Whole blood dry analysis element

Claim 2

A dry analysis element for the determination of a component in erythrocyte-containing blood which comprises at least two water permeable layers which include a reagent layer and a porous spreading layer having a liquid-accepting face, the reagent layer being arranged on the side opposite to the liquid-accepting face for the porous spreading layer, and containing a reagent composition capable of producing an optically detectable substance in the presence of an analyte in at least one of the water permeable layers, said porous spreading layer containing a compound selected from the group consisting of cholic acids, deoxycholic acids, and salts thereof, said compound being present in an amount effective to substantially prevent analysis errors due to variation in the hematocrit value of a blood sample.

Claim 3

The analysis element of claim 1 wherein said porous spreading layer contains an alkali metal salt of deoxycholic acid.

Claim 4

The analysis element of claim 1 wherein the compound is selected from the group consisting of cholic acid, lithocholic acid, taurocholic acid, glycocholic acid, deoxycholic acid, chenodeoxycholic acid, taurodeoxycholic acid, glycodeoxy-cholic acid, and their salts.

Claim 5

The analysis element of claim 3 wherein the salt is an alkali metal salt.

Claim 6

The analysis element of claim 4 wherein the alkali metal salt is selected from the group consisting of sodium and potassium.

Claim 7

The analysis element of claim 1 wherein the amount of said compound is from about 0.5 to 6 g/m 2 .

Claim 8

The analysis element of claim 6 wherein the amount of said compound is from about 1 to 4 g/m 2 .

Claim 9

In a method for the analysis of a component in an erythrocyte-containing blood sample wherein a droplet size sample of the blood is introduced to a dry analysis element and the quantity of the component is determined by optical analysis, the improvement which comprises said element having at least two water permeable layers which include a reagent layer and a porous spreading layer having a liquid-accepting face, the reagent layer being arranged on the side opposite to the liquid-accepting face of the porous spreading layer, and containing a reagent composition capable of producing an optically detectable substance in the presence of an analyte in at least one of the water-permeable layers, said porous spreading layer containing a compound selected from the group consisting of cholic acids, deoxycholic acids, and salts thereof, said compound being present in an amount effective to substantially prevent analysis errors due to variation in the hematocrit value of a blood sample.

Claim 10

In a method for the analysis of a component in an erythrocyte-containing blood sample wherein a droplet size sample of the blood is introduced to a dry analysis element and the quantity of the component is determined by optical analysis, the improvement which comprises said element having at least two water permeable layers which include a reagent layer and a porous spreading layer having a liquid-accepting face, the reagent layer being arranged on the side opposite to the liquid-accepting face of the porous spreading layer, and containing a reagent composition capable of producing an optically detectable substance in the presence of an analyte in at least one of the water-permeable layers, said porous spreading layer containing a compound selected from the group consisting of cholic acids, deoxycholic acids, and salts thereof, said compound being present in an amount effective to substantially prevent analysis errors due to variation in the hematocrit value of a blood sample.

Claim 11

The method of claim 8 wherein non-hydrophobic constituents in blood are determined.

Claim 12

The method of claim 8 wherein saccharides in blood are determined.

Claim 13

The method of claim 8 wherein glucose in blood is determined.

Claim 14

The method of claim 8 wherein said porous spreading layer contains an alkali metal salt of deoxycholic acid.

Claim 15

The method of claim 8 wherein the compound is selected from the group consisting of cholic acid, lithocholic acid, taurocholic acid, glycocholic acid, deoxycholic acid, chenodeoxycholic acid, taurodeoxycholic acid, glycodeoxycholic acid, and their salts.

Claim 16

The method of claim 8 wherein the salt is an alkali metal salt.

Claim 17

The method of claim 8 wherein the alkali metal salt is selected from the group consisting of sodium and potassium.

Claim 18

The method of claim 8 wherein the amount of said compound is from about 0.5 to 6 g/m 2 .

Claim 19

The method of claim 8 wherein the amount of said compound is from about 1 to 4 g/m 2 .

Claim 20

The method of claim 8 wherein the blood to be analyzed has a hematocrit value in the range from about 25 to 70%.