Method for measuring polyamines in erythrocytes, diagnostic method and kit for measuring polyamines in erythrocytes
AssigneeNational University Corporation Nagoya University
InventorKenji Takagi
Life of this patent
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Abstract
A method for measuring polyamines in erythrocytes in which a polyamine oxidase having a substrate specificity to spermine and spermidine or a polyamine oxidase having a substrate specificity to spermine only is used, an eluate in erythrocytes separated and purified from blood is reacted with these enzymes, and hydrogen peroxide formed is determined with a highly sensitive chromogen1 such as a diphenylamine-based chromogen. A method for measuring amounts of polyamines in erythrocytes easily with high precision. The method is effective for diagnosis of certain disease conditions or physiological conditions or the like.
Claims12
A method for measuring polyamines in erythrocytes, comprising:
- forming hydrogen peroxide by reacting an eluate of erythrocytes separated and purified from blood with at least one polyamine oxidase having a substrate specificity to spermine and spermidine, and
- measuring the hydrogen peroxide formed by reacting the hydrogen peroxide using at least one diphenylamine-based highly sensitive chromogen to measure a total amount of spermine and spermidine in the erythrocytes,
- wherein said polyamine oxidase reacts with 1 mol of spermine to relase 1 mol of hydrogen peroxide and reacts with 1 mol of spermidine to release 1 mol of hyrdrogen peroxide, and
- wherein said polyamine oxidase is an enzyme derived from a gramineous plant.
A method for measuring polyamines in erythrocytes, comprising:
- forming hydrogen peroxide by reacting an eluate of erythrocytes separated and purified from blood with a polyamine oxidase having substrate specificity to spermine, and
- measuring the hydrogen peroxide formed in the foregoing step by reacting the hydrogen peroxide with a diphenylamine-based highly sensitive chromogen to measure an amount of spermine in the erythrocytes, wherein the eluate of erythrocytes is adjusted to pH of from 4 to 5 and from 30 to 40° C., and said polyamine oxidase is a barley seedling-derived polyamine oxidase (BSPO).
A method for measuring polyamines in erythrocytes, comprising:
- obtaining a calculated value C of a spermidine amount in erythrocytes by subtracting the following measured value B from the following measured value A on the basis of the same sample of the same specimen,
- wherein measured value A is the measured value of a total amount of spermine and spermidine in erythrocytes which is obtained by forming hydrogen peroxide by reacting an eluate of erythrocytes separated and purified from blood with at least one polyamine oxidase having a substrate specificity to spermine and spermidine, and
- measuring the amount of hydrogen peroxide formed by reacting the hydrogen peroxide with at least one diphenylamine-based highly sensitive chromogen to measure a total amount of spermine and spermidine in the erythrocytes,
- wherein said polyamine oxidase reacts with 1 mol of spermine to release 1 mol of hydrogen peroxide and reacts with 1 mol of spermidine to release 1 mol of hydrogen peroxide, and
- wherein said polyamine oxidase is an enzyme derived from a gramineous plant;
- and wherein measured value B is the measured value of spermine in erythrocytes which is obtained by reacting an eluate of erythrocytes separated and purified from blood with a polyamine oxidase having substrate specificity to spermine, and determining the amount of hydrogen peroxide formed by reacting the hydrogen peroxide with a diphenylamine-based highly sensitive chromogen to measure an amount of spermine in the erythrocytes, wherein the eluate of erythrocytes is adjusted to pH of from 4 to 5 and from 30 to 40° C., and said polyamine oxidase is a barley seedling-derived polyamine oxidase (BSPO).
Dependencies are inferred from the claim text.