ON THE RELIABILITY OF THE HENDERSON-HASSELBALCH EQUATION IN ROUTINE CLINICAL ACID-BASE CHEMISTRY

This paper deals with the variability of the practical coefficient of the first ionisation equilibrium of carbonic acid as related to the CO2 in the liquid phase (Henderson-Hasselbalch equation) [Formula: see text] and that of the practical coefficient of the first ionisation equilibrium of carbonic acid as related to the CO2 in the gas phase (modified Henderson-Hasselbalch equation) [Formula: see text] </jats:p

Recommendation on mean molar activity coefficients and single ion activity coefficients of solutions for calibration of ion-selective electrodes for sodium, potassium and calcium determination (Reprinted from J Clin Chem Clin Biochem)

In principle, flame photometry measures substance concentration, and ion-selective electrodes (ISEs) measure ion activity. However, the situation regarding the comparison of results from the two techniques when applied to blood plasma is complex. The problem can be approached experimentally from the point of view of calibration of ion-selective electrodes with concentration calibrators, and similar procedures are adopted for commercial ISE-based clinical analysers. Nevertheless, there is interest in the evaluation of single ion activities in blood plasma and solutions simulating its ionic composition. Solutions are proposed for calibrating ion-selective electrodes for the determination of sodium, potassium and calcium. It is recommended that the values for single ion activities derived from the Pitzer treatment of mixed electrolyte solutions be adopted, because, although this has some empirical features, it has a sounder theoretical basis than the previously used Stokes-Robinson-Bates hydration approach