Stabilization of tetrazolium salts with cyclodextrins

This invention relates to a process for stabilizing a tetrazolium compound using cyclodextrin as an effective component.
Tetrazolium compounds such as nitrotetrazolium blue (hereinafter referred to as "NO.sub.2 -TB") are generally low in oxidation-reduction potential and when they are reduced, there are produced formazan compounds such as monoformazan compounds or diformazane compounds which exhibit an orange to blue color. Therefore, they are widely used as reagent for colorimetrically measuring dehydrogenases or as reagent for colorimetrical determination of reductive substances such as reduced type coenzymes, superoxide irons, etc., in the fields of clinical chemistry, pharmaceutical chemistry, biochemistry, food chemistry, and the like. For example, there is known a process for measuring components in a body fluid sample using a tetrazolium compound wherein superoxide ions (O.sub.2.sup.-) produced quantitatively by a reaction reduce the tetrazolium compound quantitatively to produce a formazan compound, the color of which is measured quantitatively (European Patent Publication No. 010027A.sub.2).
As an example of the reaction for producing such superoxide ions, there is known an enzymatic reaction wherein superoxide ions are produced by acting an oxidase on a substrate. In order to conduct such an enzymatic reaction practically, an oxidase is acted on a substrate preferably in the presence of a thiol compound, peroxidase or an iron complex of porphyrin or an iron chelate compound of complexane, an amine or a phenol, and preferably together with a chelating agent, to produce superoxide ions, which are used for determination of the desired components. When superoxide ions can stably be produced as they are as in the case of acting xanthine oxidase on xanthine, the presence of such reagents as mentioned above is not required.
For example, cholesterol can be determined by using such a principle as follows: ##STR1##
Since the above-mentioned reactions proceed quantitatively and specifically, the amount of cholesterol can be determined by measuring the color intensity of the formazan produced. (In the above-mentioned formulae, "X" represents a halogen.)
Generally speaking, an aqueous solution of a tetrazolium compound is not sufficiently stable, and becomes unstable when exposed to light, or kept in neutral or alkaline conditions, or by the presence of an interfering substance. For example, when there is present a reductive substance such as a thiol compound, the tetrazolium compound is gradually decomposed to produce a color, which results in raising reagent blank values with the lapse of time and causing errors in the measurement. Therefore, in the case of quantitatively measuring the color of formazan compound produced quantitatively by the reduction of tetrazolium compound with superoxide ions, the tetrazolium compound becomes unstable when exposed to light, or kept in neutral or alkaline conditions, or by the presence of a thiol compound and the solution containing the thiol compound and tetrazolium compound is colored to damage the quantitative measurement of the desired component.
It is an object of this invention to overcome the problem of the prior art process and to provide a process for stabilizing a tetrazolium compound in an aqueous solution.
This invention provides a process for stabilizing a tetrazolium compound in an aqueous solution which comprises adding at least one member selected from the group consisting of .beta.-cyclodextrin, a derivative thereof and .gamma.-cyclodextrin to the aqueous solution, said tetrazolium compound having a moiety of the formula: ##STR2##
In this invention, at least one member selected from the group consisting of .beta.-cyclodextrin, a derivative thereof and .gamma.-cyclodextrin should be used for stabilizing the tetrazolium compound having the moiety of the formula (I). In contrast, .alpha.-cyclodextrin has no effect for stabilizing the tetrazolium compound having the moiety of the formula (I). This seems to be that both .beta.-cyclodextrin, or a derivative thereof and .gamma.-cyclodextrin have a clathrate action for the tetrazolium compound, while .alpha.-cyclodextrin has no such a clathrate action.
The tetrazolium compound thus stabilized by .beta.-cyclodextrin, and/or a derivative of .beta.-cyclodextrin, and/or .gamma.-cyclodextrin can be reduced by superoxide ions with sufficiently fast reaction rate to produce a formazan compound, the color of which is measured for determining the amount of superoxide ions with sufficient sensitivity. There is no influence of the addition of .beta.-cyclodextrin, and/or a derivative of .beta.-cyclodextrin, and/or .gamma.-cyclodextrin to the tetrazolium compound on the color development rate and the increase in reagent blank value can be suppressed decisively.
The tetrazolium compound usable in this invention is those having the moiety of the formula (I).
Examples of such tetrazolium compounds are monotetrazolium compounds having the formula: ##STR3## wherein X is a halogen; and R.sup.1, R.sup.2, and R.sup.3 are independently organic residues such as a phenyl group, a phenyl group substituted by one or more halogens such as iodine, or nitro group, a group of the formula: ##STR4## etc. Typical examples of monotetrazolium compounds having the formula (II) are as follows: ##STR5##
It is also possible to use ditetrazolium compounds of the following formula as the tetrazolium compound having the moiety of the formula (I): ##STR6## wherein Y.sup.1 and Y.sup.2 are independently --NO.sub.2 or --H; Y.sup.3 is --OCH.sub.3, --I or --H; and X is a halogen. Typical examples of ditetrazolium compounds of the formula (III) are as follows: ##STR7##
As is well known, these tetrazolium compounds are reduced to form corresponding formazan compounds having specific colors which are used for colorimetrical determination.
On the other hand, it is generally known that formazan compounds produced by reducing tetrazolium compounds have strong staining properties for vessels made from such materials as glass, plastics, etc. For example, a cuvette used for measuring absorbance is often stained strongly to cause errors. Such a problem of staining vessels can be solved by using gelatin as an effective component. Gelatin can effectively inhibit staining power of the formazan compounds produced from tetrazolium compounds. That is, when gelatin is present in an aqueous solution containing a tetrazolium compound, staining caused by a formazan compound which is a reduction product of the tetrazolium compound can effectively be prevented.
The problem of staining vessels can also be solved by making the formazan compound which is a reduction product of a tetrazolium compound water-soluble. Examples of tetrazolium compounds which can form water-soluble formazan are those represented by the formula: ##STR8## wherein R.sup.4 is a nitro group or hydrogen, but at least one R.sup.4 should be a nitro group; R.sup.5 is hydrogen, a lower alkyl group, a lower alkoxy group or a halogen; R.sup.6 is hydrogen or --OR.sup.7 ; R.sup.7 is a straight- or branched-chain aliphatic hydrocarbon having 1 to 4 carbon atoms which has at least one sulfonic acid group or sulfonic acid salt group and/or carboxyl group or carboxyl salt group and can also have a hydroxyl group, provided that the number of sulfonic acid (or its salt) group or carboxyl (or its salt) group contained in R.sup.6 is 2 or more as a total and one of them forms an intramolecular salt with a tetrazolium ring; and X is a halogen. Examples of tetrazolium compounds of the formula (IV) are 2-(nitrophenyl)-3,5-di(sulfopropoxyphenyl)-2H-tetrazolium salts, etc. These tetrazolium compounds which can form water-soluble formazan compounds can be used in an amount of 1 to 40 mg/dl in the reaction solution at the time of color development irrespective of their water solubility.
The concentration of .beta.-cyclodextrin or a derivative thereof or .gamma.-cyclodextrin for stabilizing the tetrazolium compound in the aqueous solution is usually 0.01 to 1.5 weight/volume percent, preferably 0.1 to 0.5 weight/volume percent, in the case of .beta.-cyclodextrin, usually 0.01 to 10 weight/volume percent, preferably 0.1 to 5 weight/volume percent in the case of a derivative of .beta.-cyclodextrin, and usually 0.01 to 10 weight/volume percent, preferably 0.1 to 3 weight/volume percent, in the case of .gamma.-cyclodextrin. .beta.-Cyclodextrin or a derivative thereof and .gamma.-cyclodextrin can be used as a mixture thereof in any ratio within the above-mentioned range of individual concentrations.
The derivative of .beta.-cyclodextrin can be represented by the formula:
.beta.-CD(--OH).sub.21-m (--OZ.sup.1).sub.m (V)
wherein CD is a cyclodextrin residue; Z.sup.1 is --NO.sub.2, --PO.sub.3 H, --SO.sub.3 H or a group of the formula: --(CH.sub.2).sub.n Z.sup.2 ; Z.sup.2 is --SO.sub.3 H or --CO.sub.2 H; n is an integer of 1 to 4; and m is a value of 1 to 5, or represented by the formula:
.beta.-CD(--OH).sub.21-k (--OCH.sub.3).sub.k (VI)
wherein 0<k.ltoreq.21.
Examples of the derivatives of .beta.-cyclodextrin are as follows:
.beta.-CD(--OH).sub.19 (--ONO.sub.2).sub.2
.beta.-CD(--OH).sub.19.2 (--OPO.sub.3 H).sub.1.8
.beta.-CD(--OH).sub.19 (--OSO.sub.3 H).sub.2
.beta.-CD(--OH).sub.18.5 (--O--CH.sub.2 --CO.sub.2 H).sub.2.5
.beta.-CD(--OH).sub.19.3 (--O--CH.sub.2 CH.sub.2 CH.sub.2 --SO.sub.3 H).sub.1.7
.beta.-CD(--OH).sub.18.5 (--O--CH.sub.2 CH.sub.2 CH.sub.2 --SO.sub.3 H).sub.2.5
.beta.-CD(--OH).sub.18.0 (--O--CH.sub.2 CH.sub.2 CH.sub.2 --SO.sub.3 H).sub.3.0
.beta.-CD(--OH).sub.7 (--OCH.sub.3).sub.14
.beta.-CD(--OCH.sub.3).sub.21
Needless to say, the examples of the derivatives of .beta.-cyclodextrin are not limited thereto.
There derivatives of .beta.-cyclodextrin can easily be prepared by a conventional method.
The gelatin used for effectively inhibiting staining by the formazan compound produced by reducing the tetrazolium compound preferably has an average molecular weight of 20,000 to 150,000. Water-soluble gelatin having an average molecular weight of 1000 to 2000 usually does not show a particular effect for inhibiting the staining by formazan compound. But any gelatin having an inhibiting effect of staining can be used. For example, gelatin derived from animal bones and animal skins is available commercially, and any other gelatin can also be used. The gelatin concentration in the aqueous solution effective for preventing staining is usually 0.1 to 0.7 weight/volume percent, preferably 0.2 to 0.5 weight/volume percent.
As mentioned above, since the tetrazolium compound which is a color producing reagent to be reduced can be stabilized in an aqueous solution even if a thiol compound is present or exposed to light or under neutral or alkaline conditions and the staining by formazan compound can be prevented, this invention can be applied to determination of substrates, for example, in body fluid samples in clinical chemical examinations wherein a thiol compound is usually used for producing superoxide ions to be determined. In such a case, a reagent composition comprising (a) an oxidaze, (b) a peroxidase, or an iron complex of porphyrin or an iron chelate compound of complexane, (c) a phenol and/or an amine, (d) a thiol compound, (e) a tetrazolium compound which is a color producing reagent to be reduced, and if required (f) a chelating agent can be used.
Examples of the thiol compound are reduced from glutathione, thioglycolic acid, mercaptoethanol, thiosalicylic acid, cysteamine, cysteine, dimercaptosuccinic acid, etc. It is also possible to use coenzymes having a SH group therein such as CoA. The thiol compound can be used in an amount of about 1 to 50 mg/dl in the reaction solution at the stage of color development.
As the amine, there can be used conventional organic amines. Aromatic amines are more effective than aliphatic amines with a small using amount. There can be used primary amines, secondary amines and tertiary amines. Examples of these amines are aniline, N-ethylaniline, N,N-dimethylaniline, N,N-diethyl-m-toluidine, N-ethyl-N-.beta.-hydroxyethyl-m-toluidine, 3,5-dimethoxy-N-ethyl-N-(2-hydroxy-3-sodiumsulfopropyl)aniline, etc. The amine can be used in an amount of about 0.0001% to 0.2% by weight in the reaction solution at the stage of color development.
The phenol is not particularly influenced by other substituents. As the phenol, there can be used phenol, chlorophenols, dichlorophenols, naphthol sulforic acid derivatives and the like. The phenol can be used in an amount of about 0.0001% to 0.2% by weight in the reaction solution at the stage of color formation.
A phenol and an amine can be used together.
The peroxidase can be used in an amount of about 50 to 1000 units/dl in the reaction solution at the stage of color development.
As the iron complex of porphyrin used in place of peroxidase, there can be used hemin, .alpha.,.beta.,.gamma.,.delta.-tetraphenylporphyrintrisulfonic acid-iron complex, .alpha.,.beta.,.gamma.,.delta.-tetrakis(4-N-methylpyridyl)-porphyrin-iron complex, tetraphenylporphyrin-iron complex, octaethylporphyrin-iron complex, etc. The iron complex of porphyrin can used in an amount of about 0.007 to 0.06 mmol/l in the reaction solution at the stage of color development.
As the iron chelate of complexane used in place of peroxidase, there can be used iron chelated of complexanes such as ethylenediaminetetraacetic acid (EDTA), diaminopropanetetraacetic acid, trans-cyclohexanediaminetetraacetic acid, hydroxyethylethylenediaminetriacetic acid, glycol ether diaminetetraacetic acid, etc. The iron chelate of complexane can be used in an amount of about 0.01 to 0.07 mmole/l. in the reaction solution at the stage of color development.
As the chelating agent which is used for preventing autooxidation of additives such as a thiol compound, and for proceeding the reaction stably, there can be used ethylenediaminetetraacetic acid (EDTA), trans-cyclohexanediaminetetraacetic acid=trans-1,2-cyclohexanediamine-N,N,N',N'-tetraacetic acid (CyDTA), diethylenetriaminepentaacetic acid=diethylenetriamine-N,N,N',N",N"-pentaacetic acid (DTPA), etc. The chelating agent can be used in an amount of about 0.5 to 5 mmole/dl in the reaction solution at the stage of color development.
In the case of using the above-mentioned compounds in proper combination, if the final mixture to be measured on its coloring is clouded to damage the measurement, a surface active agent or solubility aid can be added thereto according to a conventional process.
Oxidases are enzymes which specifically oxidize substrates in enzymatic reactions. Substrates and corresponding specific oxidases usable in this invention can be listed as follows:
Glucose
Glucose oxidase
Cholesterol
Cholesterol oxidase
Glycerol
Glycerol oxidase
Glycerolphosphate
Glycerolphosphate oxidase
Choline
Choline oxidase
Acyl CoA
Acyl CoA oxidase
Pyruvic acid
Pyruvate oxidase
Uric acid
Uricase
Xanthine
Xanthine oxidase
Lactic acid
Lactate oxidase
Enzymatic reactions mentioned above can be applied to measuring the amounts of substrates in body fluid (samples) or measuring the activities of serum enzymes.
Examples of compositions of reagents used for such measuring are listed below:
______________________________________Determination of cholesterol:Cholesterol oxidase 10-50 units/dlNO.sub.2 --TB 10-30 mg/dl.beta.-cyclodextrin 0.1-0.5%gelatin 0.1-0.5%reduced form glutathione 0.01-0.1%a phenol or an amine 0.005-0.5%peroxidase 100-1000 units/dlor hemin 0.0005-0.002%chelating agent 0.0005-0.002%Triton X-100* 0.05-0.2%0.05-0.2 M tris or pH 7.5-8.5phosphate buffer *Octylphenoxy polyethoxyethanolavailable from Rohm and Haas Company.Determination of free fatty acid:acyl CoA synthetase 5-30 units/dlacyl CoA Oxidase 100-6000 units/dladenosine-5'-triphosphate 10-100 mg/dldisodium salt(ATP)CoA 20-50 mg/dlmagnesium chloride 0.5-3 mmole/lNO.sub.2 --TB 10-30 mg/dl.beta.-cyclodextrin 0.1-0.5%gelatin 0.1-0.5%peroxidase 100-1000 units/dla phenol or an amine 0.005-0.5%chelating agent 0.0005-0.002%Triton X-100 0.05-0.5%buffer solution pH 7.0Determination of phospholipid:phospholipase D 40-100 units/dlcholine oxidase 150-500 units/dlCaCl.sub.2.2H.sub.2 O 3-10 mg/dl.beta.-cyclodextrin 0.1-0.5%gelatin 0.1-0.5%NO.sub.2 --TB 10-30 mg/dlperoxidase 100-1000 units/dlreduced form glutathione 0.01-0.1%a phenol or an amine 0.005-0.5%chelating agent 0.0005-0.002%Triton X-100 0.05-0.5%buffer solution pH 8.0Determination of triglyceride:lipoprotein lipase 3000-6000 units/dlglycerol kinase 150-500 units/dlglycerol-3-phosphate 100-400 units/dloxidaseATP 100-300 mg/dlmagnesium acetate 3-10 mmole/l.beta.-cyclodextrin 0.1-0.5%gelatin 0.1-0.5%NO.sub.2 --TB 10-30 mg/dlperoxidase 100-1000 units/dlreduced form glutathione 0.01-0.1%a phenol or an amine 0.005-0.5%chelating agent 0.0005-0.002%Triton X-405* 0.01-0.3%buffer solution pH 7.0______________________________________ *Alkylphenoxy polyethoxythanolavailable from Rohm and Haas Company.
According to this invention, a tetrazolium compound in an aqueous solution can be stabilized by adding .beta.-cyclodextrin and/or a derivative thereof and/or .gamma.-cyclodextrin as an effective component to the aqueous solution. Particularly when a thiol compound is present in the aqueous solution wherein a substrate is acted with an oxidase to produce superoxide ions (O.sub.2.sup.-), the tetrazolium compound becomes unstable by the presence of the thiol compound; but such an unstabilizing phenomenon can effectively be prevented by the action of .beta.-cyclodextrin and/or a derivative thereof and/or .gamma.-cyclodextrin without causing any undesirable influences on the colorimetrical determination. Thus, when a desired component in a sample (e.g. a body fluid) is to be determine by applying the present invention, the increase in reagent blank values can be suppressed effectively due to the stabilization of tetrazolium compound. Therefore the present invention can widely be applied to clinical chemistry, pharmaceutical chemistry, biochemistry, food chemistry and the like, wherein the colorimetrical determination of the formazan compound which is produced by reducing a tetrazolium compound is used.

This invention is illustrated by way of the following Examples.
EXAMPLE 1
Determination of Free Cholesterol in Serum
A color producing reagent was prepared by using the following ingredients:
______________________________________NO.sub.2 --TB 20 mg/dlphenol 0.01%Triton X-100 0.1%peroxidase (available 300 units/dlfrom Toyobo Co., Ltd.)cholesterol oxidase 15 units/dl(available from AmanoPharmaceutical Co., Ltd.)glutathione (reduced form) 20 mg/dlgelatin 0.5%.beta.-cyclodextrin 0.2%0.1 M tris buffer pH 8.0______________________________________
Measurement of Free Cholesterol in Serum
To 50 .mu.l of serum, 3 ml of the color producing reagent was added and incubated at 37.degree. C. for 10 minutes. Then, absorbance at the wavelength of 560 nm was measured by using water as control. On the other hand, absorbance of deionized water in place of serum treated in the same manner as mentioned above was also measured as reagent blank.
Further, absorbance of an isopropanol solution containing cholesterol in an amount of 200 mg/dl (standard solution) was also measured in the same manner as mentioned above.
The free cholesterol concentration in the serum was calculated by the following equation: ##EQU1## wherein E.sub.S : absorbance when the serum was used
E.sub.B : reagent blank value
E.sub.std : absorbance when the standard solution was used.
COMPARATIVE EXAMPLE 1
Determination of Free Cholesterol in Serum
A color producing reagent was prepared in the same manner as mentioned in Example 1 except for not using gelatin and .beta.-cyclodextrin.
Measurement of Free Cholesterol in Serum
The procedures of Example 1 were repeated.
The result of measured values are shown in Table 1.
TABLE 1______________________________________ ReagentSerum Example 1 Comparative Example 1No. (mg/dl) (Y) (mg/dl) (X)______________________________________1 44.3 43.92 32.5 32.83 66.8 66.54 44.0 44.05 59.8 59.56 48.9 49.07 35.5 36.08 40.2 40.09 39.3 39.410 47.7 47.4Average 45.90 45.85______________________________________ .gamma. = 1.000 Y = 1.02 X - 0.79
Comparison of reagent blank values is shown in Table 2.
TABLE 2______________________________________Example No. Example 1 Comparative Example 1______________________________________Absorbance at 560 nm 0.076 0.183(water, control)______________________________________
Comparison of the degree of color development of the standard solution is shown in Table 3.
TABLE 3______________________________________Example No. Example 1 Comparative Example 1______________________________________Absorbance at 560 nm 1.267 1.271(E.sub.std -E.sub.B)______________________________________
Comparison of changes of the color producing reagents with the lapse of time stored at room temperature is shown in Table 4.
TABLE 4______________________________________ Example No.Storedtime Example 1 Comparative Example 1______________________________________0 hour Clear Clear18 Clear Clouded with a small amount of precipitation48 Clear Clouded with a large amount of precipitation72 Clear Clouded with a large amount of precipitation______________________________________
Staining of cuvettes used is compared and shown in Table 5.
TABLE 5______________________________________Example No. Example 1 Comparative Example 1______________________________________Staining No staining Whole cuvette was stained light violet______________________________________
The degree of staining was obtained by allowing a colored cholesterol standard solution in a glass cuvette to stand for 18 hours at room temperature, removing the solution, washing the cuvette with water and drying the cuvette to observe the degree of staining.
As shown in Tables 1 through 5, the presence of gelatin and .beta.-cyclodextrin do not influence the determined values of cholesterol by the enzymatic method but controls the raise of reagent blank values effectively, stabilizes the color producing reagent and prevents effectively the staining of glass cuvettes by the colored solutions.
EXAMPLE 2
Determination of Free Cholesterol in Serum
A color producing reagent was prepared in the same manner as described in Example 1 except for not using gelation.
Measurement of Free Cholesterol in Serum
The procedures of Example 1 were repeated.
The results are shown in the following Tables 6 to 8.
Comparison of reagent blank values is shown in Table 6.
TABLE 6______________________________________Example No. Example 1 Example 2______________________________________Absorbance at 560 nm 0.076 0.081(water, control)______________________________________
Changes of the color producing reagents with the lapse of time stored at room temperature are shown in Table 7.
TABLE 7______________________________________ Example No.Storedtime Example 1 Example 2______________________________________0 hour Clear Clear18 Clear Clear48 Clear Clear72 Clear Clear______________________________________
Staining of cuvettes used is compared and shown in Table 8.
TABLE 8______________________________________Example No. Example 1 Example 2______________________________________Staining No staining Whole cuvette was stained light violet______________________________________
As is clear from Tables 6 through 8, .beta.-cyclodextrin has effects for effectively control the raise of reagent blank values and for stabilizing the color producing reagents but has no effect for preventing the glass cuvettes from staining.
REFERENCE EXAMPLE 1
Determination of Free Cholesterol in Serum
A color producing reagent was prepared in the same manner as described in Example 1 except for not using .beta.-cyclodextrin.
Measurement of Free Cholesterol in Serum
The procedures of Example 1 were repeated.
The results are shown in the following Tables 9 and 10.
Comparison of reagent blank values is shown in Table 9.
TABLE 9______________________________________ ReferenceExample No. Example 2 Example 1______________________________________Absorbance at 560 nm 0.081 0.209(water, control)______________________________________
Staining of cuvettes used is compared and shown in Table 10.
TABLE 10______________________________________ ReferenceExample No. Example 2 Example 1______________________________________Staining Whole cuvette was No staining stained light violet______________________________________
As is clear from Tables 9 and 10, gelatin has no effect for controlling the raise of reagent blank values but has an effect for preventing the glass cuvette from staining.
EXAMPLE 3
Determination of Free Cholesterol in Serum
A color producing reagent was prepared in the same manner as described in Example 1 except for using 0.3% of .gamma.-cyclodextrin in place of 0.2% of .beta.-cyclodextrin.
Measurement of Free Cholesterol in Serum
The procedures of Example 1 were repeated.
COMPARATIVE EXAMPLE 2
Determination of Free Cholesterol in Serum
A color producing reagent was prepared in the same manner as described in Example 3 except for not using gelatin and .gamma.-cyclodextrin.
Measurement of Free Cholesterol in Serum
The procedures of Example 1 were repeated.
Comparison between the results obtained in Example 3 and Comparative Example 2 is shown in Tables 11 to 15.
The results of measured values are shown in Table 11.
TABLE 11______________________________________ Example No.Serum Example 3 Comparatie Example 2No. (mg/dl) (mg/dl)______________________________________1 52.7 53.02 48.1 48.0Average 50.4 50.5______________________________________
Comparison of reagent blank values is shown in Table 12.
TABLE 12______________________________________ Example No. Example 3 Comparative Example 2______________________________________Absorbance at 560 nm 0.071 0.190(water, control)______________________________________
Comparison of the degree of color development of the standard solution is shown in Table 13.
TABLE 13______________________________________ Example No. Example 3 Comparative Example 2______________________________________Absorbance at 560 nm 1.270 1.268(E.sub.std -E.sub.B)______________________________________
Comparison of changes of the color producing reagents with the lapse of time stored at room temperature is shown in Table 14.
TABLE 14______________________________________Stored Example No.time Example 3 Comparative Example 2______________________________________ 0 hour Clear Clear18 Clear Clouded with a small amount of precipitation48 Clear Clouded with a large amount of precipitation72 Clear Clouded with a large amount of precipitation______________________________________
Staining of cuvettes used is compared and shown in Table 15.
TABLE 15______________________________________ Example No. Exanple 3 Comparative Example 2______________________________________Staining No staining Whole cuvette was stained light violet.______________________________________
EXAMPLE 4
Determination of Free Cholesterol in Serum
A color producing reagent was prepared in the same manner as described in Example 1 except for using a mixture of .beta.-cyclodextrin and .gamma.-cyclodextrin (1:1 by weight) in an amount of 0.2% in place of 0.2% of .beta.-cyclodextrin.
Measurement of Free Cholesterol in Serum
The procedures of Example 1 were repeated.
COMPARATIVE EXAMPLE 3
Determination of Free Cholesterol in Serum
A color producing reagent was prepared in the same manner as described in Example 4 except for not using gelatin and the mixture of .beta.-cyclodextrin and .gamma.-cyclodextrin.
Measurement of Free Cholesterol in Serum
The procedures of Example 1 were repeated.
Comparison between the results obtained in Example 4 and Comparative Example 3 is shown in Table 16 to 20.
The results of measured values are shown in Table 16.
TABLE 16______________________________________ Example No.Serum Example 4 Comparative Example 3No. (mg/dl) (mg/dl)______________________________________l 60.5 61.12 48.9 48.33 55.2 54.74 35.5 36.15 42.6 42.3Average 48.54 48.50______________________________________
Comparison of reagent blank values is shown in Table 17.
TABLE 17______________________________________ Example No. Example 4 Comparative Example 3______________________________________Absorbance at 560 nm 0.075 0.196(water, control)______________________________________
Comparison of the degree of color development of the standard solution is shown in Table 18.
TABLE 18______________________________________ Example No. Example 4 Comparative Example 3______________________________________Absorbance at 560 nm 1.283 1.277(E.sub.std -E.sub.B)______________________________________
Comparison of changes of the color producing reagents with the lapse of time stored at room temperature is shown in Table 19.
TABLE 19______________________________________Stored Example No.time Example 4 Comparative Example 3______________________________________ 0 hour Clear Clear18 Clear Clouded with a small amount of precipitation48 Clear Clouded with a large amount of precipitation72 Clear Clouded with a large amount of precipitation______________________________________
Staining of cuvettes used is compared and shown in Table 20.
TABLE 20______________________________________ Example No. Example 4 Comparative Example 3______________________________________Staining No staining Whole cuvette was stained light violet.______________________________________
EXAMPLE 5
Measurement of Activity of Superoxide Dismutase (SOD) in Serum
______________________________________A first reagent:0.1 M phosphate buffer pH 8.0NO.sub.2 --TB 200 mg/lXanthine 0.4 mmole/lEDTA .multidot. 2Na 0.005%Triton X-100 0.1%.beta.-cyclodextrin 0.2%A second reagent:0.1 M phosphate buffer pH 8.0Xanthine oxidase 150 units/lEDTA .multidot. 2Na 0.005%Reaction stopper:0.1 N HCl solution containing 0.1% ofTriton X-100______________________________________
Measurement of Activity of SOD
To 100 .mu.l of serum, 1 ml of the first reagent was added and heated at 37.degree. C. for 3 minutes. Then, 0.1 ml of the second reagent was added thereto and incubated at 37.degree. C. for 20 minutes. Subsequently 3 ml of the reaction stopper was added to the incubated solution. Absorbance (E.sub.S) at the wavelength of 560 nm was measured using reagent blank as control. The reagent blank was prepared by adding 1 ml of the first reagent to 100 .mu.l of deionized water, heating at 37.degree. C. for 20 minutes, adding 3 ml of the reaction stopper, and adding 0.1 ml of the second reagent thereto.
Absorbance (E.sub.B) was obtained by repeating the same procedure as done in the case of serum by using deionized water in place of serum.
The activity of SOD can be represented by the damaging rate calculated by the following equation: ##EQU2##
COMPARATIVE EXAMPLE 4
Measurement of Activity of SOD
A first reagent:
Prepared in the same manner as descriped in Example 5 except for not using .beta.-cyclodextrin.
A second reagent:
The same as used in Example 5.
Measurement of activity of SOD:
The procedures described in Example 5 were repeated and the damaging rate (%) was measured.
Comparison of storage stability of the first reagents:
The degree of coloring when the first reagents were stored at room temperature (20.degree. to 25.degree. C.) was measured at the wavelength of 560 nm using water as control.
The results are as shown in Table 21.
TABLE 21______________________________________Storage Example No.days Example 5 Comparative Example 4______________________________________0 day 0.010 0.0101 0.010 0.0352 0.010 0.0713 0.010 0.1254 0.010 0.168______________________________________
As is clear from Table 21, no change is admitted in the case of Example 5, but the coloring, that is, the absorbance increases gradually in the case of Comparative Example 4 with the lapse of time due to the decomposition of NO.sub.2 --TB.
The results of SOD activities measured in Example 5 and Comparative Example 4 are shown in Table 22.
TABLE 22______________________________________Serum Example No.No. Example 5 Comparative Example 4______________________________________1 12.1 11.92 4.6 4.63 10.5 11.04 14.9 15.25 2.3 2.06 9.8 10.17 6.6 6.98 4.2 4.09 3.3 3.210 14.4 14.1Average 8.27 8.30______________________________________
As shown in Table 22, there is admitted no significant difference in measured values between Example 5 and Comparative Example 4.
EXAMPLE 6
Determination of Free Cholesterol in Serum
A color producing reagent was prepared in the same manner as described in Example 1 except for using heptakis(2,6-di-o-methyl)-.beta.-cyclodextrin in a concentration of 2% in place of .beta.-cyclodextrin.
Measurement of Free Cholesterol in Serum
The procedures of Example 1 were repeated.
The results were the same as those obtained in Example 1.
EXAMPLE 7
Measurement of Activity of SOD in Serum
A first reagent:
A first reagent was prepared in the same manner as described in Example 5 except for using heptakis(2,3,6-tri-o-methyl)-.beta.-cyclodextrin in a concentration of 3% in place of .beta.-cyclodextrin.
A second reagent:
The same as that used in Example 5.
Reaction stopper:
The same as that used in Example 5.
Measurement of activity of SOD:
The procedures of Example 5 were repeated.
The results were the same as those obtained in Example 5.

Stabilization of tetrazolium salts with cyclodextrins

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Tsou et al., J. Am. Chem. Soc, 78, pp. 6139-6144 (1956).
Nineham, "Chemical Reviews", 55 (1955), pp. 355 and 423.