Method and composition for direct determination of iron in blood serum

Claim 2

A direct method for determination of iron in blood serum comprising (a) reacting the blood serum with ferrozine in the presence of a reducing agent to bring iron ion into divalent form, thiosemicarbazide and hydrochloric acid at a pH between 1.7 and 2.1, without any addition of buffers and tensioactive agents and (b) determining colorimetrically the iron content of the specimen by means of the colored complex formed between iron ion and ferrozine against a reagent blank.

Claim 3

The method of claim 1 wherein the reducing agent is ascorbic acid.

Claim 4

The method of claim 1 wherein the concentration of hydrochloric acid in the test sample submitted to colorimetric measurement is ranging between 0.05 mol/l and 0.12 mol/l.

Claim 5

The method of claim 1 wherein the concentration of ferrozine in the test sample submitted to colorimetric determination amounts from 0.4 mg/ml to 1 mg/ml.

Claim 6

The method of claim 1 wherein the concentration of thiosemicarbazide in the test sample submitted to colorimetric determination amounts from 0.5 mg/ml to 1 mg/ml.

Claim 7

The method of claim 2 wherein the concentration of ascorbic acid in the test sample amounts to at least 1.5 mg/ml.

Claim 8

In a method for direct colorimetric determination of iron in blood serum by reacting the serum iron with ferrozine in the presence of acid and a reducing agent to release serum iron from transferrin and reduce iron ion to divalent form the improvement which comprises: carrying out the iron-ferrozine reaction in the presence of sufficient thiosemicarbazide to eliminate significant copper interference, without any addition of buffer and tensioaction agents and at a pH sufficiently low that such elimination of copper interference is obtained without significant reaction of the thiosemicarbazide with iron, said low pH also being such that substantially complete formation of a colored iron-ferrozine complex is obtained.

Claim 9

In a method for direct colorimetric determination of iron in blood serum by reacting the serum iron with ferrozine in the presence of acid and a reducing agent to release serum iron from transferrin and reduce iron ion to divalent form the improvement which comprises: carrying out the iron-ferrozine reaction in the presence of sufficient thiosemicarbazide to eliminate significant copper interference, without any addition of buffer and tensioaction agents and at a pH sufficiently low that such elimination of copper interference is obtained without significant reaction of the thiosemicarbazide with iron, said low pH also being such that substantially complete formation of a colored iron-ferrozine complex is obtained.

Claim 10

Method of claim 7 wherein the pH is from about 1.7 to about 2.1.

Claim 11

A kit for colorimetric determination of iron in blood serum without protein precipitation characterized in that the reagent mixture for colorimetric determination comprises hydrochloric acid, ascorbic acid, ferrozine and thiosemicarbazide and does not require addition of tensioactive agents, the amounts of hydrochloric acid, ferrozine and thiosemicarbazide being such that substantially complete reaction of ferrozine with iron in serum, and substantially complete elimination of copper interference without substantial reaction of iron with thiosemicarbazide is obtained.

Claim 12

A kit for colorimetric determination of iron in blood serum without protein precipitation characterized in that the reagent mixture for colorimetric determination comprises hydrochloric acid, ascorbic acid, ferrozine and thiosemicarbazide and does not require addition of tensioactive agents, the amounts of hydrochloric acid, ferrozine and thiosemicarbazide being such that substantially complete reaction of ferrozine with iron in serum, and substantially complete elimination of copper interference without substantial reaction of iron with thiosemicarbazide is obtained.

Claim 13

The kit of claim 9 whereby the reagent mixture is prepared in such a way that in the test sample submitted to colorimetric measurement the concentration of hydrochloric acid ranges between 0.05 mol/l and 0.12 mol/l, the concentration of ascorbic acid ranges between 5 mg/ml and 10 mg/ml, the concentration of ferrozine ranges between 0.4 mg/ml and 1 mg/ml and the concentration of thiosemicarbazide ranges between 0.5 mg/ml and 1/ml.

Claim 14

The kit of claim 10 whereby the reagent ferrozine is added as a concentrated solution to the reaction mixture and two photometric readings are made on the sample, one before and the other after the addition of ferrozine.

Claim 15

The kit of claim 9 whereby the reactants ferrozine and ascorbic acid and the thiosemicarbazide are added to the mixture of serum and hydrochloric acid in form of tablets.

Claim 16

A tablet for use in the kit of claim 12 which contains ferrozine and ascorbic acid together with an inert carrier.

Claim 17

A reagent composition for determination of iron in blood serum consisting essentially of ferrozine, thiosemicarbazide, ascorbic acid and sufficient hydrochloric acid to provide a pH of from about 1.7 to about 2.1.

Claim 18

A reagent composition for determination of iron in blood serum consisting essentially of ferrozine, thiosemicarbazide, ascorbic acid and sufficient hydrochloric acid to provide a pH of from about 1.7 to about 2.1.