ2 isolates the second spectral response due to pulsating arterial blood flow;

obtaining the NO measurement value R λ1, λ2 from a ratio of the value L λ1 and the value L λ2 ; and

compensating the NO measurement value R λ1, λ2 using the concentration level for at least the first species of hemoglobin to obtain the adjusted measurement value of nitric oxide.

13. The method of claim 10 , further comprising:

accessing a calibration database that includes a correlation of the adjusted measurement value of nitric oxide to a concentration level of nitric oxide (NO); and

obtaining the concentration level of NO using the calibration database.

14. The method of claim 10 , wherein determining the concentration level for at least the first species of hemoglobin comprises:

processing a third spectral response for light at a third wavelength reflected from skin tissue of the patient, wherein the third wavelength has a high absorption coefficient for at least the first species of hemoglobin; and

determining the concentration level for at least the first species of hemoglobin using the third spectral response.

15. The method of claim 14 , wherein the first species of hemoglobin is methemoglobin (MetHb).

16. The method of claim 15 , further comprising:

determining that the concentration level for MetHb is within a predetermined range; and

using the concentration level for MetHb as a known value in a Beer-Lambert matrix equation.

17. The method of claim 16 , further comprising:

processing a fourth spectral response for light at a fourth wavelength reflected from skin tissue of the patient, wherein the fourth wavelength has a high absorption coefficient for at least a second species of hemoglobin; and

determining a concentration level for the second species of hemoglobin using the Beer-Lambert matrix equation, the concentration level for MetHb and the fourth spectral response.

18. The method of claim 17 , further comprising:

obtaining the adjusted measurement value of nitric oxide by compensating the NO measurement value using the concentration level for MetHb and the concentration level for the second species of hemoglobin.