Histopathological findings in humans and extensive toxicological inves
tigation in vivo and in vitro point to an unambiguous neurotoxic poten
cy of Al(III). Experimental toxicology with aqueous Al(III) is very di
fficult owing to the complex and somewhat uncontrollable aqueous chemi
stry of the metal centre in the neutral range. The choice of neutral,
hydrolytically stable synthetic toxins makes possible both the control
of metal speciation and of analytical metal concentration down to abo
ut 1 mM in neutral buffered solutions. The employment of less stable c
omplexes like Al-2(citrate)(2)(H2O)(6) and Al(lactate)(3) or of ordina
ry salts is unavoidably complicated by the precipitation of Al(OH)(3)
under the same conditions. In spite of this, the choice of a carefully
designed protocol, based on ensuring well defined steps, enables one
to successfully control the analytical metal concentration down to 10
mu M Al(III). The control of the metal speciation at these concentrati
on levels remains an open question.