JP4250693B2 - Measuring method using redox reaction - Google Patents

Description

  The present invention relates to a method for measuring an object to be measured in a sample using an oxidation-reduction reaction.

  Conventionally, for example, measuring the amount of a measurement object in a sample using an oxidation-reduction reaction has been widely performed. For example, it is applied to the measurement of glycated protein in biochemical analysis and clinical examination.

  For example, glycated proteins in blood, in particular glycated hemoglobin (HbA1c) in erythrocytes, reflect the past history of biological blood glucose levels, and are therefore important indicators in diabetes diagnosis and treatment. For example, glycated protein in erythrocytes is measured as shown below using an oxidation-reduction reaction.

  First, a sample in which red blood cells are hemolyzed is prepared, and this hemolyzed sample is treated with an appropriate protease or the like, and then treated with fructosyl amino acid oxidase (hereinafter referred to as FAOD) to generate hydrogen peroxide. This amount of hydrogen peroxide corresponds to the amount of glycated protein in red blood cells. A peroxidase (hereinafter referred to as POD) and a reducing agent are added to the sample, and an oxidation-reduction reaction is caused between the hydrogen peroxide and the reducing agent using the POD as a catalyst. At this time, if a reducing agent that develops color when oxidized is used as the reducing agent, the amount of hydrogen peroxide can be measured by measuring the color development. As a result, the amount of glycated protein in erythrocytes can be known. it can.

  However, various reducing substances such as ascorbic acid (AsA) and bilirubin usually exist in blood, and various reducing substances such as glutathione (GSH) exist in red blood cells. By these reducing substances, the hydrogen peroxide may be reduced, the oxidation-reduction reaction may be inhibited, or the reducing agent may be reduced and faded after coloring. For this reason, there is a problem that it is difficult to accurately measure the amount of glycated protein in erythrocytes.

  Moreover, since the concentration of the reducing substance contained in each sample is not constant, there is a problem that measurement accuracy is inferior.

  In order to avoid such a problem, for example, there is a method of adding various oxidizing agents to the sample. For example, Japanese Patent Application Laid-Open No. 56-151358 (Patent Document 1) discloses a method using a halogen oxide such as iodic acid or periodic acid as an oxidizing agent. Patent Document 2), Japanese Patent Application Laid-Open No. 57-161650 (Patent Document 3), Japanese Patent Application Laid-Open No. 59-193354 (Patent Document 4), Japanese Patent Application Laid-Open No. 62-169053 (Patent Document 5), Japanese Patent Application Laid-Open No. Hei 3 Japanese Patent No. 30697 (Patent Document 6) discloses a method using a metal complex such as cobalt, iron, cerium or the like as an oxidizing agent.

However, even when these oxidants are used, the above-described influence on the measurement cannot be sufficiently avoided. In particular, when the measurement object is an erythrocyte component, the effect of the oxidant as described above is low. It was.
JP-A-56-151358 JP-A-57-13357 Japanese Unexamined Patent Publication No. 57-161650 JP 59-193354 A JP-A-62-169053 JP-A-3-30697

  Therefore, an object of the present invention is to provide a method for measuring a measurement object in a sample using an oxidation-reduction reaction, and to provide a measurement method that can obtain a measurement value with excellent reliability.

In order to achieve the above object, the measurement method of the present invention is a method for measuring an object to be measured in a sample using a redox reaction, wherein a tetrazolium compound is added to the sample prior to the redox reaction. The influence of the reducing substance contained in the sample is eliminated, and then a reducing substance or an oxidizing substance derived from the measurement object is generated, and this amount is measured by an oxidation-reduction reaction. It is characterized by determining the quantity. The tetrazolium compound has a ring structure substituent in at least two positions of the tetrazole ring, and the ring structure substituent includes a phenyl group, a tolyl group, a diphenyl group, a styrylphenyl group, a thienyl group, and Each compound is selected from the group consisting of dimethylthiazoyl groups .

  As a result of intensive studies, the present inventors have found that, according to conventional methods, for example, the influence of low molecular weight reducing substances such as GSH and AsA is not excluded, but high molecular weights such as proteins are not excluded. I found out that the effects of reducing substances were not excluded. Then, the present inventors have found that according to the tetrazolium compound, for example, the influence of not only the low molecular weight reducing substance but also other reducing substances can be eliminated, and the measurement method of the present invention has been reached. According to the measurement method of the present invention, it is possible to determine the amount of the measurement object with higher reliability, and thus it is useful for various examinations in clinical medicine, for example.

  In the measurement method of the present invention, by adding the tetrazolium compound to the sample, the influence of the reducing substance in the sample can be eliminated, so that measurement with excellent reliability can be performed. Therefore, the measurement method of the present invention can be applied to various analyzes in clinical medicine, for example, and is particularly useful for measurement of glycated proteins such as glycated hemoglobin in erythrocytes, which is important in diabetes diagnosis.

In the measurement method of the present invention, the tetrazolium compound has a ring structure substituent in at least two positions of the tetrazole ring, more preferably three positions, and the ring structure substituent includes a phenyl group, a tolyl group, a diphenyl group, Each is selected from the group consisting of a styrylphenyl group, a thienyl group, and a dimethylthiazoyl group.

  As described above, when the tetrazolium compound has a ring structure substituent in at least two positions of the tetrazole ring, it is preferable to have the substituent at the 2-position and the 3-position of the tetrazole ring. Moreover, when a tetrazolium compound has a ring structure substituent in three places, it is preferable to have the said substituent in 2nd-position, 3rd-position, and 5th-position of the said tetrazole ring.

In the method of the present invention, the ring structure of at least two ring substituents is a benzene ring. Examples of the ring structure substituent other than the benzene ring include a substituent having S or O in the ring skeleton and having a resonance structure, such as a thienyl group and a thiazoyl group.

  In the measurement method of the present invention, the tetrazolium compound has a ring structure substituent in at least three positions of the tetrazole ring, and the ring structure of at least two of the ring structure substituents is a benzene ring. Is preferred.

  In the measurement method of the present invention, it is preferable that at least one ring structure substituent has a functional group, and it is more preferable that the number of the functional groups is large.

Examples of the functional group include unsaturated hydrocarbon groups such as a phenyl group (C ₆ H ₅ —) and a styryl group (C ₆ H ₅ CH═CH—). The functional group may be ionized by dissociation.

In the measurement method of the present invention, the tetrazolium compound may have the functional group at any position (ortho-, meta-, pra) in the benzene ring. The number of functional groups is not particularly limited, and may have the same functional group or different functional groups.

In the measurement method of the present invention, the tetrazolium compound is, for example, a compound having a benzene ring structure substituent at the 2-position, 3-position and 5-position of the tetrazole ring, for example, 3,3 ′-(1,1′- biphenyl-4,4'-Gilles) - bis (2,5-diphenyl) -2H- tetrazolium salt, 2,5-diphenyl-3-(p-diphenyl) yl tetrazolium salt, 2,3-diphenyl-5- ( p-diphenyl) tetrazolium salt, 2,5-diphenyl-3- (4-styrylphenyl) tetrazolium salt, 2,5-diphenyl-3- (m-tolyl) tetrazolium salt and 2,5-diphenyl-3- (p -Tolyl) tetrazolium salt and the like.

Further, the tetrazolium compound is not limited to the above-mentioned compounds, and in addition, a compound having a benzene ring structure substituent at two positions of the tetrazole ring and another ring structure substituent at one position can be used. Examples thereof include 2,3-diphenyl-5- (2-thienyl) tetrazolium salt and 3- (4,5-dimethyl-2-thiazoyl) -2,5-diphenyl-2H-tetrazolium salt.

Further, tetrazolium compounds having a benzene ring structure substituent at two positions of the tetrazole ring and a substituent not having a ring structure at one position can also be used, for example, 2,3 -diphenyl-5-methyltetrazolium salt, 2,3-diphenyl Examples include -5-ethyltetrazolium salt.

Among the above-mentioned tetrazolium compounds, as described above, a compound having three cyclic substituted groups are preferred, more preferably the ring structure is one having three substituents is a benzene ring. Such a tetrazolium compound may be, for example, a salt or an ionized state.

  In the measurement method of the present invention, the amount of the tetrazolium compound added is not particularly limited, and can be appropriately determined depending on the type of sample and the amount of the reducing substance. Specifically, for example, the tetrazolium compound is preferably added so as to be in the range of 0.001 to 100 μmol per 1 μl of the sample, more preferably in the range of 0.005 to 10 μmol, and particularly preferably 0.00. The range is 01 to 1 μmol.

In the measurement method of the present invention, when the sample is whole blood, the tetrazolium compound is preferably added in a range of 0.001 to 10 μmol per 1 μl of whole blood, more preferably 0.005 to 5 μmol. The range is particularly preferably 0.01 to 1 μmol .

  In the measurement method of the present invention, it is preferable that the oxidation substance derived from the measurement object is hydrogen peroxide, and the measurement of the oxidation-reduction reaction is measurement of the amount of hydrogen peroxide.

  The measurement of the amount of hydrogen peroxide is preferably a measurement using an oxidase and a substrate that develops color by oxidation (hereinafter referred to as a chromogenic substrate).

The chromogenic substrate is not particularly limited. The oxidase is preferably peroxidase.

In the measurement method of the present invention, the type of the sample is a hemolyzed sample.

  In the measurement method of the present invention, examples of the measurement target include whole blood components, erythrocyte components, plasma components, serum components, urine components, and cerebrospinal fluid components, preferably erythrocyte components. is there. Examples of the erythrocyte component include glycated proteins such as glycated hemoglobin and glycated albumin, glycated peptides, glycated amino acids, glucose, uric acid, cholesterol, creatinine, sarcosine, and glycerol, and more preferably glycated proteins. For example, when measuring the red blood cell component, a sample obtained by hemolyzing whole blood as it is may be used as a sample, or a sample obtained by separating red blood cells from whole blood and hemolyzing the red blood cells may be used as a sample.

  In the measurement method of the present invention, it is preferable to generate hydrogen peroxide by oxidatively degrading the sugar portion of the glycated protein with FAOD. In addition, the glycated peptide and glycated amine are preferably allowed to act on FAOD as well. The glycated protein or glycated peptide is preferably treated with a protease before the FAOD treatment, if necessary.

  As said FAOD, it is preferable that it is FAOD which catalyzes reaction shown to following formula (1).

In the formula (1), R ¹ means a hydroxyl group or a residue (sugar residue) derived from a sugar before saccharification reaction. The sugar residue (R ¹ ) is an aldose residue when the sugar before the reaction is aldose, and is a ketose residue when the sugar before the reaction is ketose. For example, when the sugar before the reaction is glucose, the structure after the reaction takes a fructose structure due to Amadori rearrangement. In this case, the sugar residue (R ¹ ) becomes a glucose residue (aldose residue). This sugar residue (R ¹ ) is, for example,
_{- [CH (OH)] n} -CH 2 OH
N is an integer of 0-6.

In the formula (1), R ² is not particularly limited. For example, in the case of a glycated amino acid, a glycated peptide or a glycated protein, the α-amino group is glycated and the other amino groups are glycated. It differs depending on the case.

In the formula (1), when the α-amino group is glycated, R ² is an amino acid residue or a peptide residue represented by the following formula (2).

In the formula (2), R ³ represents an amino acid side chain group. R ⁴ represents a hydroxyl group, an amino acid residue, or a peptide residue, and can be represented by, for example, the following formula (3). In the following formula (3), n is an integer of 0 or more, and R ³ represents an amino acid side chain group as described above.

In the formula (1), when an amino group other than the α-amino group is saccharified (the amino acid side chain group is saccharified), R ² can be represented by the following formula (4).

In the formula (4), R ⁵ is the amino acid side chain, showing a portion other than the glycated amino group. For example, when the glycated amino acid is lysine, R ⁵ is —CH ₂ —CH ₂ —CH ₂ —CH ₂ —.
And
For example, when the glycated amino acid is arginine, R ⁵ is
—CH ₂ —CH ₂ —CH ₂ —NH—CH (NH ₂ ) —
It is.

In the formula (4), R ⁶ is hydrogen, an amino acid residue or a peptide residue, and can be represented by, for example, the following formula (5). In the following formula (5), n is an integer of 0 or more, and R ³ represents an amino acid side chain group as described above.

In the formula (4), R ⁷ is a hydroxyl group, an amino acid residue or a peptide residue, and can be represented by the following formula (6), for example. In the following formula (6), n is an integer of 0 or more, and R ³ represents an amino acid side chain group as described above.

In the measurement method of the present invention, the reducing substance in the sample is not particularly limited, but the molecular weight is 10,000 or more , preferably in the range of 10,000 to 3,000,000, more preferably. It is in the range of 10,000 to 300,000, particularly preferably in the range of 30,000 to 100,000.

Moreover, it is preferable that the said reducing substance in a sample is protein. The molecular weight of the protein, preferably, 10, the range of 000～3,000,000, more preferably in the range of 10,000 to 300,000, particularly preferably from 30,000 to 100,000. Examples of such a reducing substance include hemoglobin, globin, globulin, and albumin, and hemoglobin is preferable.

  Next, the measurement method of the present invention will be described with an example of measuring glycated protein in blood cells.

  First, whole blood is hemolyzed as it is, or a blood cell fraction is separated from whole blood by a conventional method such as centrifugation, and this is hemolyzed to prepare a hemolyzed sample. The hemolysis method is not particularly limited, and for example, a method using a surfactant, a method using ultrasonic waves, a method using a difference in osmotic pressure, and the like can be used. Among these, the method using the surfactant is preferable for reasons such as ease of operation.

  Examples of the surfactant include polyoxyethylene-pt-octylphenyl ether (Triton surfactant, etc.), polyoxyethylene sorbitan alkyl ester (Tween surfactant, etc.), polyoxyethylene alkyl ether ( Nonionic surfactants such as Brij type surfactants can be used, and specific examples include Triton X-100, Tween-20, Brij 35, and the like. The treatment conditions with the surfactant are usually such that when the blood cell concentration in the treatment solution is 1 to 10% by volume, the surfactant is adjusted so that the concentration in the treatment solution is 0.01 to 5% by weight. Add and stir at room temperature for a few seconds (about 5 seconds) to about 10 minutes.

  Next, the tetrazolium compound having the tetrazole ring structure is added to the hemolyzed sample, and the sample is pretreated.

For example, when the blood cell concentration in the pretreatment solution is 1 to 10% by volume, the tetrazolium compound is preferably added so that the concentration is in the range of 0.02 to 2000 mmol / liter, and more preferably 0.1 to 0.1%. It is in the range of ~ 1000 mmol / liter, particularly preferably in the range of 0.4 to 200 mmol / liter .

  The pretreatment is usually performed in a buffer solution. Examples of the buffer include CHES buffer, CAPSO buffer, CAPS buffer, phosphate buffer, Tris buffer, EPPS buffer, and HEPES buffer. The pH is, for example, in the range of 6 to 13, preferably in the range of 8 to 12, and more preferably in the range of 9 to 11. Moreover, the final concentration of the buffer solution in the pretreatment solution is, for example, in the range of 1 to 400 mmol / liter, and preferably in the range of 10 to 200 mmol / liter.

  The conditions for this pretreatment are not particularly limited, but are usually in the range of a temperature of 10 to 37 ° C. and a treatment time of 10 seconds to 60 minutes.

  The tetrazolium compound may be used as it is, but it is preferably used as a tetrazolium compound solution dissolved in a solvent from the viewpoint of easy operation and processing efficiency. The concentration of the solution can be appropriately determined depending on the type of tetrazolium compound (for example, molecular weight, etc.), and is, for example, in the range of 0.01 to 120 mmol / liter, preferably in the range of 0.1 to 50 mmol / liter. Is in the range of 0.2-20 mmol / liter. As the solvent, for example, distilled water, physiological saline, buffer solution, or the like can be used. As the buffer solution, for example, the same buffer solution as described above can be used. In addition, the said tetrazolium compound may be one type and may use 2 or more types together.

  Next, a protease treatment is performed on the pretreated hemolyzed sample. This is for facilitating the action of the FAOD used for the subsequent processing on the measurement object.

  The kind of the protease is not particularly limited, and for example, protease K, subtilisin, trypsin, aminopeptidase and the like can be used. The protease treatment is usually performed in a buffer solution, and the treatment conditions are appropriately determined depending on the type of protease to be used, the type of glycated protein that is a measurement target, the concentration thereof, and the like.

  Specifically, for example, when the pretreated hemolyzed sample is treated with protease K as the protease, the protease concentration in the reaction solution is usually 10 to 30,000 mg / liter, and the blood cell concentration in the reaction solution is 0. It is the range of 05-15 volume%, reaction temperature 15-37 degreeC, reaction time 1 minute-24 hours, and pH 6-12. Further, the type of the buffer solution is not particularly limited, and for example, Tris-HCl buffer solution, EPPS buffer solution, PIPES buffer solution and the like can be used.

  Next, the degradation product obtained by the protease treatment is treated with the FAOD. By this FAOD treatment, the reaction represented by the formula (1) is catalyzed.

  This FAOD treatment is preferably performed in a buffer solution as in the protease treatment. The processing conditions are appropriately determined depending on the type of FAOD to be used, the type of glycated protein that is a measurement target, its concentration, and the like.

  Specifically, for example, the FAOD concentration in the reaction solution is 50 to 50,000 U / liter, the blood cell concentration in the reaction solution is 0.01 to 1% by volume, the reaction temperature is 15 to 37 ° C., the reaction time is 1 to 60 minutes, and the pH is 6 It is the range of ~ 9. Further, the type of the buffer solution is not particularly limited, and the same buffer solution as in the protease treatment can be used.

  Next, the hydrogen peroxide generated by the FAOD treatment is measured by a redox reaction using POD and the chromogenic substrate.

  As the chromogenic substrate, for example, N- (carboxymethylaminocarbonyl) -4,4′-bis (dimethylamino) diphenylamine sodium, orthophenylenediamine (OPD), a substrate obtained by combining a Trinder reagent and 4-aminoantipyrine Etc. Examples of the Trinder reagent include phenol, phenol derivatives, aniline derivatives, naphthol, naphthol derivatives, naphthylamine, naphthylamine derivatives, and the like. In addition to the aminoantipyrine, aminoantipyrine derivatives, vanillin diamine sulfonic acid, methylbenzthiazolinone hydrazone (MBTH), sulfonated methylbenzthiazolinone hydrazone (SMBTH) and the like can also be used. Among such chromogenic substrates, as described above, N- (carboxymethylaminocarbonyl) -4,4'-bis (dimethylamino) diphenylamine sodium is particularly preferable.

  The oxidation-reduction reaction is usually performed in a buffer solution, and the conditions are appropriately determined depending on the concentration of the generated hydrogen peroxide. Usually, the POD concentration in the reaction solution is 10 to 100,000 IU / liter, the chromogenic substrate concentration is 0.005 to 30 mmol / l, the reaction temperature is 15 to 37 ° C., the reaction time is 0.1 to 30 minutes, and the pH is 5 to 9. The buffer solution is not particularly limited, and for example, the same buffer solution as the protease treatment and FAOD treatment can be used.

  In the oxidation-reduction reaction, for example, when the chromogenic substrate is used, the amount of hydrogen peroxide can be measured by measuring the degree of color development (absorbance) of the reaction solution with a spectrophotometer. For example, the amount of glycated protein in the sample can be determined using the hydrogen peroxide concentration and the calibration curve.

  The amount of hydrogen peroxide can be measured by, for example, an electrical method in addition to the enzymatic method using the POD or the like.

  In this measurement method, the pretreatment step with the tetrazolium compound is not particularly limited as long as the oxidation-reduction reaction substantially occurs as described above, but hydrogen peroxide is generated after the FAOD treatment. It is preferably performed before the FAOD treatment. Moreover, although each process process may be performed separately as mentioned above, there exists a process process which may be performed simultaneously by the combination as shown below, for example.

1: hemolysis treatment + pretreatment 2: hemolysis treatment + pretreatment + protease treatment 3: protease treatment + FAOD treatment 4: FAOD treatment + POD oxidation-reduction treatment 5: protease treatment + FAOD treatment + POD oxidation-reduction treatment The order of adding the substrates is not particularly limited.

  Thus, by contacting the sample with a tetrazolium compound, not only the influence of low molecular weight reducing substances such as GSH, AsA, dithiothreitol, cysteine, N-acetyl-cysteine, but also proteins and molecular weights as described above, for example. It is also possible to avoid the influence of the reducing substance within the range.

  In the pretreatment step with the tetrazolium compound in the measurement method of the present invention, for example, an oxidizing agent other than the tetrazolium compound may be used in combination. Examples of the oxidizing agent include halogen oxides such as sodium iodoacetate, iodoacid, and periodic acid, EDTA-Fe, ascorbate oxidase, bilirubin oxidase, and the like. The amount of the oxidizing agent added is, for example, in the range of 0.001 to 0.1 mg per 1 μl of sample.

  In the measurement method of the present invention, the measurement object is not particularly limited as long as it uses an oxidation-reduction reaction. In addition to the glycated protein, for example, as described above, a glycated peptide, a glycated amino acid, glucose, Examples include cholesterol, uric acid, creatinine, sarcosine, glycerol and the like.

  For example, when hydrogen peroxide is generated to measure the amount of each measurement object, for example, glucose oxidase for glucose, cholesterol oxidase for cholesterol, uricase for uric acid, and creatinine Sarcosine oxidase, sarcosine oxidase on the sarcosine, glycerol oxidase on the glycerol, and hydrogen peroxide may be generated. The method for measuring the amount of hydrogen peroxide can be performed in the same manner as described above. The glycated peptide and glycated amino acid can be measured in the same manner as the measurement of the glycated protein, for example.

  Further, after treatment of the reducing substance in the sample with the tetrazolium compound, a reducing substance derived from the measurement object is generated, this amount is measured by an oxidation-reduction reaction, and the amount of the measurement object is determined from this measurement value. In this case, for example, measurement can be performed as shown below.

  For example, when the measurement object is glucose, a reducing substance such as NADH or NADPH is generated using glucose dehydrogenase in the presence of NAD or NADP, for example. Then, NADH and NADPH, which are reducing substances derived from the measurement object, are measured by an oxidation-reduction reaction using, for example, diaphorase and a substrate that develops color by reduction. And as above-mentioned, the quantity of the measuring object in a sample can be calculated | required using the density | concentration of a reducing substance derived from this measuring object, a calibration curve, etc., for example. Further, for example, when the measurement object is cholesterol, cholesterol dehydrogenase can be used, and when the measurement object is sarcosine, sarcosine dehydrogenase can be used.

  The substrate that develops color by reduction is not particularly limited. For example, a color-forming tetrazolium compound added to eliminate the influence of the reducing substance in the sample may be used. Depending on each measurement wavelength, a color-developing tetrazolium compound of a different type from that used for the pretreatment of the sample may be used. In addition to the color-forming tetrazolium compound, for example, 2,6-dichlorophenolindophenol can also be used. In order to obtain a more reliable measurement value, for example, it is preferable to measure the absorbance in advance before measuring the reducing substance derived from the measurement object.

  Thus, if the sample is treated with the tetrazolium compound, the influence of not only the low molecular weight reducing substance but also the high molecular weight reducing substance such as protein as described above can be avoided. For this reason, when a reducing substance having a molecular weight of 10,000 or more or a reducing substance that is a protein is affected, the invention is not limited to the whole blood sample, and can be applied to various samples as described above. When a sample other than the whole blood sample is used, measurement can be performed in the same manner using the same reagent except that the sample is different.

  Next, examples will be described together with comparative examples.

( Reference Example 1, Comparative Example 1)
The reference example, pretreated samples below tetrazolium compounds are examples in which the influence of reducing substances in the sample. The reagents and methods used are shown below.

(Surfactant solution)
Polyoxyethylene (10) -pt-octylphenyl ether (hereinafter referred to as Triton X-100) was prepared by mixing with purified water to a concentration of 0.1% by volume.

(WST-3 solution)
In purified water, 2- (4-iodophenyl) -3- (2,4-dinitrophenyl) -5- (2,4-disulfophenyl) -2H-tetrazolium, mono was added so that the concentration was 1 mmol / liter. A sodium salt (WST-3, manufactured by Dojindo Laboratories) was dissolved and prepared.

(Fructosylvaline solution)
Fructosylvaline (hereinafter referred to as FV) was produced according to JP-A-2-69644 (hereinafter the same). The FV was prepared by adding to a 0.5 mol / liter Tris-HCl buffer (pH 8.0) to a concentration of 50 μmol / liter.

(Redox reaction solution A)
FAOD (Asahi Kasei Kogyo Co., Ltd .: The same applies below) 28.6 KU / L POD (Toyobo Co., Ltd .: The same applies below) 14.3 KU / L DA-64 (Wako Pure Chemical Industries, Ltd .: The same applies below) 28.6 μmol / L Distilled water residue Whole blood of a healthy person was centrifuged (1630 G, 10 minutes) to collect blood cells. The blood cells were diluted 20 times (volume) with the Triton X-100 solution and hemolyzed to obtain hemolyzed samples.

  After adding 50 μl of 0.5 mol / liter CHES buffer (PH9.0) to 50 μl of the sample, 100 μl of the WST-3 solution was added, and after stirring, treated at 37 ° C. for 10 minutes. After the treatment, 400 μl of the FV solution was added to the treated sample, and then 1400 μl of the oxidation-reduction reaction solution A was added to start the reaction. Then, the absorbance of the reaction solution at 726 nm was measured.

As a control, measurement was performed in the same manner as described above except that distilled water was used instead of the hemolyzed sample. As Comparative Example 1, measurement was performed in the same manner as in Reference Example 1 except that distilled water was used instead of the WST-3 solution.

  Then, these measured values were substituted into the following formula (Equation 1) to obtain a relative value (%) when the absorbance of the control was 100%. These results are shown in Table 1 below.

Thus, by treating the hemolyzed sample of blood cells with the tetrazolium compound, the influence of the reducing substance in the sample can be eliminated, and the reliability of the measurement is improved.
(Comparative Example 2 and Comparative Example 3)
Blood cells were collected in the same manner as in Reference Example 1, and this was diluted 5 times (volume) with 1.0 volume% Triton X-100 solution, and hemolyzed sample was used as a hemolyzed sample. To 50 μl of this hemolyzed sample, 150 μl of a 1.0 mol / liter sodium iodoacetate (Aldrich: hereinafter the same) solution was added, stirred, and then treated at 37 ° C. for 10 minutes. After the treatment, 400 μl of the FV solution was added to the treated sample, and then 1400 μl of the oxidation-reduction reaction solution A was added to initiate the reaction. Then, the absorbance was measured in the same manner as in Example 1, and the relative value (%) to the control was determined. This was designated as Comparative Example 2. As a control, measurement was performed in the same manner as described above except that distilled water was used instead of the hemolyzed sample.

In Comparative Example 3, measurement was performed in the same manner as in Reference Example 1 except that distilled water was added instead of the sodium iodoacetate solution. These results are shown in Table 2 below.

As shown in Table 2 above, it has been confirmed that sodium iodoacetate, which is an oxidant conventionally used, cannot avoid the influence of reducing substances in the hemolyzed sample.
(Comparative Example 4)
In this comparative example, a hemolyzed sample of red blood cells was subjected to molecular weight fractionation and then treated with sodium iodoacetate.
Ten milliliters of healthy human blood to which heparin was added was centrifuged (1630 G, 10 minutes), and the plasma layer and leukocyte layer were removed with a pipette. To the obtained erythrocyte layer, physiological saline was added, and the mixture was slowly mixed so that the erythrocytes would not be hemolyzed, followed by centrifugation as described above to remove the supernatant. This series of washing operations was repeated three times. Next, after adding the same amount (volume) of distilled water to the obtained erythrocytes to completely hemolyze them, centrifugation (4530 G, 10 minutes) is performed again, and the solution from which the membrane components have been removed is referred to as Sample 1. did.

  Next, the sample 1 was ultrafiltered by centrifuging (1630G, 4 hours) using CENTRIPREP 30 (Millipore). The fraction having a molecular weight of 30,000 or more remaining in the CENTRIPREP 30 was designated as sample 2, and the filtrate was designated as sample 3.

  Next, the sample 3 was further ultrafiltered by centrifugation (1630 G, 2 hours) using CENTRIPREP 10 (manufactured by Millipore). The fraction remaining in the CENTRIPREP 10 with a molecular weight of 10,000 or more and less than 30,000 was designated as sample 4, and the filtrate was designated as sample 5.

  Then, 400 μl of the FV solution was added to 200 μl of a diluted solution obtained by diluting each sample with distilled water, and then 1400 μl of the oxidation-reduction reaction solution A was added to start the reaction. Then, the absorbance was measured in the same manner as in Example 1, and the relative value (%) to the control was determined. The samples 1 and 2 were diluted 80 times with distilled water, and the samples 3 to 5 were diluted 10 times. As a control, measurement was performed in the same manner as described above except that distilled water was used instead of the hemolyzed sample.

Further, 150 μl of the sodium iodoacetate solution was added to 50 μl of the diluted solution of each sample, and the mixture was stirred and treated at 37 ° C. for 10 minutes. Then, 400 μl of the FV solution was added to the processed diluted sample, and then 1400 μl of the oxidation-reduction reaction solution A was added to start the reaction. Absorbance was measured in the same manner as in Reference Example 1, and a relative value (%) to the control was determined. These results are shown in Table 3 below.

As shown in Table 3, almost no measurement was possible for sample 1 (unfractionated) and sample 2 (fraction with a molecular weight of 30,000 or more). Similarly, even when Sample 1 and Sample 2 were treated with sodium iodoacetate, almost no measurement was possible. From this, it was found that sodium iodoacetate can hardly avoid the influence of 10,000 or more, especially 30,000 or more reducing substances.
( Example 1 and Comparative Example 5)
In this example, blood samples were treated with various tetrazolium compounds to eliminate the influence of reducing substances in the samples. The compound names and structures of the tetrazolium compounds used are shown below.

  (1-8) D0883: 2,5-diphenyl-3- (p-diphenyl) tetrazolium chloride

(1-9) D0884: 2,3-diphenyl-5- (p-diphenyl) tetrazolium chloride

(1-10) D0915: 2,5-diphenyl-3- (4-styrylphenyl) tetrazolium chloride

(1-11) T324: 2,5-diphenyl-3- (m-tolyl) tetrazolium chloride

(1-12) T326: 2,5-diphenyl-3- (p-tolyl) tetrazolium chloride

(2) Tetrazolium compound having a benzene ring structure substituent at two positions on the tetrazole ring and another ring structure substituent at one position (2-1) B0325 : 2,3-diphenyl-5- (2-thienyl) ) Tetrazolium chloride

(2-4) MTT: 3- (4,5-dimethyl-2-thiazoyl) -2,5-diphenyl-2H-tetrazolium chloride

(3) A tetrazolium compound having a benzene ring structure substituent at two positions on the tetrazole ring and a substituent other than the ring structure at one position.

(3-3) B313: 2,3-diphenyl-5-methyltetrazolium chloride

(3-4) B319: 2,3-diphenyl-5-ethyltetrazolium chloride

These compounds are manufactured by Tokyo Chemical Industry Co., Ltd.
(FV solution)
The FV was prepared by adding 0.145 mol / liter KPB (pH 7.0) to a concentration of 10 μmol / liter.
(Redox reaction solution B)
FAOD 73 KU / L POD 219 KU / L DA-64 146 μmol / L Distilled water Residue 1.0 mol / L In CAPSO buffer (pH 10.0) 25 μL, the 10 vol% Triton X-100 solution 41.3 μL 1.65 μl of whole blood was added and quantified to 250 μl with distilled water. And what diluted this 3 times (volume) with purified water was made into the hemolysis sample.

150 μl of various tetrazolium compound solutions were added to 250 μl of the hemolyzed sample, stirred, and then treated at 37 ° C. for 60 minutes. Then, 55 μl of the FV solution was added to 25 μl of the processed sample, and then 15 μl of the redox reaction solution B was added to start the reaction. And the light absorbency was measured like the said reference example 1, and the relative value (%) with respect to control was calculated | required. The concentration of the tetrazolium compound solution was 0.5 mmol / liter for WST-5, and the concentration of the other solutions was 5 mmol / liter.

As a control, measurement was performed in the same manner as described above except that distilled water was used instead of the hemolyzed sample. As Comparative Example 5, measurement was performed in the same manner as in Example 1 except that distilled water was used instead of the tetrazolium compound solution. These results are shown in Table 4 below.

As shown in Table 4, the reliability of the measured values was improved by treating the hemolyzed sample with the various tetrazolium compounds. In particular, according to the tetrazolium compounds (1-8) to (1-12) having a benzene ring structure substituent at three positions on the tetrazole ring, it was possible to obtain a more reliable measurement value .

Claims (15)

A method for measuring an object to be measured in a sample using a redox reaction, wherein the sample is a hemolytic sample, and prior to the redox reaction, a tetrazolium compound is added to the sample and the reduction contained in the sample After eliminating the influence of the substance, a reducing substance or an oxidizing substance derived from the measurement object is generated, and this amount is measured by a redox reaction in the presence of a chromogenic substrate other than the tetrazolium compound. Determining the amount of the measurement object from
The tetrazolium compound has a ring structure substituent in at least two positions of the tetrazole ring, and the ring structure substituent is composed of a phenyl group, a tolyl group, a diphenyl group, a styrylphenyl group, a thienyl group, and a dimethylthiazoyl group. Each selected from a group,
The measurement method wherein the molecular weight of the reducing substance in the sample is 10,000 or more . The measurement method according to claim 1, wherein the at least two ring structure substituents are phenyl groups . 3. The ring structure according to claim 1, wherein the tetrazolium compound has a ring structure substituent in at least three positions of the tetrazole ring, and the ring structure of at least two ring structure substituents among the ring structure substituents is a phenyl group . Measuring method. Tetrazolium compound
2,5-diphenyl-3- (p-diphenyl) tetrazolium salt,
2,3-diphenyl-5- (p-diphenyl) tetrazolium salt,
2,5-diphenyl-3- (4-styrylphenyl) tetrazolium salt,
2,5-diphenyl-3- (m-tolyl) tetrazolium salt,
2,5-diphenyl-3- (p-tolyl) tetrazolium salt,
2,3-diphenyl-5- (2-thienyl) tetrazolium salt,
3- (4,5-dimethyl-2-thiazoyl) -2,5-diphenyl-2H-tetrazolium salt,
2,3-diphenyl-5-methyltetrazolium salt and
The measurement method according to any one of claims 1 to 3 , which is at least one compound selected from the group consisting of 2,3-diphenyl-5-ethyltetrazolium salt .   A tetrazolium compound is 2,5-diphenyl-3- (p-diphenyl) tetrazolium salt, 2,3-diphenyl-5- (p-diphenyl) tetrazolium salt,
The compound is at least one compound selected from the group consisting of 2,5-diphenyl-3- (4-styrylphenyl) tetrazolium salt and 2,5-diphenyl-3- (m-tolyl) tetrazolium salt. The measuring method in any one of. The measurement method according to claim 1 , wherein the tetrazolium compound is added so as to have a concentration in a range of 0.001 to 100 μmol per 1 μl of a sample. The measurement method according to claim 1 , wherein the sample is whole blood, and the tetrazolium compound is added so as to have a concentration in the range of 0.001 to 10 μmol per μl of whole blood. The measurement method according to claim 1 , wherein the oxidation substance derived from the measurement target is hydrogen peroxide, and the measurement of the oxidation-reduction reaction is measurement of the amount of hydrogen peroxide. The measurement method according to claim 8 , wherein the measurement of the amount of hydrogen peroxide is measurement using peroxidase and a substrate that develops color by oxidation. The measurement method according to claim 9 , wherein the substrate is sodium N- (carboxymethylaminocarbonyl) -4,4′-bis (dimethylamino) diphenylamine. The measurement method according to claim 1 , wherein the measurement object is a component in red blood cells. The measurement method according to claim 8 , wherein the measurement object is a glycated protein in erythrocytes, and hydrogen peroxide is generated by oxidative decomposition of a sugar portion of the glycated protein with fructosyl amino acid oxidase. The measuring method according to claim 1 , wherein the reducing substance in the sample is a protein. The measuring method according to claim 1 , wherein the reducing substance in the sample is hemoglobin. The measurement method according to any one of claims 12 to 14 , wherein the glycated protein is glycated hemoglobin.