Metal Nanoparticles/Nanocellulose Composites-Based Non-Enzymatic Electrochemical glucose sensor and Preparation Method Thereof

Abstract

The invention discloses a metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor, comprising a three-electrode system composed of a working electrode, a counter electrode, and a reference electrode. The surface of the working electrode is coated with a metal nanoparticles/nanocellulose composites. The surface of the nanocellulose is modified with a strong cationic conducting polymer. The invention promotes the sensitivity and selectivity of glucose sensing with the linear range of 4 μM-15 mM and the detection limit of 1.4 μM. Therefore, the sensor possesses high sensitivity, high response speed, stable performance and high anti-interference ability. The preparation method of the metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor is simple and the cost is low. And enzyme is introduced into the preparation process.

Claims

1. A metal nanoparticle/nanocellulose composites-based non-enzymatic electrochemical glucose sensor is composed of a three-electrode system consisting of a working electrode, a counter electrode, and a reference electrode; the surface of the working electrode is coated with the metal nanoparticles/nanocellulose composites; and the surface of the nanocellulose is modified with a strong cationic conducting polymer; a loading capacity of the metal nanoparticles is 1%-20%, and the loading capacity of the metal nanoparticles is the ratio between the weight of the metal nanoparticles and the total weight of the composites; the cationic conducting polymer is polydiallyldimethylammonium chloride; the metal nanoparticles is Au or Pt nanoparticles, and the particle size is 2-10 nm.

2. The metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor of claim 1, wherein the rod-shaped nanocellulose is negatively charged, with a length of 150-200 nm and a diameter of 10-20 nm.

3. The metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor of claim 1, wherein the metal nanoparticles are obtained from a metal precursor, and the metal precursor is AuCl.sub.4.sup.− or PtCl.sub.6.sup.2−.

4. The metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor of claim 1, wherein the working electrode is a glassy carbon electrode, the counter electrode is a platinum wire or a platinum sheet, and the reference electrode is Ag/ AgCl electrode.

5. A preparation method of a metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor of claim 1, comprising: (1) carrying out oxidation treatment on microcrystalline cellulose by ammonium persulfate, and obtaining 0.1 wt % nanocellulose suspensions through dialysis, homogeneity and rotary evaporation; (2) mixing 500 ml of nanocellulose suspensions obtained in step (1) with 2.5-5.0 g of 20 wt % strong cationic conducting polymer, and ultrasonic dispersing for 1-2 hour and stirring for 12-24 hours; then adding 2.5-5.0 g of sodium chloride to the suspensions and continually stirring for 12-24 hours; centrifugal washing the suspensions for 5-8 times to obtaining 0.05 wt % strong cation conducting polymer-nanocellulose suspensions; (3) mixing 200 ml of strong cationic conducting polymer-nanocellulose suspension obtained in step (2) with 1.01-25.00 ml anion metal precursor aqueous solution, and the metal content in the metal precursor water solution is 1 mg/ml; ultrasonic dispersing the suspensions for 1-2 hour, and dropwise adding excessive NaBH.sub.4 aqueous solution to the suspensions under stirring; dialyzing the suspensions to obtaining metal nanoparticles/nanocellulose composites; (4) polishing and ultrasonic washing the working electrode; coating the surface of the working electrode with the metal nanoparticles/nanocellulose composites obtained in step (3) and drying the working electrode to obtaining the metal nanoparticles/nanocellulose composites modified working electrode; (5) composing metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor with the metal nanoparticles/nanocellulose composites obtained in step (4) modified working electrode, the counter electrode and the reference electrode.

6. The preparation method of the metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor of claim 5, wherein the process for step (1) further comprising: adding 5 g of microcrystalline cellulose into 300-500 ml ammonium persulfate solution, and the concentration of the ammonium persulfate solution is 1-2 mol/l; and stirring for 6-16 hours under 60-70° C. at a stirring speed of 500-600 r/min.

7. The preparation method of the metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor of claim 5, wherein in step (3), the metal precursor is AuCl.sub.4.sup.− or PtCl.sub.6.sup.2−; the concentration of the NaBH.sub.4 solution is 0.05 mol/l, and the dropwise adding quantity is 30-60 ml; and the dialysis is completed when an electric conductivity of dialysate is constant.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0025] FIG. 1 is a transmission electron microscopy image of Au/PDDA-CNCs composites of embodiment 1.

[0026] FIG. 2 shows the i-t curves of embodiment 1.

[0027] FIG. 3 shows the linear relationship diagram between a response current and glucose concentration.

[0028] FIG. 4 is a transmission electron microscope image of Pt/PDDA-CNCs composites of embodiment 2.

[0029] FIG. 5 shows the i-t curve under interfering substance of embodiment 2.

DETAILED DESCRIPTION OF THE INVENTION

[0030] The invention is further described in combination with drawings and embodiments.

Embodiment 1

[0031] A metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor was composed of a three-electrode system consisting of a glassy carbon electrode, a platinum wire and a Ag/AgCl electrode. The surface of the glassy carbon electrode was coated with the metal nanoparticles/nanocellulose composites. The rod-shaped nanocellulose was negatively charged by modifying with poly (diallyldimethylammonium chloride) (PDDA), with the length of 150-200 nm and the diameter of 10-20 nm. The metal nanoparticles in the composites is Au nanoparticles, with the particle size distribution range of 2.6-4.9 nm, and the average particle size of 3.75 nm. The loading capacity of Au nanoparticles was 5%.

[0032] The preparation method comprises:

[0033] (1) adding 5 g microcrystalline cellulose into 350 ml of 1 mol/l ammonium persulfate solution, and stirring for 16 hours under 60° C. at a stirring speed of 600 r/min; placing the suspensions in a dialysis tubing to dialyze until the suspension conductivity reached a stable value; carrying out homogeneity on the suspensions after dialyzing for 5 times under 25000 Psi; then carrying out rotary evaporation on the suspensions under 56° C. to obtaining 0.1 wt % nanocellulose (CNCs) suspensions;

[0034] (2) mixing 500 ml CNCs suspensions obtained in step (1) with 3.0 g of 20 wt % PDDA, and ultrasonic dispersing for 1 hour and stirring for 12 hours; adding 3.0 g of sodium chloride to the suspensions and continually stirring for 24 hours; centrifuging the suspensions for 20 min at a rotate speed of 17000 r/min for 5 times, and dispersing the suspensions with deionized water to obtaining 0.05 wt % PDDA-CNCs suspensions;

[0035] (3) mixing 200 ml PPDA-CNCs suspension obtained in step (2) with 5.26 ml of 1 mg Au/mL chloroauric acid aqueous solution, and ultrasonic dispersing for 1.5 hours; dropwise adding 40 ml 0.05 mol/1 NaBH.sub.4 solution to the suspension under magnetic stirring at a rotate speed of 500 r/min, and continually stirring for 2 hours; placing the suspensions in a dialysis tubing to dialyze until the suspension conductivity reached a stable value to obtaining Au/PDDA-CNCs composites;

[0036] (4) polishing the glassy carbon electrode with 0.5 μm and 0.05 μm alumina slurry, and ultrasonic washing with deionized water and ethyl alcohol sequentially; modifying the glassy carbon electrode by coating 5 μL of Au/PDDA-CNCs composites (the content is 1 mg/mL) obtained in step (3) with pipette; drying the electrode by infrared lamp to obtaining the glassy carbon electrode modified by Au/PDDA-CNCs compound;

[0037] (5) composing Au/PDDA-CNCs composites-based non-enzymatic electrochemical glucose sensor by taking the Au/PDDA-CNCs composites obtained in step (4) modified glassy carbon electrode as the working electrode, a platinum wire as the counter electrode, and a Ag/AgCl electrode as the reference electrode.

Embodiment 2

[0038] A metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor was composed of a three-electrode system consisting of a glassy carbon electrode, a platinum wire and a Ag/AgCl electrode. The surface of the glassy carbon electrode was coated with the metal nanoparticles/nanocellulose composites. The rod-shaped nanocellulose was negatively charged by modifying with poly (diallyldimethylammonium chloride) (PDDA), with the length of 150-200 nm and the diameter of 10-20 nm. The metal nanoparticles in the composites is Pt nanoparticles, with the particle size distribution range of 3.8-9.7 nm, and the average particle size of 6.1 nm. The loading capacity of Pt nanoparticles was 10%.

[0039] The preparation method comprises:

[0040] (1) adding 5 g microcrystalline cellulose into 400 ml of 1 mol/l ammonium persulfate solution, and stirring for 6 hours under 70° C. at a stirring speed of 600 r/min; placing the suspensions in a dialysis tubing to dialyze until the suspension conductivity reached a stable value; carrying out homogeneity on the suspensions after dialyzing for 5 times under 25000 Psi; then carrying out rotary evaporation on the suspensions under 56° C. to obtaining 0.1 wt % nanocellulose (CNCs) suspensions;

[0041] (2) mixing 500 ml CNCs suspensions obtained in step (1) with 4.0 g of 20 wt % PDDA, and ultrasonic dispersing for 1 hour and stirring for 24 hours; adding 4.0 g of sodium chloride to the suspensions and continually stirring for 24 hours; centrifuging the suspensions for 20 min at a rotate speed of 17000 r/min for 5 times, and dispersing the suspensions with deionized water to obtaining 0.05 wt % PDDA-CNCs suspensions;

[0042] (3) mixing 200 ml PPDA-CNCs suspension obtained in step (2) with 11.11 ml of 1 mg Pt/mL chloroplatinic acid aqueous solution, and ultrasonic dispersing for 2 hours; dropwise adding 50 ml 0.05 mol/1 NaBH.sub.4 solution to the suspension under magnetic stirring at a rotate speed of 500 r/min, and continually stirring for 2 hours; placing the suspensions in a dialysis tubing to dialyze until the suspension conductivity reached a stable value to obtaining Pt/PDDA-CNCs composites;

[0043] (4) polishing the glassy carbon electrode with 0.5 μm and 0.05 μm alumina slurry, and ultrasonic washing with deionized water and ethyl alcohol sequentially; modifying the glassy carbon electrode by coating 5 μL of Pt/PDDA-CNCs composites (the content is 1 mg/mL) obtained in step (3) with pipette; drying the electrode by infrared lamp to obtaining the glassy carbon electrode modified by Pt/PDDA-CNCs compound; (5) composing Pt/PDDA-CNCs composites-based non-enzymatic electrochemical glucose sensor by taking the Pt/PDDA-CNCs composites obtained in step (4) modified glassy carbon electrode as the working electrode, a platinum wire as the counter electrode, and a Ag/AgCl electrode as the reference electrode.

Embodiment 3

[0044] A metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor was composed of a three-electrode system consisting of a glassy carbon electrode, a platinum wire and a Ag/AgCl electrode. The surface of the glassy carbon electrode was coated with the metal nanoparticles/nanocellulose composites. The rod-shaped nanocellulose was negatively charged by modifying with poly (diallyldimethylammonium chloride) (PDDA), with the length of 150-200 nm and the diameter of 10-20 nm. The metal nanoparticles in the composites is Au nanoparticles, with the particle size distribution range of 2.2-3.9 nm, and the average particle size of 2.9 nm. The loading capacity of Pt nanoparticles was 1%.

[0045] For the preparation method, the differences with embodiment 1 are 300 ml of 1 mol/l ammonium persulfate solution in step (1), 2.5 g of 20 wt % PDDA, 2.5 g of sodium chloride, and continually stirring for 12 hours in step (2), 1.01 ml of 1 mgAu/mL chloroauric acid solution, 30 ml of NaBH.sub.4 solution, and ultrasonic dispersing for 1 hour in step (3). And other steps are of the same with embodiment 1.

Embodiment 4

[0046] A metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor was composed of a three-electrode system consisting of a glassy carbon electrode, a platinum wire and a Ag/AgCl electrode. The surface of the glassy carbon electrode was coated with the metal nanoparticles/nanocellulose composites. The rod-shaped nanocellulose was negatively charged by modifying with poly (diallyldimethylammonium chloride) (PDDA), with the length of 150-200 nm and the diameter of 10-20 nm. The metal nanoparticles in the composites is Pt nanoparticles, with the particle size distribution range of 6.8-16.3 nm, and the average particle size of 12.4 nm. The loading capacity of Pt nanoparticles was 20%.

[0047] For the preparation method, the differences with embodiment 2 are 500 ml of 1 mol/l ammonium persulfate solution in step (1), 5.0 g of 20 wt % PDDA, 5.0 g of sodium chloride, and ultrasonic dispersing for 2 hours in step (2), 25 ml of 1 mg Pt/mL chloroplatinic acid solution, and 60 ml of NaBH.sub.4 solution in step (3). And other steps are of the same with embodiment 2.

Embodiment 5

[0048] It is found that the obtained compound has good dispersion and no agglomeration by observing the metal nanoparticles/nanocellulose composites of embodiments 1-4 from transmission electron microscope.

[0049] FIG. 1 is a transmission electron microscope image of metal nanoparticles/nanocellulose composites of embodiment 1. As shown in FIG. 1, the CNCs were 150-200 nm in length and 10-20 nm in diameter. The particle size distribution range of Au nanoparticles was 2.6-4.9 nm, with the average particle size of 3.7 nm.

[0050] FIG. 4 is a transmission electron microscope image of metal nanoparticles/nanocellulose composites of embodiment 2. As shown in FIG. 4, the CNCs were 150-200 nm in length and 10-20 nm in diameter. The particle size distribution range of Pt nanoparticles was 3.8-9.7 nm, with the average particle size of 6.1 nm.

Embodiment 6: Performance Test

[0051] 6.1 Electrochemical Testing of Non-Enzymatic Electrochemical Glucose Sensor of Embodiment 1

[0052] Testing method: the electrochemical testing was performed on a electrochemical workstation by i-t operation mode at an applied potential of 0.2 V in 30 mL of 0.1M sodium hydroxide solution under 200 rpm magnetic stirring; the response current signals were recorded by adding a certain concentration of glucose at intervals of 50 s; as shown in FIG. 2 and FIG. 3, the time for reaching steady-state current after adding of glucose was less than 5 s, indicating that the electrochemical glucose sensor can detect glucose rapidly and sensitively.

[0053] As shown in FIG. 2 and FIG. 3, the non-enzymatic electrochemical glucose sensor of embodiment 1 exhibited the glucose sensing ability with a linear range of 4 μM-9.5 mM, high sensitivity of 62.8 μA mM.sup.−1 cm.sup.−2, a low detection limit of 1.4 μM (S/N=3) (related coefficient is 0.9994). It can be seen that the non-enzymatic electrochemical glucose sensor of embodiment 1 has wide detection linear range, high sensitivity, low detection limit for glucose sensing.

[0054] 6.2 Selectivity of Non-Enzymatic Electrochemical Glucose Sensor on Glucose Detection of Embodiment 2 Under Interference

[0055] Testing method: the electrochemical testing was performed on a electrochemical workstation by i-t operation mode at an applied potential of 0.2 V in 30 mL of 0.1M sodium hydroxide solution under 200 rpm magnetic stirring; the response current signals were recorded by adding a certain concentration of ascorbic acid, uric acid and glucose at intervals of 50 s, as shown in FIG. 5.

[0056] As shown in FIG. 5, the non-enzymatic electrochemical glucose sensor of embodiment 2 showed very small response current on ascorbic acid and uric acid. The response current of ascorbic acid and uric acid are negligible compared with that of glucose, suggesting the high selectivity of embodiment 2 for glucose detection.