Graphene for the Building of Electroanalytical Enzyme-Based Biosensors. Application to the Inhibitory Detection of Emerging Pollutants

Graphene and its derivates offer a wide range of possibilities in the electroanalysis field, mainly owing to their biocompatibility, low-cost, and easy tuning. This work reports the development of an enzymatic biosensor using reduced graphene oxide (RGO) as a key nanomaterial for the detection of contaminants of emerging concern (CECs). RGO was obtained from the electrochemical reduction of graphene oxide (GO), an intermediate previously synthesized in the laboratory by a wet chemistry top-down approach. The extensive characterization of this material was carried out to evaluate its proper inclusion in the biosensor arrangement. The results demonstrated the presence of GO or RGO and their correct integration on the sensor surface. The detection of CECs was carried out by modifying the graphene platform with a laccase enzyme, turning the sensor into a more selective and sensitive device. Laccase was linked covalently to RGO using the remaining carboxylic groups of the reduction step and the carbodiimide reaction. After the calibration and characterization of the biosensor versus catechol, a standard laccase substrate, EDTA and benzoic acid were detected satisfactorily as inhibiting agents of the enzyme catalysis obtaining inhibition constants for EDTA and benzoic acid of 25 and 17 mmol·L−1, respectively, and a maximum inhibition percentage of the 25% for the EDTA and 60% for the benzoic acid.


Introduction
A chemical sensor is defined by IUPAC as a device that transforms chemical information into an useful analytical signal [1]. The use of sensors has progressed over the years with the constant development of new technologies and devices. Researchers try to improve the selectivity of these designs with a wide range of techniques, such as the modification of the transducer material, the use of chemometric data processing, or the inclusion of sample pretreatment. An example of the former is the concept of biosensors. A biosensor may be described as a sensor combined with a recognition element from the biological world, which is the one responsible for conferring paramount selectivity. Actually, this is what makes the difference from common sensors and grants their success. Since the discovery of graphene and its derived products, they have been gaining importance in the sensors and biosensors field [2]; one of the reasons for this is due to their synergistic effect when they are implemented as transducing materials [3,4]. It can be proven that the usage of graphene is becoming widespread when you search how many publications exist with "graphene" as a keyword, since 2004, when graphene was strictly discovered. Almost 150,000 publications can be listed in total; from these, 14,117 can be found using the "graphene + sensor" keyword combination (data according to Scopus database).
Among others, graphene and its derivates have gained popularity in electroanalysis due to their interesting inherent properties, such as biocompatibility, low-cost raw materials, and their easy tuning [3,4]. In this work, graphene is used not only as a key material to New pollutants, also named emerging pollutants or contaminants of emerging concern (CECs), are appearing continuously. These chemicals have become an increasing problem over the years. Fortunately, at the same time, technology has been developed which has introduced new and improved methods to isolate and/or detect CECs in human consumption products. However, the existing commercial techniques are time-consuming and expensive, which encourages researchers to find new alternatives. Moreover, it must be considered that at this moment there are no reference methods in the European legislation to control the presence of these compounds in water. Nevertheless, different factors will force their consideration in the near future. The first reason is the conclusions from recently published articles, which determine that certain CECs, in special endocrine disruptors, interfere in the human and animal endocrine system [36][37][38]. The second reason is that these pollutants are not only found in water but also in soil and marine species such as shellfish and oily fish, increasing the contact of humans with these compounds with still unknown long-term effects. This work reports the preparation and characterization of a laccase-graphene biosensor for the detection of CECs (EDTA and benzoic acid) by the inhibition of the laccase enzyme.

Chemical and Reagents
All reagents were of an analytical grade and all solutions were prepared using deionized water from Milli-Q system (Millipore, Billerica, MA, USA). Samples for electrochemical measurements were prepared on phosphate buffer in the presence of KCl as a background electrolyte, reagents purchased from Merck KGaA (Darmstadt, Germany).
Finally, catechol, acid benzoic, and EDTA were purchased from Merck KGaA.

Electrochemical Measurements
Voltammetric measurements were performed on a AUTOLAB PGSTAT30 (Ecochemie, Netherlands) controlled by GPES software. Electrochemical Impedance Spectroscopy (EIS) experiments were performed on a Bas-Zahner IM6e (Kronach, Germany) potentiostat controlled by Thales software. For both electrochemical techniques a typical three electrode circuit was used. In the used assembly it can be found: the working electrode based on a graphite epoxy composite (electrode already optimized in our laboratory [39][40][41]), an Ag/AgCl (0.1 mol·L −1 KCl) electrode as a reference and a Pt electrode as a counter. All measurements were carried out at room temperature without stirring using as an electrolyte solution phosphate buffer 50 mmol·L −1 + KCl 100 mmol·L −1 at pH 7.4.
Parameters for the cyclic voltammetry (CV) measurement were optimized for its use; at the end, a scan rate of 10 mV·s −1 and a step potential of 0.001 V was applied. The analysis of CV was performed with the GPES software, in particular using the inset tool to calculate the base line and the corresponding peak height of the recorded data.

Sensor Characterization
Morphological characterization of the raw materials was carried essentially by Transmission Electron Microscopy (TEM); TEM images were obtained using a JEOL JEM-2011 microscope. Moreover, X-ray photoelectron spectroscopy (XPS) analysis was carried out to describe the structure of the synthetized GO; a SPECS PHOIBOS 150 hemispherical energy analyzer with monochromatic Cu-Kα radiation was used. CasaXPS software was used to acquire the fitted values.
Surface roughness assessment was done by processing of topographic atomic force microscopy (AFM) images obtained using a Veeco Dimension 3100 AFM Microscope (Bruker, Billerica, MA, USA).

Graphene Synthesis and Characterization
A top-down synthesis based on a modified Hummers' method was used for the synthesis of GO [16,18,42]. In short, the protocol consists of the addition of 1.5 g of graphite and 4.5 g of NaNO 3 to 35 mL of sulfuric acid (98%) cooled at 0 • C. Afterwards, 4.5 g of KMnO 4 in fine powder form was added in small portions over a period of 2 h, avoiding temperature from rising and the mixture was stirred for an additional 4 h. The resulting mixture was heated at 35 • C for 30 min and the oxidation process was completed by slowly adding 75 mL of deionized water. In this highly exothermic step, it is important to avoid boiling. The reaction finishes 15 min after being kept at 70 • C. In order to eliminate unreacted oxidizing compounds, the solution was treated with 300 mL of 10% hydrogen peroxide. The resulting brown paste (the densest GO) was washed multiple times with deionized water, recovering the solid by centrifugation at 6000 rpm. This process was repeated several times, till the pH approached neutrality. With a pH close to 7, the sample of GO was treated with cation and anion exchange resins to eliminate the remaining salt impurities. This was done just by placing in contact, under vigorous stirring, the sample and resin for 30 min. The separation was achieved by using a 50 µm sieve. Sulfate ions were eliminated with Ba(NO 3 ) 2 . Finally, the obtained slurry was dried in a vacuum oven at 60 • C for 48 h.

Graphene Oxide Modification and Immobilization of the Enzyme for the Biosensor Building
The graphite epoxy composite (GEC) electrode, used as base transducer, had an average geometric area of 28 mm 2 (Ø = 6 mm), as it is specified in the reference bibliography [39,40,43]; the composite conductive paste was added in an assembly formed by an electrical connector and a PVC tube. Afterwards, the conductive material was hardened in an oven at 40 • C. Finally, the electrode was polished with different grain sandpapers until a homogeneous and pristine surface was obtained. The polishing step can be applied when needed to regenerate the surface and obtain again the bare platform. Figure 1 sketches the construction process. the base line and the corresponding peak height of the recorded data.

Sensor Characterization
Morphological characterization of the raw materials was carried essentially by Transmission Electron Microscopy (TEM); TEM images were obtained using a JEOL JEM-2011 microscope. Moreover, X-ray photoelectron spectroscopy (XPS) analysis was carried out to describe the structure of the synthetized GO; a SPECS PHOIBOS 150 hemispherical energy analyzer with monochromatic Cu-Kα radiation was used. CasaXPS software was used to acquire the fitted values.
Surface roughness assessment was done by processing of topographic atomic force microscopy (AFM) images obtained using a Veeco Dimension 3100 AFM Microscope (Bruker, Billerica, MA, USA).

Graphene Synthesis and Characterization
A top-down synthesis based on a modified Hummers' method was used for the synthesis of GO [16,18,42]. In short, the protocol consists of the addition of 1.5 g of graphite and 4.5 g of NaNO3 to 35 mL of sulfuric acid (98%) cooled at 0 °C. Afterwards, 4.5 g of KMnO4 in fine powder form was added in small portions over a period of 2 h, avoiding temperature from rising and the mixture was stirred for an additional 4 h. The resulting mixture was heated at 35 °C for 30 min and the oxidation process was completed by slowly adding 75 mL of deionized water. In this highly exothermic step, it is important to avoid boiling. The reaction finishes 15 min after being kept at 70 °C. In order to eliminate unreacted oxidizing compounds, the solution was treated with 300 mL of 10% hydrogen peroxide. The resulting brown paste (the densest GO) was washed multiple times with deionized water, recovering the solid by centrifugation at 6000 rpm. This process was repeated several times, till the pH approached neutrality. With a pH close to 7, the sample of GO was treated with cation and anion exchange resins to eliminate the remaining salt impurities. This was done just by placing in contact, under vigorous stirring, the sample and resin for 30 min. The separation was achieved by using a 50 µm sieve. Sulfate ions were eliminated with Ba(NO3)2. Finally, the obtained slurry was dried in a vacuum oven at 60 °C for 48 h.

Graphene Oxide Modification and Immobilization of the Enzyme for the Biosensor Building
The graphite epoxy composite (GEC) electrode, used as base transducer, had an average geometric area of 28 mm 2 (Ø = 6 mm), as it is specified in the reference bibliography [39,40,43]; the composite conductive paste was added in an assembly formed by an electrical connector and a PVC tube. Afterwards, the conductive material was hardened in an oven at 40 °C. Finally, the electrode was polished with different grain sandpapers until a homogeneous and pristine surface was obtained. The polishing step can be applied when needed to regenerate the surface and obtain again the bare platform. Figure 1 sketches the construction process.  Once the conductive element of the proposed biosensor was ready, it was modified with GO. The selected technique to modify the electrode surface was drop casting, based on the physical adsorption of the GO to the base carbon material. Firstly, 40 µL of the GO dispersion (1 mg·mL −1 in deionized water) was deposited on the GEC electrode. It may be noted that the GO suspension must be sonicated previously for 1 h and centrifugated for 1 min at 800 rpm to use only the part of the dispersion that content the flakes with fewer layers. After this, the electrode was dried at 40 • C to promote physisorption. The RGO was obtained by the electrochemical reduction of the previous electrode. As it was first optimized [43], the reduction was carried out via CV; in particular, 10 cycles were applied in a potential range going from +1.90 V to −2.30 V at 0.1 V·s −1 .
The laccase enzyme was covalently bonded to the RGO via carbodiimide (EDAC, N-(3-dimethylaminopropyl)-N -ethylcarbodiimide hydrochloride) chemistry. The EDAC reaction proved to be the most suitable strategy to immobilize the enzyme since it is able to react (through a free amino group) with the remaining carboxylic groups from RGO (that were not reduced in the reduction step) to obtain the amide bond. Concretely, after the reduction, a solution of 10 mg·mL −1 of laccase in water was prepared, where 100 µL of EDAC solution (1000 ppm) and 50 µL of sulfo-NHS solution (1000 ppm) were added. Once the solution was homogenized, the RGO electrode was incubated overnight in an Eppendorf tube [44][45][46][47]. The last step was to clean the non-bonded compounds from the surface of the electrode by rinsing it for 1 h in the working phosphate buffer.
As Figure 2 depicts, the EDAC coupling agent is used to activate the carboxylic groups from the RGO surface and form an intermediate complex that can react with the primary amine group from the laccase chain. In this article, sulfo-NHS was additionally used to obtain a more stable and efficient intermediate complex.
Once the conductive element of the proposed biosensor was ready, it was modified with GO. The selected technique to modify the electrode surface was drop casting, based on the physical adsorption of the GO to the base carbon material. Firstly, 40 µL of the GO dispersion (1 mg·mL −1 in deionized water) was deposited on the GEC electrode. It may be noted that the GO suspension must be sonicated previously for 1 h and centrifugated for 1 min at 800 rpm to use only the part of the dispersion that content the flakes with fewer layers. After this, the electrode was dried at 40 °C to promote physisorption. The RGO was obtained by the electrochemical reduction of the previous electrode. As it was first optimized [43], the reduction was carried out via CV; in particular, 10 cycles were applied in a potential range going from +1.90 V to −2.30 V at 0.1 V·s −1 .
The laccase enzyme was covalently bonded to the RGO via carbodiimide (EDAC, N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride) chemistry. The EDAC reaction proved to be the most suitable strategy to immobilize the enzyme since it is able to react (through a free amino group) with the remaining carboxylic groups from RGO (that were not reduced in the reduction step) to obtain the amide bond. Concretely, after the reduction, a solution of 10 mg·mL −1 of laccase in water was prepared, where 100 µL of EDAC solution (1000 ppm) and 50 µL of sulfo-NHS solution (1000 ppm) were added. Once the solution was homogenized, the RGO electrode was incubated overnight in an Eppendorf tube [44][45][46][47]. The last step was to clean the non-bonded compounds from the surface of the electrode by rinsing it for 1 h in the working phosphate buffer.
As Figure 2 depicts, the EDAC coupling agent is used to activate the carboxylic groups from the RGO surface and form an intermediate complex that can react with the primary amine group from the laccase chain. In this article, sulfo-NHS was additionally used to obtain a more stable and efficient intermediate complex. Step 1: activation of the RGO using EDAC (and NHS to increase the efficiency), Step 2: bonding creation between the primary amine from the enzyme and the intermediate complex of the RGO surface. Finally, the catalytic reaction is described.

Study of the Synthesized Graphene Oxide
The obtained GO was characterized by TEM. Figure 3 shows some representative images resulting from this technique. Herein, the main part of graphene flakes was thin and transparent enough to see the CuTEM grid through them. The presence of GO was corroborated when its characteristic wrinkles were identified, present, for example, in Figure 3A,B,D [48,49]. The main presence of few layers of aggregates, which is supported because not only the transparency is achieved but also clear borders, is also noticed. Particularly, in Figure 3A,D can be seen clear and sharp edges, whereas in Figure 3B the presence of a large number of layers can be deduced from the multiple grey shades at the edge of the flake. These hypotheses were compared with the literature, where other researchers have similar TEM images [22,50,51]. The opaque materials in Figure 3C may be associated with the graphite residues coming from the starting synthesis reagents. Step 1: activation of the RGO using EDAC (and NHS to increase the efficiency), Step 2: bonding creation between the primary amine from the enzyme and the intermediate complex of the RGO surface. Finally, the catalytic reaction is described.

Study of the Synthesized Graphene Oxide
The obtained GO was characterized by TEM. Figure 3 shows some representative images resulting from this technique. Herein, the main part of graphene flakes was thin and transparent enough to see the CuTEM grid through them. The presence of GO was corroborated when its characteristic wrinkles were identified, present, for example, in Figure 3A,B,D [48,49]. The main presence of few layers of aggregates, which is supported because not only the transparency is achieved but also clear borders, is also noticed. Particularly, in Figure 3A,D can be seen clear and sharp edges, whereas in Figure 3B the presence of a large number of layers can be deduced from the multiple grey shades at the edge of the flake. These hypotheses were compared with the literature, where other researchers have similar TEM images [22,50,51]. The opaque materials in Figure 3C may be associated with the graphite residues coming from the starting synthesis reagents.  In addition to TEM, XPS analysis was carried out to study the obtained GO ( Figure  4). Table 1 presents the dominating groups assigned to C 1s core level after its deconvolution. Different groups could be found in the material, corresponding to the wide range of oxygen functional groups from the synthetic pathway. To confirm this hypothesis, the oxygen and carbon ratio was calculated, being equal to 2.14. Normally, the approved ratio values range between 2.1 and 2.9 for GPO samples [16].   In addition to TEM, XPS analysis was carried out to study the obtained GO ( Figure 4). Table 1 presents the dominating groups assigned to C 1s core level after its deconvolution. Different groups could be found in the material, corresponding to the wide range of oxygen functional groups from the synthetic pathway. To confirm this hypothesis, the oxygen and carbon ratio was calculated, being equal to 2.14. Normally, the approved ratio values range between 2.1 and 2.9 for GPO samples [16]. In addition to TEM, XPS analysis was carried out to study the obtained GO (Figur 4). Table 1 presents the dominating groups assigned to C 1s core level after its deconvolu tion. Different groups could be found in the material, corresponding to the wide range o oxygen functional groups from the synthetic pathway. To confirm this hypothesis, the oxygen and carbon ratio was calculated, being equal to 2.14. Normally, the approved ratio values range between 2.1 and 2.9 for GPO samples [16].    Briefly, the resulting material of the modified Hummers' method has similar properties and characteristics to comparable works in the literature [17,20,22,52], reflecting then the good performance.

Modification and Characterization of the Graphene Sensor
The optimization of the sensor assembly was carefully addressed. First, the optimal amount of GO solution to be deposited onto the electrode was studied. In this case, dropcasting was chosen as the modification method, due to its rapid and easy application. The effect of four different volumes (20,30,40, and 50 µL) of a 1 mg·mL −1 GO dispersion (in deionized water) was studied. As mentioned above, GO is not conductive. For this reason, after the deposition, it was reduced to RGO to analyze its response using electrochemical techniques. The analytical performance was studied by using a CV technique, by measuring the height of the oxidative peak at a potential of 0.18 V (vs. Ag/AgCl reference electrode) in the electrochemical standard [Fe(CN) 6 ] 3-/4-5 mmol·L −1 (diluted in phosphate buffer 50 mmol·L −1 at pH 7.4) as analyte. The goal was to find a volume that covers all the electrode surface and did not saturate the response. As can be observed in Figure 5A, the obtained results, together with visual checking, demonstrate that smaller volumes did not cover the whole area of the electrode, but at the same time volumes higher than 40 µL formed aggregates too large to be stacked in the surface for long periods of time, deteriorating any graphene benefits in the electrochemical responses. At the sight of these results, 40 µL was the selected volume for preparing the graphene-modified electrode. Briefly, the resulting material of the modified Hummers' method has similar properties and characteristics to comparable works in the literature [17,20,22,52], reflecting then the good performance.

Modification and Characterization of the Graphene Sensor
The optimization of the sensor assembly was carefully addressed. First, the optimal amount of GO solution to be deposited onto the electrode was studied. In this case, dropcasting was chosen as the modification method, due to its rapid and easy application. The effect of four different volumes (20,30,40, and 50 µL) of a 1 mg·mL −1 GO dispersion (in deionized water) was studied. As mentioned above, GO is not conductive. For this reason, after the deposition, it was reduced to RGO to analyze its response using electrochemical techniques. The analytical performance was studied by using a CV technique, by measuring the height of the oxidative peak at a potential of 0.18 V (vs. Ag/AgCl reference electrode) in the electrochemical standard [Fe(CN)6] 3-/4-5 mmol·L −1 (diluted in phosphate buffer 50 mmol·L −1 at pH 7.4) as analyte. The goal was to find a volume that covers all the electrode surface and did not saturate the response. As can be observed in Figure 5A, the obtained results, together with visual checking, demonstrate that smaller volumes did not cover the whole area of the electrode, but at the same time volumes higher than 40 µL formed aggregates too large to be stacked in the surface for long periods of time, deteriorating any graphene benefits in the electrochemical responses. At the sight of these results, 40 µL was the selected volume for preparing the graphene-modified electrode. The electrode surface was characterized also topographically via AFM, in order to visualize how the graphene was distributed onto the electrochemical platform. Figure 6A shows the surface of a bare GEC electrode, and Figure 6B,C is a representative region of a GO modified GEC electrode, all images have a scanned surface of 10 × 10 µm. As it can be seen in Figure 6A, the GEC electrode presents a crumpled surface with a root mean square roughness (RRMS) of 73.5 nm; meanwhile, the surface modified with GO has a RRMS of 123.3 nm. Those values, along with the AFM images, verify the presence of graphene flakes. Moreover, the 3D AFM image ( Figure 6C) indicates the presence of multiple and separated GO flakes, some of them clearly with less height than the others. Even in image 6C (marked with an arrow), it is possible to notice the GO wrinkles, also observed in TEM images ( Figure 3). To sum up, AFM images demonstrated the correct stacking of GO, which lays in the surface increasing the rugosity, and consequently, the active sites of the electrode surface. The electrode surface was characterized also topographically via AFM, in order to visualize how the graphene was distributed onto the electrochemical platform. Figure 6A shows the surface of a bare GEC electrode, and Figure 6B,C is a representative region of a GO modified GEC electrode, all images have a scanned surface of 10 × 10 µm. As it can be seen in Figure 6A, the GEC electrode presents a crumpled surface with a root mean square roughness (R RMS ) of 73.5 nm; meanwhile, the surface modified with GO has a R RMS of 123.3 nm. Those values, along with the AFM images, verify the presence of graphene flakes. Moreover, the 3D AFM image ( Figure 6C) indicates the presence of multiple and separated GO flakes, some of them clearly with less height than the others. Even in image 6C (marked with an arrow), it is possible to notice the GO wrinkles, also observed in TEM images (Figure 3). To sum up, AFM images demonstrated the correct stacking of GO, which lays in the surface increasing the rugosity, and consequently, the active sites of the electrode surface. One essential step for the building of the biosensor is the correct reduction of GO to RGO; in this work, the electrochemical reduction step was followed via CV, and verified with EIS by the comparison of the different surfaces. In Figure 5B, the CV plot corresponding to the electrochemical reduction of the GO to RGO is shown. Specifically, the good performance of the process was assessed through the oxidation and reduction peaks that appear in the range of −1.0 V to −0.5 V (vs. Ag/AgCl) (see insert on Figure 5B). According to the literature, these peaks are related to the reduction of oxygen groups present in the deposited GO in aqueous medium and neutral pH [20,53]. An EIS technique was also used to confirm the efficiency of the electrochemical reduction. The differences in the electrode surface of the sensors can give information on the electron transfer and thus demonstrates the increment in conductivity of the RGO. In this case, the impedance characterization experiments were carried out in [Fe(CN)6] 3-/4-5 mmol·L −1 between 0.5 MHz and 0.1 Hz at a sinusoidal voltage perturbation of 10 mV amplitude. Figure 5C shows the Nyquist plot for each modification phase; the bare GEC electrode, the electrode when the GO material was deposited and finally when the last material, RGO, was obtained. In the same figure is inserted the Randles' equivalent circuit, which includes: (i) Rs, the ohmic resistance of the bulk solution; (ii) Rct, the charge transfer resistance, which describes the difficulty of the electrochemical reaction; and (iii) CPE, a constant phase element, the component that gives information on the double layer capacitance. Figure 5C shows a smaller Rct for RGO-GEC electrode (206 Ω) than for GEC (1638 Ω) and GO-GEC (2256 Ω), indicating that the conductivity of graphene is regenerated with the electrochemical method applied in this work. Additionally, the data demonstrate the better conductivity of the RGO-modified electrode than the non-modified one.
These observations allowed us to confirm that GO is deposited correctly onto the GEC surface using 40 µL; moreover, it could be assumed that the reduction method is good enough to recover the conductive properties of graphene and proceed to covalently immobilize the enzyme via the EDAC reaction.

Electrochemical Response of the Laccase Biosensor
Once the enzyme was immobilized, EIS was used to compare and contrast the biosensor against the already-evaluated platform.
The results of Table 2 compare Rs, Rct and CPE values for the most significant steps of the electrode modification. The most characteristic value in impedance results is the Rct; in this case, it is easy to see the little difference between the electrodes, RGO (206 Ω) and the laccase-RGO (231 Ω) electrodes, which expose less resistance to the current flow than the bare one (1638 Ω). The effects seen in Rct of the laccase-RGO electrode could be explained with the negative charge formed in the carboxylic groups of the amino acids, which are deprotonated at pH 7.4, generating a minimal increase in the electronic transference between the electrode surface and the negative complex used as analyte. One essential step for the building of the biosensor is the correct reduction of GO to RGO; in this work, the electrochemical reduction step was followed via CV, and verified with EIS by the comparison of the different surfaces. In Figure 5B, the CV plot corresponding to the electrochemical reduction of the GO to RGO is shown. Specifically, the good performance of the process was assessed through the oxidation and reduction peaks that appear in the range of −1.0 V to −0.5 V (vs. Ag/AgCl) (see insert on Figure 5B). According to the literature, these peaks are related to the reduction of oxygen groups present in the deposited GO in aqueous medium and neutral pH [20,53]. An EIS technique was also used to confirm the efficiency of the electrochemical reduction. The differences in the electrode surface of the sensors can give information on the electron transfer and thus demonstrates the increment in conductivity of the RGO. In this case, the impedance characterization experiments were carried out in [Fe(CN) 6 ] 3-/4-5 mmol·L −1 between 0.5 MHz and 0.1 Hz at a sinusoidal voltage perturbation of 10 mV amplitude. Figure 5C shows the Nyquist plot for each modification phase; the bare GEC electrode, the electrode when the GO material was deposited and finally when the last material, RGO, was obtained. In the same figure is inserted the Randles' equivalent circuit, which includes: (i) Rs, the ohmic resistance of the bulk solution; (ii) Rct, the charge transfer resistance, which describes the difficulty of the electrochemical reaction; and (iii) CPE, a constant phase element, the component that gives information on the double layer capacitance. Figure 5C shows a smaller Rct for RGO-GEC electrode (206 Ω) than for GEC (1638 Ω) and GO-GEC (2256 Ω), indicating that the conductivity of graphene is regenerated with the electrochemical method applied in this work. Additionally, the data demonstrate the better conductivity of the RGO-modified electrode than the non-modified one.
These observations allowed us to confirm that GO is deposited correctly onto the GEC surface using 40 µL; moreover, it could be assumed that the reduction method is good enough to recover the conductive properties of graphene and proceed to covalently immobilize the enzyme via the EDAC reaction.

Electrochemical Response of the Laccase Biosensor
Once the enzyme was immobilized, EIS was used to compare and contrast the biosensor against the already-evaluated platform.
The results of Table 2 compare Rs, Rct and CPE values for the most significant steps of the electrode modification. The most characteristic value in impedance results is the Rct; in this case, it is easy to see the little difference between the electrodes, RGO (206 Ω) and the laccase-RGO (231 Ω) electrodes, which expose less resistance to the current flow than the bare one (1638 Ω). The effects seen in Rct of the laccase-RGO electrode could be explained with the negative charge formed in the carboxylic groups of the amino acids, which are deprotonated at pH 7.4, generating a minimal increase in the electronic transference between the electrode surface and the negative complex used as analyte. Moreover, CPE, a complex value with empirical significance, was adjusted. The results indicate changes that may be related to the double layer capacitance thickens the decrease. Rs, as mentioned above, describes the bulk features of the solution and the diffusion characteristics; therefore, it may not be affected by the modifications on the electrode surface as can be observed in the table, indicating the ideal situation. Finally, the resulting biosensor was tested versus a phenolic compound, catechol, which is a standard substrate of the laccase enzyme. In Figure 7A is shown the excellent performance of the enzyme by the comparison of the responses of each sensor against different concentrations of catechol. Note that the anodic peak was used as the analytical signal in the following experiments since, contrary to what was expected, it is the part where the synergistic effect of all the system elements was best [54][55][56]. In the calibration curves, observed a linear trend from 2 to 100 µmol·L −1 for the biosensor and a wider range for the bare and the RGO electrodes was observed, which goes from 2 to 1500 µmol·L −1 and from 2 to 800 µmol·L −1 respectively. In the same image is also noted a clear enhancement in the sensitivity of the system, increasing by more than threefold the initial slope value.
indicate changes that may be related to the double layer capacitance thickens the decrease. Rs, as mentioned above, describes the bulk features of the solution and the diffusion characteristics; therefore, it may not be affected by the modifications on the electrode surface as can be observed in the table, indicating the ideal situation. Finally, the resulting biosensor was tested versus a phenolic compound, catechol, which is a standard substrate of the laccase enzyme. In Figure 7A is shown the excellent performance of the enzyme by the comparison of the responses of each sensor against different concentrations of catechol. Note that the anodic peak was used as the analytical signal in the following experiments since, contrary to what was expected, it is the part where the synergistic effect of all the system elements was best [54][55][56]. In the calibration curves, observed a linear trend from 2 to 100 µmol·L −1 for the biosensor and a wider range for the bare and the RGO electrodes was observed, which goes from 2 to 1500 µmol·L −1 and from 2 to 800 µmol·L −1 respectively. In the same image is also noted a clear enhancement in the sensitivity of the system, increasing by more than threefold the initial slope value. Figure 7B compares GEC, RGO, and Lac-RGO responses against the same concentration of catechol. In the figure, as expected from the previous characterization, a current enhancement can be observed when the GEC electrode is modified with graphene. On the other side, some differences are appreciated when RGO and Lac-RGO responses are compared, which leads us to assume the laccase activity. Two of the most characteristic changes are observed in the oxidation baseline and the reduction peak. These facts are caused by the catalysis of the anodic reaction, and consequently there is a significant enlargement of the cathodic pathway.

Analytical Characterization of the Biosensor
Once the biosensor operation was confirmed, their analytical properties were studied in detail. The properties studied were the linear range, limit of detection (LOD), limit of quantification (LOQ), repeatability, intermediate precision, selectivity, and lifetime. Moreover, CPE, a complex value with empirical significance, was adjusted. The results indicate changes that may be related to the double layer capacitance thickens the decrease. Rs, as mentioned above, describes the bulk features of the solution and the diffusion characteristics; therefore, it may not be affected by the modifications on the electrode surface as can be observed in the table, indicating the ideal situation. Finally, the resulting biosensor was tested versus a phenolic compound, catechol, which is a standard substrate of the laccase enzyme. In Figure 7A is shown the excellent performance of the enzyme by the comparison of the responses of each sensor against different concentrations of catechol. Note that the anodic peak was used as the analytical signal in the following experiments since, contrary to what was expected, it is the part where the synergistic effect of all the system elements was best [54][55][56]. In the calibration curves, observed a linear trend from 2 to 100 µmol·L −1 for the biosensor and a wider range for the bare and the RGO electrodes was observed, which goes from 2 to 1500 µmol·L −1 and from 2 to 800 µmol·L −1 respectively. In the same image is also noted a clear enhancement in the sensitivity of the system, increasing by more than threefold the initial slope value. Figure 7B compares GEC, RGO, and Lac-RGO responses against the same concentration of catechol. In the figure, as expected from the previous characterization, a current enhancement can be observed when the GEC electrode is modified with graphene. On the other side, some differences are appreciated when RGO and Lac-RGO responses are compared, which leads us to assume the laccase activity. Two of the most characteristic changes are observed in the oxidation baseline and the reduction peak. These facts are caused by the catalysis of the anodic reaction, and consequently there is a significant enlargement of the cathodic pathway.

Analytical Characterization of the Biosensor
Once the biosensor operation was confirmed, their analytical properties were studied in detail. The properties studied were the linear range, limit of detection (LOD), limit of quantification (LOQ), repeatability, intermediate precision, selectivity, and lifetime.  Figure 7B compares GEC, RGO, and Lac-RGO responses against the same concentration of catechol. In the figure, as expected from the previous characterization, a current enhancement can be observed when the GEC electrode is modified with graphene. On the other side, some differences are appreciated when RGO and Lac-RGO responses are compared, which leads us to assume the laccase activity. Two of the most characteristic changes are observed in the oxidation baseline and the reduction peak. These facts are caused by the catalysis of the anodic reaction, and consequently there is a significant enlargement of the cathodic pathway.

Analytical Characterization of the Biosensor
Once the biosensor operation was confirmed, their analytical properties were studied in detail. The properties studied were the linear range, limit of detection (LOD), limit of quantification (LOQ), repeatability, intermediate precision, selectivity, and lifetime.
The linear range is generally defined as the area in the calibration curve where the signals are directly proportional to the concentration. This parameter is typically evaluated using the correlation coefficient. As can be observed in the inset of Figure 7A, the linear range found spanned from 2 to 100 µmol·L −1 . The correlation coefficient for this range was 0.992, indicating a satisfactory linearity.
Regarding the LOD and LOQ, there are multiple ways to calculate them, such as the use of the calibration curve for the target analyte (see Equation (1), where m is the slope of the calibration curve and σ the standard deviation of the response at a 95% confidence level), the measure of signal/noise ratio or by the use of the blank standard deviation [57,58]. In this work, we used the first option, obtaining an LOD of 2.1 µmol·L −1 and a LOQ of 7.7 µmol·L −1 .
The repeatability is defined for the European Medicines Agency (EMEA) as the "term that expresses the precision under the same operating conditions over a short interval of time" [59]. In this case, 10 consecutive measurements of a 50 µmol·L −1 catechol solution were performed, obtaining a relative standard deviation (RSD) value equal to 8%. Moreover, a second repeatability test was done to check the reliability of the biosensor during the day. For this purpose, 3 calibration experiments were repeated in 3 different time instants of the day (9 a.m., 1 p.m. and 4 p.m., see Figure 8A). The results showed an RSD for each point of the curve not larger than 8%. All repeatability tests were taken as positive, considering that a group of data is significantly equal when the RSD value is lower than 10%. In the EMEA guideline, is also defined the intermediate precision [59]. This term expresses "the within-laboratories variations, for example, when considering different days of analysis, different analyst or analysis in different equipment". This test measured, across three different days, three different calibration curves, from three regenerated biosensors, checking at the same time two parameters, the difference between days and the difference of the electrode surface regeneration procedure (see Figure 8B). The findings indicated that there were no differences between the regenerated electrodes or the measurements on different days (RSD = 6%). The last studied parameter was the lifetime of the biosensor (or the intermediate precision of different days). To perform this test, an electrode was stored in the fridge at 4 • C in a closed Eppendorf and a measurement was done every day (without regeneration of the surface) using a 50 µmol·L −1 catechol solution. The RSD results were 3% (n = 3).
To visualize the selectivity of the biosensor, a Principal Component Analysis (PCA) (executed in Matlab R2020a) was carried out to show the ability of the biosensor to distinguish between the different substances considered. In particular, six substances from different families were analyzed with a Lac-RGO-modified electrode. As can be seen in Figure 9, the score plot shows that substances without phenols in their molecular structure as ibuprofen and cadaverine have similar behaviors to the buffer response. This fact demonstrates then the correct performance against the specific substrates.
indicated that there were no differences between the regenerated electrodes or the mea urements on different days (RSD = 6%). The last studied parameter was the lifetime of th biosensor (or the intermediate precision of different days). To perform this test, an ele trode was stored in the fridge at 4°C in a closed Eppendorf and a measurement was don every day (without regeneration of the surface) using a 50 µmol·L −1 catechol solution. Th RSD results were 3% (n = 3). To visualize the selectivity of the biosensor, a Principal Component Analysis (PCA (executed in Matlab R2020a) was carried out to show the ability of the biosensor to disti guish between the different substances considered. In particular, six substances from d ferent families were analyzed with a Lac-RGO-modified electrode. As can be seen  Figure 9, the score plot shows that substances without phenols in their molecular structure as ibuprofen and cadaverine have similar behaviors to the buffer response. This fact demonstrates then the correct performance against the specific substrates. Figure 9. PCA Score plot for the three principal components of 6 different molecules, acetaminophen, cadaverine, catechin, 4-Ethylguaiacol, and ibuprofen. Table 3 was built to compare the results in the presented work with the others in the literature. From here, it can be concluded that our biosensor has a similar behavior to devices with similar properties, even if it is compared with electrodes that include more than one catalytic material.   Table 3 was built to compare the results in the presented work with the others in the literature. From here, it can be concluded that our biosensor has a similar behavior to devices with similar properties, even if it is compared with electrodes that include more than one catalytic material.

Kinetic and Inhibition Study
The kinetics in enzymatic studies is one of the most interesting features as it is unique for each enzyme and substrate. For this reason, this issue is normally studied in detail; Leonor Michaelis and Maud Menten developed one of the most common models. This relates the enzyme substrate concentration ([S]) with the reaction rate (V). In this model, the enzyme rate depicts a saturation curve arriving to a steady state situation. At this point, the reaction rate achieves its maximum (V max ). This typical behavior is clearly observable in Figures 7A and 8B. From here, Michaelis and Menten deduced their equation (Equation (2)), where K M is the Michaelis-Menten's constant, defined as the concentration of substrate needed to reach half of the maximum rate [71]. It is important to take into account that the K M and V max values will be unique for each pair of enzyme and substrate.
To determine experimentally these parameters, the Lineweaver-Burk linearization is normally used (see its tailored version in Equation (3)) [72]. However, to assure that the Michaelis-Menten kinetics are valid for the studied system, first, the Hills coefficient (h, see Equation (4)) is commonly calculated. In this way, when h results are being close to 1, a Michaelis-Menten model can be assumed.
In this work, the h estimated value from the catechol calibration curve was 0.99 ± 0.09, demonstrating that the Lac-RGO biosensor followed the already explained kinetics. The rate parameters K M and V max , obtained from Equation (4), were 2.62 ± 0.50 µmol·L −1 and 1.90 × 10 −4 ± 0.13 × 10 −4 A, respectively.
As commented in the introduction section, there are common household products that have been used for a long period of time, that are now under scrutiny due to their possible effects on the environment and health. Examples are the emerging pollutants found in cosmetics, processed food, or pharmaceutical compounds. The inhibition study of the Lac-RGO biosensor was carried out using benzoic acid and EDTA, two examples of CECs. Benzoic acid is a colorless crystalline compound that is widely used in pharmaceutical products either as an active product ingredient (for its antifungal properties) or as an excipient (as a lubricant in tablets). Both in the food and cosmetics industry, it is used as a preservative [73,74]. On the other hand, EDTA is a colorless and soluble product used in various and distinct applications; for example, in the paper industry as a metal chelate agent or in the food and cleaning industries as a preservative [75,76]. Regarding the legislated limits for the herein target compounds, there is not an individual value. Nevertheless, the WHO made preliminary studies that recommend as maximum values 5 mg·kg −1 for the benzoic acid and 600 µg·L −1 for the EDTA (values for drinking-water) [77,78].
Any substance that in a particular context can decrease the kinetics of an enzyme will be considered as an enzymatic inhibitor. As mentioned before, the Michaelis-Menten constants (Equation (2)) are unique for a specific enzyme-substrate system, so the presence of inhibitors will lead to renaming the K M and V max to K' M and V' max .
There are three modelled scenarios [23]. The first situation is competitive inhibition, where the inhibitor and the substrate compete for the same active site; thus, K M < K' M and V max = V' max . The second situation is named non-competitive inhibition; in this case, the inhibitor is not a direct competitor but is bound in an allosteric site that deactivates the enzyme. The changes in the constants are noted as K M = K' M and V max > V' max . Finally, the last scenario is the uncompetitive inhibition, where the inhibitor is bound, producing a bigger affinity between the substrate and the enzyme, leading to fewer active sites in the system, in that case K M > K' M and V max = V' max [72].
Experimentally, the changes can be elucidated comparing the Lineweaver-Burk linearization for different concentrations of inhibitor. In this sense, Figures 10 and 11 show the inhibition effects of different concentrations of benzoic acid and EDTA in a Lac-RGO electrode. Both figures show a typical behavior of the first scenario: a competitive inhibition. Figures 10A and 11A depict the calibration curves of catechol using a Lac-RGO electrode in the presence of different concentrations of benzoic acid and EDTA, respectively. Zone 1 highlighted the steady V max and zone 2 in the increase in K M with the inhibitor concentration. In Table 4 there are complementary data used to corroborate the conclusions from Figures 10A and 11A; concretely, it includes the slopes from the K' M and V' max (calculated from the linear regressions on Figures 10A and 11A), when inhibitor concentrations are varied. In this table, positive slopes confirm the Michaelis constant increase (significant variation of K' M with slope values above uncertainties), and the constant trend for the maximum velocity (the uncertainties include the zero-slope value). This state is supported by Figure 10B,C and Figure 11B,C, where the calculated K M ' and V max ' values, and their trends, are plotted.      Moreover, the inhibition constant (K I ) for each inhibitor. Table 4 shows the higher affinity of benzoic acid (25 mmol·L −1 ) to Laccase than EDTA (17 mmol·L −1 ). To calculate K I values, expression (5), corresponding to competitive inhibition, was used.
On a further visualization of the inhibition effect, Figure 12B,D shows the percentage of the inhibition achieved for each pollutant in 800 µmol·L −1 of catechol. A bigger effect for benzoic acid, as expected from the previous comments, was fulfilled. In detail, a maximum ≈ 60% of inhibition was reached for the benzoic acid system in front of the ≈25% for EDTA. Voltammograms presented in Figure 12A,C shows the biosensor response in front of the catechol in the presence or absence of the inhibitor. In each case, the shape of the RGO voltammogram profile is recovered ( Figure 7B) when benzoic acid and EDTA are in solution, indicating that laccase has lost its activity when they are present. To sum up, the expected inhibition effect was verified, permitting the quantification of EDTA and benzoic acid in controlled samples.
of the inhibition achieved for each pollutant in 800 µmol·L −1 of catechol. A bigger effect for benzoic acid, as expected from the previous comments, was fulfilled. In detail, a maximum ≈ 60% of inhibition was reached for the benzoic acid system in front of the ≈25% for EDTA. Voltammograms presented in Figure 12A,C shows the biosensor response in front of the catechol in the presence or absence of the inhibitor. In each case, the shape of the RGO voltammogram profile is recovered ( Figure 7B) when benzoic acid and EDTA are in solution, indicating that laccase has lost its activity when they are present. To sum up, the expected inhibition effect was verified, permitting the quantification of EDTA and benzoic acid in controlled samples.

Conclusions
The reported work has shown the capabilities of graphene as a nanomaterial to improve and facilitate the development of electrochemical biosensors, specifically those employing redox enzymes. The advantages observed can be attributed to two factors: the first one is the amelioration of the electrochemical transduction properties, thanks to inherent electrical characteristics of graphene. The second, the conjunction with the chemical properties of the material, as it serves as a linkage platform for immobilization of biomolecules such as enzymes.
All this makes this combination an unbeatable choice for electrochemical biosensing. The case specified in here, the biosensing of catechol, has demonstrated an improvement of sensitivity of ca. 30%, which in turn improves the direct determination of phenolic compounds or opens the door to consider inhibition. In this inhibitory biosensing application, two different chemicals, EDTA and benzoate, have been verified as inhibitors of the

Conclusions
The reported work has shown the capabilities of graphene as a nanomaterial to improve and facilitate the development of electrochemical biosensors, specifically those employing redox enzymes. The advantages observed can be attributed to two factors: the first one is the amelioration of the electrochemical transduction properties, thanks to inherent electrical characteristics of graphene. The second, the conjunction with the chemical properties of the material, as it serves as a linkage platform for immobilization of biomolecules such as enzymes.
All this makes this combination an unbeatable choice for electrochemical biosensing. The case specified in here, the biosensing of catechol, has demonstrated an improvement of sensitivity of ca. 30%, which in turn improves the direct determination of phenolic compounds or opens the door to consider inhibition. In this inhibitory biosensing application, two different chemicals, EDTA and benzoate, have been verified as inhibitors of the enzyme reaction, which may constitute the basis for a future analytical device or system to monitor CECs in water.