Sensor devices

Abstract

To provide a sensor device capable of comparatively easily detecting an acetyl compound such as diacetyl in a sample.SOLUTION: A sensor device is the device for detecting an acetyl compound in a sample. The sensor device includes: a storage part for storing the sample; a sensor part to have contact with the sample inside the storage part so as to detect a change of an ion density; and an amino compound fixed to the sensor part.SELECTED DRAWING: Figure 1

Description

Technical Field

[0001] Embodiments of the present invention relate to a sensor device for detecting acetyl compounds.

Background Art

[0002] Acetyl compounds, such as organic compounds having an acetyl group like diacetyl, for example, diacetyl, are contained in alcoholic beverages, fermented beverages, dairy products, meats, and the like. There is a need for a sensor device that can relatively easily detect these acetyl compounds.

Prior Art Documents

Patent Documents

[0003]

Patent Document 1

Summary of the Invention

Problems to be Solved by the Invention

[0004] An object of the present invention is to provide a sensor device that can relatively easily detect acetyl compounds such as diacetyl.

Means for Solving the Problems

[0005] The sensor device according to the embodiment detects an acetyl compound in a sample, and includes a housing portion that houses the sample, a sensor portion that contacts the sample in the housing portion and detects a change in ion density, and an amino compound fixed to the sensor portion. A supply mechanism for supplying the sample to the storage section, and comprises The amino compound comprises a cyclic aromatic amino compound, and the cyclic aromatic amino compound comprises 1-pyrenebutyrate hydrazide. .

Brief Description of the Drawings

[0006] [Figure 1] FIG. 1 is a schematic cross - sectional view showing the sensor device of the first embodiment.

[0007] [Figure 2]Figure 2 is a schematic plan view of the sensor device shown in Figure 1.

[0008] [Figure 3] Figure 3 is a schematic cross-sectional view showing a sensor device according to the second embodiment. [Modes for carrying out the invention]

[0009] A sensor device according to one embodiment is a sensor device for detecting acetyl compounds in a sample. The sensor device comprises a housing for containing the sample. The sensor device further comprises a sensor unit that comes into contact with the sample within the housing and detects changes in ion density, and an amino compound fixed to the sensor unit. The sensor unit detects changes in ion density based on the reaction between acetyl groups and amino groups. A sensor device according to one or more embodiments includes a substrate, a sensitive film provided on the substrate, a first electrode connected to one end of the sensitive film, a second electrode connected to the other end of the sensitive film, and an amino compound fixed to the sensitive film.

[0010] In one or more embodiments, the sensor device further comprises a supply mechanism for supplying a sample to the housing.

[0011] In one or more embodiments, the sensor unit detects changes in ion density as changes in pH value, potential, or current. Changes in pH value can be detected by a pH meter. Changes in potential or current can be detected by field-effect transistors (FETs) such as ion-selective field-effect transistors (ISFETs) or graphene field-effect transistors (graphene FETs), charge-coupled devices (CCDs), etc.

[0012] In one or more embodiments, the sensor portion has a graphene FET structure in which a graphene film constitutes a channel region. The graphene film has an amino compound having one or more amino groups immobilized on its surface.

[0013] In one or more embodiments, the amino compound includes a cyclic aromatic amino compound. The cyclic aromatic amino compound has an aromatic moiety fixed to the surface of the graphene film by π-π interaction and a functional moiety having an amino group bonded to the aromatic moiety. Such cyclic aromatic amino compounds may be 1-pyrene butyrate hydrazides. The aromatic moiety is, for example, pyrene. The functional moiety is, for example, butyrate hydrazide. The functional moiety can include, for example, hydrazine structures, hydrazone structures, hydrazide structures, and substituted structures thereof, all containing an amino group. Amino compounds having an amino group structure of (-NR-NH2) (where R is any substituent, e.g., a carbon substituent or H) react strongly with acetyl compounds. In one or more embodiments, the amino compound has two or more amino groups, with each of two adjacent carbon atoms having an amino group. The amino groups on each of the two carbon atoms react with the two acetyl groups of diacetyl to form a cyclization, thereby stabilizing the product. The functional part of such an amino compound may be ortho-phenylenediamine. The two adjacent carbon atoms may be two adjacent carbon atoms in an aromatic ring, or two carbon atoms linked by a double bond in an alkenyl having two amino groups at the cis position. For example, the reaction of an ortho-phenylenediamine structure or a diaminoalkenyl (-CNH2=CRNH2) structure with diacetyl forms an aromatic cyclic structure in the product, thus stabilizing the product (see Formula 2 below as an example).

[0014] When the sensor has a graphene FET structure, cyclic aromatic amino compounds can be immobilized on the surface of the graphene film by π-π interactions. The amino compound does not need to be an aromatic compound as long as it is immobilized on the surface of the graphene film. The amino compound may be adsorbed onto the graphene film by the π electrons of its double bond, or it may be immobilized by covalent or electrostatic bonding with the graphene film.

[0015] In one or more embodiments, the sample in the accommodating portion is in an acidic state. Due to the sample being in an acidic state, the amino group (-NH2) of the amino compound fixed on the surface of the graphene film is protonated (-NH3

[0021] , , , ).

[0016] In one or more embodiments, one or more amino groups are in a form protected by a protecting group respectively. Such protecting groups can be a chloro group, a butoxycarbonyl group, a benzyloxycarbonyl group, a fluorenylmethyloxycarbonyl group, a trichloroethoxycarbonyl group, an allyloxycarbonyl group, a phthaloyl group, or a toluenesulfonyl group. By the amino group being protected by a protecting group, the sensor portion is stabilized over a long period. The amino group and the protecting group are, for example, condensed. The protecting group detaches in an acidic environment (for example, the sample in the accommodating portion in an acidic state). The amino group liberated by the detachment of the protecting group is protonated as described above.

[0017] In one or more embodiments, the sample coexists with a Schiff base in the accommodating portion. The Schiff base can be, for example, sodium cyanoborohydride (SCB). In one or more embodiments, the sample coexists with an amino group-modified charge-labeled molecule in the accommodating portion.

[0018] In one or more embodiments, the sample is in a liquid form in the accommodating portion.

[0019] In one or more embodiments, the sample is in a gaseous form in the accommodating portion.

[0020] <000009​​​​Figure 1 is a schematic cross-sectional view showing the sensor device 10 of the first embodiment, and Figure 2 is a schematic plan view of the sensor device 10 shown in Figure 1. Note that in Figure 2, the liquid sample supply mechanism 110 and the liquid sample discharge mechanism 120 for discharging the liquid sample as shown in Figure 1 are omitted, and on the other hand, the heater 20 shown in Figure 2 is not shown in Figure 1.

[0022] As will be described in detail below, in the sensor device 10, the sensor portion has a graphene FET structure.

[0023] The sensor device 10 includes a substrate 11. The substrate 11 is, for example, a rectangular plate. The substrate 11 is formed from, for example, silicon, glass, ceramics, polymer material, or metal. The size of the substrate 11 is not limited, but for example, it is 1 to 10 mm × 1 to 10 mm × 0.1 to 0.7 mm (width × length × thickness).

[0024] The substrate 11 may, for example, have an insulating film (not shown) on the surface 11a side. Such an insulating film can be formed from an electrically insulating material such as silicon oxide, silicon nitride, aluminum oxide, polymer material, or a self-assembled film of organic molecules.

[0025] A graphene film 12 is formed on the surface 11a of the substrate 11 as a sensitive film. The graphene film 12 is a single layer of graphene with a thickness of one carbon atom, but it can also be composed of multiple layers of graphene. The size of the graphene film 12 is not limited, but for example, it can be 0.1 to 500 μm × 0.1 to 500 μm (width × length). In practical terms, it is easy to manufacture if it is 10 to 100 μm × 10 to 100 μm.

[0026] A source electrode 13 is provided on the surface 11a of the substrate 11, connected to one end of the graphene film 12. A drain electrode 14 is provided on the surface 11a of the substrate 11, connected to the other end of the graphene film 12.

[0027] The source electrode 13 and drain electrode 14 are formed from metals such as gold (Au), silver (Ag), copper (Cu), palladium (Pd), platinum (Pt), nickel (Ni), titanium (Ti), chromium (Cr), or aluminum (Al), or from conductive materials such as zinc oxide (ZnO), indium tin oxide (ITO), indium gallium zinc oxide (IGZO), or conductive polymers.

[0028] The source electrode 13 and the drain electrode 14 are electrically connected to a power supply (not shown). When a voltage (source-drain voltage (Vsd)) is applied from the power supply, for example, a current (source-drain current (Isd)) flows from the source electrode 13 to the drain electrode 14 through the graphene film 12. At this time, the graphene film functions as a channel for the source electrode 13 and the drain electrode 14.

[0029] A peripheral wall 15 is erected on the surface 11a of the substrate 11. The peripheral wall 15 surrounds the graphene film 12 and covers the outer surfaces of the source electrode 13 and the drain electrode 14. Inside the peripheral wall 15, a housing section 15a for housing a sample is defined. The bottom of the housing section 15a is made up of the graphene film 12.

[0030] The peripheral wall 15 is formed of an electrically insulating material, such as a polymer substance like acrylic resin, polyimide, polybenzoxazole, epoxy resin, phenolic resin, polydimethylsiloxane, or fluororesin, or an inorganic insulating film such as silicon oxide, silicon nitride, or aluminum oxide, or a self-assembled film of organic molecules.

[0031] A lid 16 is provided, supported by the peripheral wall 15, to seal the housing section 15a. The lid 16 can be made of an insulating material as shown above.

[0032] Now, an amino compound 17 having one or more amino groups 17a is immobilized on the surface 12a of the graphene film 12. If the amino compound 17 is a cyclic aromatic amino compound having one or more aromatic rings (e.g., benzene rings), then the amino compound can be immobilized on the surface 12a of the graphene film 12 by π-π interactions with the graphene film 12. One example of such an amino compound is 1-pyrene butyrate hydrazide, which has a condensed aromatic ring and one amino group. Another example of such an amino compound is an ortho-phenylenediamine compound (ortho-phenylenediamine or its derivatives) in which an amino group is bonded to each of two adjacent carbon atoms in a benzene ring. Other amino compounds (e.g., diaminoalkenyls, etc.) have already been described above. One or more amino groups 17a may be in a protected form by a protecting group. Such protecting groups have already been described above.

[0033] The sensor device 10 detects the presence or absence of acetyl compounds in a sample in solution form (liquid sample). Therefore, the sensor device 10 further includes a liquid sample supply mechanism 110 that supplies the liquid sample to the storage section 15a.

[0034] The liquid sample supply mechanism 110 includes a first container (bottle) 112 containing a liquid sample 111, which is a liquid sample supply source installed away from the peripheral wall 15. One end of a capillary tube 113 is inserted into the liquid sample 111 in the bottle 112. The other end of the capillary tube 113 is inserted into the containment section 15a, passing through the lid 16. The capillary tube 113 delivers the liquid sample 111 from the bottle 112 to the containment section 15a. The capillary tube 113 may be made of a material such as glass, and its inner surface may be hydrophilic. The liquid sample introduced into the containment section 15a is the direct sample to be detected and is indicated by reference numeral 18 (Figures 1 and 2).

[0035] The supply of the liquid sample 111 in the bottle 112 to the containment section 15a via the capillary tube 113 can be carried out using capillary action. When using capillary action, it is preferable that the inner surface of the capillary tube 113 is hydrophilic. The capillary tube 113 is fitted with a stopcock 114 that opens and closes the flow path inside the capillary tube 113.

[0036] After detection is complete, the liquid sample 18 in the containment section 15a is discharged by the liquid sample discharge mechanism 120. The liquid sample discharge mechanism 120 includes a second container 121 for collecting the discharged liquid sample, which is installed separated from the peripheral wall 15. One end of a capillary tube 122 is inserted into the second container 121. The other end of the capillary tube 122 penetrates the lid 16 and is inserted into the liquid sample 18 in the containment section 15a. The capillary tube 122 is made of a material such as glass, and the inner surface of the capillary tube 122 may be hydrophilic. The discharge of the liquid sample 18 from the containment section 15a into the second container 121 via the capillary tube 122 can utilize capillary action. When using capillary action, it is preferable that the inner surface of the capillary tube 113 is hydrophilic. A stopcock 123 for opening and closing the flow path inside the capillary tube 122 is interposed in the capillary tube 122.

[0037] The use of stopcocks 114 and 123 should be obvious to those skilled in the art.

[0038] The acetyl compounds to be detected, such as diacetyl, are found in alcoholic beverages, fermented drinks, dairy products, meat, etc. The sensor device 10 can detect acetyl compounds contained in such products. If the analyte is itself a liquid, such as an alcoholic beverage or fermented drink, it can be introduced into the first bottle 112 as a liquid sample 111. If the analyte is in a gaseous state, such as air, breath, or gas generated from living organisms or solid products (raw meat, etc.), or air around solid products, the gas can be blown into a solvent that dissolves the acetyl compound, and the resulting solution can be introduced into the first bottle 112. For example, diacetyl is soluble in water, alcohol, ether, or mixtures thereof.

[0039] Incidentally, although not shown in Figure 1, as shown in Figure 2, the sensor device 10 may have a heater 20 connected to the peripheral wall 15 for heating the sample 18 in the containment section 15a. By heating the sample in the containment section 15a with the heater 20, the reaction between the amino compound 17 and the acetyl compound in the sample 18 can be accelerated, allowing for faster detection. The heater 20 can also be installed inside the peripheral wall 15. The heater 20 can heat the liquid sample 18 in the containment section 15a to, for example, about 30°C to 85°C.

[0040] The amino compound can be immobilized onto the graphene film 12, for example, by introducing a solution (amino compound fixative) obtained by dissolving the amino compound in an aqueous solution of alcohol (e.g., isopropyl alcohol) into the containment section 15a and bringing it into contact with the graphene film 12. As long as the amino compound in the solution has one or more aromatic rings (e.g., benzene rings), it will be immobilized on the surface 12a of the graphene film 12 by π-π interactions, as described above.

[0041] Once the amino compound is fixed onto the graphene film 12, the amino compound fixative solution is discharged from the containment section 15a, and then an acid such as hydrochloric acid is introduced into the containment section 15a. This causes the amino group of the amino compound fixed onto the graphene film 12 to protonate, resulting in -NH3 + This is how it works. At that time, the Id (drain current) - Vg (gate voltage) in the graphene FET is measured. For example, the minimum value of Id is read and reported as the charge neutral point (CNP) (first CNP).

[0042] Next, the liquid sample is introduced, but if an acetyl compound is present in the liquid sample, the reaction will occur. [ka] This reduces the ion density in the amino compound. In any case, after introducing the liquid sample 18 into the containment section 15a, the Id (drain current) - Vg (gate voltage) in the graphene FET is measured, its minimum value is read, and this value is reported as the charge neutral point (CNP) (second CNP).

[0043] Furthermore, if there is no substantial difference between the first CNP value and the second CNP value, it can be determined that no acetyl compounds are present in sample 18. On the other hand, if there is a substantial difference between the first CNP value and the second CNP value, it can be determined that acetyl compounds are present in sample 18.

[0044] Incidentally, the reaction product produced according to Equation 1 undergoes dehydration to produce a Schiff base: RN=CCH3. This generated Schiff base undergoes hydrolysis in an aqueous medium to revert back to the original R-NHCCH3(OH)-R' (reversible reaction), making measurement (detection) unstable. Therefore, by introducing the Schiff base simultaneously when introducing the liquid sample into the containment section 15a, the reversible reaction can be prevented, enabling stable measurement. For example, sodium borohydride (SCB) can be used as the Schiff base.

[0045] Furthermore, after the reaction between the amino compound and the acetyl compound in the containment section 15a, an amino group-modified charge-labeled molecule can be added to the reaction solution in the containment section 15a. When such an amino group-modified charge-labeled molecule is present, if the amino compound has one amino group and an acetyl compound with multiple acetyl groups (e.g., diacetyl) is present in the sample, one amino group of the amino compound reacts with one acetyl group of the acetyl compound with multiple acetyl groups, but the remaining acetyl groups remain unchanged. These remaining acetyl groups bind to the amino group-modified charge-labeled molecule, and the amino compound becomes charge-labeled. When an acetyl compound with only one acetyl group (e.g., acetaldehyde) is present in the sample, the acetyl compound reacts with the amino compound, and the charge of the amino compound disappears. Therefore, by comparing the CNP value at that time (second CNP value) with the first CNP value, if there is a significant difference between the two, it can be determined that the difference is due to an acetyl compound with multiple acetyl groups. In other words, it is possible to detect only acetyl compounds with multiple acetyl groups in the sample. Examples of such charge-labeled compounds include peptides in which the C-terminus containing a single polar amino acid is modified to prevent reaction with the amino group. Alternatively, aptamers or antibodies that capture charge-labeled amino compounds can also be used.

[0046] Incidentally, as mentioned earlier, an amino compound to be immobilized on the graphene film 12 can be immobilized on the surface 12a of the graphene film 12 by π-π interactions, provided it has one or more aromatic rings (e.g., benzene rings). As mentioned above, a compound having one amino group, such as 1-pyrene butyrate hydrazide, can be used as such a compound. However, if a cyclic aromatic amino compound has amino groups on each of two adjacent carbon atoms in one aromatic ring, a ring structure is formed by reaction with an acetyl compound having multiple acetyl groups, such as diacetyl. An example of the reaction to produce this compound is shown below, taking the case where the cyclic aromatic amino compound is ortho-phenylenediamine and the acetyl compound having multiple acetyl groups is diacetyl (Equation 2 below).

[0047] [ka] The reaction in Equation 2 is an irreversible reaction, unlike the reversible reaction shown earlier. Therefore, when an acetyl compound with multiple acetyl groups (e.g., diacetyl) and an acetyl compound with only one acetyl group (e.g., acetaldehyde) coexist in a liquid sample, acetaldehyde can only react with one of the two amino groups of ortho-phenylenediamine. This reaction is ultimately reversible, as described above, and the amino group of ortho-phenylenediamine that reacts with acetaldehyde is cationized by a reversible reaction into a cationized amino group (-NH3). + ). Therefore, if the CNP value at that time (second CNP value) is significantly different from the first CNP value (CNP value before reaction with acetyl compound) as described above, it can be confirmed that diacetyl is present in the sample.

[0048] Figure 3 is a schematic cross-sectional view of the sensor device 20 according to the second embodiment. The sensor device 20 shown in Figure 3 is for detecting a sample in gaseous form and has basically the same configuration as the sensor device 10 of the first embodiment. However, the sensor device 20 has a third container 112a for containing a sample 111a in gaseous form instead of the first container 112 for containing a liquid sample 111 in the sensor device 10, and instead of a capillary tube 113 equipped with a stopcock 114, it has a thin tube 113a that does not need to be a capillary tube, with one end inserted into the third container 112a and the other end passing through the lid 16 and facing the containment section 15a. A pump P1 is interposed in the thin tube 113a to supply the sample in gaseous form from the third container 112a to the containment section 15a. Furthermore, instead of the capillary tube 122 equipped with a stopcock 123 in the sensor device 10, a thin tube 122a is provided, which does not need to be a capillary tube. One end of the thin tube 122a penetrates the lid 16 and faces the housing section 15a, and the other end is inserted into the fourth container 121a. A pump P2 is interposed in the thin tube 122a to supply the sample in gaseous form from the housing section 15a to the fourth container 121a.

[0049] For samples in gaseous form, amino compounds can be cationized using, for example, moisture in the air. In this case, it is preferable that the amino compound is protected with an ionically dissociable protecting group. An example of such a protecting group is a chloro group, which detaches from the amino group to become a chloride ion. The ionically dissociable protecting group contributes to stable detection by detaching from the amino group of the amino compound to become an anion, thereby maintaining a constant ion concentration.

[0050] Here, we briefly summarize the method for detecting acetyl compounds using the sensor devices shown in Figures 1 and 2.

[0051] First, a predetermined amino compound is dissolved in an amino compound-soluble solvent (for example, an aqueous alcohol solution), and the resulting amino compound solution is introduced into the containment section 15a. The solution is then left to stand to fix the amino compound to the surface 12a of the graphene film 12.

[0052] Next, the acetyl compound solution is discharged from the containment section 15a, and then an acid such as hydrochloric acid is introduced into the containment section 15a, and the CNP value (first CNP value) is determined in that state.

[0053] After measurement, the acid is discharged from the containment section 15a.

[0054] Subsequently, the sample in which the presence or absence of the acetyl compound is to be detected is dissolved in an acetyl compound-soluble solvent such as alcohol, and the resulting acetyl compound solution is introduced into the containment section 15a and left to stand to allow the reaction between the amino compound and the acetyl compound to proceed sufficiently. In this case, if necessary, a Schiff base may be added to the acetyl compound solution.

[0055] Next, after draining the reaction solution from the containment section 15a, an acid such as hydrochloric acid is introduced into the containment section 15a, and the CNP value (second CNP value) is determined in that state. At this time, an amino group-modified charge-labeled molecule may also be added to the containment section 15a simultaneously.

[0056] As mentioned above, the CNP value is the minimum value obtained by measuring Id (drain current) - Vg (gate voltage) in a graphene FET.

[0057] Next, we will describe an example of an experiment.

[0058] Experimental Example 1 The sensor device shown in Figure 1 was prepared before immobilizing the amino compound on the graphene membrane 12 and before introducing the liquid sample. A 10 mM solution of 1-pyrene butyrate hydrazide (1-PH) in an aqueous solution of pure water to isopropyl alcohol (IPA) with a volume ratio of 1:1 was introduced into the containment section 15a, and the solution was allowed to stand for 30 minutes to immobilize 1-PH on the graphene membrane 12. After draining the 1-PH solution from the containment section 15a, 0.001 M hydrochloric acid was introduced into the containment section 15a, and Id-Vg was measured. The minimum value read was 229.86 mV (first CNP value).

[0059] Next, after draining the hydrochloric acid from the containment section 15a, a sample solution consisting of 200 μM diacetyl and 2 μM sodium borohydride (SCB) was introduced into the containment section 15a and allowed to stand for 30 minutes. After that, the sample solution was drained from the containment section 15a, and then 0.001 M hydrochloric acid was introduced into the containment section 15a, and Id-Vg was measured. The minimum value read was 247.57 mV (second CNP value).

[0060] A significant difference (difference: 17.71 mV) was observed between the first and second CNP values, indicating that diacetyl was detected in this experiment.

[0061] Experimental Example 2 The experiment was conducted in the same manner as in Experimental Example 1, except that a 10 mM ortho-phenylenediamine (o-PDA) solution was used instead of a 10 mM 1-PH solution, and the 0.001 M hydrochloric acid used twice was replaced with 0.01 M hydrochloric acid.

[0062] The first CNP value was 228.50 mV, and the second CNP value was 258.50 mV.

[0063] A significant difference (difference: 30mV) was observed between the first and second CNP values, indicating that diacetyl was detected in this experiment.

[0064] Although several embodiments of the present invention have been described above, these embodiments are presented as examples and are not intended to limit the scope of the invention. These novel embodiments can be implemented in various other forms, and various omissions, substitutions, and modifications can be made without departing from the spirit of the invention. These embodiments and their variations are included in the scope and spirit of the invention, as well as in the claims of the invention and its equivalents. [Explanation of symbols]

[0065] 10, 30... Sensor devices 11… Circuit board 12... Graphene membrane 13…Source electrode 14…Drain electrode 15...Peripheral wall 15a... Containment area 16... Lid 17…Amino compounds 10 18…Liquid sample 18a...Gaseous sample 20... Heater 110...Liquid sample supply mechanism 110a...Gas sample supply mechanism 120...Liquid sample discharge mechanism 120a...Gas sample discharge mechanism

Claims

1. A sensor device for detecting acetyl compounds in a sample, A storage section for housing the aforementioned sample, A sensor unit that comes into contact with the sample within the storage unit and detects changes in ion density, An amino compound fixed to the sensor part, A supply mechanism for supplying the sample to the storage section, Equipped with, The amino compound includes a cyclic aromatic amino compound, The sensor device comprises the cyclic aromatic amino compound 1-pyrenebutyrate hydrazide.

2. A sensor device for detecting acetyl compounds in a sample, A storage section for housing the aforementioned sample, A sensor unit that comes into contact with the sample within the storage unit and detects changes in ion density, An amino compound fixed to the sensor part, A supply mechanism for supplying the sample to the storage section, Equipped with, The amino compound includes a cyclic aromatic amino compound, The sensor device wherein the cyclic aromatic amino compound has an amino group on each of two adjacent carbon atoms.

3. The sensor device according to claim 2, wherein the cyclic aromatic amino compound comprises an ortho-phenylenediamine compound.

4. The sensor device according to any one of claims 1 to 3, wherein the sensor unit detects the change in ion density as a change in pH value, a change in potential, or a change in current.

5. The sensor device according to any one of claims 1 to 3, wherein the sensor portion has a graphene field-effect transistor structure in which a graphene film constitutes a channel region, and the graphene film has the amino compound fixed on its surface.

6. The sensor device according to claim 5, wherein each amino group of the amino compound is protected by a protecting group.

7. The sensor device according to claim 6, wherein the protecting group is a chloro group, a butoxycarbonyl group, a benzyloxycarbonyl group, a fluorenylmethyloxycarbonyl group, a trichloroethoxycarbonyl group, an allyloxycarbonyl group, a phthaloyl group, or a toluenesulfonyl group.

8. The sensor device according to any one of claims 1 to 3, wherein the sample is in an acidic state within the containment section.

9. The sensor device according to any one of claims 1 to 3, wherein the sample is in liquid form within the containment section.

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