Determination of urinary sodium and potassium by ion-selective electrodes and flame photometry compared.

1982 ◽  
Vol 28 (7) ◽  
pp. 1710-1711 ◽  
Author(s):  
R G Burr
1994 ◽  
Vol 40 (6) ◽  
pp. 869-872 ◽  
Author(s):  
M Sampson ◽  
M Ruddel ◽  
R J Elin

Abstract We compared five ion-selective electrodes (ISEs; AVL 985S, Baxter Lytening 2Z, Beckman EL-ISE, Ciba-Corning 654 Na/K/Li, and Nova CRT 11) and a colorimetric method (Ektachem) for determination of lithium with flame atomic absorption and atomic emission spectroscopy. We evaluated precision, recovery, interference by drugs (procainamide, N-acetylprocainamide, quinidine, lidocaine, carbamazepine, and valproic acid) and inorganic analytes (Na, K, Ca, Mg, and Br), and performance with sera from patients receiving lithium. Imprecision was < 5% (CV) for all analyzers except Ektachem and Beckman. Analytical recovery was 100% +/- 5% for all analyzers except Ektachem and Baxter. Some drug interference was seen with all analyzers except AVL and Corning. Calcium caused interference with AVL, Corning, and Ektachem analyzers, and sodium and potassium interfered with the Ektachem analyzer. The results with the Baxter, Beckman, and Corning analyzers were closest to those by flame atomic emission (mean differences, 0.01 to 0.02 mmol/L); the AVL and Nova analyzers gave lower results (mean differences, -0.11 to -0.13 mmol/L) and the Ektachem gave higher results (mean difference, 0.08 mmol/L).


1975 ◽  
Vol 15 (3) ◽  
pp. 217-222 ◽  
Author(s):  
John H. Puffer ◽  
Robert S. Cohen

RSC Advances ◽  
2021 ◽  
Vol 11 (57) ◽  
pp. 36215-36221
Author(s):  
Liubov V. Pershina ◽  
Andrei R. Grabeklis ◽  
Ludmila N. Isankina ◽  
Ekaterina V. Skorb ◽  
Konstantin G. Nikolaev

Supramolecular assemblies based on polyelectrolyte complexes made it possible to create complex interfaces with predictable properties. Polyelectrolyte complexes serve as a pseudo-liquid contact in ion-selective electrodes.


1956 ◽  
Vol 2 (2) ◽  
pp. 112-116 ◽  
Author(s):  
R L Dryer

Abstract A method for the determination of serum sodium and potassium involving only a single serum dilution is described. Samples of 0.1 ml. of serum suffice for both determinations, but larger samples may also be used. By careful control of the lithium concentration and the dilution factor the mean relative photometric error may be held to no more than 1 per cent under normal circumstances of operation.


1981 ◽  
Vol 27 (8) ◽  
pp. 1435-1438 ◽  
Author(s):  
G B Levy

Abstract The advent of ion-selective electrodes made possible the potentiometry of sodium in serum and plasma. These methods were based on dilution of serum, as done in flame photometry, and the results were identical. Analysis of whole blood precludes dilution and so "direct" potentiometry was developed. Results by this technique are variable but tend to compensate for the spurious hyponatremias found by the "indirect" dilution methods due to displacement of volume by lipids and protein. However, there is no unambiguous theoretical basis on which to choose between the various direct ion-selective-electrode techniques and instruments. As an alternative, I propose use of current indirect methods, with numerical correction for the shift in normal sodium values in the presence of abnormal lipid and (or) protein. A table was constructed for making such corrections.


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