JP3064635B2 - Glucose biosensor - Google Patents

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

The present invention relates to a glucose biosensor. More specifically, the present invention relates to a glucose biosensor having improved durability.

[0002]

2. Description of the Related Art In conventional biosensors, when a film is to be further formed on an enzyme-immobilized film, the material is mainly cellulose acetate. The purpose of forming such a cellulose acetate-based membrane is to limit the diffusion of the substrate,
The purpose is to extend the calibration range. However, protein,
When trying to measure the amount of glucose in a solution containing lipids, carbohydrates, blood cells, etc., for example, in blood, these components adhere to the membrane surface and coagulate, resulting in a poor response and poor durability. There was a problem of inferiority.

[0003]

SUMMARY OF THE INVENTION An object of the present invention is to measure the amount of glucose in a solution containing proteins, lipids, carbohydrates, blood cells, etc. It is an object of the present invention to provide a glucose biosensor which does not adhere to or coagulate with the glucose biosensor, and therefore does not have a problem such that a response is inhibited or durability is poor.

[0004]

SUMMARY OF THE INVENTION The object of the present invention is as follows.
Sustained release of sodium ethylenediaminetetraacetate aqueous solution
This is achieved by a glucose biosensor in which a functional microcapsule is immobilized on a glucose oxidase-immobilized electrode and used as a working electrode.

[0005] Sodium ethylenediaminetetraacetate has a function of capturing calcium ions and preventing coagulation of blood and the like. Sodium ethylenediaminetetraacetate having such a function is encapsulated in a sustained-release microcapsule, and coagulation of blood or the like at a glucose oxidase-immobilized electrode in which it is immobilized is performed by sustained release of sodium ethylenediaminetetraacetate through the capsule wall. In this case, the durability of the glucose sensor response is improved.

[0006] The microencapsulation is carried out by a commonly used interfacial polymerization method, phase separation method, or the like. The formed microcapsules are made of gum arabic-gelatin, polyamide, polyimide, etc., and their particle size is generally not particularly limited to about 0.1 to 1000 μm, and an aqueous solution of sodium ethylenediaminetetraacetate encapsulated therein. Is not particularly limited.

[0007] The sustained-release microcapsules enclosing an aqueous solution of sodium ethylenediaminetetraacetate are immobilized on a glucose oxidase-immobilized electrode. As the electrode, a platinum electrode, a gold electrode, and the like are generally used. When immobilizing glucose oxidase on these electrode surfaces, it is preferable that the electrode surfaces are once covered with a vinyl chloride resin film and then immobilized.

[0008] The formation of the vinyl chloride resin film on the electrode is performed as follows. That is, a copolymer obtained by copolymerizing polyvinyl chloride or vinyl chloride with a small amount of ethylene, vinyl acetate, etc., is dissolved in a solvent such as dimethylformamide, cyclohexanone, tetrahydrofuran,
A solution of about 0.1 to 20% by weight dissolved in methyl ethyl ketone or the like is generally dropped directly on the electrode surface at room temperature and then air-dried, or the electrode surface is immersed in the solution,
After pulling up, air dry, wash with water and dry.

After the electrode surface is coated with the vinyl chloride resin film in this manner, it is immersed in a glucose oxidase aqueous solution having a concentration of about 1 to 200 mg / ml at 4 ° C. for about 1 to 120 minutes, pulled up and washed with water. Dry and immobilize glucose oxidase. Such a method for immobilizing glucose oxidase is not only simple, but also has excellent adhesion to the electrode surface of the vinyl chloride resin membrane and immobilization of glucose oxidase, and excellent results in terms of responsiveness. Is shown.

[0010] Immobilization of the sustained-release microcapsules encapsulating an aqueous solution of sodium ethylenediaminetetraacetate on such a glucose oxidase-immobilized electrode can be performed using a suitable adhesive substance such as a water-soluble photocrosslinkable resin, albumin, fibrinogen, chitosan, or the like. After dispersing the microcapsules in the solution, it is applied by a method of applying and curing.

To measure the glucose amount, a sensor having the working electrode obtained in this manner as a working electrode is connected to an ammeter, and a counter electrode (silver electrode, silver / silver chloride electrode) and a reference electrode of the ammeter (silver electrode). )
And applying a potential to the working electrode, and measuring the response to the glucose solution.

[0012]

According to the present invention, proteins, lipids, carbohydrates,
Even when used in a solution containing blood cells and the like, a glucose biosensor excellent in durability is provided.

[0013]

Next, the present invention will be described with reference to examples.

EXAMPLE A 0.5 μl dope solution consisting of a 10% by weight solution of polyvinyl chloride in cyclohexanone was applied on a platinum electrode (1.0 × 1.5 mm), left at room temperature for 1 minute, immersed in water and gelled. ,
A polyvinyl chloride film was formed.

This platinum electrode coated with a polyvinyl chloride film was immersed in a 1 mg / ml aqueous solution of glucose oxidase (manufactured by Sigma) at 4 ° C. for 24 hours to adsorb and immobilize glucose oxidase on the membrane surface.

[0016] Separately, a sustained-release microcapsule containing an aqueous solution of sodium ethylenediaminetetraacetate is
It was manufactured as follows. Aqueous solution containing 0.4 mol of 1,6-hexanediamine, 0.45 mol of sodium carbonate and 0.2 mol of sodium ethylenediaminetetraacetate 7.
After adding an equal amount of water to 5 ml, 15 ml of this diluted aqueous solution is
Chloroform in which 5% by volume of surfactant (Span 85) is dissolved
-It is added to 75 ml of a mixed solvent solution of cyclohexane (volume ratio 1: 4), and is stirred well to emulsify to form a W / O emulsion.

Five minutes after the emulsification, 0.6 g of terephthalic acid dichloride dissolved in 75 ml of the above mixed solvent is added while stirring (400 rpm) is continued at 4 ° C. This causes a condensation polymerization reaction between equimolar amounts of terephthalic acid dichloride and 1,6-hexanediamine on the surface of the water droplets in the emulsion,
A condensation polymer is obtained. Sodium carbonate is a neutralizing agent for the hydrogen chloride generated in this reaction. The resulting microcapsules (5 μm diameter) were centrifuged and collected.

0.5 ml of this sustained-release microcapsule encapsulating an aqueous solution of sodium ethylenediaminetetraacetate and an aqueous solution of a water-soluble photocrosslinkable resin (Toyo Gosei Kogyo, 11.1% aqueous solution of polyvinyl alcohol containing styrylpyridinium group)
Then, 0.5 μl of the mixture was applied on the glucose oxidase-immobilized polyvinyl chloride membrane-coated platinum electrode, and dried at 25 ° C. for 1 hour.
Irradiation was performed for 0 second, and after washing with water, ultraviolet irradiation was further performed for 30 seconds.

The electrode thus obtained was used as a working electrode. At an applied voltage of 0.7 V, a counter electrode consisting of a silver / silver chloride electrode was short-circuited to a reference electrode of an ammeter. The response to glucose was measured by measuring with LC-4B.

Specifically, the steady-state current value of the response to fresh swine blood immediately after blood collection was measured, and the measured value (150 nA) was calculated as 100%.
And The sensor is washed with saline after measurement and
Saved in. Such an operation was performed once a day.
After a day, the steady-state current value still maintained 95% of the initial value.

Comparative Example In the examples, a sustained-release microcapsule containing an aqueous solution of sodium ethylenediaminetetraacetate was not used, and only an aqueous solution of a water-soluble photocrosslinkable resin was applied on a platinum electrode coated with a glucose oxidase-immobilized polyvinyl chloride film, It was dried and irradiated with ultraviolet light.

When the response to glucose was similarly measured using the working electrode thus obtained, the steady-state current decreased to 10% of the initial value on the second day, and no response was observed on the third day. Was.

Claims (2)

(57) [Claims] 1. A glucose biosensor in which a sustained release microcapsule enclosing an aqueous solution of sodium ethylenediaminetetraacetate is fixed on a glucose oxidase-immobilized electrode, and used as a working electrode. 2. The glucose biosensor according to claim 1, wherein a glucose oxidase-immobilized vinyl chloride resin membrane-coated electrode is used as the glucose oxidase-immobilized electrode.