Hippuric acid (HA) originating from the conjugation of benzoic acid with gl
ycine is a physiological component of human urine. Findings suggest that HA
inhibits calcium oxalate (CaOx) growth and considerably enhances the CaOx
solubility in artificial urine. Thus, it is assumed that HA is a major modi
fier of CaOx formation. However, only a slight CaOx growth inhibition of 1-
8 % was also reported. These values were also derived from artificial urine
. The key mechanism, which led HA to be of interest in urolithiasis researc
h is the fact that in presence of Ca2+ ions HA can form a hippurate complex
. By forming such a complex, Ca2+ concentration in urine decreases, and as
a consequence, CaOx formation is inhibited.
This study was performed in order to clarify the role of HA in native and a
rtificial urine. Biochemical analyses to calculate the relative CaOx supers
aturations and crystallisation experiments using an in-line laser probe wer
e examined. BONN Risk Indices indicating the risk of CaOx crystallisation w
ere calculated from the results of the crystallisation experiments.
The results obtained from artificial as well as from native urines showed t
hat HA has no significant effects on CaOx formation. We suggest that HA pla
ys only a minor role as a crystallisation modifier in human urine.