Time-dependent speciation studies have been carried out on the ternary Al-I
II-citrate (A)-phosphate (B) system in order to clarify the solution state
of Al-III in blood serum. The potentiometric results indicate that ternary
complexes predominate both in freshly prepared mixtures and at equilibrium.
The ternary species AlAB and AlABH(-1) and the binary species AlAH(-1) and
AlBH-1 are present at physiological pH. As the solution ages the amount of
the trinuclear species [Al-3(AH(-1))(3)(OH)](4-) increases at the expense
of the mononuclear binary and ternary complexes. P-31 NMR spectra measured
at neutral pH provide corroborating evidence of the formation of the ternar
y complexes ALAB and AlABH(-1) and binary species AlBH-1 and Al2BH-3 found
potentiometrically. Time-dependent H-1 NMR measurements show that monodenta
te phosphate can slowly displace citrate from the otherwise very stable str
ucture of the trinuclear species [Al-3(AH(-1))(3)(OH)](4-). At blood serum
concentrations [c(Al-III) = 3 muM], Al-III is mostly bound to citrate eithe
r in binary species or in the ternary species formed with phosphate. Howeve
r, with increasing Al-III concentrations binding to phosphate becomes more
important.