Aluminium hydroxide (AH) and aluminium phosphate (AP) adjuvants, label
led with Al-26, were injected intramuscularly (i.m.) in New Zealand Wh
ite rabbits. Blood and urine samples were collected for 28 days and an
alysed for Al-26 using accelerator mass spectrometry to determine the
absorption and elimination of AH and AP adjuvants. Al-26 was present i
n the first blood sample (1 h) for both adjuvants. The area under the
blood level curve for 28 days indicates that three times more aluminiu
m was absorbed from AP adjuvant than AH adjuvant. The distribution pro
file of aluminium to tissues was the same for both adjuvants (kidney >
spleen > liver > heart > lymph node > brain). This study has demonstr
ated that in vivo mechanisms are available to eliminate aluminium-cont
aining adjuvants after i.m. administration. In addition, the pharmacok
inetic profiles of AH and AP adjuvants are different. (C) 1997 Elsevie
r Science Ltd.