Method and system for non-invasive detection of zinc protoporphyrin in erythrocytes

• US 4,178,917 A
• Filed: 01/03/1979
• Issued: 12/18/1979
• Est. Priority Date: 01/03/1979
• Status: Expired due to Term

• Current Assignee: Howard M. Shapiro
• Original Assignee: Howard M. Shapiro
• Inventors: Shapiro, Howard M.
• Primary Examiner(s): Cohen, Lee S.
• Application Number:
  US05/866,788
• Time in Patent Office: 349 Days
• Field of Search: 128/2 R, 128/2 A, 128/2 G, 128/2 L, 356/39-41, 356/317, 356/318
• US Class Current: 600/322
• CPC Class Codes: A61B 5/0071 by measuring fluorescence emission
• CPC Class Codes: A61B 5/14556 by fluorescence A61B5/14555 takes precedence
• CPC Class Codes: G01N 2015/012 Red blood cells
• CPC Class Codes: G01N 2015/0222 from dynamic light scattering, e.g. photon correlation spectroscopy
• CPC Class Codes: G01N 2021/6484 Optical fibres
• CPC Class Codes: G01N 21/274 Calibration, base line adjustment, drift correction
• CPC Class Codes: G01N 21/64 Fluorescence; Phosphorescence
• CPC Class Codes: G01N 33/72 involving blood pigments, e.g. haemoglobin, bilirubin or other porphyrins; involving occult blood

Abstract

A method and system for the non-invasive detection of zinc protoporphyrin (ZPP) in erythrocytes. Light at least partially within the fluorescence excitation spectrum of ZPP is directed onto the skin of a patient. The resultant incident light reflection and ZPP fluorescence from the region underlying the irradiated skin are detected. Signals representative of the detected light are generated and combined to provide a signal representative of the ZPP concentration in the erythrocytes within the sample region.

Claims

1. A system for the non-invasive detection of zinc protoporphyrin (ZPP) in erythrocytes in a region underlying a sample surface of a patient, comprising:

A. source means for generating excitation light in a predetermined spectrum, said predetermined spectrum being outside the characteristic fluorescence emission spectrum of ZPP and at least a portion of said predetermined spectrum being in the characteristic fluorescence excitation spectrum of ZPP,

B. first detection means for generating a first signal representative of the intensity of light incident thereon and in said characteristic fluorescence emission spectrum of ZPP,

C. second detection means for generating a second signal representative of the intensity of light incident thereon and within said predetermined spectrum,

D. transfer means for directing said excitation light to be incident on said sample surface, and for directing light emitted from said sample surface to be incident on said first and second detection means,

E. circuit means responsive to said first and second signals to generate a signal representative of the concentration of ZPP in said erythrocytes.

2. The system according to claim 1 further comprising:

third detection means for generating an excitation level signal representative of the intensity of light incident thereon and in said fluorescence excitation spectrum,

monitor transfer means for directing a predetermined portion of said excitation light to be incident on said third detection means,

wherein said excitation level signal is representative of the intensity of said excitation light.

3. The system according to claim 2 further comprising:

source control means responsive to said excitation level signal to adaptively control said source means whereby the intensity of said light incident in said third detection means is substantially constant.

4. The system according to claim 1 wherein said circuit means comprises:

means responsive to said first signal to generate a third signal representative of the amplitude of the a.c. component of said first signal,

means responsive to said second signal to generate a fourth signal representative of the amplitude of the a.c. component of said second signal,

means responsive to said third and fourth signals to generate a fifth signal representative of the ratio of said third and fourth signals, said fifth signal being representative of the concentration of ZPP in said erythrocytes.

5. The system according to claim 1 wherein said circuit means comprises means responsive to said first and second signals to generate a ZPP signal representative of the ratio of said first and second signals, said ZPP signal being representative of the concentration of ZPP in said erythrocytes.

6. The system according to claim 1 wherein said source means is adapted to generate said excitation light at wavelengths substantially in the range 420-430 nm.

7. The system according to claim 6 wherein said first detection means is adapted to be responsive to incident light having wavelengths substantially in the range 590-680 nm.

8. The system according to claim 7 wherein said second detection means is adapted to be responsive to incident light having wavelengths substantially in the range 420-430 nm.

9. The system according to claim 6 wherein said first detection means is adapted to be responsive to incident light having wavelengths substantially in a relatively narrow range including 590 nm.

10. The system according to claim 9 wherein said second detection means is adapted to be responsive to incident light having wavelengths substantially in the range 420-430 nm.

11. The system according to claim 6 wherein said first detection means is adapted to be responsive to incident light having wavelengths substantially in a relatively narrow range including 640 nm.

12. The system according to claim 11 wherein said second detection means is adapted to be responsive to incident light having wavelengths substantially in the range 420-430 nm.

13. The system according to claim 1 wherein said predetermined spectrum is substantially all within said characteristic excitation spectrum.

14. The system according to claim 1 wherein said predetermined spectrum includes at least a portion outside said characteristic excitation spectrum and wherein said second detection means is adapted whereby said second signal is representative of the intensity of light incident thereon and in said portion outside said characteristic excitation spectrum.

15. Method for the non-invasive detection of zinc protoporphyrin (ZPP) in erythrocytes in a region underlying a sample surface of a patient, comprising the steps of:

A. generating excitation light in a predetermined spectrum, said predetermined spectrum being outside the characteristic fluorescence emission spectrum of ZPP and at least partially in the characteristic fluorescence excitation spectrum of ZPP,

B. directing said excitation light to be incident on said sample surface,

C. detecting light emitted from said sample surface in said characteristic fluorescence emission spectrum of ZPP and generating a first signal representative of the intensity thereof,

D. detecting light emitted from said sample surface in said predetermined spectrum and generating a second signal representative of the intensity thereof,

E. combining said first and second signals generating a signal representative of the concentration of ZPP in said erythrocytes.

16. The method according to claim 15 comprising the further step of:

generating an excitation level signal representative of the intensity of a predetermined portion of said excitation light.

17. The method according to claim 16 comprising the further step of:

adaptively controlling said step of generating of excitation light in response to said excitation level signal whereby the intensity of said light incident on said sample surface is substantially constant.

18. The method according to claim 15 wherein said combining step comprises:

generating a third signal from said first signal, said third signal being representative of the amplitude of the a.c. component of said first signal,

generating a fourth signal from said second signal, said fourth signal being representative of the amplitude of the a.c. component of said second signal,

combining said third and fourth signals to generate a fifth signal representative of the ratio of said third and fourth signals, said fifth signal being representative of the concentration of ZPP in said erythrocytes.

19. The method according to claim 15 wherein said combining step comprises combining said first and second signals to generate a ZPP signal representative of the ratio of said first and second signals, said ZPP signal being representative of the concentration of ZPP in said erythrocytes.

20. The method according to claim 15 wherein said predetermined spectrum is substantially within said characteristic fluorescence excitation spectrum of ZPP.

21. The method according to claim 15 wherein said predetermined spectrum is at least partially outside said characteristic excitation spectrum, and wherein said step D comprises the step of:

detecting light in the portion of said predetermined spectrum outside said characteristic excitation spectrum and generating said second signal representative of the intensity thereof.