Electro-chemical sensor and coating method, production method and corresponding uses

Abstract

The invention relates to an electro-chemical sensor and coating method, production method and corresponding uses. The coating method of an electro-chemical sensor comprises the following steps: coating a carbon-rich substrate, with a carbon content greater than or equal to 0 wt. % in relation to the total weight of the substrate, and with an organic polymer; and applying a cold plasma treatment to said coating. This method permits the production of electro-chemical sensors with a carbon-rich substrate, with a carbon content greater or equal to 50 wt. % in relation to the total weight of the substrate, and a modified organic polymer coating. These new sensors are suitable for the detection of, inter alia, dopamine, glucose, uric acid and ascorbic acid.

Claims

1. An electrochemical sensor coating method, comprising the steps of: coating a carbon-rich substrate of the electrochemical sensor with an organic low density polyethylene (LDPE) coating, the substrate having a carbon content greater than or equal to 50% by weight with respect to the total weight of the substrate, and applying a cold plasma treatment to said coating thereby converting at least a portion of the LDPE coating surface into active species of carbon and oxygen, wherein the carbon-rich substrate is made of a material from the group consisting of graphite, glassy carbon, nanostructured carbons, and fullerenes.

2. The method according to claim 1, wherein said plasma is an atmospheric plasma, a vacuum plasma, or a corona energy plasma comprising between 0.1 mJ/cm.sup.2 and 100 J/cm.sup.2 in an atmosphere with oxygen, or nitrogen, or another inert gas.

3. The method according to claim 1, wherein the plasma application time is more than 1 s.

4. The method according to claim 3, wherein the plasma application time is more than 15 s.

5. The method according to claim 1, wherein the plasma application time is less than 120 s.

6. The method of claim 1, wherein the electrochemical sensor is for detection of dopamine, glucose, uric acid or ascorbic acid.

7. The method according to claim 1, wherein the nanostructured carbons comprise graphene or carbon nanotubes.

8. A production method for producing an electrochemical sensor comprising a carbon-rich substrate with a carbon content greater than or equal to 50% by weight with respect to the total weight of the substrate, wherein the method comprises the steps of claim 1.

9. An electrochemical sensor, comprising a carbon-rich substrate having a carbon content greater than or equal to 50% by weight with respect to the total weight of the substrate, and an organic low density polyethylene (LDPE) coating deposited on the carbon-rich substrate, wherein said LDPE coating has been treated by a cold plasma and the treated LDPE coating comprises carbon and oxygen as active species on its surface; wherein the carbon-rich substrate is made of a material from the group consisting of graphite, glassy carbon, nanostructured carbons, and fullerenes.

10. A method for detecting an analyte selected from the group consisting of dopamine, glucose, uric acid, and ascorbic acid, the method comprising contacting the analyte with the electrochemical sensor of claim 9.

11. The electrochemical sensor of claim 9, wherein the electrochemical sensor is for detection of dopamine, glucose, uric acid or ascorbic acid.

12. The electrochemical sensor of claim 9, wherein cold plasma is atmospheric plasma, air plasma, oxygen plasma, or nitrogen plasma.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) Other advantages and features of the invention can be seen from the following description in which preferred embodiments of the invention are described in a non-limiting manner in reference to the attached drawings. The drawing show:

(2) FIG. 1. Control voltammograms of 100 μM DA, 100 μM UA, and 100 μM AA in a 0.1 M phosphate-buffered saline (PBS) solution recorded using untreated substrates (electrodes): glassy carbon (GCE) bare GCE, poly(3,4-ethylenedioxythiophene)-coated GCE (PEDOT), and poly(N-cyanoethylpyrrole)-coated GCE (PNCPy).

(3) FIG. 2. Control voltammograms of 100 μM DA, 100 μM UA, and 100 μM AA in a 0.1 M phosphate buffer (PBS) solution recorded using plasma-air-treated substrates (electrodes): bare GCE, poly(3,4-ethylenedioxythiophene)-coated GCE (PEDOT), and poly(N-cyanoethylpyrrole)-coated GCE (PNCPy).

(4) FIG. 3. Control voltammograms of 100 μM DA in 0.1 M PBS collected in PEDOT-coated GCE treated with cold plasma prepared using different plasma-air application times (t.sub.cp).

(5) FIG. 4. Determination of the DA detection limit of PEDOT- and PNCPy-coated GCEs with plasma-air treatment.

(6) FIG. 5. Variation of anodic peak intensity (i.sub.p) in PEDOT-coated GCEs with cold plasma treatment with respect to plasma application time (t.sub.cp).

(7) FIG. 6. Control voltammogram of 1 mM DA in 0.1 M PBS in low-density polyethylene (LDPE)-coated GCE with and without plasma-air treatment. The first and third cycle for the electrode that is treated with plasma-air is shown.

(8) FIG. 7. Control voltammograms of 100, 10, and 1 μM DA in LPDE-coated GCEs treated with plasma-air. Right: Complete voltammograms; Left: Enlargement of the area associated with DA oxidation. In all the cases: scan rate: 100 mV/s; final and initial potentials: −0.40; Reversal potential: +0.80 V.

(9) FIG. 8. Micrograph obtained by means of scanning electron microscopy (SEM) of PEDOT-coated GCE not treated with plasma.

(10) FIG. 9. SEM micrograph of the PEDOT-coated GCE treated with plasma.

(11) FIG. 10. Cyclic voltammetries of 10 μM dopamine in a urine-like chemical using an LDPE-coated GCE treated with plasma-air.

(12) FIG. 11. Enlargement of the cyclic voltammetries in the area of oxidation of 10 μM dopamine in a urine-like chemical using an LDPE-coated GCE treated with plasma-air.

(13) FIG. 12. Oxidation peak intensity of urea with respect to oxidation and reduction cycles in a urine-like chemical using an LDPE-coated GCE treated with plasma-air.

(14) FIG. 13. Oxidation peak intensity of dopamine with respect to oxidation and reduction cycles in a urine-like chemical using an LDPE-coated GCE treated with plasma-air.

(15) FIG. 14. Enlargement of the cyclic voltammetries in the area of oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using an LDPE-coated GCE treated with plasma-air.

(16) FIG. 15. Oxidation peak intensity of DA with respect to oxidation and reduction cycles in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using an LDPE-coated GCE treated with plasma-air.

(17) FIG. 16: Absolute intensity and peak intensity of DA using GCE coated with conventional polymer and treated with plasma-air.

(18) FIG. 17. Oxidation peak intensity of DA using GCE coated with conventional polymer and treated with plasma-air.

(19) FIG. 18. Oxidation potential of DA using GCE coated with conventional polymer and treated with plasma-air.

(20) FIG. 19. Cyclic voltammetry of the oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using an isotactic polypropylene-coated GCE treated with and without plasma-air. The results are compared with GCE treated with and without plasma-air.

(21) FIG. 20. Cyclic voltammetry of the oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using a polyvinylpyrrolidone-treated (approximate mean molecular weight: 40,000) GCE treated with and without plasma-air. The results are compared with GCE treated with and without plasma-air.

(22) FIG. 21. Cyclic voltammetry of the oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using a poly(ethylene oxide)-coated (approximate mean molecular weight: 600,000) GCE treated with and without plasma-air. The results are compared with GCE treated with and without plasma-air.

(23) FIG. 22. Cyclic voltammetry of the oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using a poly(4-vinylphenol)-coated (approximate mean molecular weight: 25,000) GCE treated with and without plasma-air. The results are compared with GCE treated with and without plasma-air.

(24) FIG. 23. Cyclic voltammetry of the oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using a polycaprolactone-coated (approximate mean molecular weight: 7,000) GCE treated with and without plasma-air. The results are compared with GCE treated with and without plasma-air.

(25) FIG. 24. Cyclic voltammetry of the oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using a nylon 66 (polyamide PA 66)-coated GCE treated with and without plasma-air. The results are compared with GCE treated with and without plasma-air.

(26) FIG. 25. Cyclic voltammetry of the oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using a polystyrene-coated (from the manufacturer, Polymer Additives) GCE treated with and without plasma-air. The results are compared with GCE treated with and without plasma-air.

(27) FIG. 26. Cyclic voltammetry of the oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using a polyacrylic acid-coated (25% by weight in water, approximate mean molecular weight: 240,000) GCE treated with and without plasma-air. The results are compared with GCE treated with and without plasma-air.

(28) FIG. 27. Cyclic voltammetry of the oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using a poly(butylene succinate)-coated (sold under the brand name Bionolle®) GCE treated with and without plasma-air. The results are compared with GCE treated with and without plasma-air.

(29) FIG. 28. Cyclic voltammetry of the oxidation of 10 μM DA in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using an LDPE-coated GCE treated with cold plasma in oxidizing and reducing atmosphere.

(30) FIG. 29. Current vs. time density graph for the chronoamperometric detection of 1 mM glucose using a PEDOT-coated GCE treated with plasma-air on which the glucose oxidase enzyme has been immobilized. Injection of glucose into the detection cell starts at 300 s and is performed every 100 s.

(31) FIG. 30. Current vs. time density graph for the chronoamperometric detection of 1 mM glucose, 1 mM UA, 1 mM AA, and 1 mM DA using a PEDOT-coated GCE treated with plasma-air on which the glucose oxidase enzyme has been immobilized. Injection of glucose and different interfering substances into the detection cell starts at 500 s and is performed every 100 s.

(32) FIG. 31. Determination of the glucose detection limit of the GCE coated with PEDOT and with a plasma-air treatment. The glucose oxidase enzyme was immobilized on the surface of the electrode.

DETAILED DESCRIPTION OF SEVERAL EMBODIMENTS OF THE INVENTION

(33) Part One

(34) One of the surprising results of the present invention is the application of a cold plasma (plasma in which the ions and electrons are not in thermal equilibrium) as a very simple and effective technique for preparing electrochemical DA (dopamine) sensors. The experiments were initially performed using two conductive polymers, specifically PEDOT and PNCPy, which were deposited on bare GCE electrodes by means of chronoamperometry. The response of the two CPs with respect to DA was completely different. The selective and simultaneous detection of DA, UA (uric acid), and AA (ascorbic acid) using PNCPy is difficult because the oxidation peaks of each of these organic substances are weak and partially overlap one another, whereas, in contrast, the oxidation peaks are well resolved when PEDOT-coated electrodes are used. The behavior of PNMPy improves when the film is covered with gold nanoparticles (AuNPs), which demonstrates the electrocatalytic activity that the latter promote. In contrast, the properties of the PEDOT electrodes for the selective detection of DA remain virtually unchanged after the incorporation of AuNPs.

(35) Both the PEDOT films and the PNCPy films generated by anodic polymerization on a CGE electrode were modified by means of applying cold plasma surface treatment (corona plasma in ambient atmosphere at about 0.5 J/cm.sup.2 for 2 minutes).

(36) DA, UA, and AA detection assays (100 μM each) were carried out by means of cyclic voltammetry (CV) using a glass cell containing 10 ml of 0.1 M PBS (phosphate-buffered saline solution) at room temperature. FIGS. 1 to 5 show the voltammetric response of PNCPy- and PEDOT-coated GCEs not treated and treated with plasma. The voltammograms recorded using bare GCEs have been included for comparative purposes. Although plasma treatment causes a significant reduction in anodic peak intensity at 0.70 V for all the systems, it must be indicated that this effect is relatively small for anodic intensities associated with the oxidation of the three analytes. Furthermore, as can be seen, both the electrode with PEDOT and the electrode with PNCPy treated with plasma are capable of selectively detecting DA, UA, and AA oxidation, whereas PNCPy that is not treated is not capable of selectively distinguishing one from the other. As regards the bare GCE, it is not capable of selectively detecting the presence of AA in the mixture, regardless of the plasma treatment. In the case of electrodes treated with plasma, small or even imperceptible peaks have been identified in some voltammograms (marked with arrows in FIG. 1). These peaks, which are shifted with respect to the identified oxidation peaks, have been associated with the oxidation processes of AA (PNCPy, PEDOT, and bare GCE) or UA (only PNCPy) by means of non-predominant reactive species created during cold plasma treatment.

(37) FIGS. 1 and 2 show the control voltammograms of 100 μM DA, 100 μM UA, and 100 μM AA in 0.1 M PBS for bare GCE, PEDOT-coated GCE, and PNMPy-coated GCE. The arrows indicate oxidation processes. Scan rate: 100 mV/s. Initial and final potentials: −0.40 V; Reversal potential: +0.80 V.

(38) An important question is the influence the time during which plasma power (t.sub.cp) is applied has on the effective detection of DA. For this purpose, PEDOT-coated GCEs were treated considering different t.sub.cp values (i.e., from 15 to 120 s). FIG. 3 compares the voltammograms of 100 μM DA in 0.1 M PBS with these treated electrodes. As can be seen, t.sub.cp has zero influence on oxidation peak potential (E=0.176 V in all the cases). Similarly, t.sub.cp has very little influence on anodic peak intensity (i.sub.p). This is reflected in FIG. 5 which depicts the mean of the i.sub.p taking into account four different samples, with respect to t.sub.cp. Therefore, i.sub.p increases from 1.50 to 1.63 μA when t.sub.cp increases from 15 to 120 s. According to these results, t.sub.cp is not a decisive factor for the detection process once exceeding 15 s.

(39) FIG. 4 shows the determination of the DA detection limit (in the absence of UA, and AA) of PEDOT- and PNCPy-coated GCEs with cold plasma treatment by means of CV using a scan rate of 50 mV.Math.s.sup.−1. The results were derived from the standard addition of 10 μL of DA in 10 ml of 0.1 M PBS (i.e., a linear interval of 0.5 to 100 μM DA). The anodic peak intensity (ip) increases with the concentration of DA for the two electrodes. The detection limit, which was determined using a calibration curve for the concentration of DA comprised between 0.5 and 5 μM (box) was comprised between 140 and 750 nM for PEDOT and PNCPy, respectively. These values are significantly lower than those obtained for the untreated samples, and prove an improvement not of the resolution alone (particularly for PNCPy).

(40) Experimental Methods:

(41) Materials. 3,4-ethylenedioxythiophene (EDOT), N-(2-cyanoethyl)pyrrole (NCPy), acetonitrile, anhydrous salt lithium perchlorate (LiClO.sub.4), DA hydrochloride (3-hydroxytyramine hydrochloride), AA (L-configuration, crystalline), UA (crystalline) of analytical reagent grade. All chemicals acquired from the company Sigma Aldrich (Spain) were used without further purification. The 0.1 M phosphate buffer solution (PBS) with pH=7.4 was prepared as an electrolyte solution by mixing four stock solutions of NaCl, KCl, NaHPO.sub.4, and KH.sub.2PO.sub.4. High-purity nitrogen was used for the de-aeration of the prepared aqueous solutions.

(42) Conductive polymer synthesis. PEDOT and PNCPy films were prepared by means of chronoamperometry (CA) under a constant potential of 1.40 V using a two-compartment, three-electrode cell under nitrogen atmosphere (99.995% of purity) at 25° C. A bare glassy carbon electrode (GCE) with a diameter of 2 mm was used as the working electrode, whereas a AISI 316 steel sheet with a area of 1 cm.sup.2 was used as the counter electrode. The surface of the glassy carbon electrode was polished with alumina powder and cleaned by means of ultrasonication before depositing the polymer. The reference electrode was an Ag|AgCl electrode containing a saturated aqueous KCl solution (E°=0.222 V vs. standard hydrogen electrode at 25° C.) which was connected with the working compartment through a saline bridge containing the electrolyte solution. All electrochemical experiments were performed in an AUTOLAB PGSTAT302N potentiostat-galvanostat (Ecochimie, The Netherlands) equipped with the ECD module for measuring very low current densities (100 μA-100 μA), which was connected with a computer controlled by means of the NOVA 1.6 software.

(43) PEDOT and PNCPy films were obtained using 10 mM of a monomer solution in acetonitrile with 0.1 M of LiClO.sub.4 and a polymerization period comprised between 6 and 10 s, respectively.

(44) Cold plasma treatment. PEDOT- and PNCPy-coated GCEs were prepared with a corona discharge in ambient atmosphere using a BD-20AC from the company Electro-Technic Products. The BD-20AC works at a very high frequency in the MHz range, generating an electric field that is created around the electrode which is used for polymer surface treatment. The unit consists of a power control unit and a separate high-voltage handle. What differentiates it from other models is that it generates an adjustable high-voltage output comprised between 10,000 and 45,000 volts at a high frequency of 4.5 MHz. The polymers were treated using a spring tip wire electrode and a voltage of 45,000 volts at a high frequency of 4.5 MHz in all cases. After plasma treatment, the coated GCE electrodes were used for DA detection experiments within a period of 24 hours.

(45) Electrochemical measurements for the detection of DA. Electromechanical detection was carried out by means of cyclic voltammetry (CV) using the Autolab PGSTAT302N equipment described above. All electrochemical experiments were carried out in a glass cell containing 10 ml of 0.1 M PBS (pH=7.4) at room temperature and equipped with saturated Ag|AgCl as the reference electrode and a platinum (Pt) wire as the counter electrode. Voltammograms were recorded in the potential interval comprised between −0.40 and 0.80 V at a scan rate of 50 mV.Math.s.sup.−1 unless another scan rate is explicitly specified. All the electrodes were in contact with the electrolyte solution for 5 minutes before CV measurements.

(46) Part Two

(47) As a proof of concept, sensors made of GCEs coated with a very cost-effective and electrochemically inert polymer, i.e., low-density polyethylene, were produced and verified. Low-density polyethylene (LDPE) was deposited on the GCE by means of solution (34.4 mg of LDPE dissolved in 10 ml of dichlorobenzene at 95° C. by means of stirring for 4 hours). For the LDPE-coated GCE without cold plasma treatment, the cyclic voltammogram recorded in a 0.1 M PBS solution with 1 mM of DA does not provide any oxidation peak (FIG. 6) indicating that, as expected, LDPE is not able to detect said neurotransmitter. In contrast, the voltammogram recorded using an electrode produced in the same way, but applying a cold plasma treatment for 1 minute, shows a considerable potential at 0.20 V which corresponds to DA oxidation (FIG. 6). Considering that the concentration of DA estimated in the synapse is 1.6 mM, this result corroborates that efficient detectors can be produced by combining an organic matrix with a simple plasma-air treatment. Furthermore, this detector is very stable since it only decreases ˜2 μA (FIG. 6) after three consecutive oxidation-reduction cycles (i.e., detection cycles).

(48) FIG. 6 shows the control voltammogram of 1 mM DA in 0.1 M PBS in the LDPE-coated GCE. The voltammograms recorded using untreated electrodes (solid line) and electrodes treated with cold plasma (dash-dot: first detection cycle; dash-dash-dot: third detection cycle (Scan rate: 100 mV/s. Initial and final potentials: −0.40 V; Reversal potential: +0.80 V) As can be seen, LDPE-coated electrodes treated with a simple plasma-air for 1 minute are capable of detecting concentrations of DA similar to those estimated for the synapse for several cycles.

(49) Additional assays were carried out with LDPE-coated GCEs treated with cold plasma using concentrations of DA of 100, 10, and 1 μM. The results shown in FIG. 7 indicate that the oxidation of DA molecules was detected as a clear oxidation peak for the 100 μM solution (i.sub.p=0.033 μA and E=0.007 μA and E=0.164 V). Unfortunately, although the detection of the neurotransmitter was almost imperceptible in the 1 μM solution, the results shown in FIG. 7 are very promising given the simplicity of the electrode. Therefore, it should be emphasized that the limit for the electromechanical detection of DA in sophisticated 3-layer films made from PEDOT (outer and inner layer) and poly(N-methylpyrrole) (intermediate layer to create a dielectric effect) coated with AuNPs on the outer layer was 2 μM, whereas the limit in a GCE coated with a CP particularly designed to detect DA, i.e., poly(hydroxymethyl-3,4-ethylenedioxythiophene), was slightly higher.

(50) The surface of PEDOT-coated GCEs treated and untreated with plasma was examined using a scanning electron microscope (SEM) and energy dispersive X-ray spectroscopy (EDX). FIGS. 8 and 9 show the SEM micrographs of the PEDOT-coated GCE that is not treated and treated with plasma, respectively. The relatively compact morphology of the untreated samples (FIG. 8) which contains C, S, O, and Cl (chlorine is due to perchlorate dopant) transforms into a highly porous network of active species made up only of C and O (FIG. 10). Therefore, the electrochemical activity of polymer-coated GCEs treated with plasma could probably be attributed essentially to the surface incorporation of active species, which are possibly responsible for the detection of oxidized and reduced analytes. Similar characteristics have been observed in LDPE-coated GCEs.

(51) Part Three

(52) 1. GCE-LDPE with Plasma: Stability and Detection of 10 μM DA in a Urine-Like Chemical

(53) The pH of the urine-like chemical is 6.2, and the chemical composition is indicated below:

(54) TABLE-US-00001 Component mM Urea 200 Uric acid 1 Na.sub.3C.sub.6H.sub.5O.sub.7 5 NaCl 54 KCl 30 NH.sub.4Cl 15 CaCl.sub.2 3 MgSO.sub.4 2 NaHCO.sub.3 2 Na.sub.2C.sub.2O.sub.4 0.1 Na.sub.2SO.sub.4 9 KH.sub.2PO.sub.4 3.6 Na.sub.2HPO.sub.4 0.4 FeSO.sub.4 0.005 Lactic acid 1

(55) FIG. 11 shows the enlargement of the cyclic voltammetries in the area of oxidation of 10 μM dopamine in a urine-like chemical using an LDPE-coated GCE treated with plasma-air. FIG. 10 shows the cyclic voltammetries in the complete scan. The oxidation potential of dopamine is between 0.230-0.237 V, whereas the oxidation peak of urea and other components is at 0.418-0.425 V.

(56) FIG. 12 shows the oxidation peak intensity of urea and other compounds with respect to oxidation and reduction cycles in a urine-like chemical using an LDPE-coated GCE treated with plasma-air. The oxidation potential of urea and other compounds is between 0.418 and 0.425 V. The total cycles applied to the system are 10. The intensity loss after 10 oxidation/reduction cycles is about 18%.

(57) FIG. 13 shows the oxidation peak intensity of dopamine with respect to oxidation and reduction cycles in a urine-like chemical using an LDPE-coated GCE treated with plasma-air. The oxidation potential of dopamine is between 0.230 and 0.237 V. The total cycles applied to the system are 10. In this case, there is no intensity loss but there is indeed an increase of 25% after applying 10 oxidation/reduction cycles.

(58) 2. GCE-LDPE with Plasma: Stability and Detection of 10 μM DA in PBS

(59) FIG. 14 shows the enlargement of the cyclic voltammetries in the area of oxidation of 10 μM dopamine in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using an LDPE-coated GCE treated with plasma-air. The inserted box shows the cyclic voltammetries in the complete scan. The oxidation potential of dopamine is between 0.171 and 0.174 V.

(60) FIG. 15 shows the oxidation peak intensity of dopamine with respect to oxidation and reduction cycles in 0.1 M PBS (phosphate-buffered saline, pH 7.2) using an LDPE-coated GCE treated with plasma-air. The oxidation potential of dopamine is between 0.171 and 0.174 V. The total cycles applied to the system are 10. The intensity loss after 10 oxidation/reduction cycles is about 17%.

(61) 3. Alternative Substrates with Polyethylene

(62) Inorganic base substrates, i.e., substrates not rich in carbon (i.e., with less than 50% by weight of carbon with respect to the total weight of the substrate) have been tested. Specifically, ITO (indium tin oxide) substrate and AISI 316 stainless steel substrate have been tested, coated in both cases with a low-density polyethylene. In both cases, the substrates are negatively affected by plasma application and favorable results are not obtained.

(63) 4. Alternative Polymers

(64) Other conventional polymers applied on a GCE not treated and treated with plasma under the same conditions as LDPE have been assayed for the detection of 10 μM DA in PBS. The following table shows the assayed polymers, the solvent and amount of polymer used in the preparation of the film being indicated.

(65) TABLE-US-00002 AMOUNT OF POLYMER POLYMER SOLVENT (MG) o-dichlorobenzene, 10 ml 52.4 Isotactic polypropylene chloroform, 10 ml 43 Polyvinylpyrrolidone chloroform, 10 ml 43.6 Poly(ethylene oxide) methanol,  4 ml 11.8 Poly(4-vinylphenol) chloroform, 10 ml 46.5 Polycaprolactone hydrochloric acid, 10 ml 43.5 Nylon 66 chloroform, 10 ml 33.5 Polystyrene water 25 wt % Polyacrylic acid chloroform/ dichloromethane (50/50), 10 ml 47.6 poly(butylene succinate)

(66) The following table shows the intensities, labs (absolute, without baseline), and Ipeak (with baseline), and the oxidation potential obtained in the detection of 10 μM dopamine in 0.1 M PBS for GCE coated with conventional polymer and treated with cold plasma (oxidizing atmosphere).

(67) TABLE-US-00003 10 μM dopamine PLASMA Ipeak (μA) labs (μA) Eox (V) GCE - plasma 1.44E−01 3.12E−01 0.174 Poly(butylene succinate) - plasma 5.57E−02 2.49E−01 0.203 Polypropylene - plasma 1.14E−01 3.32E−01 0.174 Polyvinylpyrrolidone - plasma 1.14E−01 3.15E−01 0.174 Poly(ethylene oxide) - plasma 1.04E−01 2.17E−01 0.174 Poly(4-vinylphenol) - plasma 1.55E−01 3.81E−01 0.179 Polycaprolactone - plasma 1.91E−01 3.88E−01 0.171 Nylon 66 - plasma 9.81E−02 1.96E−01 0.179 Polystyrene - plasma 1.21E−01 3.05E−01 0.184 Polyacrylic acid - plasma 2.99E−02 1.89E−01 0.208

(68) FIGS. 16 to 27 show the results that are obtained. As can be seen, the application of plasma-air on other conventional polymers produces effects similar to those obtained with LDPE.

(69) 5. Non-Oxidizing Atmosphere

(70) Assays have been performed with non-oxidizing atmospheres, specifically with N.sub.2 atmosphere, with LDPE-coated GCE obtained according to the preceding conditions.

(71) The results that are obtained are shown in FIG. 29 and in the following table:

(72) TABLE-US-00004 Oxidizing Non-oxidizing atmosphere atmosphere Oxidation potential (V) 0.174 0.171 Peak intensity (μA) 2.03E−1 1.09E−1 Absolute intensity (μA) 6.27E−1   6E−1

(73) As can be seen, the use of non-oxidizing atmosphere in the application of cold plasma produces effects similar to those described with oxidizing atmosphere.

(74) Part Four

(75) Monitoring glucose levels in the human body is fundamental for the diagnosis and treatment of diabetes which has become a public health problem worldwide. Furthermore, monitoring glucose metabolism through the detection of changes in the concentration of this analyte can improve the treatment of brain diseases, such as, for example, tumors and brain injuries. The detection of glucose is also very important in the food processing, fermentation, and bio-fuel cell industry.

(76) Another surprising result of the present invention is the preparation of electrochemical glucose sensors by means of applying cold plasma surface treatment (corona plasma in ambient atmosphere at about 0.5 J/cm.sup.2 for 2 minutes) to polymer films deposited on a CGE.

(77) The selective and simultaneous detection of DA, UA (uric acid), and AA (ascorbic acid) using PNCPy is difficult because the oxidation peaks of each of these organic substances are weak and partially overlap one another, whereas, in contrast, the oxidation peaks are well resolved when PEDOT-coated electrodes are used. The behavior of PNMPy improves when the film is covered with gold nanoparticles (AuNPs), which demonstrates the electrocatalytic activity that the latter promote. In contrast, the properties of the PEDOT electrodes for the selective detection of DA remain virtually unchanged after the incorporation of AuNPs.

(78) Both the PEDOT films and the PNCPy films generated by anodic polymerization on a CGE electrode were modified by means of applying cold plasma surface treatment (corona plasma in ambient atmosphere at about 0.5 J/cm.sup.2 for 2 minutes). Glucose detection assays in the absence and presence of interfering substances (1 mM DA, UA, and AA) were carried out by means of chronoamperometry at room temperature. FIGS. 29 to 30 show the chronoamperometric response of the PEDOT-coated GCEs treated with plasma. As can be seen, the electrodes treated with plasma are capable of selectively detecting glucose oxidation. FIG. 31 shows the determination of the glucose detection limit of the GCE coated with PEDOT and with cold plasma treatment by means of chronoamperometry. The results were derived from successive standard injection of glucose. The detection limit which was determined using the calibration line obtained for a maximum concentration of glucose 14 mM was 1 mM.

(79) In conclusion, several very simple methods have been described for the electrochemical detection of DA or glucose, for example. Said methods have resulted in sensors with a resolution and sensitivity similar to those achieved by means of sophisticated chemical modifications, such as, for example, the incorporation of AuNPs to CP coatings, the preparation of multilayer CP compounds, or the functionalization of monomers. Furthermore, it has been demonstrated that these new methods were a success when applied not only to CPs, but also to layers of other non-electrochemically active polymers, such as LDPE, for example. This paves the way to a quick, easy, and simple way of producing sensitive detectors, for example, DA detectors, glucose detectors, etc., which can be implemented as very cost-effective diagnostic tests.