The present invention relates to an SPR sensor cell and an SPR sensor. More specifically, the present invention relates to an SPR sensor cell including an optical waveguide and an SPR sensor.
Hitherto, in the fields of chemical analysis, biochemical analysis, and the like, a surface plasmon resonance (SPR) sensor including an optical fiber has been used. In the SPR sensor including an optical fiber, a metal thin film is formed on an outer circumferential surface of a tip end portion of the optical fiber, and an analysis sample is fixed to the optical fiber into which light is guided. Among the light to be guided, light having a particular wavelength generates surface plasmon resonance in the metal thin film, and light intensity thereof is attenuated. In such an SPR sensor, the wavelength of the light generating surface plasmon resonance generally varies depending on a refractive index of an analysis sample to be fixed to the optical fiber. Therefore, if a wavelength at which light intensity is attenuated after the generation of surface plasmon resonance is measured, the wavelength of the light generating surface plasmon resonance can be identified. Further, if a change in the wavelength at which light intensity is attenuated is detected, it can be confirmed that the wavelength of the light generating surface plasmon resonance has changed, and hence a change in refractive index of the analysis sample can be confirmed. As a result, such an SPR sensor can be used for various chemical analyses and biochemical analyses such as measurement of a sample concentration and detection of an immunoreaction.
For example, in the case where the sample is a solution, the refractive index of the sample (solution) depends on a concentration of the solution. Therefore, the concentration of the sample can be detected by measuring the refractive index of the sample (solution) with the SPR sensor in which the sample (solution) is in contact with the metal thin film, and further, it can be confirmed that the concentration of the sample (solution) has changed by confirming a change in the refractive index. In analysis of the immunoreaction, for example, an antibody is fixed onto the metal thin film of the optical fiber in the SPR sensor through intermediation of a dielectric film, an analyte is brought into contact with the antibody, and surface plasmon resonance is generated. In this case, if the antibody and the analyte perform the immunoreaction, the refractive index of the sample changes. Therefore, it can be determined that the antibody and the analyte have performed the immunoreaction by confirming that the refractive index of the sample has changed before and after the contact between the antibody and the analyte.
In the SPR sensor including an optical fiber, the tip end portion of the optical fiber has a fine cylindrical shape, and hence there is a problem in that it is difficult to form the metal thin film and fix an analysis sample to the optical fiber. In order to solve the problem, for example, there has been proposed an SPR sensor cell including a core through which light is transmitted and a clad covering the core, in which a through-hole extending to a surface of the core is formed at a predetermined position of the clad, and a metal thin film is formed on the surface of the core at a position corresponding to the through-hole (for example, Patent Literature 1). In such an SPR sensor cell, it is easy to form the metal thin film for generating surface plasmon resonance on the surface of the core and fix the analysis sample onto the surface.
However, in recent years, in chemical analysis and biochemical analysis, there is an increasing demand for detection of a minute change and/or a trace amount of component, and thus further enhancement of detection sensitivity of the SPR sensor cell is being demanded.
The present invention has been made in view of solving the conventional problem, and an object of the present invention is to provide an SPR sensor cell having very excellent detection sensitivity and an SPR sensor.
The SPR sensor cell of the present invention includes a detection unit and a sample mounting portion adjacent to the detection unit, wherein: the detection unit includes an under clad layer, a core layer provided so that at least a part thereof is adjacent to the under clad layer, and a metal layer covering the core layer; and the core layer has a refractive index of 1.43 or less and an absorption coefficient of 9.5×10−2 (mm−1) or less.
In a preferred embodiment, the refractive index of the core layer is 1.33 or more.
In a preferred embodiment, the refractive index of the core layer is larger than a refractive index of the under clad layer, and the refractive indices have a difference of 0.010 or more.
According to another aspect of the present invention, an SPR sensor is provided. The SPR sensor includes the SPR sensor cell.
According to the present invention, the SPR sensor cell having very excellent detection sensitivity and the SPR sensor can be provided by optimizing the refractive index and absorption coefficient of a core layer of an optical waveguide as a detection unit.
A. SPR Sensor Cell
As illustrated in
The under clad layer 11 is formed in a shape of a plate having a substantially rectangular shape in a plan view, with a predetermined thickness. The thickness of the under clad layer (thickness from an upper surface of the core layer) is, for example, 5 μm to 400 μm.
The core layer 12 is formed substantially in a square column shape (more specifically, a rectangular shape in a cross-section flattened in a width direction) extending in a direction orthogonal to both a width direction (horizontal direction of the drawing surface of
The core layer 12 is disposed so that the upper surface thereof is exposed from the under clad layer 11. Preferably, the core layer 12 is disposed so that the upper surface thereof is flush with an upper surface of the under clad layer 11. The metal layer 14 can be disposed efficiently only on an upper side of the core layer 12 by disposing the core layer so that the upper surface thereof is flush with the upper surface of the under clad layer. Further, the core layer 12 is disposed so that both end surfaces thereof in the extending direction are flush with both end surfaces of the under clad layer in the extending direction.
In the present invention, the refractive index of the core layer 12 is 1.43 or less, preferably 1.41 or less, more preferably 1.39 or less. The detection sensitivity can be enhanced remarkably by setting the refractive index of the core layer to 1.43 or less. Adopting the core layer having a very low refractive index as described above is one of the features of the present invention. The lower limit of the refractive index of the core layer is preferably 1.33. When the refractive index of the core layer is 1.33 or more, SPR can be excited even in an aqueous solution-based sample (refractive index of water: 1.33), and a general-purpose material can be used. Note that the refractive index as used herein refers to a refractive index at a wavelength of 830 nm.
In the present invention, the absorption coefficient of the core layer 12 is 9.5×10−2 (mm−1) or less, preferably 8.5×10−2 (mm−2) or less, more preferably 7.0×10−2 (mm−2) or less, still more preferably 5.0×10−2 (mm−1) or less, particularly preferably 3.0×10−2 (mm−1) or less. When the absorption coefficient of the core layer is 9.5×10−2 (mm−1) or less, the refractive index of the core layer can be decreased to enhance sensitivity, and an ensuing decrease in signal-to-noise (S/N) ratio can be suppressed. More specifically, when the sensitivity is enhanced by decreasing the refractive index of the core layer, an SPR absorption peak is generated in a wavelength region shifted to a long wavelength side (near-infrared region). In the near-infrared region, C-H vibration absorption is present, and light intensity at an excitation wavelength decreases due to the absorption. As a result, the S/N ratio may decrease or a waveguide mode may exert its influence. On the other hand, by setting the absorption coefficient in the above-mentioned range, the light amount to be absorbed in the optical waveguide becomes small and transmittance increases, and hence the S/N ratio can be prevented from decreasing. The lower limit of the absorption coefficient is preferably 0 (zero). Note that the absorption coefficient as used herein refers to an absorption coefficient at a wavelength of 1,200 nm. By optimizing the absorption coefficient in the near-infrared region of the core layer, the transmittance of light in the near-infrared region is enhanced in the optical waveguide, and the S/N ratio in the SPR absorption peak detection can be enhanced.
The refractive index of the core layer 12 is higher than that of the under clad layer 11. The difference between the refractive index of the core layer and that of the under clad layer is preferably 0.010 or more, more preferably 0.020 or more. When the difference between the refractive index of the core layer and that of the under clad layer is in such a range, the optical waveguide of the detection unit can be set to a so-called multimode. Thus, the amount of light transmitted through the optical waveguide can be increased, and as a result, the S/N ratio can be enhanced.
As a material for forming the core layer 12, any suitable material can be used as long as the above-mentioned refractive index and absorption coefficient are obtained. Specific examples thereof include a fluorine resin, an epoxy resin, a polyimide resin, a polyamide resin, a silicone resin, an acrylic resin, and modified products thereof (for example, a fluorene-modified product, a heavy hydrogen-modified product, and a fluorine-modified product in the case of the resins other than the fluorine resin). These resins may be used alone or in combination. These resins each can be used as a photosensitive material preferably by being blended with a photosensitizing agent. The under clad layer 11 can be formed of a material that is similar to that for forming the core layer and is adjusted so that the refractive index thereof becomes lower than that of the core layer.
The protective layer 13 is formed as a thin film in the same shape as that of the under clad layer in a plan view so as to cover all the upper surfaces of the under clad layer 11 and the core layer 12, as necessary. By providing the protective layer 13, for example, in the case where a sample is a liquid, the core layer and/or the clad layer can be prevented from being swollen with the sample. As a material for forming the protective layer 13, for example, silicon dioxide and aluminum oxide may be utilized. These materials each can be adjusted preferably so that the refractive index thereof becomes lower than that of the core layer 12. The thickness of the protective layer 13 is preferably 1 nm to 100 nm, more preferably 5 nm to 20 nm.
As illustrated in
As a material for forming the metal layer 14, gold, silver, platinum, copper, aluminum, and alloys thereof may be utilized. The metal layer 14 may be a single layer or may have a laminate structure of two or more layers. The thickness (total thickness of all the layers in the case of the laminate structure) of the metal layer 14 is preferably 40 nm to 70 nm, more preferably 50 nm to 60 nm.
As a material for forming the easy-adhesion layer, chromium or titanium may typically be utilized. The thickness of the easy-adhesion layer is preferably 1 nm to 5 nm.
As illustrated in
As a material for forming the over clad layer 15, for example, the materials for forming the core layer and the under clad layer, and silicone rubber may be utilized. The thickness of the over clad layer is preferably 5 μm to 2,000 μm, more preferably 25 μm to 200 μm. The refractive index of the over clad layer is preferably lower than that of the core layer. In one embodiment, the refractive index of the over clad layer is equal to that of the under clad layer. Note that, in the case of forming a protective layer having a refractive index lower than that of the core layer, the refractive index of the over clad layer is not necessarily required to be lower than that of the core layer.
Although the SPR sensor cell according to the preferred embodiment of the present invention has been described, the present invention is not limited thereto. For example, in the relationship between the core layer and the under clad layer, at least a portion of the core layer has only to be adjacent to the under clad layer. For example, although a configuration in which the core layer is buried in the under clad layer is described in the above-mentioned embodiment, the core layer may be provided so as to pass through the under clad layer. Alternatively, the core layer may be formed on the under clad layer so that a predetermined portion of the core layer is surrounded by the over clad layer.
Further, the number of core layers in the SPR sensor cell may be changed depending on the purpose. Specifically, a plurality of the core layers may be formed at a predetermined interval in the width direction of the under clad layer. With such a configuration, a plurality of samples can be analyzed simultaneously, and hence analysis efficiency can be enhanced. As the shape of the core layer, any suitable shape (for example, a semicircular column shape or a convex column shape) can be adopted depending on the purpose.
Further, a lid may be provided on an upper portion of the SPR sensor cell 100 (sample mounting portion 20). With such a configuration, a sample can be prevented from coming into contact with ambient air. Further, in the case where the sample is a solution, a change in concentration caused by evaporation of a solvent can be prevented. In the case of providing a lid, an injection port for injecting a liquid sample into the sample mounting portion and a discharge port for discharging the liquid sample from the sample mounting portion may be provided. With such a configuration, the sample can be allowed to flow and to be supplied to the sample mounting portion continuously, and hence the characteristics of the sample can be measured continuously.
The above-mentioned embodiments may be combined appropriately.
B. Method of Producing SPR Sensor Cell
The SPR sensor cell of the present invention can be produced by any suitable method. As an example, a method of producing an SPR sensor cell adopting a stamper system as a method of forming a core layer on an under clad layer is described. As the method of forming a core layer on an under clad layer, for example, photolithography (direct exposure system) using a mask as well as the stamper system may be utilized. Note that the photolithography is well known.
a) to 3(h) are schematic sectional views illustrating the method of producing an SPR sensor cell adopting a stamper system as a method of forming a core layer on an under clad layer. First, as illustrated in
Then, as illustrated in
As necessary, as illustrated in
Next, as illustrated in
Finally, as illustrated in
Accordingly, the SPR sensor cell can be produced by the method described above.
C. SPR Sensor
As the light source 110, any suitable light source can be adopted. Specific examples of the light source include a white light source and a monochromatic light source. The optical measuring instrument 120 is connected to any suitable arithmetic processing device, and enables accumulation, display and processing of data.
The light source 110 is connected to a light source side optical fiber 112 through a light source side optical connector 111. The light source side optical fiber 112 is connected to one side end portion in a propagation direction of the SPR sensor cell 100 (core layer 12) through a light source side fiber block 113. A measuring instrument side optical fiber 115 is connected to the other side end portion in the propagation direction of the SPR sensor cell 100 (core layer 12) through a measuring instrument side fiber block 114. The measuring instrument side optical fiber 115 is connected to the optical measuring instrument 120 through a measuring instrument side optical connector 116.
The SPR sensor cell 100 is fixed by any suitable sensor cell fixing device (not shown). The sensor cell fixing device is movable in a predetermined direction (for example, a width direction of the SPR sensor cell), and thus the SPR sensor cell can be disposed at a desired position.
The light source side optical fiber 112 is fixed by a light source side optical fiber fixing device 131, and the measuring instrument side optical fiber 115 is fixed by a measuring instrument side optical fiber fixing device 132. The light source side optical fiber fixing device 131 and the measuring instrument side optical fiber fixing device 132 are each fixed to any suitable six-axis movable stage (not shown) so as to be movable in the propagation direction of the optical fiber, width direction (direction orthogonal to the propagation direction in a horizontal direction) and thickness direction (direction orthogonal to the propagation direction in a perpendicular direction), and rotatable about axes in the above-mentioned respective directions.
In the SPR sensor as described above, the light source 110, the light source side optical fiber 112, the SPR sensor cell 100 (core layer 12), the measuring instrument side optical fiber 115, and the optical measuring instrument 120 can be arranged on one axis, and light can be guided from the light source 110 so as to be transmitted therethrough.
An example of the manner of use of such an SPR sensor is described below.
First, a sample is mounted on the sample mounting portion 20 of the SPR sensor cell 100, and the sample and the metal layer 14 are brought into contact with each other. Then, predetermined light from the light source 110 is guided to the SPR sensor cell 100 (core layer 12) through the light source side optical fiber 112 (see an arrow L1 of
For example, in the case of using a white light source as the light source 110, a change in refractive index of the sample can be confirmed by measuring the wavelength of light whose light intensity is attenuated after the transmission through the SPR sensor cell 100 (wavelength of light generating surface plasmon resonance) with the optical measuring instrument 120 and detecting a change in wavelength of the light whose light intensity is attenuated. Further, for example, in the case of using a monochromatic light source as the light source 110, a change in wavelength of light generating surface plasmon resonance can be confirmed and a change in refractive index of the sample can be confirmed by measuring a change (attenuation degree) in light intensity of monochromatic light after the transmission through the SPR sensor cell 100 with the optical measuring instrument 120 and detecting a change in attenuation degree.
As described above, such an SPR sensor cell can be used, for example, for various chemical analyses and biochemical analyses such as the measurement of a sample concentration and the detection of an immunoreaction, based on a change in refractive index of the sample. More specifically, for example, in the case where the sample is a solution, the refractive index of the sample (solution) depends on the concentration of the solution, and hence the concentration of the sample can be measured by detecting the refractive index of the sample. Further, a change in concentration of the sample can be confirmed by detecting a change in refractive index of the sample. Further, for example, in the detection of an immunoreaction, an antibody is fixed onto the metal layer 14 of the SPR sensor cell 100 through intermediation of a dielectric film, and an analyte is brought into contact with the antibody. If the antibody and the analyte perform an immunoreaction, the refractive index of the sample changes. Therefore, it can be determined that the antibody and the analyte have performed an immunoreaction by detecting a change in refractive index of the sample before and after the contact between the antibody and the analyte.
The present invention is hereinafter described specifically by way of Examples. However, the present invention is not limited thereto. Note that, unless otherwise specified, the measurement wavelength for a refractive index is 830 nm and a measurement wavelength for an absorption coefficient is 1,200 nm in the Examples and the Comparative Examples.
An optical waveguide was formed through use of the stamper system as illustrated in
Then, SiO2 was sputtered onto the entire surface of an upper surface (core layer exposed surface) of the optical waveguide film thus obtained to form a protective layer (thickness: 10 nm). The optical waveguide film with the protective layer formed thereon was subjected to dice cutting to a length of 20 mm and a width of 20 mm. After that, chromium and gold were sputtered onto the cut optical waveguide film in the stated order through a mask with an opening having a length of 6 mm and a width of 1 mm, and thus an easy-adhesion layer (thickness: 1 nm) and a metal layer (thickness: 50 nm) were formed in the stated order so as to cover the core layer through intermediation of the protective layer. Finally, a frame-shaped over clad layer was formed by a method similar to that for forming the under clad layer through use of the same material as the material for forming an under clad layer. Thus, an SPR sensor cell as illustrated in
The SPR sensor cell obtained as described above, a halogen light source (“HL-2000-HP” (trade name) manufactured by Ocean Optics, Inc.), and a spectroscope (“USB4000” and “NIRQuest512” (trade names) manufactured by Ocean Optics, Inc.) were arranged on one axis and connected to each other to produce an SPR sensor as illustrated in
An SPR sensor cell and an SPR sensor were produced in the same way as in Example 1 except for forming a core layer having a refractive index of 1.399 and an absorption coefficient of 2.90×10−2 (mm−1) through use of a fluorine-based UV curable resin (“OP40Z” (trade name) manufactured by DIC Corporation) as the material for forming a core layer. The SPR sensor thus obtained was evaluated in the same way as in Example 1. Table 1 shows the results.
An SPR sensor cell and an SPR sensor were produced in the same way as in Example 1 except for forming a core layer having a refractive index of 1.414 and an absorption coefficient of 8.46×10−2 (mm−1) through use of a composition prepared by stirring and dissolving 70 parts by weight of a UV curable resin (“FNR-061” manufactured by Nagase ChemteX Corporation), 30 parts by weight of a UV curable resin (“FNR-062” manufactured by Nagase ChemteX Corporation), and 1 part by weight of a photo-acid generator (“CPI-200K” manufactured by San-Apro Ltd.) as the material for forming a core layer. The SPR sensor thus obtained was evaluated in the same way as in Example 1. Table 1 shows the results.
An SPR sensor cell and an SPR sensor were produced in the same way as in Example 1 except for forming a core layer having a refractive index of 1.425 and an absorption coefficient of 9.42×10−2 (mm−1) through use of a composition prepared by stirring and dissolving 60 parts by weight of a UV curable resin (“FNR-061” manufactured by Nagase ChemteX Corporation), 40 parts by weight of a UV curable resin (“FNR-062” manufactured by Nagase ChemteX Corporation), and 1 part by weight of a photo-acid generator (“CPI-200K” manufactured by San-Apro Ltd.) as the material for forming a core layer. The SPR sensor thus obtained was evaluated in the same way as in Example 1. Table 1 shows the results.
An SPR sensor cell and an SPR sensor were produced in the same way as in Example 1 except for forming a core layer having a refractive index of 1.423 and an absorption coefficient of 9.62×10−2 (mm−1) through use of a composition prepared by stirring and dissolving 100 parts by weight of epoxy-modified silicone oil (“X-22-163” (trade name) manufactured by Shin-Etsu Chemical Co., Ltd.) and 1 part by weight of a photo-acid generator (“CPI-200K” manufactured by San-Apro Ltd.) as the material for forming a core layer. The SPR sensor thus obtained was evaluated in the same way as in Example 1. Table 1 shows the results.
An SPR sensor cell and an SPR sensor were produced in the same way as in Example 1 except for forming a core layer having a refractive index of 1.439 and an absorption coefficient of 9.70×10−2 (mm−1) through use of a composition prepared by stirring and dissolving 40 parts by weight of a UV curable resin (“FNR-061” manufactured by Nagase ChemteX Corporation), 60 parts by weight of a UV curable resin (“FNR-062” manufactured by Nagase ChemteX Corporation), and 1 part by weight of a photo-acid generator (“CPI-200K” manufactured by San-Apro Ltd.) as the material for forming a core layer. The SPR sensor thus obtained was evaluated in the same way as in Example 1. Table 1 shows the results.
An SPR sensor cell and an SPR sensor were produced in the same way as in Example 1 except for forming a core layer having a refractive index of 1.458 and an absorption coefficient of 6.97×10−2 (mm−1) through use of a composition prepared by stirring and dissolving 80 parts by weight of epoxy-modified silicone oil (“XF-101” (trade name) manufactured by Shin-Etsu Chemical Co., Ltd.), 20 parts by weight of an epoxy compound (“ADEKA RESIN EP-4080E” (trade name) manufactured by ADEKA CORPORATION), and 1 part by weight of a photo-acid generator (“CPI-200K” manufactured by San-Apro Ltd.) as the material for forming a core layer. The SPR sensor thus obtained was evaluated in the same way as in Example 1. Table 1 shows the results.
An SPR sensor cell and an SPR sensor were produced in the same way as in Example 1 except for forming a core layer having a refractive index of 1.463 and an absorption coefficient of 9.93×10−2 (mm−1) through use of a composition prepared by stirring and dissolving 100 parts by weight of a UV curable resin (“FNR-062” manufactured by Nagase ChemteX Corporation) and 1 part by weight of a photo-acid generator (“CPI-200K” manufactured by San-Apro Ltd.) as the material for forming a core layer. The SPR sensor thus obtained was evaluated in the same way as in Example 1. Table 1 shows the results.
An SPR sensor cell and an SPR sensor were produced in the same way as in Example 1 except for forming a core layer having a refractive index of 1.509 and an absorption coefficient of 11.08×10−2 (mm−1) through use of a composition prepared by stirring and dissolving 100 parts by weight of a UV curable resin (“EHPE3150” (trade name) manufactured by Daicel Corporation) and 1 part by weight of a photo-acid generator (“CPI-200K” manufactured by San-Apro Ltd.) as the material for forming a core layer. The SPR sensor thus obtained was evaluated in the same way as in Example 1. Table 1 shows the results.
As is apparent from Table 1, the detection sensitivity of each of the SPR sensor cells of the Examples is more excellent than that of the Comparative Examples. In particular, it is understood that the detection sensitivity of each of the SPR sensor cells of Examples 1 and 2 is remarkably excellent as compared to that of the Comparative Examples. Thus, the SPR sensor cells and SPR sensors of the Examples are capable of realizing the detection of a minute change and/or a trace amount of component. Further,
The SPR sensor cell and SPR sensor of the present invention can be used suitably in various chemical analyses and biochemical analyses such as the measurement of a sample concentration and the detection of an immunoreaction.
Number | Date | Country | Kind |
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2011-070443 | Mar 2011 | JP | national |
2011-159580 | Jul 2011 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP2012/054066 | 2/21/2012 | WO | 00 | 9/27/2013 |