Analysis element and method for analyzing glycated hemoglobin content ratio

• US 5,882,935 A
• Filed: 10/17/1995
• Issued: 03/16/1999
• Est. Priority Date: 10/19/1994
• Status: Expired due to Fees

• Current Assignee: Fuji Photo Film Co Limited (Fujifilm Holdings Corporation)
• Original Assignee: Fuji Photo Film Co Limited (Fujifilm Holdings Corporation)
• Inventors: Ogawa, Masashi, Hirai, Kikuo, Makino, Yoshihiko, Shinoki, Hiroshi
• Primary Examiner(s): Hutzell, Paula K.
• Assistant Examiner(s): BAKALYAR, HEATHER
• Application Number:
  US08/544,133
• Time in Patent Office: 1,246 Days
• Field of Search: 435/7.9, 435/287.27, 435/7.91, 435/28, 436/66, 436/67, 436/523, 422/82.05
• US Class Current: 436/67
• CPC Class Codes: G01N 33/721 Haemoglobin
• CPC Class Codes: G01N 33/723 Glycosylated haemoglobin

Abstract

An analysis element for analyzing both amounts of glycated hemoglobin and total hemoglobin in an aqueous liquid sample to determine glycated hemoglobin content ratio in the sample. The element comprises a substrate layer for receiving a reaction mixture after the completion of an immunological reaction between the glycated hemoglobin in the sample and an enzyme-labelled antibody against the glycated hemoglobin, and a reagent layer. The substrate layer contains a non-diffusible substrate which forms a diffusible material in the presence of the enzyme of the enzyme-labelled antibody, the activity of the enzyme being effected relative to the steric hindrance due to the immunological reaction. The reagent layer contains a reagent composition for reacting with the diffusible material to form a dye detectable colorimetrically in a wavelength range which is not effected by an absorption spectrum of the hemoglobin. The total hemoglobin retained in the substrate layer and the dye formed in the reagent layer are colorimetrically analyzed separately, and the glycated hemoglobin content ratio is calculated from respective values. An analysis method using this analysis element is also provided.

Claims

1. An analysis method for simultaneously analyzing both amounts of glycated hemoglobin and total hemoglobin in a single aqueous liquid sample so as to calculate glycated hemoglobin content ratio in the sample, the method comprising the steps of:

(a) mixing the entire single aqueous liquid sample containing hemoglobin including glycated hemoglobin with an enzyme-labelled antibody against the glycated hemoglobin to allow the antigen-antibody reaction between the glycated hemoglobin and the enzyme-labelled antibody;

(b) supplying the reaction mixture after the completion of said antigen-antibody reaction to a substrate layer containing a non-diffusible substrate which forms a diffusible material in the presence of the enzyme of said enzyme-labelled antibody, the activity of said enzyme being effected relative to the steric hindrance due to said antigen-antibody reaction;

(c) allowing said diffusible material formed in said substrate layer to migrate to a reagent layer which contains a reagent composition for reacting with the diffusible material to form a dye, the formed dye being detectable colorimetrically in a wavelength range which is not affected by an absorption spectrum of the hemoglobin, the diffusion resistance of said reagent layer being larger than the diffusion resistance of said substrate layer;

(d) measuring colorimetrically the amount of the formed dye in the reagent layer to analyze quantitatively the amount of glycated hemoglobin contained in the sample;

(e) measuring the amount of the total hemoglobin retained in the substrate layer by the colorimetrical determination at a wavelength range in which the hemoglobin has its inherent absorption, to analyze quantitatively the amount of total hemoglobin in the sample; and

(f) calculating the ratio of the glycated hemoglobin amount to the total hemoglobin amount so as to determine the glycated hemoglobin content ratio in the sample.

2. The analysis method according to claim 1, wherein said glycated hemoglobin is glycosylated hemoglobin HbA_1c.

3. The analysis method according to claim 1, wherein the colorimetric determination of total hemoglobin in said step (e) is done precedently to the formation of said pigment in the reagent layer in said step (c).

4. The analysis method according to claim 1, wherein said reagent layer is composed of a non-porous medium and said substrate layer is composed of a porous medium.

5. The analysis method according to claim 1, wherein said reagent layer contains a fragmenting enzyme for further fragmenting said diffusible material into a lower molecular weight product.

6. The analysis method according to claim 5, wherein said non-diffusible material is a high polymer polysaccharide, said enzyme of the enzyme-labelled antibody is an endo-active glucosidase, and said fragmenting enzyme is an exo-active glucosidase.

7. The analysis method according to claim 6, wherein said lower molecular weight product is glucose.

8. The analysis method according to claim 7, wherein said reagent composition reacts with said lower molecular weight product to form a peroxide.

9. The analysis method according to claim 8, wherein said reagent composition contains a leuco dye.

10. The analysis method according to claim 9, wherein said reagent layer contains a hydrophilic binder, and wherein said reagent composition contains a dispersion of a solution of said leuco dye in a water-insoluble solvent in the hydrophilic binder.

11. The analysis method according to claim 10, wherein said reagent composition contains glucose oxidase, peroxidase and the leuco dye.

12. An analysis method for simultaneously analyzing both amounts of glycated hemoglobin and total hemoglobin in a single aqueous liquid sample so as to calculate glycated hemoglobin content ratio in the sample, the method comprising the steps of:

(a) mixing the entire single aqueous liquid sample containing hemoglobin including glycated hemoglobin with an enzyme labelled antibody against the glycated hemoglobin to allow the antigen-antibody reaction between the glycated hemoglobin and the enzyme-labelled antibody;

(b) supplying the reaction mixture after the completion of said antigen-antibody reaction to a substrate layer containing a non-diffusible substrate which forms a diffusible material in the presence of the enzyme of said enzyme-labelled antibody, the activity of said enzyme being effected relative to the steric hindrance due to said antigen-antibody reaction, the diffusible material being detectable colorimetrically in a wavelength range which is not affected by an absorption spectrum of the hemoglobin;

(c) allowing said diffusible material formed in said substrate layer to migrate to a detection layer, the diffusion resistance of said detection layer being larger than the diffusion resistance of said substrate layer;

(d) measuring colorimetrically the amount of the diffusible material in the detection layer to analyze quantitatively the amount of glycated hemoglobin contained in the sample;

(e) measuring the amount of the total hemoglobin retained in the substrate layer by the colorimetrical determination at a wavelength range in which the hemoglobin has its inherent absorption, to analyze quantitatively the amount of total hemoglobin in the sample; and

(f) calculating the ratio of the glycated hemoglobin amount to the total hemoglobin amount so as to determine the glycated hemoglobin content ratio in the sample.

13. The analysis method according to claim 12, wherein said non-diffusible substrate is a dye-starch.

14. The analysis method according to claim 12, wherein said detection layer is composed of a non-porous medium and said substrate layer is composed of a porous medium.

15. The analysis method according to claim 12, wherein said glycated hemoglobin is glycosylated hemoglobin HbA_1c.

16. The analysis method according to claim 12, wherein the colorimetric determination of total hemoglobin in said step (e) is done precedently to the migration of said diffusible material to the detection layer in said step (c).