L. Graff et D. Burnel, A POSSIBLE NON-ALUMINUM ORAL PHOSPHATE BINDER - A COMPARATIVE-STUDY ON DIETARY PHOSPHORUS ABSORPTION, Research communications in molecular pathology and pharmacology, 89(3), 1995, pp. 373-388
The aim of this study was to highlight a possible new non-aluminum pho
sphate-binder to limit hyperphosphatemia in patients with renal failur
e. Lanthanum chloride hydrate was evaluated as a dietary phosphate bin
der in rats. Aluminum chloride hexahydrate was evaluated as a referenc
e. Animals were divided in five groups (6 animals per group): 1 contro
l group (C), 2 aluminum groups (Al-1 and Al-2), receiving different do
ses of aluminum chloride hexahydrate and 2 lanthanum groups (La-1 and
La-2), receiving different doses of lanthanum chloride hydrate. During
the treatment, urine and stools were collected. At the end of the tre
atment animals were sacrificed and plasma and different organs were co
llected (liver, spleen, kidneys, brain and femur). To highlight the po
ssible transfer of lanthanum in rat tissues, a long-term (100 days) st
udy was carried with a high dose. At the end of the treatment, lanthan
um determinations were carried out on several tissues (liver, spleen,
kidneys, brain, femur and lungs). Determinations of phosphorus and cal
cium levels in plasma indicated that lanthanum chloride hydrate showed
as good results as aluminum chloride hexahydrate. Lanthanum chloride
hydrate significantly (p < 0.01) reduced the bone phosphorus burden. D
ecreases of urinary excretion and increases in fecal excretion of phos
phorus indicated a severe phosphorus depletion in all treatments (Al a
nd La). Unfortunately, in the long-term study, lanthanum traces could
only be determined in the different tissues but not in plasma. However
, in comparison with the equivalent aluminum treatment, the transfer o
f lanthanum was less important than aluminum transfer. Consequently, l
anthanum could provide a possible alternative to aluminum.