Immunoassay using insoluble carrier particles and reagent therefor
The present invention provides a reagent for an immunoassay comprising insoluble carrier particles which can give the values to be determined with high accuracy and reliability, and can be stored for a long time; an immunoassay using the reagent; and a method for keeping the reagent stable. The present invention provides an immunoassay which comprises carrying out an antigen-antibody reaction using insoluble carrier particles in an aqueous medium comprising a buffer having its buffer capacity in a neutral or alkaline region (except for a carbonate-based buffer) and a carbonic acid compound releasing a bicarbonate ion; a reagent for an immunoassay comprising a buffer having its buffer capacity in a neutral or alkaline region (except for a carbonate-based buffer), a carbonic acid compound releasing bicarbonate ion, and insoluble carrier particles; and a method for keeping the reagent for an immunoassay comprising insoluble carrier particles stable, which comprises allowing insoluble carrier particles to co-exist in an aqueous medium comprising a buffer having its buffer capacity in a neutral or alkaline region (except for a carbonate-based buffer) and a carbonic acid compound releasing a bicarbonate ion.
1. A nephelometric immunoassay, which comprises the steps of:
1) preparing a suspension by adding insoluble carrier particles carrying neither a substance to be determined nor antibodies to the substance to an aqueous medium consisting essentially of a buffer having its buffer capacity in a neutral or alkaline region except for a carbonate-based buffer and a carbonic acid compound releasing a bicarbonate ion;
2) keeping the suspension of step 1);
3) reacting the suspension comprising the insoluble carrier particles with a sample comprising substance to be determined;
4) adding a reagent comprising antibodies reactive with the substance to be determined to the mixture of step 3); and
5) measuring agglutination of insoluble carrier particles formed in step 4).
2. The immunoassay according to claim 1 , wherein the substance to be determined is hemoglobin A1c.
3. The immunoassay according to claim 1 , wherein the carbonic acid compound releasing a bicarbonate ion is an alkali metal compound.
4. The immunoassay according to claim 1 , wherein the concentration of the bicarbonate ion is 0.05 to 500 mmol/L.
5. The immunoassay according to claim 1 , wherein the concentration of the buffer having its buffer capacity in a neutral or alkaline region is 0.1 to 500 mmol/L.
6. The immunoassay according to claim 1 , wherein the insoluble carrier particles are latex.