A method for determination of serum iron, total iron binding capacity and iron in urine by atomic absorption spectrophotometry with manganese as internal standard

1974 ◽  
Vol 50 (1) ◽  
pp. 35-41 ◽  
Author(s):  
C. Pronk ◽  
H. Oldenziel ◽  
H.C. Lequin
1974 ◽  
Vol 20 (3) ◽  
pp. 360-364 ◽  
Author(s):  
Yu-Yan Yeh ◽  
Paulus Zee

Abstract Because of the large quantities of venous blood required, assays of total iron-binding capacity (TIBC) and serum iron are often omitted in diagnostic tests involving small children. As an alternative to the conventional method of assessing TIBC, we developed a micromethod based on flameless atomic absorption spectrophotometry (flameless AAS). Additionally, the standard microprocedure for determining serum iron was modified so that iron concentration could be estimated from the same iron standards used to calculate TIBC. With these procedures, only 20 µl of serum is required to prepare protein-free supernate for measurement of TIBC or serum iron with an atomic absorption spectrophotometer equipped with a graphite furnace and a recorder. The resulting TIBC, serum iron, and computed transferrin saturation values compared well with those obtained by conventional flame atomic absorption spectrophotometry. The correlation was statistically significant at the 99% confidence level. These flameless AAS micromethods provide an accurate and sensitive means of determining both TIBC and serum iron in a total of 40 µl of serum, a quantity easily collected from a fingertip puncture, and hence are appropriate for routine laboratory work in pediatric clinics and for large-scale nutrition surveys.


1969 ◽  
Vol 15 (6) ◽  
pp. 438-444 ◽  
Author(s):  
Arthur D Olson ◽  
W B Hamlin

Abstract A new, atomic absorption spectrophotometric method for serum iron and iron-binding capacity is described, which utilizes 20% (w/v) TCA plus heating at 90° for 15 min. This procedure liberates the ferric iron; precipitates the protein, facilitating removal by centrifugation; and avoids significant interferences by contaminating hemoglobin iron. The method is highly specific, accurate, and has the additional feature of requiring less time than most colorimetric or atomic absorption methods employing chelation and extraction.


1978 ◽  
Vol 24 (2) ◽  
pp. 374-376 ◽  
Author(s):  
A N Fudge ◽  
C G Fraser

Abstract We describe an evaluation of the "RES-OMAT FE-59" radiometric kit (Mallinckrodt Australia Pty. Ltd.) for determination of total iron-binding capacity and unsaturated iron-binding capacity; serum iron may be calculated from total iron-binding capacity and unsaturated iron-binding capacity. Values obtained on patients' sera were compared with those obtained by continuous-flow analysis; correlation coefficients were 0.92, 0.93, and 0.88 for total iron-binding capacity, unsaturated iron-binding capacity, and iron, respectively. Precision between-run and within-run was almost identical and compares very favorably with that reported by Dixon [Ann. Clin. Biochem. 10, 127 (1973)] and that achieved in inter-laboratory surveys. Analytical recovery averaged only 83.5%, but results of analyses of sera with assigned or consensus values showed good accuracy. Satisfactory performance cannot be achieved with lyophilzed bovine quality-control materials. The kit has significant technical advantages over colorimetric methods and good short- and long-term analytical performance.


1970 ◽  
Vol 16 (2) ◽  
pp. 92-96 ◽  
Author(s):  
John A O’Malley ◽  
Anne Hassan ◽  
Judith Shiley ◽  
Henry Traynor

Abstract 2,4,6-Tripyridyl-s-triazine (TPTZ) is a color reagent for ferrous ion in the pH range 2 to 10, when ascorbic acid is used as the reducing agent. In this range TPTZ and ferrous ion combine in the ratio of two to one. Tris buffer is commonly used to maintain an alkaline pH, but it reacts with other reducing agents, rendering them ineffective. These observations suggested a method for the joint determination of serum iron and total iron-binding capacity (TIBC), all done in a single tube and with one color reagent. The method is compared with those of Peters et al. The standard deviation of the difference between the serum iron methods is less than 6 µg/100 ml, between the TIBC methods, less than 19 µg/100 ml.


Sign in / Sign up

Export Citation Format

Share Document