CN111896601B - Lactate dehydrogenase electrode and preparation method and application thereof - Google Patents
Lactate dehydrogenase electrode and preparation method and application thereof Download PDFInfo
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- CN111896601B CN111896601B CN202010682884.9A CN202010682884A CN111896601B CN 111896601 B CN111896601 B CN 111896601B CN 202010682884 A CN202010682884 A CN 202010682884A CN 111896601 B CN111896601 B CN 111896601B
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Abstract
The invention provides a lactate dehydrogenase electrode and a preparation method and application thereof. Chemical means of coenzyme factor small molecule NAD + Chemically modifying the inactive site, and chemically modifying the NAD + Covalently linked with chitosan carrier to obtain NAD + Modifying a carbon nano tube on the surface of the substrate electrode by using the chitosan compound, and using the carbon nano tube as a substrate material for detecting NADH; electrodeposition of ABTS on electrodes, use of ABTS as an electron mediator to achieve NAD + In-situ regeneration; dropping NAD + Chitosan complex, effecting NAD + Fixing on the surface of the electrode; connecting dehydrogenase enzyme to a chitosan carrier through glutaraldehyde crosslinking to obtain a dehydrogenase electrode; the NAD + The immobilization and regeneration method can be combined with different dehydrogenases to prepare various dehydrogenase electrodes/biosensors. The invention has wide practical application value in the field of biosensor preparation.
Description
The application is a divisional application with the title of 'a coenzyme factor compound, an enzyme electrode, an enzyme sensor, a preparation method and an application thereof' of application No. 2020101521251, 3/6/2020.
Technical Field
The invention belongs to the technical field of detection and analysis, and particularly relates to a lactate dehydrogenase electrode as well as a preparation method and application thereof.
Background
The information in this background section is only for enhancement of understanding of the general background of the invention and is not necessarily to be construed as an admission or any form of suggestion that this information forms the prior art that is already known to a person of ordinary skill in the art.
The oxidoreductases are the most abundant enzymes in nature, and 30-35% of the six types of enzymes are oxidoreductases. Oxidase-dependent biosensors are well-developed products, but suffer from disadvantages such as the need for oxygen consumption during the course of action of the oxidase, susceptibility to O 2 Interference of (2); most of the reaction products of oxidase are H 2 O 2 ，H 2 O 2 Accumulation can have an effect on sensor detection. Dehydrogenases are more abundant in nature, and nearly 400 natural dehydrogenases have been reported. The dehydrogenase biosensor completes reaction by means of coenzyme, and the coenzyme can directly participate in the reaction and is free from O 2 Interference and more sensitive and rapid response. Therefore, dehydrogenase biosensors have been a focus of research and play an important role in medical detection, food fermentation control, and the like. Gamellaa et al monitored the malate-lactate fermentation process during wine brewing by making a malate dehydrogenase electrochemical biosensor. Vinay Narwal et al used a gold electrode modified by the preparation of lactate dehydrogenase nanoparticles for lactate determination. Beam Yuyu et al developedGlutamate dehydrogenase voltammetric sensors for sensitive ammonium ion determination.
Nicotinoyl-type coenzymes [ NAD ] are required for the performance of most dehydrogenase catalysis + ，NADH]It binds to the enzyme in the enzymatic reaction and participates directly as an oxidizing or reducing agent. Among nicotinoyl-type coenzymes, NAD + In the oxidized state, NADH is in the reduced state, and the oxidized coenzyme and the reduced coenzyme are mutually converted through the redox reaction of hydrogenation or dehydrogenation. NAD (nicotinamide adenine dinucleotide) + Is not internally wrapped by enzyme molecules while performing an electron transfer function. Therefore, the conventional dehydrogenase electrode needs to be prepared by adding free NAD to the reaction system + The reaction of the dehydrogenase with the substrate is effected. But free NAD + Cannot be reused, and requires repeated addition of free NAD for each measurement + 。NAD + Is expensive, generally much more expensive than the product obtained in the enzymatic reaction, and requires about $ 100/g. Addition of free NAD + The disadvantages of long time consumption and complex operation are also existed, which is not favorable for convenient use and popularization of the dehydrogenase electrode. To coenzyme NAD + It is necessary to carry out immobilization and regeneration for recycling. Coenzyme NAD + Immobilization and efficient regeneration techniques at the electrode surface are two key techniques for constructing dehydrogenase electrodes/sensors. Dehydrogenase electrode NAD + Only hundreds of molecular weight, the traditional method is difficult to fix the coenzyme, the coenzyme is difficult to embed in a semipermeable membrane, and the problem can be solved if the coenzyme is combined with a polymer carrier to make the coenzyme high molecular weight. Another key issue in achieving electrode cycling of dehydrogenases is NAD + Regeneration of (2). However, the inventor finds that NADH has high oxidation overpotential, slow electron transfer rate and undesirable kinetic characteristics, and dimers are generated in the electrochemical oxidation process and deposited on the surface of an electrode to passivate the electrode, so that NADH can be directly measured and NAD can be directly measured + Becomes very difficult, and NAD is regenerated by oxidation-reduction based on an electron mediator + Is an effective regeneration method, can reduce the oxidation potential of NADH, improve the electron transfer rate on the surface of the electrode and realize NAD in the use process of dehydrogenase electrode + And (4) regenerating.
Disclosure of Invention
Aiming at the defects of the prior art, the invention provides a coenzyme factor compound, an enzyme electrode, an enzyme sensor, a preparation method and application thereof. The invention firstly uses chemical means to make coenzyme factor small molecule NAD + Chemically modifying the inactive site; chemically modifying NAD by chemical means + Covalently linked with chitosan carrier to obtain NAD + Chitosan complex (coenzyme factor complex). On the basis, an enzyme electrode is prepared by the following steps: modifying a carbon nano tube on the surface of a substrate electrode, and using the carbon nano tube as a substrate material for detecting NADH; electrodeposition of ABTS on electrodes, use of ABTS as an electron mediator to achieve NAD + In-situ regeneration; dropwise prepared NAD + Chitosan complex, effecting small molecule NAD + Fixing; and (3) connecting dehydrogenase to the chitosan carrier through glutaraldehyde crosslinking to obtain the dehydrogenase electrode. Utilizing the NAD + The immobilization and regeneration methods are respectively combined with different dehydrogenases, so that various dehydrogenase electrodes/biosensors can be prepared, and the detection of various substrates such as malic acid, glucose, lactic acid and the like can be realized. Thus, immobilization and in situ regeneration of NAD in the present invention + The technical method and the electrode preparation technology can be widely applied to the preparation process of the dehydrogenase electrode/sensor, so that the dehydrogenase electrode can be recycled, and an effective technical approach is provided for constructing the dehydrogenase electrode/biosensor.
In order to achieve the technical purpose, the technical scheme adopted by the invention is as follows:
in a first aspect of the present invention, a coenzyme factor complex is provided, wherein the coenzyme factor complex is obtained by complexing a coenzyme factor and a loading material.
It should be noted that the complex means that the coenzyme factor and the carrier are attached to, bound to, integrated with, or linked to each other. Thus, they are not physically separate components, but rather can be compounded together as a single component (covalently or ionically bonded complex).
The coenzyme factor may be a natural coenzyme or an artificial coenzyme. "coenzyme" or "redox cofactor" means to act asEnzymatically transferred redox equivalents (e.g., hydride (H) - ) A redox equivalent of the enzymatic transfer from a substrate (e.g., a target analyte) to an enzyme to a coenzyme. As used herein, "redox equivalents" refers to concepts commonly used in redox chemistry, which are well known to those skilled in the art.
In particular, it relates to the transfer of electrons from a substrate of a coenzyme-dependent enzyme (i.e., a target analyte) to the coenzyme or from the coenzyme to an electrode or an indicator reagent. Examples of coenzymes include, but are not limited to, NAD, NADP, PQQ, thio-NAD, thio-NADP, and the like.
In some cases, the coenzyme is an artificial coenzyme. Examples of artificial coenzymes include, but are not limited to, artificial NAD (P)/NAD (P) H compounds that are chemical derivatives of natural NAD/NADH or natural NADP/NADPH.
Specifically, the artificial coenzyme can be chemically modified at the inactive site of the natural coenzyme, so that the coenzyme carries a chemical group for fixation under the condition of not influencing the activity and the function of the coenzyme factor, and the coenzyme is further fixed.
In some cases, the amino group on NAD adenine may be modified to obtain the artificial coenzyme NAD + A compound is provided.
The load material may be a polymer carrier, and examples of the load material include, but are not limited to, chitosan, agarose, sodium alginate, polyethylene glycol, and the like; preferably, the chitosan is a high molecular water-soluble polysaccharide with free amino, has good film forming property and can be used as a carrier of coenzyme factors; more preferably, the chitosan is medium viscosity chitosan (200-400 mPa.s).
In some cases, the coenzyme factor complex of the invention may be NAD + -chitosan complex, the NAD + Chitosan complex by para-NAD + Modifying amino on adenine to obtain artificial NAD + Coenzyme, then covalently linked with chitosan to prepare the coenzyme, thereby actually realizing NAD + Immobilization of (2).
In particular, the NAD + The preparation method of the chitosan complex comprises the following steps:
1) to NAD + Adding iodoacetic acid into the aqueous solution, and heating to react to obtain n 1-carboxymethyl-NAD + ；
2) At n 1-carboxymethyl-NAD + Adding a sodium thiosulfate solution into the aqueous solution, adjusting the pH to be alkaline, heating to react to obtain n 1-carboxymethyl-NADH, and simultaneously carrying out Dimroth rearrangement under a strong alkali condition to obtain n 6-carboxymethyl-NADH;
3) adding formaldehyde, heating and reacting to obtain c 6-carboxymethyl NAD + 。
4) Adjusting the pH of the reaction system to be neutral, adding N-hydroxysuccinimide (NHS) and (1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride) (EDC), adding a chitosan solution, and heating for reaction to obtain chitosan-NAD + And (3) a compound.
In some cases, in the step 1), the heating reaction is preferably water bath heating, and the water bath reaction condition is that the reaction is carried out for 0.5-3 h at the temperature of 60-80 ℃, and preferably for 1h at the temperature of 70 ℃;
in some cases, in the step 2), the pH is adjusted to be strong alkaline, preferably 10-11, the heating reaction is preferably heating in a water bath, and the water bath reaction condition is that the reaction is carried out for 0.5-3 h at the temperature of 60-80 ℃, preferably for 1h at the temperature of 70 ℃;
in some cases, in the step 3), the heating reaction is preferably water bath heating, and the water bath reaction condition is that the reaction is carried out for 0.5-3 h at the temperature of 60-80 ℃, and preferably for 1h at the temperature of 70 ℃;
in some cases, in the step 4), the heating reaction is preferably water bath heating, and the water bath reaction condition is that the reaction is carried out for 0.5-3 h at the temperature of 60-80 ℃, and preferably for 1h at the temperature of 70 ℃.
In a second aspect of the invention, there is provided the use of the above-described coenzyme factor complex in an enzyme electrode and/or in the preparation of an enzyme electrode.
In a third aspect of the present invention, there is provided an enzyme electrode comprising:
a base electrode, and a base material carried by the base electrode.
The substrate electrode includes, but is not limited to: a Glassy Carbon (GCE) electrode, a gold electrode, a graphite electrode, a carbon paste electrode, preferably GCE. The GCE has good mechanical stability, light stability and high conductivity.
The substrate material is a carbon material including, but not limited to: the electrode material comprises activated carbon, graphene, carbon nanofibers, carbon nanospheres, glassy carbon, carbon aerogel and Carbon Nanotubes (CNTs), and preferably the carbon nanotubes have large specific surface area and small internal resistance, so that the analysis performance of the chemically modified electrode can be remarkably improved, and the electrode material has good conductivity and chemical stability.
The carbon nano tube not only comprises a multi-wall carbon nano tube and a single-wall carbon nano tube, but also comprises a functionalized carbon nano tube modified by amination, carboxylation and the like.
In some cases, the enzyme electrode comprises: a GCE electrode, and CNTs loaded on the GCE electrode. Wherein, the loading can be carried out by adopting a dripping mode.
In some cases, the enzyme electrode comprises:
the substrate electrode is loaded with a substrate material, a medium is deposited on the surface of the substrate material, and the surface of the medium is coated with a coenzyme factor compound and an enzyme.
The substrate electrode includes, but is not limited to: a Glassy Carbon (GCE) electrode, a gold electrode, a graphite electrode, a carbon paste electrode, preferably GCE. The GCE has good mechanical stability, light stability and high conductivity.
The substrate material is a carbon material including, but not limited to: the electrode material comprises activated carbon, graphene, carbon nanofibers, carbon nanospheres, glassy carbon, carbon aerogel and Carbon Nanotubes (CNTs), and preferably the carbon nanotubes have large specific surface area and small internal resistance, so that the analysis performance of the chemically modified electrode can be remarkably improved, and the electrode material has good conductivity and chemical stability.
The carbon nano tube not only comprises a multi-wall carbon nano tube and a single-wall carbon nano tube, but also comprises a functionalized carbon nano tube modified by amination, carboxylation and the like.
In the present invention, the "mediator" refers to a compound that increases the reactivity of a reduced coenzyme obtained by reaction with an analyte and transfers electrons to an electrode system or a suitable optical indicator/optical indicator system.
The mediator can be any chemical species (typically electrochemically active) that can participate in a reaction scheme involving an analyte, a coenzyme-dependent enzyme, a coenzyme, and reaction products thereof to produce a detectable electrochemically active reaction product. In general, participation of the mediator in the reaction involves a change in its oxidation state upon interaction with any of the analyte, the coenzyme-dependent enzyme, the coenzyme, or a species that is a reaction product of one of these (e.g., the coenzyme reacts to a different oxidation state). The media may also be stable in its oxidized form, may optionally exhibit reversible redox electrochemistry, may exhibit good solubility in aqueous solutions, and may react rapidly to produce electrochemically active reaction products.
Examples of such mediators include, but are not limited to, 2,2' -diaza bis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS), azo compounds or azo precursors, benzoquinone, prussian blue, nitrosoaniline or nitrosoaniline-based precursors, thiazine or thiazine derivatives, transition metal complexes such as potassium ferricyanide, ruthenium complexes such as hexylamine ruthenium chloride, osmium derivatives, quinones or quinone derivatives, phenazine or phenazine-based precursors, and combinations of phenazine derivatives and ruthenium hexamine chloride, and derivatives thereof.
In some cases, when the coenzyme is NAD/NADH, the mediator may be 2,2' -diaza-bis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS). In the present invention, carbon nanotubes are mixed with ABTS + The carbon nano tube is modified on the surface of a GCE electrode, and can realize the catalytic oxidation of NADH (nicotinamide adenine dinucleotide), ABTS (adenosine triphosphate), and + electron transfer can be increased. Simultaneous ABTS + Oxidation reduction occurs with NADH, the 4-position of pyridine ring in NADH and ABTS + Radical cation reaction, ABTS + The hydrogen ion is converted into ABTS, NADH is oxidized into NAD + Effecting NAD + And (4) in-situ regeneration. After the above process, ABTS loses electrons, and ABTS is generated at the positive electrode of the electrode + And entering the next cycle.
In the present invention, the "enzyme" refers specifically to a coenzyme-dependent enzyme, and the "coenzyme-dependent enzyme" refers to an enzyme requiring an organic or inorganic cofactor called a coenzyme for catalytic activity.
In some cases, the coenzyme-dependent enzyme can be a dehydrogenase. As used herein, "dehydrogenase" refers to a compound capable of passing a hydride (H) as a redox equivalent (redox equivalent) - ) A protein or polypeptide that is transferred to a receptor molecule to catalyze the oxidation of a substrate. Examples of dehydrogenases include, but are not limited to, glucose dehydrogenase, alcohol dehydrogenase, glycerol dehydrogenase, lactate dehydrogenase, L-amino acid dehydrogenase, malate dehydrogenase, sorbitol dehydrogenase, or the like, especially nad (p)/nad (p) H-dependent dehydrogenase.
In a fourth aspect of the present invention, there is provided the above-mentioned enzyme electrode preparation method, which is not particularly limited, but the enzyme electrode may be formed by being applied on one surface of a base electrode or by being coated in the form of a film using the following method: such as drop coating, electrodeposition, sputtering, e-beam, thermal deposition, spin coating, screen printing, ink jet printing, doctor blading or gravure printing.
In some cases, the method of making comprises:
1) dripping a substrate material on the surface of the substrate electrode;
2) depositing a medium on the substrate electrode loaded with the substrate material prepared in the step 1) by adopting an electrochemical deposition method;
3) dripping a coenzyme factor compound on the material prepared in the step 2);
4) loading enzyme on the material prepared in the step 3).
In the step 1) of the method, the steps of,
in some cases, the base electrode includes, but is not limited to: a Glassy Carbon (GCE) electrode, a gold electrode, a graphite electrode, a carbon paste electrode, preferably GCE. The GCE has good mechanical stability, light stability and high conductivity.
The substrate material is a carbon material including, but not limited to: the electrode material comprises activated carbon, graphene, carbon nanofibers, carbon nanospheres, glassy carbon, carbon aerogel and Carbon Nanotubes (CNTs), and preferably the carbon nanotubes have large specific surface area and small internal resistance, so that the analysis performance of the chemically modified electrode can be remarkably improved, and the electrode material has good conductivity and chemical stability.
The carbon nano tube not only comprises a multi-wall carbon nano tube and a single-wall carbon nano tube, but also comprises a functionalized carbon nano tube modified by amination, carboxylation and the like.
In the step 2), the step (c) is carried out,
"mediator" refers to a compound that increases the reactivity of a reduced coenzyme obtained by reaction with an analyte and transfers electrons to an electrode system or a suitable optical indicator/optical indicator system.
The mediator can be any chemical species (typically electrochemically active) that can participate in a reaction scheme involving an analyte, a coenzyme-dependent enzyme, a coenzyme, and reaction products thereof to produce a detectable electrochemically active reaction product. In general, participation of the mediator in the reaction involves a change in its oxidation state (e.g., reduction) upon interaction with any of the analyte, the coenzyme-dependent enzyme, the coenzyme, or a species that is a reaction product of one of these (e.g., the coenzyme reacts in a different oxidation state). A variety of media exhibit suitable electrochemical behavior. The mediator may also be stable in its oxidized form, may optionally exhibit reversible redox electrochemistry, may exhibit good solubility in aqueous solutions, and may react rapidly to produce electrochemically active reaction products.
Examples of such mediators include, but are not limited to, ABTS, azo compounds or azo precursors, benzoquinone, prussian blue, nitrosoaniline or nitrosoaniline-based precursors, thiazine or thiazine derivatives, transition metal complexes such as potassium ferricyanide, ruthenium complexes such as hexylamine ruthenium chloride, osmium derivatives, quinone or quinone derivatives, phenazine or phenazine-based precursors, and combinations of phenazine derivatives and ruthenium hexammine chloride, and derivatives thereof.
In some cases, when the coenzyme factor is NAD/NADH, the mediator may be 2,2' -diaza-bis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS).
In the step 3), the step (c),
in some cases, a coenzyme factor complex, the coenzyme factor complex being complexed from a coenzyme factor and a support material.
It should be noted that the complex means that the coenzyme factor and the carrier are attached to, bound to, integrated with, or linked to each other. Thus, they are not physically separate components, but rather can be compounded together as a single component (covalently or ionically bonded complex).
The coenzyme factor may be a natural coenzyme or an artificial coenzyme. As used herein, "coenzyme" or "redox cofactor" refers to a redox equivalent (e.g., hydride (H) ion) that can act as an enzymatic transfer - ) A redox equivalent of the enzymatic transfer from a substrate (e.g., a target analyte) to an enzyme to a coenzyme. "Redox equivalents" refers to concepts commonly used in redox chemistry, which are well known to those skilled in the art.
In particular, it relates to the transfer of electrons from a substrate of a coenzyme-dependent enzyme (i.e., a target analyte) to the coenzyme or from the coenzyme to an electrode or an indicator reagent. Examples of coenzymes include, but are not limited to, NAD, NADP, PQQ, thio-NAD, thio-NADP, and the like.
In some cases, the coenzyme is an artificial coenzyme. Examples of artificial coenzymes include, but are not limited to, artificial NAD (P)/NAD (P) H compounds, which are chemical derivatives of natural NAD/NADH or natural NADP/NADPH.
Specifically, the artificial coenzyme can be chemically modified at the inactive site of the natural coenzyme, so that the coenzyme carries a chemical group for fixation under the condition of not influencing the activity and the function of the coenzyme factor, and the coenzyme is further fixed.
In some cases, the amino group on NAD adenine can be modified to obtain an artificial coenzyme NAD compound.
In some cases, the support material may be a polymeric carrier, examples of which include, but are not limited to, chitosan, agarose, sodium alginate, polyethylene glycol, and the like; preferably, the chitosan is a high molecular water-soluble polysaccharide with free amino, has good film forming property and can be used as a carrier of coenzyme factors; more preferably, the chitosan is medium viscosity chitosan (200-400 mPa.s).
In some cases, the coenzyme factor complex of the invention may be NAD + -chitosan complex, said NAD + -chitosan complex, said NAD + Chitosan complex by para-NAD + Modifying amino on adenine to obtain artificial NAD + Coenzyme, then covalently linked with chitosan to prepare the coenzyme, thereby actually realizing NAD + Immobilization of (2).
In the step 4), the step of mixing the raw materials,
in some cases, the "enzyme" refers specifically to a coenzyme-dependent enzyme, and "coenzyme-dependent enzyme" refers to an enzyme that requires an organic or inorganic cofactor, called a coenzyme, for catalytic activity.
In some cases, the coenzyme-dependent enzyme can be a dehydrogenase. As used herein, "dehydrogenase" refers to a compound capable of passing a hydride (H) as a redox equivalent (redox equivalent) - ) A protein or polypeptide that is transferred to a receptor molecule to catalyze the oxidation of a substrate. Examples of dehydrogenases include, but are not limited to, glucose dehydrogenase, alcohol dehydrogenase, glycerol dehydrogenase, lactate dehydrogenase, L-amino acid dehydrogenase, malate dehydrogenase, sorbitol dehydrogenase, or the like, especially nad (p)/nad (p) H-dependent dehydrogenase.
It should be noted that, in the step 4), the enzyme is loaded on the material prepared in the step 3), and the cross-linking effect of the glutaraldehyde on the enzyme can be realized. Specifically, when the loading material of the coenzyme factor compound in the step 3) is chitosan, the free amino group of the chitosan and one free aldehyde on glutaraldehyde are covalently connected to synthesize a Schiff base structure under the action of glutaraldehyde, and the other free aldehyde of the glutaraldehyde is connected with an enzyme to realize the immobilization of the enzyme.
In a fifth aspect of the present invention, there is provided a method for regenerating a coenzyme factor, the method comprising:
1) dripping a substrate material on the surface of the substrate electrode;
2) depositing a medium on the substrate electrode loaded with the substrate material prepared in the step 1) by adopting an electrochemical deposition method.
In the step 1), the step (A) is carried out,
in some cases, the base electrode includes, but is not limited to: a Glassy Carbon (GCE) electrode, a gold electrode, a graphite electrode, a carbon paste electrode, preferably GCE. The GCE has good mechanical stability, light stability and high conductivity.
The substrate material is a carbon material including, but not limited to: the electrode material comprises activated carbon, graphene, carbon nanofibers, carbon nanospheres, glassy carbon, carbon aerogel and Carbon Nanotubes (CNTs), and preferably the carbon nanotubes have large specific surface area and small internal resistance, so that the analysis performance of the chemically modified electrode can be remarkably improved, and the electrode material has good conductivity and chemical stability.
The carbon nano tube not only comprises a multi-wall carbon nano tube and a single-wall carbon nano tube, but also comprises a functionalized carbon nano tube modified by amination, carboxylation and the like.
In the step 2), the step (c) is carried out,
"mediator" refers to a compound that increases the reactivity of a reduced coenzyme obtained by reaction with an analyte and transfers electrons to an electrode system or a suitable optical indicator/optical indicator system.
The mediator can be any chemical species (typically electrochemically active) that can participate in a reaction scheme involving an analyte, a coenzyme-dependent enzyme, a coenzyme, and reaction products thereof to produce a detectable electrochemically active reaction product. In general, participation of the mediator in the reaction involves a change in its oxidation state (e.g., reduction) upon interaction with any of the analyte, the coenzyme-dependent enzyme, the coenzyme, or a species that is a reaction product of one of these (e.g., the coenzyme reacts in a different oxidation state). A variety of media exhibit suitable electrochemical behavior. The media may also be stable in its oxidized form, may optionally exhibit reversible redox electrochemistry, may exhibit good solubility in aqueous solutions, and may react rapidly to produce electrochemically active reaction products.
Examples of such mediators include, but are not limited to, ABTS, azo compounds or azo precursors, benzoquinones, prussian blue, nitrosoanilines or nitrosoaniline-based precursors, thiazine or thiazine derivatives, transition metal complexes such as potassium ferricyanide, ruthenium complexes such as hexylamine ruthenium chloride, osmium derivatives, quinones or quinone derivatives, phenazine or phenazine-based precursors, and combinations of phenazine derivatives and ruthenium hexammine chloride, and derivatives thereof.
In some cases, when the coenzyme factor is NAD, the mediator may be 2,2' -biazobis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS). In the present invention, carbon nanotubes are mixed with ABTS + The carbon nano tube is modified on the surface of a GCE electrode, and can realize the catalytic oxidation of NADH (nicotinamide adenine dinucleotide), ABTS (adenosine triphosphate), and + electron transfer can be increased. Simultaneous ABTS + Oxidation reduction occurs with NADH, the 4-position of pyridine ring in NADH and ABTS + Radical cation reaction, ABTS + The obtained hydrogen ions are converted into ABTS, NADH is oxidized into NAD + Effecting NAD + And (4) in-situ regeneration. After the above process, ABTS loses electrons, and ABTS is generated at the positive electrode of the electrode + And entering the next cycle.
In a sixth aspect of the present invention, there is provided a use of the above-described method for regenerating a coenzyme factor in an enzyme electrode and/or an enzyme sensor.
In a seventh aspect of the present invention, there is provided the use of the above-described coenzyme factor complex and/or enzyme electrode for the production of an enzyme sensor.
In an eighth aspect of the present invention, there is provided an enzyme sensor comprising at least two electrodes comprising at least the above-described coenzyme factor complex and/or the above-described enzyme electrode. The enzyme sensor has the advantages of high detection sensitivity, high detection repeatability and long-term storage stability.
In some cases, the enzyme sensor comprises two or three electrodes, and accordingly, the enzyme sensor is a two-electrode or three-electrode enzyme sensor.
In some cases, a sensor consisting of two electrodes (i.e., a two-electrode enzyme sensor), the electrodes being a working electrode and a counter electrode; wherein the working electrode is the coenzyme factor complex and/or the enzyme electrode.
In some cases, a sensor consisting of three electrodes (i.e., a three-electrode enzyme sensor), the electrodes being a working electrode, a counter electrode, and a reference electrode; wherein the working electrode is the coenzyme factor complex and/or the enzyme electrode.
In some cases, in a three-electrode enzyme sensor, the counter electrode is a platinum electrode; the reference electrode is an Ag/AgCl electrode.
In a ninth aspect of the invention, there is provided a method of electrochemically measuring the concentration or presence of a target analyte to be measured, the method comprising: and (3) contacting the enzyme electrode and/or the enzyme sensor with a liquid sample having or suspected of having a target analyte to be detected, measuring the response current intensity of the target analyte to be detected, and analyzing the concentration or the existence of the target analyte.
In some cases, the target analyte includes, but is not limited to, amino acids, glucose, ethanol, glycerol, lactic acid, malic acid, pyruvic acid, sorbitol, triglycerides, and uric acid.
In a tenth aspect of the present invention, there is provided a malate dehydrogenase electrode comprising: the GCE electrode is loaded with carbon nanotubes, ABTS is deposited on the surface of the carbon nanotubes, and chitosan-NAD is loaded on the surface of the ABTS + Complexes and malate dehydrogenase.
In some cases, the method of making a malate dehydrogenase electrode comprises:
1) dropping carbon nanotubes on the surface of the GCE electrode;
2) depositing ABTS on the substrate electrode loaded with the substrate material prepared in the step 1) by adopting an electrochemical deposition method;
3) dripping chitosan-NAD (nicotinamide adenine dinucleotide) on the material prepared in the step 2) + A complex;
4) loading malate dehydrogenase on the material prepared in the step 3).
In some cases, the method of making a malate dehydrogenase electrode comprises:
the carbon nanotube dispersion (0.1%) was drop-coated onto the working surface of the GCE electrode, and dried to obtain CNTs/GCE.
And (2) soaking the CNTs/GCE into the ABTS deposition storage solution, and performing Cyclic Voltammetry (CV) scanning for different times within a potential range of-200 mV to 600mV at a scanning rate of 50mV/s, wherein the electrode is ABTS/CNTs/GCE. ABTS cation free radicals deposited on the surface of the electrode can participate in NADH oxidation process to realize NAD + And (4) regenerating.
Wherein the ABTS deposition stock solution comprises: 2.5mmol/L FeCl 3 、2.5mmol/L K 3 Fe(CN) 6 200mmol/L HCl and 1mmol/L ABTS.
NAD prepared by dropwise adding on ABTS/CNTs/GCE surface + -chitosan complex, dried, electrode CTS-NAD + /ABTS/CNTs/GCE。
Wherein, NAD + -the preparation process of the chitosan complex comprises:
taken 5mL of NAD + Adding 1mL of iodoacetic acid (1mg/mL) into the aqueous solution (1mg/mL), and reacting in a water bath at 70 ℃ for 1h to obtain n 1-carboxymethyl-NAD + 。
② in the above NAD + Adding 1mL of sodium thiosulfate solution (1.3mmol/L) into the aqueous solution, adjusting the pH value to 11, reacting in a water bath at 70 ℃ for 1h to obtain n 1-carboxymethyl-NADH, and simultaneously carrying out Dimroth rearrangement under a strong alkali condition to obtain n 6-carboxymethyl NADH.
③ adding 1mL of formaldehyde into the mixture to react for 1h in 70 ℃ water bath to obtain c 6-carboxymethyl NAD + 。
Fourthly, after the pH value of the reaction system is adjusted to be neutral, 10mg of NHS and 10mg of EDC are added, 10mL of chitosan solution (0.1%) is added, and the mixture is reacted in water bath at 70 ℃ for 1h to obtain the chitosan-NAD + And (c) a complex.
Converting CTS-NAD + Immersing the/ABTS/CNTs/GCE working surface in 25% glutaraldehyde aqueous solution, taking out after 1h, and fully cleaning with deionized water. Subsequently, the working surface of the electrode is immersed in a solution of malate dehydrogenase (240U/mL), taken out after 1h, and sufficiently washed to take out the loosely bound enzyme molecules, the electrode being MDH/CTS-NAD + /ABTS/CNTs/GCE。
In some cases, the malate dehydrogenase sensor comprises: the malic dehydrogenase electrode is used as the working electrode; the counter electrode is a platinum electrode; the reference electrode was an Ag/AgCl electrode.
In an eleventh aspect of the present invention, there is provided a glucose dehydrogenase electrode comprising: the GCE electrode is loaded with carbon nanotubes, ABTS is deposited on the surface of the carbon nanotubes, and chitosan-NAD is loaded on the surface of the ABTS + A complex and glucose dehydrogenase.
In some cases, the method of making a glucose dehydrogenase electrode comprises:
1) dropping carbon nanotubes on the surface of the GCE electrode;
2) depositing ABTS on the substrate electrode loaded with the substrate material prepared in the step 1) by adopting an electrochemical deposition method;
3) dripping chitosan-NAD (nicotinamide adenine dinucleotide) on the material prepared in the step 2) + A complex;
4) loading glucose dehydrogenase on the material prepared in the step 3).
In some cases, the method of making a glucose dehydrogenase electrode comprises:
and (3) dripping the carbon nano tube dispersion liquid (0.1%) on the working surface of the GCE electrode, and drying to obtain the CNTs/GCE electrode.
And (2) soaking the CNTs/GCE into the ABTS deposition storage solution, and performing Cyclic Voltammetry (CV) scanning for different times within a potential range of-200 mV to 600mV at a scanning rate of 50mV/s, wherein the electrode is ABTS/CNTs/GCE. ABTS cation free radicals deposited on the surface of the electrode can participate in NADH oxidation process to realize NAD + And (4) regenerating.
Wherein the ABTS deposition stock solution comprises: 2.5mmol/L FeCl 3 、2.5mmol/L K 3 Fe(CN) 6 200mmol/L HCl and 1mmol/L ABTS.
NAD prepared by dropwise adding on ABTS/CNTs/GCE surface + -chitosan complex, dried, electrode CTS-NAD + /ABTS/CNTs/GCE。
Wherein, NAD + -the preparation process of the chitosan complex comprises:
taken 5mL of NAD + 1mL of iodoacetic acid (1mg/mL) was added to the aqueous solution (1mg/mL), and the mixture was reacted in a 70 ℃ water bath for 1 hour to give n 1-carboxymethyl-NAD + 。
② in the above NAD + Adding 1mL of sodium thiosulfate solution (1.3mmol/L) into the aqueous solution, adjusting the pH value to 11, reacting in a water bath at 70 ℃ for 1h to obtain n 1-carboxymethyl-NADH, and simultaneously carrying out Dimroth rearrangement under a strong alkali condition to obtain n 6-carboxymethyl NADH.
③ adding 1mL of formaldehyde into the mixture to react for 1h in 70 ℃ water bath to obtain c 6-carboxymethyl NAD + 。
Fourthly, after the pH value of the reaction system is adjusted to be neutral, 10mg of NHS and 10mg of EDC are added, 10mL of chitosan solution (0.1%) is added, and the mixture is reacted in water bath at 70 ℃ for 1h to obtain the chitosan-NAD + And (c) a complex.
Converting CTS-NAD + Immersing the/ABTS/CNTs/GCE working surface in 25% glutaraldehyde aqueous solution, taking out after 1h, and fully cleaning with deionized water. The working surface of the electrode was then immersed in a solution of glucose dehydrogenase (240U/mL) for 1h, removed, washed thoroughly to remove the loosely bound enzyme molecules, and the electrode was MDH/CTS-NAD + /ABTS/CNTs/GCE。
In some cases, the glucose dehydrogenase sensor comprises: a working electrode, a counter electrode and a reference electrode, wherein the glucose dehydrogenase electrode is used as the working electrode; the counter electrode is a platinum electrode; the reference electrode was an Ag/AgCl electrode.
In a twelfth aspect of the present invention, there is provided a lactate dehydrogenase electrode comprising: the GCE electrode is loaded with carbon nanotubes, ABTS is deposited on the surface of the carbon nanotubes, and the surface of the ABTS comprises chitosan-NAD + A complex and lactate dehydrogenase.
In some cases, the lactate dehydrogenase electrode is prepared by a method comprising:
1) dropping carbon nanotubes on the surface of the GCE electrode;
2) depositing ABTS on the substrate electrode loaded with the substrate material prepared in the step 1) by adopting an electrochemical deposition method;
3) dripping chitosan-NAD (nicotinamide adenine dinucleotide) on the material prepared in the step 2) + A complex;
4) loading lactate dehydrogenase on the material prepared in the step 3).
In some cases, the lactate dehydrogenase electrode is prepared by a method comprising:
and (3) dripping the carbon nano tube dispersion liquid (0.1%) on the working surface of the GCE electrode, and drying to obtain the CNTs/GCE electrode.
The CNTs/GCE is immersed in ABTS deposition stock solution, Cyclic Voltammetry (CV) scanning is carried out for different times within the potential range of-200 mV to 600mV at the scanning speed of 50mV/s, and the electrode is ABTS/CNTs/GCE. ABTS cation free radicals deposited on the surface of the electrode can participate in NADH oxidation process to realize NAD + And (4) regenerating.
Wherein the ABTS deposition stock solution comprises: 2.5mmol/L FeCl 3 、2.5mmol/L K 3 Fe(CN) 6 200mmol/L HCl and 1mmol/L ABTS.
NAD prepared by dropwise adding on ABTS/CNTs/GCE surface + -chitosan complex, dried, electrode CTS-NAD + /ABTS/CNTs/GCE。
Wherein, NAD + -the preparation process of the chitosan complex comprises:
taken 5mL of NAD + Adding 1mL of iodoacetic acid (1mg/mL) into the aqueous solution (1mg/mL), and reacting in a water bath at 70 ℃ for 1h to obtain n 1-carboxymethyl-NAD + 。
② in the above NAD + Adding 1mL of sodium thiosulfate solution (1.3mmol/L) into the aqueous solution, adjusting the pH value to 11, reacting in a water bath at 70 ℃ for 1h to obtain n 1-carboxymethyl-NADH, and simultaneously carrying out Dimroth rearrangement under a strong alkali condition to obtain n 6-carboxymethyl NADH.
③ adding 1mL of formaldehyde into the mixture to react for 1h in 70 ℃ water bath to obtain c 6-carboxymethyl NAD + 。
Fourthly, after the pH value of the reaction system is adjusted to be neutral, 10mg of NHS and 10mg of EDC are added, 10mL of chitosan solution (0.1%) is added, and the mixture is reacted in water bath at 70 ℃ for 1h to obtain the chitosan-NAD + And (c) a complex.
Converting CTS-NAD + the/ABTS/CNTs/GCE working surface is immersed in a solution containing 25 percentAnd taking out the solution after 1h in glutaraldehyde aqueous solution, and fully washing the solution with deionized water. The working surface of the electrode was then immersed in a solution of lactate dehydrogenase (240U/mL) for 1h, removed, and thoroughly washed to remove the loosely bound enzyme molecules, the electrode being MDH/CTS-NAD + /ABTS/CNTs/GCE。
In some cases, the lactate dehydrogenase sensor comprises: a working electrode, a counter electrode and a reference electrode, wherein the lactate dehydrogenase electrode is used as the working electrode; the counter electrode is a platinum electrode; the reference electrode was an Ag/AgCl electrode.
The invention has the beneficial technical effects that:
(1) the present invention uses simple NAD + Modification technology for preparing chitosan-NAD + The complex (coenzyme factor complex) is used for the preparation of dehydrogenase electrodes. The complex is to NAD + The amino group on adenine is modified without affecting NAD + The activity function is exerted, and the immobilized NAD is effectively improved + Activity of (2). The coenzyme factor compound is dripped on the surface of an electrode to realize NAD (nicotinamide adenine dinucleotide) + The coenzyme factor complex is immobilized on the surface of an electrode, and provides a chitosan binding site on the surface of the electrode for dehydrogenase, so that the coenzyme factor complex has wide application value in the field of coenzyme-dependent enzyme electrodes/biosensors.
(2) The invention uses ABTS as an electron mediator, and realizes NAD through electron transfer of an electrode + And (4) regenerating. In situ regeneration of NAD by electrochemical means + Not only is convenient and fast, but also can avoid the influence of byproducts.
(3) The invention utilizes NAD + The immobilized and in-situ regeneration technology prepares the dehydrogenase electrode which can be repeatedly used. In addition, compared with the traditional dehydrogenase electrode, the electrode has higher detection sensitivity, higher detection repeatability and better storage stability, thereby having good practical application value.
Drawings
The accompanying drawings, which are incorporated in and constitute a part of this specification, are included to provide a further understanding of the invention, and are incorporated in and constitute a part of this specification, illustrate exemplary embodiments of the invention and together with the description serve to explain the invention and not to limit the invention.
FIG. 1 shows chitosan-NAD prepared in example 1 of the present invention + Compound structural change and corresponding ultraviolet absorption spectrogram; wherein FIG. 1(I) is NAD + Exhibits a maximum uv absorption peak at 260 nm; FIG. 1(II) is N1-carboxymethyl-NAD + Exhibits a maximum uv absorption peak at 250 nm; FIG. 1(III) is C6-carboxymethyl NAD + Maximum ultraviolet absorption peaks at 250nm and 340 nm; FIG. 1(IV) is chitosan-NAD + The composite showed a maximum uv absorption peak at 260 nm.
FIG. 2 is a schematic diagram of an electrode for malate dehydrogenase in example 2 of the present invention.
FIG. 3 is a schematic diagram of the process of preparing malate dehydrogenase according to example 2 of the present invention and a scanning electron microscope image; wherein, fig. 3(I) is a scanning electron microscope image of the carbon nanotube modified electrode; FIG. 3(II) is a scanning electron micrograph of the electrode after ABTS deposition; FIG. 3(III) is a scanning electron micrograph of the modified chitosan-NAD complex; FIG. 3(IV) is a scanning electron micrograph showing malate dehydrogenase immobilized on an electrode.
FIG. 4 is a graph showing the repetitive results of the malate dehydrogenase electrode prepared in example 2 of the present invention.
FIG. 5 is a graph showing the results of the linear range of the malate dehydrogenase electrode prepared in example 2 of the present invention.
FIG. 6 is a graph showing the results of electrode stability of malate dehydrogenase prepared in example 2 of the present invention.
FIG. 7 is a graph showing the results of the linear range of the glucose dehydrogenase electrode prepared in example 3 of the present invention.
FIG. 8 is a graph showing the results of the reproducibility of the glucose dehydrogenase electrode prepared in example 3 of the present invention.
FIG. 9 is a graph showing the results of electrode stability of glucose dehydrogenase prepared in example 3 of the present invention.
FIG. 10 is a graph showing the results of the linear range of the lactate dehydrogenase electrode prepared in example 4 of the present invention.
FIG. 11 is a graph showing the results of reproducibility of the lactate dehydrogenase electrode prepared in example 4 according to the present invention.
FIG. 12 is a graph showing the results of stability of the lactate dehydrogenase electrode prepared in example 4 of the present invention.
FIG. 13 is a graph showing the results of detecting malic acid by using the electrode of dehydrogenase of unmodified ABTS in example 5 of the present invention.
FIG. 14 is a graph showing the results of NADH detection using CNTs-GCE and a bare electrode in example 6 of the present invention.
FIG. 15 shows the immobilization of NAD in example 7 of the present invention + Electrode response to malic acid with free NAD + Compare the figures.
FIG. 16 is a graph showing the intensity of response current in measuring malic acid using a malate dehydrogenase electrode prepared using Prussian blue as an electron enzyme mediator in example 8 of the present invention.
FIG. 17 is a graph showing the intensity of response current in measuring malic acid using a malate dehydrogenase electrode prepared using agarose as a supporting material in example 9 of the present invention.
FIG. 18 is a graph comparing the intensity of response current of a malate dehydrogenase electrode prepared using other types of chitosan (high viscosity chitosan) and standard chitosan (medium viscosity chitosan) as a support material in example 10 of the present invention to measure standard malate. Firstly, dissolving chitosan (high viscosity) to modify an electrode; ② standard chitosan (medium viscosity) modified electrode.
Detailed Description
It is to be understood that the following detailed description is exemplary and is intended to provide further explanation of the invention as claimed. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.
It is noted that the terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of exemplary embodiments according to the invention. As used herein, the singular forms "a", "an" and "the" are intended to include the plural forms as well, and it should be understood that when the terms "comprises" and/or "comprising" are used in this specification, they specify the presence of stated features, steps, operations, devices, components, and/or combinations thereof, unless the context clearly indicates otherwise. It is to be understood that the scope of the invention is not to be limited to the specific embodiments described below; it is also to be understood that the terminology used in the examples is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention.
The invention takes carbon nano-tube as substrate material, ABTS as electron mediator, and utilizes chitosan/chemical modification NAD + Chitosan-NAD formed under the action of carbodiimide + The composite film and the crosslinking effect of glutaraldehyde on dehydrogenase produce a dehydrogenase electrode which can be reused. The chitosan is a high molecular water-soluble polysaccharide with free amino group, has good film forming property, and can be used as NAD + And (3) a carrier. Free amino groups on chitosan and chemically modified NAD after EDC/NHS treatment + The free carboxyl group on the amino group forms a urea derivative to complete the immobilization of NAD + . Through the action of glutaraldehyde, the free amino group of chitosan and one free aldehyde on glutaraldehyde are covalently linked to synthesize a Schiff base structure, and the other free aldehyde of glutaraldehyde is linked to dehydrogenase, so that the dehydrogenase is immobilized.
The invention is further illustrated by the following examples, which are not to be construed as limiting the invention thereto. It should be understood that these examples are for illustrative purposes only and are not intended to limit the scope of the present invention.
Example 1 Chitosan-NAD + Preparation of the Complex
Taking NAD + 5mL (1mg/mL) of the aqueous solution was added with 1mL of iodoacetic acid (1mg/mL), and the mixture was reacted in a 70 ℃ water bath for 1 hour. In the above-mentioned NAD + To the aqueous solution, 1mL (1.3mM) of a sodium thiosulfate solution was added, the pH was adjusted to 11 with 1M NaOH, and the mixture was reacted in a water bath at 70 ℃ for 1 hour. Then adding 1mL formaldehyde into 70 ℃ water bath for reaction for 1 h. The pH of the reaction system was adjusted to neutral using 1M HCl, NHS (10mg), EDC (10mg) were added, and 10mL of a 0.1% chitosan solution [ chitosan was medium viscosity chitosan (200-400mPa. s) ]was added]And reacting in water bath at 70 ℃ for 1 h. And carrying out ultraviolet absorption full-wavelength scanning test on the key steps.
Chitosan-NAD + The results of the UV absorption wavelength in the preparation of the complex are shown in FIG. 1, and we mainly utilize NAD + Covalent linkage with chitosan with good water solubility and film-forming property to realize NAD + And (4) immobilizing. NAD was used in this experiment + To start with, NAD + The maximum UV absorption peak is shown at 260nm (FIG. 1-I). Firstly, iodoacetic acid is used as an alkylating reagent to NAD in an acidic environment + Alkylation of adenine 1-position nitrogen atom to obtain N1-carboxymethyl-NAD + . With NAD + In contrast, N1-carboxymethyl-NAD + There was a blue shift peak showing the largest UV absorption peak at 250nm (FIG. 1-II). Sodium thiosulfate as reducing agent to N1-carboxymethyl-NAD + The reduction is carried out to obtain N1-carboxymethyl-NADH which is more stable under alkaline conditions. Then carrying out Dimroth rearrangement under the strong alkali condition to obtain C6-carboxymethyl NADH with the amino group on the 6-position carbon modified. The Cannizzaro reaction of formaldehyde takes place under alkaline conditions, while the rearrangement product C6-carboxymethyl NADH is oxidized to C6-carboxymethyl NAD + . As shown in FIGS. 1-III, the compound showed the maximum UV absorption peaks at 250nm and 340nm, and NADH showed the maximum UV absorption peak at 340nm, indicating that NAD is present during this reaction + And NADH derivatives. C6-carboxymethyl NAD was then treated with EDC/NHS + And chitosan. Free amino groups on chitosan and C6-carboxymethyl NAD after EDC treatment + The free carboxyl group on the (A) forms an unstable urea derivative, and then the stability of a carbodiimide cross-linked product can be enhanced through NHS treatment, so that NAD is realized + Covalent bond connection with chitosan carrier to complete the immobilization of NAD + As shown in FIGS. 1-IV, NAD + The macromolecule shows the maximum ultraviolet absorption peak at 260nm, and the result shows that NAD + The reactive groups are not affected by the immobilization process.
Example 2 preparation method of malate dehydrogenase electrode
(1) Preparation of Chitosan-NAD + Composite material
Taking NAD + 5mL (1mg/mL) of the aqueous solution was added with 1mL of iodoacetic acid (1mg/mL), and the mixture was reacted in a 70 ℃ water bath for 1 hour. In the above-mentioned NAD + To the aqueous solution, 1mL (1.3mM) of a sodium thiosulfate solution was added, the pH was adjusted to 11 with 1M NaOH, and the mixture was reacted in a water bath at 70 ℃ for 1 hour. Then adding 1mL of formaldehyde into a 70 ℃ water bath for reaction for 1 h. The pH of the reaction system was adjusted to neutral using 1M HCl, NHS (10mg), EDC (10mg) were added, and 10mL of a 0.1% chitosan solution [ chitosan was medium viscosity chitosan (200-400mPa. s) ]was added]Reaction in 70 ℃ water bath 1h。
(2) Preparation of malate dehydrogenase electrode
All electrochemical measurements were performed in a typical three-electrode system (CHI 760D, CH instrument). The three-electrode system comprises: the platinum electrode is used as a counter electrode, the Ag/AgCl electrode is used as a reference electrode, and the glassy carbon electrode is used as a working electrode. During the experiment, a glassy carbon electrode with the diameter of 3mm is sequentially coated with Al with a certain particle size 2 O 3 Polishing the slurry on polishing cloth to mirror surface, removing surface dirt after each polishing, cleaning in ultrasonic water bath for 1min for three times, and sequentially adding 1:1 ethanol and 1:1NHO 3 And (4) ultrasonic cleaning. After thorough washing, the mixture was washed with 0.20mol/L KNO 3 Middle record 1X 10 -3 mol/L K 3 Fe(CN) 6 The cyclic voltammetry curve of the solution is used for testing the performance of the electrode, the scanning speed is 50mV/s, and the scanning range is 0.6 to-0.2V. The peak potential difference in the cyclic voltammogram obtained under laboratory conditions is below 80mV and as close as possible to 64mV, and the electrode can be used.
5 mu L of 0.1% carbon nanotube dispersion liquid is dripped on the pretreated working surface of the electrode, and the electrode is dried. The electrodes were immersed in an ABTS deposition stock solution (ABTS deposition stock solution containing 2.5mM/L FeCl) 3 、2.5mM/L K 3 Fe(CN) 6 200mM/L HCl and 1mM/L ABTS, used only on the day), different numbers of Cyclic Voltammetry (CV) scans were performed over a potential range of-200 to 600mV at a scan rate of 50 mV/s. The redox peaks in the interface are seen to increase once with the number of passes scanned and eventually approach coincidence, indicating that ABTS has been deposited on the electrode. Fully cleaning the working electrode and the working surface of the counter electrode by deionized water, and dripping 10 mu L of chitosan-NAD (nicotinamide adenine dinucleotide) on the working surface + And (5) drying the compound at room temperature again. Immersing the newly prepared working surface of the electrode in an aqueous solution containing 25% of glutaraldehyde, taking out after 1 hour, and fully cleaning with deionized water to introduce a certain amount of active aldehyde groups into the chitosan modification layer on the surface of the electrode. The electrode working face was then immersed in a malate dehydrogenase solution (240U/mL) and after 1h removed, and washed thoroughly to remove loosely bound enzyme molecules.
The working principle of the malate dehydrogenase electrode is as follows:
as shown in FIG. 2, malate dehydrogenase catalyzes the conversion of malate to oxaloacetate to form NADH. Therefore, the malic acid content can be quantitatively analyzed by measuring the NADH content. Mixing carbon nanotubes with ABTS + The carbon nano tube is modified on the surface of the electrode, and can realize catalytic oxidation of NADH, ABTS + Electron transfer can be increased. Simultaneous ABTS + Oxidation reduction occurs with NADH, the 4-position of pyridine ring in NADH and ABTS + Radical cation reaction, ABTS + The hydrogen ion is converted into ABTS, NADH is oxidized into NAD + Effecting NAD + And (4) in-situ regeneration. After the process, ABTS loses electrons and generates ABTS at the positive electrode + And entering the next cycle.
(3) Detection of malate dehydrogenase electrode Performance
Standard malic acid solutions with the concentrations of 1, 2, 4, 6, 8 and 10mmol/L are respectively prepared, the response current intensity of the standard malic acid is measured by using the prepared malic acid dehydrogenase electrode, and the linear range of the electrode is analyzed. The measurement of current was repeated 10 times in 1, 2, 4, 6, 8, 10mmol/L malic acid solution, respectively, and the reproducibility of the electrode was analyzed. The prepared malate dehydrogenase electrode was stored at 4 ℃ and the electrode response was measured at a 4mmol/L malic acid solution every day to analyze the stability of the electrode.
FIG. 3 shows a scanning electron microscope of the preparation process of the malate dehydrogenase electrode, and FIG. 3-I shows a carbon nanotube modified electrode with a significant distribution of tube bundles on the surface of the electrode. After depositing ABTS, as shown in FIG. 3-II, the electrode surface has a distinct film structure after electrochemically depositing ABTS on the carbon nanotubes. As shown in fig. 3-III, the membrane structure on the surface of the electrode was significantly thickened after the modification of the chitosan-NAD complex. As shown in FIGS. 3-IV, the electrode surface had a distinct protrusion, indicating that malate dehydrogenase was immobilized on the electrode surface.
In order to examine the reusability of the dehydrogenase electrode, the current was repeatedly measured 10 times in 1, 2, 4, 6, 10mmol/L malic acid solution, respectively, and the reproducibility of the electrode was analyzed. After each measurement, the electrode surface was thoroughly cleaned for the next reaction. The results of electrode reproducibility tests are shown in FIG. 4. The Relative Standard Deviations (RSD) of the current response values were all below 5%, averaging 4.40%. These values indicate that the experimentally prepared malate dehydrogenase electrodes have good reproducibility.
In order to examine the linear range of the dehydrogenase electrode, standard malic acid solutions with concentrations of 1, 2, 4, 6, 8 and 10mmol/L were prepared, and the response current intensity of the standard malic acid was measured using the prepared malate dehydrogenase electrode, and the linear range of the electrode was analyzed. As shown in FIG. 5, the correlation coefficient of the redox peak current and its concentration was 0.9836 at malic acid contents of 1-10mmol/L, and the linear fit was good. According to the 3 sigma principle, when the signal-to-noise ratio is 3(S/N ═ 3), the apple detection limit is 0.0278 mmol/L.
The prepared malate dehydrogenase electrode was stored at 4 ℃ and the electrode response was measured at a 4mmol/L malic acid solution every day to analyze the stability of the electrode. As shown in fig. 6, during the 25 day test, no significant fluctuation in current intensity occurred before day 20, indicating that the electrode remained stable for 20 days.
Example 3 preparation of glucose dehydrogenase electrode
(1) Preparation of glucose dehydrogenase electrode
All electrochemical measurements were performed in a typical three-electrode system (CHI 760D, CH instrument). The three-electrode system comprises: the platinum electrode is used as a counter electrode, the Ag/AgCl electrode is used as a reference electrode, and the glassy carbon electrode is used as a working electrode. During the experiment, a glassy carbon electrode with the diameter of 3mm is sequentially coated with Al with a certain particle size 2 O 3 Polishing the slurry on polishing cloth to mirror surface, removing surface dirt after each polishing, cleaning in ultrasonic water bath for 1min for three times, and sequentially adding 1:1 ethanol and 1:1NHO 3 And (4) ultrasonic cleaning. After thorough washing, at 0.20mol/L KNO 3 Middle record 1X 10 -3 mol/L K 3 Fe(CN) 6 The cyclic voltammetry curve of the solution is used for testing the performance of the electrode, the scanning speed is 50mV/s, and the scanning range is 0.6 to-0.2V. The peak potential difference in the cyclic voltammogram obtained under laboratory conditions is below 80mV and as close as possible to 64mV, and the electrode can be used.
5 mu L of 0.1% carbon nano-particles are dripped on the working surface of the pretreated electrodeAnd (5) pipe dispersion liquid, and drying. The electrodes were immersed in ABTS deposition stock solution and different number of Cyclic Voltammetric (CV) scans were performed at a scan rate of 50mV/s over a potential range of-200 to 600 mV. The redox peaks in the interface are seen to increase once with the number of passes scanned and eventually approach coincidence, indicating that ABTS has been deposited on the electrode. Fully cleaning the working electrode and the working surface of the counter electrode by deionized water, and dripping 10 mu L of chitosan-NAD (nicotinamide adenine dinucleotide) on the working surface + And (5) drying the compound at room temperature again. And immersing the newly prepared working surface of the electrode in an aqueous solution containing 25% of glutaraldehyde, taking out after 1h, and fully cleaning with deionized water to introduce a certain amount of active aldehyde groups into the chitosan modification layer on the surface of the electrode. The working surface of the electrode was then immersed in a solution of glucose dehydrogenase and after 1h removed, and washed thoroughly to remove the loosely bound enzyme molecules.
(2) Detection of electrode Performance of glucose dehydrogenase
Standard glucose solutions with concentrations of 0.55, 11, 22, 33, 44 and 55mmol/L were prepared, and the response current intensity of standard glucose was measured using the prepared glucose dehydrogenase electrode, and the linear range of the electrode was analyzed. The current was measured repeatedly 10 times in 1, 10, 20, 30, 40, 50mmol/L glucose solution, respectively, and the reproducibility of the electrode was analyzed. The prepared glucose dehydrogenase electrode was stored at 4 ℃ and the electrode response was measured at 30mmol/L glucose solution every day to analyze the stability of the electrode.
In order to examine the linear range of the dehydrogenase electrode, standard glucose solutions were prepared at concentrations of 0.55, 11, 22, 33, 44, and 55mmol/L, respectively, and the response current intensity of standard glucose was measured using the prepared glucose dehydrogenase electrode, and the linear range of the electrode was analyzed. As shown in FIG. 7, the correlation coefficient of the redox peak current and its concentration was 0.9954 at glucose contents of 0.55-55mmol/L, and the linear fit was good. According to the 3 σ principle, when the signal-to-noise ratio is 3(S/N — 3), the apple detection limit is 0.00347 mmol/L.
To examine the reusability of the dehydrogenase electrode, the measurement of current was repeated 10 times in 1, 10, 20, 30, 40, 50mmol/L glucose solutions, respectively, and the reproducibility of the electrode was analyzed. After each measurement, the electrode surface was thoroughly cleaned for the next reaction. The results of electrode reproducibility tests are shown in FIG. 8. The Relative Standard Deviation (RSD) of the current response values were all below 5%, with an average of 3.80%. These values indicate that the experimentally prepared glucose dehydrogenase electrode has good reproducibility.
The prepared glucose dehydrogenase electrode was stored at 4 ℃ and the electrode response was measured at 30mmol/L glucose solution every day to analyze the stability of the electrode. As shown in fig. 9, during the 20 day test, no significant fluctuation in current intensity occurred before day 15, indicating that the electrode remained stable for 15 days.
Example 4 preparation method of lactate dehydrogenase electrode
(1) Preparation of lactate dehydrogenase electrode
All electrochemical measurements were performed in a typical three-electrode system (CHI 760D, CH instrument). The three-electrode system comprises: the platinum electrode is used as a counter electrode, the Ag/AgCl electrode is used as a reference electrode, and the glassy carbon electrode is used as a working electrode. In the experiment, a glassy carbon electrode with the diameter of 3mm is sequentially coated with Al with a certain particle size 2 O 3 Polishing the slurry on polishing cloth to mirror surface, removing surface dirt after each polishing, cleaning in ultrasonic water bath for 1min for three times, and sequentially adding 1:1 ethanol and 1:1NHO 3 And (4) ultrasonic cleaning. After thorough washing, the mixture was washed with 0.20mol/L KNO 3 Middle record 1X 10 -3 mol/L K 3 Fe(CN) 6 The cyclic voltammetry curve of the solution is used for testing the performance of the electrode, the scanning speed is 50mV/s, and the scanning range is 0.6 to-0.2V. The peak potential difference in the cyclic voltammogram obtained under laboratory conditions is below 80mV and as close as possible to 64mV, and the electrode can be used.
5 mu L of 0.1% carbon nanotube dispersion liquid is dripped on the pretreated working surface of the electrode, and the electrode is dried. The electrodes were immersed in ABTS deposition stock solution and different number of Cyclic Voltammetric (CV) scans were performed at a scan rate of 50mV/s over a potential range of-200 to 600 mV. The redox peaks in the interface are seen to increase once with the number of passes scanned and eventually approach coincidence, indicating that ABTS has been deposited on the electrode. Fully cleaning working electrode and counter electrode with deionized waterFace, 10. mu.L of chitosan-NAD was drop-coated onto the work surface + And (5) drying the compound at room temperature again. And immersing the newly prepared working surface of the electrode in an aqueous solution containing 25% of glutaraldehyde, taking out after 1h, and fully cleaning with deionized water to introduce a certain amount of active aldehyde groups into the chitosan modification layer on the surface of the electrode. The working surface of the electrode was then immersed in a solution of lactate dehydrogenase for 1h and then removed, and washed thoroughly to remove the loosely bound enzyme molecules.
(2) Lactate dehydrogenase electrode performance detection
Standard lactic acid solutions with the concentrations of 2, 4, 6, 8 and 10mmol/L are respectively prepared, the response current intensity of the standard lactic acid is measured by using the prepared lactate dehydrogenase electrode, and the linear range of the electrode is analyzed. The measurement of current was repeated 10 times in 2, 3, 4, 5, 6, 8mmol/L lactic acid solution, respectively, and the reproducibility of the electrode was analyzed. The prepared lactate dehydrogenase electrode was stored at 4 ℃ and the electrode response was measured at 6mmol/L lactate solution every day to analyze the stability of the electrode.
In order to examine the linear range of the dehydrogenase electrode, standard lactic acid solutions having concentrations of 2, 4, 6, 8, and 10mmol/L were prepared, respectively, and the linear range of the electrode was analyzed by measuring the response current intensity of the standard lactic acid using the prepared lactate dehydrogenase electrode. As shown in FIG. 10, the correlation coefficient of the redox peak current and its concentration was 0.9977 at lactic acid contents of 2 to 10mmol/L, and the linear fit was good. According to the 3 σ principle, when the signal-to-noise ratio is 3 (S/N-3), the detection limit of lactic acid is 0.0609 mmol/L.
To examine the reusability of the dehydrogenase electrode, the measurement of current was repeated 10 times in 2, 3, 4, 5, 6, 8mmol/L lactate solutions, respectively, and the reproducibility of the electrode was analyzed. After each measurement, the electrode surface was thoroughly cleaned for the next reaction. The results of the electrode reproducibility test are shown in FIG. 11. The Relative Standard Deviations (RSD) of the current response values were all below 5%, averaging 2.14%. These values indicate that the experimentally prepared lactate dehydrogenase electrode has good reproducibility.
The prepared lactate dehydrogenase electrode was stored at 4 ℃ and the electrode response was measured at 6mmol/L lactate solution every day to analyze the stability of the electrode. As shown in fig. 12, during the 28 day test, no significant fluctuation in current intensity occurred before day 21, indicating that the electrode remained stable for 21 days.
Example 5 Effect of ABTS in preparation of malate dehydrogenase electrode (unmodified ABTS, NAD) + Can not regenerate)
(1) Preparation of Chitosan-NAD + Composite material
Taking NAD + 5mL (1mg/mL) of the aqueous solution was added with 1mL of iodoacetic acid (1mg/mL), and the mixture was reacted in a 70 ℃ water bath for 1 hour. In the above-mentioned NAD + To the aqueous solution, 1mL (1.3mM) of a sodium thiosulfate solution was added, the pH was adjusted to 11 with 1M NaOH, and the mixture was reacted in a water bath at 70 ℃ for 1 hour. Then adding 1mL formaldehyde into 70 ℃ water bath for reaction for 1 h. The reaction system was adjusted to neutral pH with 1M HCl, NHS (10mg) and EDC (10mg) were added thereto, 10mL of 0.1% chitosan solution was added thereto, and the mixture was reacted in a 70 ℃ water bath for 1 hour.
(2) Preparation of malate dehydrogenase electrode
All electrochemical measurements were performed in a typical three-electrode system (CHI 760D, CH instrument). The three-electrode system comprises: the platinum electrode is used as a counter electrode, the Ag/AgCl electrode is used as a reference electrode, and the glassy carbon electrode is used as a working electrode. During the experiment, a glassy carbon electrode with the diameter of 3mm is sequentially coated with Al with a certain particle size 2 O 3 Polishing the slurry on polishing cloth to mirror surface, removing surface dirt after each polishing, cleaning in ultrasonic water bath for 1min for three times, and sequentially adding 1:1 ethanol and 1:1NHO 3 And (4) ultrasonic cleaning. After thorough washing, the mixture was washed with 0.20mol/L KNO 3 Middle record 1X 10 -3 mol/L K 3 Fe(CN) 6 The cyclic voltammetry curve of the solution is used for testing the performance of the electrode, the scanning speed is 50mV/s, and the scanning range is 0.6 to-0.2V. The peak potential difference in the cyclic voltammogram obtained under laboratory conditions is below 80mV and as close as possible to 64mV, and the electrode can be used.
5 mu L of 0.1% carbon nanotube dispersion liquid is dripped on the pretreated working surface of the electrode, and the electrode is dried. Drop-coating 10. mu.L of chitosan-NAD onto the working surface + And (5) drying the compound at room temperature again. Immersing the newly prepared electrode working surface in 25% glutaraldehyde aqueous solution, taking out after 1h, and fully cleaning with deionized water to ensure thatA certain amount of active aldehyde groups are introduced into the chitosan modification layer on the surface of the electrode. The electrode working face was then immersed in a solution of malate dehydrogenase (240U/mL), removed after 1h, and washed thoroughly to remove loosely bound enzyme molecules. Preparing a standard malic acid solution with the concentration of 10mmol/L, and measuring the response current intensity of the standard malic acid by using the prepared malate dehydrogenase electrode.
The experimental results are as follows:
as shown in fig. 13, the current gradually decreased with the number of scanning cycles in the malic acid solution. Indicating that NAD was immobilized on the surface of the electrode as the reaction proceeded + Consumption and inability to regenerate, thus modifying ABTS versus NAD on the electrode surface + Plays a key role.
EXAMPLE 6 NADH-DETECTING SCHEME OF CNTs ELECTRODES
(1) Preparation of malate dehydrogenase electrode
All electrochemical measurements were performed in a typical three-electrode system (CHI 760D, CH instrument). The three-electrode system comprises: the platinum electrode is used as a counter electrode, the Ag/AgCl electrode is used as a reference electrode, and the glassy carbon electrode is used as a working electrode. During the experiment, a glassy carbon electrode with the diameter of 3mm is sequentially coated with Al with a certain particle size 2 O 3 Polishing the slurry on polishing cloth to mirror surface, removing surface dirt after each polishing, cleaning in ultrasonic water bath for 1min for three times, and sequentially adding 1:1 ethanol and 1:1NHO 3 And (4) ultrasonic cleaning. After thorough washing, the mixture was washed with 0.20mol/L KNO 3 Middle record 1X 10 -3 mol/L K 3 Fe(CN) 6 The cyclic voltammetry curve of the solution is used for testing the performance of the electrode, the scanning speed is 50mV/s, and the scanning range is 0.6 to-0.2V. The peak potential difference in the cyclic voltammogram obtained under laboratory conditions is below 80mV and as close as possible to 64mV, and the electrode can be used.
5 mu L of 0.1% carbon nanotube dispersion liquid is dripped on the pretreated working surface of the electrode, and the electrode is dried. Denoted CNTs-GCE.
NADH solutions with the concentrations of 2, 6 and 10mmol/L are prepared respectively, and the prepared CNTs-GCE is used for measuring the response current intensity of standard NADH. The NADH electrical signal was detected using a bare electrode and compared to the above CNTs electrode results.
The experimental results are as follows:
the result of detecting NADH by using CNTs-GCE is shown in FIG. 14, and the result shows that the response current is gradually increased along with the increase of NADH concentration, which indicates that the prepared CNTs-GCE has good linear response to NADH, and the CNTs-GCE electrode response current intensity is obviously higher than the GCE bare electrode response current intensity, and the potential is obviously lower than the bare electrode response potential, which indicates that CNTs is an ideal substrate material for preparing dehydrogenase electrodes.
Example 7 immobilization of NAD + With free NAD + Comparison
(1) Preparation of Chitosan-NAD + Composite material
Taking NAD + 5mL (1mg/mL) of the aqueous solution was added with 1mL of iodoacetic acid (1mg/mL), and the mixture was reacted in a 70 ℃ water bath for 1 hour. In the above-mentioned NAD + To the aqueous solution, 1mL (1.3mM) of a sodium thiosulfate solution was added, the pH was adjusted to 11 with 1M NaOH, and the mixture was reacted in a water bath at 70 ℃ for 1 hour. Then adding 1mL formaldehyde into 70 ℃ water bath for reaction for 1 h. The reaction system was adjusted to neutral pH with 1M HCl, NHS (10mg) and EDC (10mg) were added thereto, 10mL of 0.1% chitosan solution was added thereto, and the mixture was reacted in a 70 ℃ water bath for 1 hour.
(2) Preparation of malate dehydrogenase electrode
All electrochemical measurements were performed in a typical three-electrode system (CHI 760D, CH instrument). The three-electrode system comprises: the platinum electrode is used as a counter electrode, the Ag/AgCl electrode is used as a reference electrode, and the glassy carbon electrode is used as a working electrode. During the experiment, a glassy carbon electrode with the diameter of 3mm is sequentially coated with Al with a certain particle size 2 O 3 Polishing the slurry on polishing cloth to mirror surface, removing surface dirt after each polishing, cleaning in ultrasonic water bath for 1min for three times, and sequentially adding 1:1 ethanol and 1:1NHO 3 And (6) ultrasonic cleaning. After thorough washing, the mixture was washed with 0.20mol/L KNO 3 Middle record 1X 10 -3 mol/L K 3 Fe(CN) 6 The cyclic voltammetry curve of the solution is used for testing the performance of the electrode, the scanning speed is 50mV/s, and the scanning range is 0.6 to-0.2V. The peak potential difference in the cyclic voltammogram obtained under laboratory conditions is below 80mV and as close as possible to 64mV, and the electrode can be used.
And 5 mu L of 0.1% carbon nano tube dispersion liquid is dripped on the pretreated working surface of the electrode, and the electrode is dried. The electrodes were immersed in an ABTS deposition stock solution (ABTS deposition stock solution containing 2.5mM/L FeCl) 3 、2.5/LmM K 3 Fe(CN) 6 200mM/L HCl and 1mM/L ABTS, used only on the day), different numbers of Cyclic Voltammetry (CV) scans were performed over a potential range of-200 to 600mV at a scan rate of 50 mV/s. The redox peaks in the interface are seen to increase once with the number of passes scanned and eventually approach coincidence, indicating that ABTS has been deposited on the electrode. Fully cleaning the working electrode and the working surface of the counter electrode by deionized water, and dripping 10 mu L of chitosan-NAD (nicotinamide adenine dinucleotide) on the working surface + And (5) drying the compound at room temperature again. And immersing the newly prepared working surface of the electrode in an aqueous solution containing 25% of glutaraldehyde, taking out after 1h, and fully cleaning with deionized water to introduce a certain amount of active aldehyde groups into the chitosan modification layer on the surface of the electrode. The electrode working face was then immersed in a solution of malate dehydrogenase (240U/mL), removed after 1h, and washed thoroughly to remove loosely bound enzyme molecules. A10 mmol/L standard malic acid solution is prepared, and the response current intensity of the standard malic acid is measured by using the prepared malic acid dehydrogenase electrode.
Separately preparing an unmodified immobilized NAD + The other steps are the same as the above process. Addition of 1mg/mL free NAD to a 10mmol/L standard malic acid solution + And using the free NAD + Electrode detection of response current of standard malic acid solution, with the immobilized NAD + And comparing the electrode detection results.
The results of the experiment are shown in FIG. 15, using non-immobilized NAD + In free NAD + When malic acid is detected in the environment, the electrode can generate a response signal at about 0.2V, but the signal intensity is low. With free NAD + Compared with the electrical signal of the electrode, the immobilized NAD prepared by the method + The working signal of the electrode is obviously enhanced, and NAD is immobilized + The electrode is significantly superior to free NAD + The electrode preparation technology is an ideal method for preparing dehydrogenase electrodes and dehydrogenase biosensors.
Example 8 Prussian blue regeneration of NAD + Preparation of dehydrogenase electrode (other kinds of electronic enzyme mediators/mediators do not make NAD available + Regeneration)
(1) Preparation of Chitosan-NAD + Composite material
Taking NAD + 5mL (1mg/mL) of the aqueous solution was added with 1mL of iodoacetic acid (1mg/mL), and the mixture was reacted in a 70 ℃ water bath for 1 hour. In the above-mentioned NAD + To the aqueous solution, 1mL (1.3mM) of a sodium thiosulfate solution was added, the pH was adjusted to 11 with 1M NaOH, and the mixture was reacted in a water bath at 70 ℃ for 1 hour. Then adding 1mL of formaldehyde into a 70 ℃ water bath for reaction for 1 h. The reaction system was adjusted to neutral pH with 1M HCl, NHS (10mg) and EDC (10mg) were added thereto, 10mL of 0.1% chitosan solution was added thereto, and the mixture was reacted in a 70 ℃ water bath for 1 hour.
(2) Preparation of malate dehydrogenase electrode
All electrochemical measurements were performed in a typical three-electrode system (CHI 760D, CH instrument). The three-electrode system comprises: the platinum electrode is used as a counter electrode, the Ag/AgCl electrode is used as a reference electrode, and the glassy carbon electrode is used as a working electrode. During the experiment, a glassy carbon electrode with the diameter of 3mm is sequentially coated with Al with a certain particle size 2 O 3 Polishing the slurry on polishing cloth to mirror surface, removing surface dirt after each polishing, cleaning in ultrasonic water bath for 1min for three times, and sequentially adding 1:1 ethanol and 1:1NHO 3 And (4) ultrasonic cleaning. After thorough washing, the mixture was washed with 0.20mol/L KNO 3 Middle record 1X 10 -3 mol/L K 3 Fe(CN) 6 The cyclic voltammetry curve of the solution is used for testing the performance of the electrode, the scanning speed is 50mV/s, and the scanning range is 0.6 to-0.2V. The peak potential difference in the cyclic voltammogram obtained under laboratory conditions is below 80mV and as close as possible to 64mV, and the electrode can be used.
5 mu L of 0.1% carbon nanotube dispersion liquid is dripped on the pretreated working surface of the electrode, and the electrode is dried. The electrode was immersed in a Prussian blue deposition stock solution (containing 2.5mM/L FeCl in deionized water 3 ，2.5mM/L K 3 Fe(CN) 6 100mM/L KCl, 200mM/L HCl and 100mM/L EDTA Na 2 As a stock solution, the solution is effective within 3 days, preferably the current preparation), and the scanning speed of 50mV/s is different in the potential range of-200 mV to 600mVA number of Cyclic Voltammetry (CV) scans. The redox peaks in the interface can now be seen to increase once with the number of scans and eventually to coincide closely, indicating that prussian blue has been deposited on the electrode. Fully cleaning the working electrode and the working surface of the counter electrode by deionized water, and dripping 10 mu L of chitosan-NAD (nicotinamide adenine dinucleotide) on the working surface + And (5) drying the aqueous solution at room temperature again. And immersing the newly prepared working surface of the electrode in an aqueous solution containing 25% of glutaraldehyde, taking out after 1h, and fully cleaning with deionized water to introduce a certain amount of active aldehyde groups into the chitosan modification layer on the surface of the electrode. The electrode working face was then immersed in a solution of malate dehydrogenase (240U/mL), removed after 1h, and washed thoroughly to remove loosely bound enzyme molecules. A10 mmol/L standard malic acid solution is prepared, and the response current intensity of the standard malic acid is measured by using the prepared malic acid dehydrogenase electrode.
The results are shown in FIG. 16, where no signal is detected by the electrode, indicating that Prussian blue as an electronic enzyme mediator is unable to immobilize NAD on the surface of the electrode + And (4) regenerating.
Example 9 agarose-NAD + Study of Complex preparation of dehydrogenase electrode (other species NAD) + Macromolecular complexes not usable for electrode modification
(1) Preparation of agarose-NAD + Composite material
Taking NAD + 5mL (1mg/mL) of the aqueous solution was added with 1mL of iodoacetic acid (1mg/mL), and the mixture was reacted in a 70 ℃ water bath for 1 hour. In the above NAD + To the aqueous solution was added 1mL (1.3mM) of sodium thiosulfate, the pH was adjusted to 11 with 1M NaOH, and the mixture was reacted in a 70 ℃ water bath for 1 hour. Then adding 1mL of formaldehyde into a 70 ℃ water bath for reaction for 1 h. The reaction system was adjusted to neutral pH using 1M HCl, NHS (10mg), EDC (10mg) were added thereto, 1g of 1% agarose gel was added, and the mixture was reacted in a 70 ℃ water bath for 1 hour.
(2) Preparation of malate dehydrogenase electrode
All electrochemical measurements were performed in a typical three-electrode system (CHI 760D, CH instrument). The three-electrode system comprises: the platinum electrode is used as a counter electrode, the Ag/AgCl electrode is used as a reference electrode, and the glassy carbon electrode is used as a working electrode. In the experiment, glassy carbon electrodes with the diameter of 3mm are used in sequenceAl of particle size 2 O 3 Polishing the slurry on polishing cloth to mirror surface, removing surface dirt after each polishing, cleaning in ultrasonic water bath for 1min for three times, and sequentially adding 1:1 ethanol and 1:1NHO 3 And (4) ultrasonic cleaning. After thorough washing, the mixture was washed with 0.20mol/L KNO 3 Middle record 1X 10 -3 mol/L K 3 Fe(CN) 6 The cyclic voltammetry curve of the solution is used for testing the performance of the electrode, the scanning speed is 50mV/s, and the scanning range is 0.6 to-0.2V. The difference in peak potential in the cyclic voltammogram obtained under laboratory conditions is below 80mV and as close to 64mV as possible, and the electrode is usable.
5 mu L of 0.1% carbon nanotube dispersion liquid is dripped on the pretreated working surface of the electrode, and the electrode is dried. The electrodes were immersed in an ABTS deposition stock solution (ABTS deposition stock solution containing 2.5mM/L FeCl) 3 、2.5mM/L K 3 Fe(CN) 6 200mM/L HCl and 1mM/LABTS, used only for the day), different numbers of Cyclic Voltammetric (CV) scans were performed at a scan rate of 50mV/s over a potential range of-200 to 600 mV. The redox peaks in the interface are seen to increase once with the number of passes scanned and eventually approach coincidence, indicating that ABTS has been deposited on the electrode. Fully cleaning the working surfaces of the working electrode and the counter electrode by deionized water, and dripping agarose-NAD (nicotinamide adenine dinucleotide) on the working surfaces + And (5) drying the compound at room temperature again. agarose-NAD on the surface of the electrode + And immersing the compound in an aqueous solution containing 25% of glutaraldehyde, taking out after 1h, and fully washing with deionized water to introduce a certain amount of active aldehyde groups into the agarose modification layer on the surface of the electrode. The agarose-NAD is then added + The complex was immersed in a solution of malate dehydrogenase (240U/mL), removed after 1h, and washed thoroughly to remove the loosely bound enzyme molecules. A10 mmol/L standard malic acid solution is prepared, and the response current intensity of the standard malic acid is measured by using the prepared malic acid dehydrogenase electrode.
The results are shown in FIG. 17, where no signal is detected by the electrode, indicating agarose-NAD + The complex cannot be applied to the preparation of dehydrogenase electrodes.
Example 10 Effect of chitosan species on malate dehydrogenase electrode Performance
(1) Preparation of high viscosity chitosan-NAD + Composite material
5mL (1mg/mL) of NAD + aqueous solution was taken, 1mL of iodoacetic acid (1mg/mL) was added, and the mixture was reacted in a 70 ℃ water bath for 1 hour. To the above NAD + aqueous solution was added 1mL (1.3mM) of sodium thiosulfate solution, ph was adjusted to 11 with 1M NaOH, and the mixture was reacted in a water bath at 70 ℃ for 1 hour. Then adding 1mL of formaldehyde into a 70 ℃ water bath for reaction for 1 h. After the pH of the reaction system was adjusted to neutral by 1M HCl, NHS (10mg) and EDC (10mg) were added thereto, 10mL of a 0.1% solution of another type of chitosan (the other type of chitosan was a high-viscosity chitosan, and the viscosity thereof was 30-3000mpa. s) was added thereto, and the reaction was carried out in a 70 ℃ water bath for 1 hour.
(2) Preparation of malate dehydrogenase electrode
All electrochemical measurements were performed in a typical three-electrode system (CHI 760D, CH instrument). The three-electrode system comprises: the platinum electrode is used as a counter electrode, the Ag/AgCl electrode is used as a reference electrode, and the glassy carbon electrode is used as a working electrode. During the experiment, a glassy carbon electrode with the diameter of 3mm is sequentially coated with Al with a certain particle size 2 O 3 Polishing the slurry on polishing cloth to mirror surface, removing surface dirt after each polishing, cleaning in ultrasonic water bath for 1min for three times, and sequentially adding 1:1 ethanol and 1:1NHO 3 And (4) ultrasonic cleaning. After thorough washing, the mixture was washed with 0.20mol/L KNO 3 Middle record 1X 10 -3 mol/L K 3 Fe(CN) 6 The cyclic voltammetry curve of the solution is used for testing the performance of the electrode, the scanning speed is 50mV/s, and the scanning range is 0.6 to-0.2V. The difference in peak potential in the cyclic voltammogram obtained under laboratory conditions is below 80mV and as close to 64mV as possible, and the electrode is usable.
5 mu L of 0.1% carbon nanotube dispersion liquid is dripped on the pretreated working surface of the electrode, and the electrode is dried. The electrodes were immersed in an ABTS deposition stock solution (ABTS deposition stock solution containing 2.5mM/L FeCl) 3 、2.5mM/L K 3 Fe(CN) 6 200mM/L HCl and 1mM/L ABTS, used only for the day), different numbers of Cyclic Voltammetry (CV) scans were performed at a scan rate of 50mV/s over a potential range of-200 to 600 mV. The redox peaks in the interface are seen to increase once with the number of passes scanned and eventually approach coincidence, indicating that ABTS has been deposited on the electrode.And fully cleaning the working electrode and the working surface of the counter electrode by using deionized water, dripping 10 mu L of chitosan-NAD + aqueous solution on the working surface, and drying at room temperature. Immersing the newly prepared working surface of the electrode in an aqueous solution containing 25% of glutaraldehyde, taking out after 1 hour, and fully cleaning with deionized water to introduce a certain amount of active aldehyde groups into the chitosan modification layer on the surface of the electrode. The electrode working face was then immersed in a solution of malate dehydrogenase (240U/mL), removed after 1h, and washed thoroughly to remove loosely bound enzyme molecules. A10 mmol/L standard malic acid solution was prepared, and the response current intensity of the standard malic acid was measured using the prepared malate dehydrogenase electrode and compared with the electrode prepared from medium viscosity chitosan in example 2.
The experimental results are as follows:
the cyclic voltammetry curve shows (fig. 18) that the electric signals of other types of chitosan (high viscosity) solution modified electrodes (i) are obviously smaller than the electric signals of standard chitosan (medium viscosity) modified electrodes (ii), which indicates that the types of chitosan play an important role in the electrode modification process.
It should be noted that the above examples are only used to illustrate the technical solutions of the present invention and not to limit them. Although the present invention has been described in detail with reference to the examples given, those skilled in the art can modify the technical solution of the present invention as needed or equivalent substitutions without departing from the spirit and scope of the technical solution of the present invention.
Claims (13)
1. A method for preparing a lactate dehydrogenase electrode, the lactate dehydrogenase electrode comprising:
the substrate electrode is loaded with a substrate material, a medium is deposited on the surface of the substrate material, and the surface of the medium is coated with a coenzyme factor compound and lactate dehydrogenase;
the substrate material is selected from carbon materials;
the medium is 2,2' -dinitrobis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt;
the coenzyme factor complex is NAD + -chitosan complex, said NAD + The chitosan complex is formed by the reaction of NAD + Modifying amino on adenine to obtain artificial NAD coenzyme, and then covalently connecting the artificial NAD coenzyme with chitosan to prepare the artificial NAD coenzyme;
the preparation method of the lactate dehydrogenase electrode specifically comprises the following steps:
1) dripping a substrate material on the surface of the substrate electrode;
2) depositing a medium on the substrate electrode loaded with the substrate material prepared in the step 1) by adopting an electrochemical deposition method;
3) dripping a coenzyme factor compound on the material prepared in the step 2);
4) loading lactic dehydrogenase on the material prepared in the step 3);
in the step 4), enzyme is loaded on the material prepared in the step 3) and the cross-linking effect of glutaraldehyde on the enzyme is realized;
in the step 3), the coenzyme factor compound is NAD + -chitosan complex, specifically prepared by a process comprising:
3-1) to NAD + Adding iodoacetic acid into the aqueous solution, heating and reacting to obtain n 1-carboxymethyl-NAD + ；
3-2) at n 1-carboxymethyl-NAD + Adding a sodium thiosulfate solution into the aqueous solution, adjusting the pH to be alkaline, heating to react to obtain n 1-carboxymethyl-NADH, and simultaneously carrying out Dimroth rearrangement under a strong alkali condition to obtain n 6-carboxymethyl-NADH;
3-3) adding formaldehyde, heating and reacting to obtain c 6-carboxymethyl NAD + ；
3-4) adjusting the pH of the reaction system to be neutral, adding NHS and EDC, adding a chitosan solution, and heating to react to obtain chitosan-NAD + And (c) a complex.
2. The method of claim 1, wherein the substrate electrode is selected from a glassy carbon electrode, a gold electrode, a graphite electrode, and a carbon paste electrode.
3. The method of claim 2, wherein the substrate electrode is a glassy carbon electrode.
4. The method of claim 1, wherein the substrate material is selected from the group consisting of activated carbon, graphene, carbon nanofibers, carbon nanospheres, glassy carbon, carbon aerogel, and carbon nanotubes.
5. The method of claim 4, wherein the substrate material is carbon nanotubes.
6. The method for preparing a lactate dehydrogenase electrode according to claim 1, wherein the chitosan is medium-viscosity chitosan, and the viscosity is 200-400 mPa.s.
7. The method for preparing a lactate dehydrogenase electrode according to claim 1, wherein in the step 3-1), the heating reaction is water bath heating, and the water bath reaction condition is that the reaction is carried out at 60-80 ℃ for 0.5-3 h;
in the step 3-2), the pH is adjusted to be strong alkaline, the heating reaction is water bath heating, and the water bath reaction condition is that the reaction is carried out for 0.5-3 h at the temperature of 60-80 ℃;
in the step 3-3), the heating reaction is water bath heating, and the water bath reaction condition is that the reaction is carried out for 0.5-3 h at the temperature of 60-80 ℃;
in the step 3-4), the heating reaction is water bath heating, and the water bath reaction condition is that the reaction is carried out for 0.5-3 h at the temperature of 60-80 ℃.
8. The method for preparing a lactate dehydrogenase electrode according to claim 7, wherein in the step 3-1), the water bath reaction conditions are 70 ℃ for 1 hour;
in the step 3-2), the pH is adjusted to 10-11, and the water bath reaction conditions are 70 ℃ for 1 hour;
in the step 3-3), the water bath reaction condition is 70 ℃ for 1 h;
in the step 3-4), the water bath reaction condition is 70 ℃ for 1 h.
9. Use of the lactate dehydrogenase electrode prepared by the method according to any one of claims 1 to 8 in the preparation of a lactate dehydrogenase sensor.
10. A lactate dehydrogenase sensor comprising at least two electrodes, wherein at least one of the electrodes is the lactate dehydrogenase electrode produced by the production method according to any one of claims 1 to 8.
11. The lactate dehydrogenase sensor of claim 10, wherein the lactate dehydrogenase sensor comprises two or three electrodes;
in the lactate dehydrogenase sensor consisting of two electrodes, the electrodes are a working electrode and a counter electrode; wherein the working electrode is a lactate dehydrogenase electrode prepared by the preparation method of any one of claims 1 to 8;
in the lactate dehydrogenase sensor consisting of three electrodes, the electrodes are a working electrode, a counter electrode and a reference electrode; wherein the working electrode is the lactate dehydrogenase electrode prepared by the preparation method of any one of claims 1 to 8.
12. The lactate dehydrogenase sensor according to claim 11, wherein in the three-electrode enzyme sensor, the counter electrode is a platinum electrode; the reference electrode is an Ag/AgCl electrode;
the lactate dehydrogenase electrode includes: the carbon nanotube-based composite membrane electrode comprises a glassy carbon electrode, wherein a carbon nanotube is loaded on the glassy carbon electrode, 2 '-dinitrogen bis (3-ethylbenzthiazoline-6-sulfonic acid) diammonium salt is deposited on the surface of the carbon nanotube, and chitosan-NAD (nicotinamide adenine dinucleotide) is loaded on the surface of the 2,2' -dinitrogen bis (3-ethylbenzthiazoline-6-sulfonic acid) diammonium salt + A complex and lactate dehydrogenase.
13. A method of electrochemically measuring the concentration or presence of lactic acid, the method comprising: contacting the lactate dehydrogenase sensor of any one of claims 10-12 with a liquid sample having or suspected of having lactate, measuring the intensity of the response current of the target analyte to be measured, and analyzing the concentration or presence of the target analyte.
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