GB2268800A - Optical sensor - Google Patents

Optical sensor Download PDF

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Publication number
GB2268800A
GB2268800A GB9214758A GB9214758A GB2268800A GB 2268800 A GB2268800 A GB 2268800A GB 9214758 A GB9214758 A GB 9214758A GB 9214758 A GB9214758 A GB 9214758A GB 2268800 A GB2268800 A GB 2268800A
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GB
United Kingdom
Prior art keywords
light
sensor
lines
bands
components
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
GB9214758A
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GB9214758D0 (en
Inventor
Rosemary Cush
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BAE Systems Electronics Ltd
Original Assignee
GEC Marconi Ltd
Marconi Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by GEC Marconi Ltd, Marconi Co Ltd filed Critical GEC Marconi Ltd
Priority to GB9214758A priority Critical patent/GB2268800A/en
Publication of GB9214758D0 publication Critical patent/GB9214758D0/en
Publication of GB2268800A publication Critical patent/GB2268800A/en
Withdrawn legal-status Critical Current

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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/55Specular reflectivity
    • G01N21/552Attenuated total reflection
    • G01N21/553Attenuated total reflection and using surface plasmons

Abstract

An optical sensor for testing a biochemical sample includes a resonant mirror device 1 and a prism 2 for coupling an input beam of light to the device 1. The input beam having a single line spectrum is produced by a source 10 and polarized by a polarizer 4 to provide equal TE and TM components. The resonant mirror device is arranged in the path of said input beam such that the resonance is excited for at least one of said components. The light reflected from the device 1 is projected onto an analyser and thereafter passed through a diffraction grating 13 for producing an output beam having a spectrum including a series of bright and/or dark lines or bands. When a sensing layer is sensitized by the chemical sample, an angular shift in the resonance angle takes place and this causes the lines or bands of the output spectrum to be swept across a reference point where detector means 14 is located to count the number of lines or bands or parts thereof swept across the reference point. <IMAGE>

Description

monomode light and to make use of the fact that light polarized perpendicularly to the plane of incidence (TE polarized) undergoes resonance at a different angle to the orthogonal component (TM polarized). An optical sensor incorporating this technique is disclosed in GB Patent Application No. 9020965.1. A part of the incident light is launched into each polarization direction, and the two components are made to interfere at the output using an analyser aligned to the input polarisation. The phase difference between the two components is measured and, by using a compensator to remove the background phase difference, the phase difference is made to be zero away from the resonance and at a maximum of 11 radians on resonance. This results in an intensity variation in the output beam, which is maximum away from the resonance and drops to zero at the resonant angles.By rotating the analayser by off/2 radians, a phase shift of 11 is added to one component, resulting in the output beam intensity being zero away from resonance and maximum on resonance.
The sensor may be used with a collimated beam (rotating the prism to vary the incident angle) or with a focused or wedge beam as disclosed in GB Application No.9020965.1. In the latter case the projected output beam is of the form of two black lines, corresponding to the resonances, on a bright background (or alternatively, two bright bands on a dark backgroundss The positions of these resonances are measured using a detector array, for example, a CCD array. Although it would be possible to measure small peak shifts using a single detector, the initial angular position will vary from sample to sample, and so detectors are required over the full range over which a resonance may occur.
The use of detector arrays results in a large number of data points being analysed in order to determine the position of the peak, so requiring complex processing. Whilst this is necessary when dealing with small angle shifts, for larger angle shifts an alternative, simpler technique may be used which utilizes a multiple beam splitting device, to produce a comb of peaks at the output.
In addition, the sensor of the present invention is particularly useful in a situation where small angular shifts in the output (i.e. of less than the output spectral spacing) are to be measured. The existence of a comb spectrum allows the use of a smaller detector/detector array than with a single line output for a given angular resolution. This is because, despite shifts in the zero position of the output arising from variability of the sensor device, there is always one measurable peak within an angular range corresponding to the comb spectrum spacing. Therefore the angular range covered by the detector/detector array need only be that of the comb spectrum spacing. By keeping the spacing to the mime mum required to separate adjacent peaks, the angular sensitivity of the detector/detector array may be maximised.
According to the invention there is provided a method of testing a biochemical sample, the method comprising providing an optical evanescent wave sensor device having a dielectric cavity and a sensing layer, providing an input beam of light having a single line or narrow band spectrum, coupling said beam of light to said device to excite resonance in said device and passing l-ight reflected from said device through an analyser and multiple beam splitting element for producing an output beam of light having an angular spectrum of a series of bright and/or dark lines or bands, sensitizing the sensing layer by the test sample, thereby causing an angular shift in the resonance angle, said lines or bands in the output beam being swept across a reference point as a result of said angular shift in the resonance angle and counting said lines or bands or parts thereof swept across said reference point, said angular shift in the resonance angle being equal to the product of the counted number of lines or bands swept across the reference point and the distance between two adjacent lines or bands in the output spectrum.
Further according to the invention there is provided an optical sensor for testing a biochemical sample, said sensor comprising means for providing an input beam of light having a single line or narrow band spectrum, an optical evanascent wave sensor device having a dielectric cavity and a sensing layer, means for coupling said beam of light to said sensor device and passing light reflected from said device through an analyser and multiple beam splitting element for producing an output beam of light having an angular spectrum of a series of bright and/or dark lines or bands, said sensing layer being sensitized by the test sample, when the optical sensor is in use, thereby causing an angular shift in the resonance angle, said lines or bands in the output spectrum being swept across a reference point as a result of said angular shift in the resonance angle and means for counting said lines or bands or parts thereof swept across said reference point.
Preferably the multiple beam splitting element is a diffraction grating. The light reflected from the sensing device is first projected onto the analyser and thereafter passed through the multiple beam splitting element. Alternatively the light reflected from the sensing device is first projected onto the multiple beam splitting element and thereafter passed through the analyser.
Preferably the input beam of light has coherent TE and TM components and said device is arranged in the path of said input beam of light such that one of said components excites resonance in said device. The device may be arranged in the path of the input beam of light such that resonance is excited for both of said TE and TM components.
By TE component is meant a component whose electric vector is perpendicular to the plane of incidence of the beam of light and by TM component is meant a component whose electric vector is in the plane of incidence of the beam of light.
The sensor device may be a resonant mirror device arranged in combination with coupling means for coupling light into said device. The resonant mirror device which may be used in the optical sensor embodying the invention is simple in construction, consisting of a prism structure onto which one low and one high index dielectric film is deposited. These form a resonant cavity on the totally internally reflecting face of the prism. Antibodies for the species to be detected are immobilized onto this surface.
Light is reflected off this surface within the prism and the phase of the reflected light is monitored. As the detected species binds to the antibody layer the angle at which resonance occurs changes, and this can be detected as a measure of the concentration of the detected species in the test sample.
Preferably the input beam of light is linearly polarized with TE and TM components by a polarizer arranged in the path of the beam of light.
The polarizer may be arranged at 45 to the TE and TM transmission axes for providing equal components of TE and TM light and the analyser may be arranged at 90 to the polarizer for providing a series of bright lines and bands in the output spectrum.
The output optics for the reflected light may include a compensator disposed adjacent said analyser to remove any phase difference which is introduced between the TE and TM components on total internal reflection and by birefringence in the device.
Preferably a detector or detector array is disposed at the reference point for detecting the lines or bands or parts thereof swept across the reference point.
Further an array of detectors may be disposed in the path of said output beam to count lines or bands or parts thereof swept across two or more than two referance points.
The invention will now be described further by way of example with reference to the accompanying drawing in which: Figure 1 illustrates an optical sensor according to the invention for use with a resonant mirror device; Referring to the drawings, the resonant mirror device and the coupling device disposed adjacent thereto are mounted on a rotatable platform. The coupling device is a prism 2 as shown in the drawing. The prism 2 couples light into the device at an angle of incidence depending on the angular position of the rotatable platform relative to the beam of light.
The input optics, provides a wedge beam of light allowing a range of input angles of incidence to be monitored. The input beam of light is produced by a source 10 of a single line spectrum.
The input beam of light is passed on to a polarizer 4 through a beam expander 12. The polarizer is arranged to produce a linearly polarized light with two components transverse electric (TE) and transverse magnetic (TM). The polarizer is set at 45* to the TE and TM transmission axes and thus provides equal components of TE and TM light. TE component undergoes a phase change on reflection which is different compared with TM component.
As with all SP and resonant mirror devices there is a resonance at some angle '0', at which a plane wave incident the structure will produce a maximum intensity in the resonant film.
This maximum will typically be many (102+) times the intensity produced at other angles of incidence. All the light is reflected for any angle of incidence, so the resonance is detected because of the effect on the phase of the reflected wave. Reference is made to GB Application No: 9106102.8 for further explanation of resonance for TE and TM components of the input beam of light and construction of the resonance mirror device.
The linearly polarized light produced by a polarizer 4 is reflected by a mirror 5 and thereafter focused by a cylindrical lens 6 on the device 1. The beam of light focused on the device is in the form of a wedge beam as shown in the drawing thus allowing a range of angles to be monitored simultaneously. The platform on which the prism 2 is mounted can be rotated so that the angles of incidence at which both components are coupled into the device can be adjusted. The prism is rotated so that the beam coupled into the device strikes the device at angles of incidence at which a resonance is excited for at least one of the TE and TM components.
The prism may be rotated to a position where the resonance is excited for both of said TE and TM components.
The reflected light from the device 1 is passed on to an analyser and compensator 11 through an output optics including reflector 7 and a cylindrical lens 8 and thereafter the light is passed through a diffraction grating 13. The analyser 11 is arranged at 90 to the polarizer. The two components are interfered at the analyser to allow the phase change on resonance to be detected. Off resonance both components undergo a similar phaseshift on total internal reflection and the relative phase between the components is adjusted by the compensator to give zero transmission through the analyser. This will apply for all angles except near resonance. Near resonance of either component, the phase shift between the TE and TM components will vary rapidly with angle, resulting in a maximum throughput of the analyser at resonance when all the light is transmitted.On rotating the analyser 90', a series of dark lines or bands appears on a bright background. On passing through the diffraction grating, the diffraction of the beam into the multiple diffraction orders of the grating results in an output beam which consists of a comb of lines for both TE + TM resonance. Changes in the sensing layer cause the comb spectrum to be swept across the detector. As the angular spacing of the output spectrum is known, simply counting the number of maxima allows the shift in the angle to be measured. This counting system is very easily realized using simple digital electronics and results in only one data value to determine the resonance position. This gives advantages in speed and cost of the instrument.
When a sensing layer of the resonant mirror device is sensitized by a test sample, there is an angular shift in the resonance angle, because of change in the angle of resonance. The series of lines or bands in the output spectrum are swept across a reference point as a result of the angular shift in the resonance angle. The series of lines or bands swept across the reference point are detected by a detector 14. Preferably the detector 14 is a silicon photodiode located at the reference point. The angular shift in the resonance angle is equal to the product of the counted number of lines or bands detected by the detector 14 and the distance between two adjacent lines or bands in the output spectrum.
When a plurality of different test samples are tested simultaneously, by sensitizing different parts across the width of the resonant mirror device in a direction perpendicular to the plane of incidence, a linear detector is used in the path of the output beam for determining an angular shift corresponding to each of the test samples, again aligned in a direction perpendicular to the plane of incident.
The compensator consists of two quarter wave plates which are manually adjusted to remove any phase difference which is introduced between the TE and TM components on total internal reflection and by birefringence in the optical path.

Claims (29)

1. A method of testing a biochemical sample, the method comprising providing an optical evanescent wave sensor device having a dielectric cavity and a sensing layer, providing an input beam of light having a single line or narrow band spectrum, coupling said beam of light to said device to excite resonance in said device and passing light reflected from said device through an analyser and multiple wave splitting element for producing an output beam of light having an angular spectrum of a series of bright and/or dark lines or bands, sensitizing the sensing layer by the test sample, thereby causing an angular shift in the resonance angle, said lines or bands in the output spectrum being swept across a reference point as a result of said angular shift in the resonance angle and counting said lines or bands or parts thereof swept across said reference point, said angular shift in the resonance angle being equal to the product of the counted number of lines or bands or parts thereof swept across the reference point and the distance between two adjacent lines or bands in the output spectrum.
2. A method as claimed in Claim 1, in which said the light reflected from said device is first projected onto the analyser and thereafter projected onto the multiple beam splitting element.
3. A method as claimed in Claim 1, in which the light reflected from said device is first projected onto the multiple beam splitting element and thereafter the multiple beam from said element is projected onto the analyser.
4. A method as claimed in any one of Claims 1 to 3, in which the multiple beam splitting element is a diffraction grating.
5. A method as claimed in any one of Claims 1 to 3, in which said input beam of light has coherent TE and TM components and said device is arranged in the path of said input beam of light such that one of said components excites resonance in said device.
6. A method as claimed in Claim 5, in which said device is arranged in the path of the input beam of light such that resonance is excited for both of said components.
7. A method as claimed in any one of Claims 5 or 6, in which said input beam of light is linearly polarized with TE and TM components by a polarizer arranged in the path of the input beam of light.
8. A method as claimed in Claim 7, in which the polarizer is arranged at 45' to the TE and TM transmission axis for providing equal components of TE and TM light and the analyzer is arranged at 90 to the polarizer for providing said series of bright lines or bands in the output spectrum.
9. A method as claimed in any one of the preceding claims, in which the sensor device is a resonant mirror device and a prism is disposed adjacent the mirror device for coupling light to the mirror device.
10. A method as claimed in any one of Claims 5 to 9, in which a compensator is disposed adjacent said analyser to remove any off resonance phase difference which is introduced between the TE and TM components on total internal reflection and by birefringence in the device.
11. A method as claimed in any one of the preceding claims, in which a detector is disposed at the reference point for detecting the lines or bands swept across the reference point.
12. A method as claimed in Claim 11, in which said detector is a silicon photodiode.
13. A method as claimed in any one of Claims 1 to 9, in which an array of detectors is disposed in the path of said output beam to count lines or bands swept across two or more than two spaced reference points.
14. An optical sensor for testing a biochemical sample, said sensor comprising means for providing an input beam of light having a single line or narrow band spectrum, an optical evanascent wave sensor device having a dielectric cavity and a sensing layer, means for coupling said beam of light to said sensor device and passing light reflected from said device through an analyser and a multiple beam splitting element for producing an output beam of light having an angular spectrum of a series of bright and/or dark lines or bands, said sensing layer being sensitized by the test sample, when the optical sensor is in use, thereby causing an angular shift in the resonance angle, said lines or bands in the output spectrum being swept across a reference point as a result of said angular shift in the resonance angle and means for counting said lines or bands or parts thereof swept across said reference point.
15. A sensor as claimed in Claim 14, in which the multiple beam splitting element is a diffraction grating.
16. A sensor as claimed in Claim 14 or 15, in which said input beam of light has coherent TE and TM components, and said sensor device is arranged in the path of said input beam of light such that one of said components excites resonance in said device.
17. A sensor as claimed in Claim 16, in which said device is arranged in the path of the beam of light such that resonance is excited for both of said components.
18. A sensor as claimed in Claim 17, including a lens arranged in the path of said beam of light for focusing the beam of light onto the device.
19. A sensor as claimed in any one of Claims 16 to 18, in which said beam of light is linearly polarized with TE and TM components by a plarizer arranged in the path of the input beam of light.
20. A sensor as claimed in Claim 19, in which the polarizer is arranged at 45 to the TE and TM transmission axis, for providing equal components of TE and TM light and the analyser is arranged at 90 to the polarizer for providing said series of bright lines or bands.
21. A sensor as claimed in any one of Claims 14 to 20, in which said device is a resonant mirror device.
22. A sensor as claimed in Claim 20, in which said coupling means is a prism.
23. A sensor as claimed in Claim 22, in which said device is fabricated on a surface of said prism.
24. A sensor as claimed in any one of claims 14 to 23, including a compensator disposed adjacent said analyser to remove any off resonance phase difference which is introduced between the TE and TM components on total internal reflection and by birefringence in the device.
25. A sensor as claimed in any one of Claims 14 to 24, in which a detector is disposed at the reference point for detecting the lines in the output spectrum swept across the reference point.
26. A sensor as claimed in Claim 25, in which said detector is a photodiode.
27. A sensor as claimed in any one of claims 14 to 24 including an array of detectors disposed in the path of said output beam to count lines swept across two or more than two spaced reference points.
28. An optical sensor substantially as hereinbefore described with reference to, and as illustrated in, the accompanying drawing.
29. A method of testing a biochemical sample substantially as hereinbefore described with reference to the accompanying drawing.
GB9214758A 1992-07-10 1992-07-10 Optical sensor Withdrawn GB2268800A (en)

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GB9214758A GB2268800A (en) 1992-07-10 1992-07-10 Optical sensor

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GB2268800A true GB2268800A (en) 1994-01-19

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998057149A1 (en) * 1997-06-11 1998-12-17 Petr Ivanovich Nikitin A method of examining biological, biochemical, and chemical characteristics of a medium and apparatus for its embodiment
WO2005050181A1 (en) * 2003-11-19 2005-06-02 Beanor Oy Method and device for carrying out surface plasmon resonance measurement
CN104237170A (en) * 2014-10-11 2014-12-24 重庆医科大学 Surface plasma resonance imaging sensor detection system

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2254415A (en) * 1991-03-22 1992-10-07 Marconi Gec Ltd An optical sensor

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2254415A (en) * 1991-03-22 1992-10-07 Marconi Gec Ltd An optical sensor

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998057149A1 (en) * 1997-06-11 1998-12-17 Petr Ivanovich Nikitin A method of examining biological, biochemical, and chemical characteristics of a medium and apparatus for its embodiment
US6628376B1 (en) 1997-06-11 2003-09-30 Petr Ivanovich Nikitin Method of examining biological, biochemical, and chemical characteristics of a medium and apparatus for its embodiment
WO2005050181A1 (en) * 2003-11-19 2005-06-02 Beanor Oy Method and device for carrying out surface plasmon resonance measurement
US7701582B2 (en) 2003-11-19 2010-04-20 Beanor Oy Method and device for carrying out surface plasmon resonance measurement
CN1894576B (en) * 2003-11-19 2010-04-28 比恩诺尔股份公司 Method and apparatus for actuating surface plasma resonance measuring
CN104237170A (en) * 2014-10-11 2014-12-24 重庆医科大学 Surface plasma resonance imaging sensor detection system
CN104237170B (en) * 2014-10-11 2017-01-18 重庆医科大学 Surface plasma resonance imaging sensor detection system

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