Method for optically ascertaining parameters of species in a liquid analyte

• US 4,818,710 A
• Filed: 12/06/1985
• Issued: 04/04/1989
• Est. Priority Date: 12/10/1984
• Status: Expired due to Term

• Current Assignee: Prutec Ltd. (Mutual Life Assurance Co. of Canada)
• Original Assignee: Prutec Ltd. (Mutual Life Assurance Co. of Canada)
• Inventors: Dahne, Claus, Sutherland, Ranald M., Revillet, Georges
• Primary Examiner(s): NOT, DEFINED
• Application Number:
  US06/805,903
• Time in Patent Office: 1,215 Days
• Field of Search: 436/805, 436/67, 436/165, 436/172, 436/527, 250/227, 250/302, 250/365, 422/57, 422/68, 422/58
• US Class Current: 436/527
• CPC Class Codes: G01N 21/648 using evanescent coupling or surface plasmon coupling for the excitation of fluorescence
• CPC Class Codes: G01N 21/7703 using reagent-clad optical fibres or optical waveguides using measurement of total internal reflection or attenuated total reflection G01N21/552; optical fibres or waveguides per se G02B
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: Y10S 436/805 Optical property

Abstract

An optical waveguide with one or more coatings of reactants specific to species to be analyzed in a liquid analyte immersed therein. A light signal carried by the waveguide undergoes interaction either with the bulk analyte whereby a first signal in connection with the bulk analyte is obtained and, simultaneously, with a layer of complex resulting from the reaction of one of said specific reactant with one of said species or with two or more complex layers corresponding to two or more of said species, this generating a second (or more) signal to provide the required analytical information on said species.

Claims

1. A method of determining the presence of more than one component in a single liquid sample by use of multiple internal reflections of excitation radiation in a waveguide comprising the steps of:

coating a surface of a waveguide with a reactant specific to a first component contained in the sample;

exposing said coated surface to the sample, thereby allowing formation of a layer of a complex formed by the reaction of said reactant and said first component;

illuminating an input end of said waveguide with an optical excitation signal in a manner such that an evanescent component of said signal penetrates a sufficient distance into said sample to interact with said complex layer with a second component in the bulk of said sample;

collecting the optical signal after said interaction; and

subsequently analyzing said signal to determine the presence or quantity of each of said first and second components in the sample.

2. The method of claim 1 wherein said signal interaction results from absorption, scattering or the generation of fluorescence.

3. The method of claim 2 wherein the excitation signal interacts with said complex layer during the formation thereof so as to provide a time dependent response on said first component and an instant response on said second component.

4. The method of claim 2 wherein said waveguide is an optical slide or an optical fiber.

5. The method of claim 1 for substantially simutaneously determining in a blood sample total hemoglobin and further hemoglobin factors or derivatives thereof relative to said total hemoglobin, the method comprising:

(a) Coating at least part of the surface of an optical waveguide system of a refractive index greater than that of the sample with one or more coatings of complexing reactants, each coating being of a reactant specific to that factor or derivative of hemoglobin and capable of building up a layer of said complex upon reaction with said hemoglobin factor or derivative;

(b) Illuminating said waveguide at an input end with a beam of light and collecting the exiting light at an output end, said beam being transmitted along said guide by a multiple internal reflection mechanism at an angle such that the effective range of action outside the guide of an evanescent light component associated with said beam exceeds that of said complex layer;

(c) Contacting together said blood sample and said illuminated waveguide whereby, on one hand, part of the light traveling in the guide is initially absorbed by interaction of the evanescent wave component with the hemoglobin of the bulk sample, this resulting in an instantaneous sharp dip (I) in the exiting light from said output end and, on the second hand, an immuno-type reaction develops between said glycosylated hemoglobin or other factor in said blood sample and corresponding reactant on the waveguide with consecutive build-up of said complex layer, such build up resulting in a relatively slower change of signal of said exiting light, said relatively slower change of signal being due to the interaction of said evanescent wave component with said complex layer in formation;

(d) Observing, measuring and/or recording said sudden optical absorption drop (I) occurring to the transmitted light collected from said output end, said measured drop being quantitatively related with the concentration of the total hemoglobin of the sample;

(e) Observing, measuring and/or recording said relatively lower change, the magnitude (M) and rate (K) of which quantitatively relates to the amount of glycosylated hemoglobin or other factor in the sample;

(f) Effecting the required computations to express the results obtained from the values of I and M or K in terms of concentration of total hemoglobin and/or ratio of glycosylated hemoglobin or other factor to hemoglobin in the sample.

6. The method of claim 5, wherein the steps (d) and (e) are both effected on the signal resulting from the interaction of the incident light and the sample at the area of the waveguide bearing the reactant coated thereon.

7. The method of claim 5 wherein the blood factor determined is glycosylated hemoglobin.

8. The method of claim 5, wherein step (d) is effected on the component of the output signal resulting from said interaction on a part of the waveguide not coated with the reactant.

9. The method of claim 8, wherein there is used a dual type waveguide, one portion of which is coated with reactant and another portion of which is not coated with reactant.

10. The method of claim 9, wherein said other portion is coated with a blocking protein for minimizing the possible deposition of hemoglobin on the waveguide uncoated surface area.

11. The method of claim 9, which comprises using as a dual waveguide an analytical cuvette whose main opposite walls are light conductive and made of a transparent material of suitable refractive index greater than that of the blood sample, this material serving as the waveguide.

12. A method determining the presence of more than one component in a single liquid sample by use of multiple internal reflections of excitation radiation in a waveguide, said method comprising the steps of:

coating a first surface of said waveguide with a reactant specific to a first component in said sample;

exposing said first coated surface, and a second surface of said waveguide, to said sample thereby allowing formation of a layer of complex on the first surface, said layer formed by the reaction of said reactant and said first component;

illuminating an input and of said waveguide with an optical excitation signal in a manner such that the evanescent component of said signal interacts with said complex layer at said first surface, and with the bulk solution of said sample at said second surface;

collecting the optical signal after said interactions; and

subsequently processing said signal to ascertain the presence or quantity of each of said first and second components.

13. The method of claim 12 wherein the first and second surfaces are part of separately illuminated waveguide elements.

14. The method of claim 12 wherein said collecting step further comprises separating the effect from each interaction by separating the signal as to wavelength.

15. The method of claim 12 wherein the first and second surfaces are alternately exposed to the excitation signal.

16. An apparatus for the combined determination of hemoglobin and at least one hemoglobin factor in a blood sample comprising

waveguide means for carrying an optical signal;

light source means for providing said optical signal to an input end of said waveguide means;

holding means for containing said blood sample;

light detecting means for collecting said optical signal exiting from an output end of said waveguide means, and for generating an electrical signal in response to said optical signal; and

computing means for processing said electrical signal and for providing output information in response thereto;

wherein the waveguide means is coated along a portion thereof with a reactant specific to a hemoglobin factor so as to form a layer of complex from said reactant and said factor when said waveguide is exposed to said sample; and

wherein a second portion of said waveguide means is untreated or treated with a hemoglobin factor blocking agent;

so that when the light signal interacts with said reactant coated portion, information is gathered for the determination of a hemoglobin factor, and where the light signal interacts with said untreated or blocked portion, information is gathered for the determination of hemoglobin.

17. The apparatus of claim 16, wherein the waveguide means has a dualtype structure and comprises two independent optical elements to simultaneously or alternately carry said optical signal, one of said elements being reactant coated and the other being bare or blocked.

18. The apparatus of claim 17, in which said light source means comprise two independent alternately flashing light sources the output of which is focussed each on one optical end of said elements via beam splitting means and in which the other end of said elements is made totally reflective so that the light signal carried by said elements travels forwards and backwards therein.

19. The apparatus of claim 17, using as the waveguide means an optical cell or cuvette of which two oppositely facing walls operate as said waveguide elements.

20. The apparatus of claim 19, in which said light source means comprises chopper means to alternately inject the signal light into the two elements of the dual-waveguide.

21. The apparatus of claim 20, in which said chopper means are either a rotating mirror or a chopper disk.

22. An apparatus for the substantially simultaneous determination in more than one component of a liquid sample comprising:

waveguide means for carrying an optical signal;

light source means for providing said optical signal to an input end of said waveguide means;

holding means for containing said liquid sample;

light detecting means for collecting said optical signal from an output end of said waveguide means, and for generating an electrical signal in response to said optical signal;

computing means for processing said electrical signal and providing output information in response thereto;

wherein said waveguide means is coated along a portion thereof with a reactant specific to a first component in said sample so as to form a layer of complex from said reactant and said component when said waveguide is exposed to said sample; and

wherein said light source means and said waveguide means are arranged such that an evanescent component of said light source means interacts with both said reactant/component complex and the bulk of said sample so that information is obtained substantially simultaneously from each both the reactant/component complex and the bulk of said sample.