Lipid formulations of amphotericin B have demonstrated reduced toxicit
y compared with conventional amphotericin B desoxycholate, allowing hi
gher daily dosages, Three preparations with entirely different pharmac
okinetic properties are currently approved in several countries: ampho
tericin B lipid complex (Abelcet(R)), liposomal amphotericin B (AmBiso
me(R)) and amphotericin B colloidal dispersion (Amphocil(R)). Ait thre
e lipid formulations of amphotericin B share a decreased nephrotoxicit
y even at dosages of 5 mg/kg. These drugs may therefore be given succe
ssfully in patients intolerant to conventional amphotericin B, althoug
h the rates of acute infusion-related reactions may differ between the
m. Although several animal studies showed a higher therapeutic index,
high dosages were needed for treatment to be effective, It is unclear
whether and at what dose these formulations would have a better effica
cy than amphotericin B in clinical use, In-vitro studies, animal exper
iments and some clinical data suggest that one should avoid low dosage
s (1 mg/kg) of the current lipid formulations in the initial treatment
of acute fulminant fungal infections, because the efficacy may be inf
erior compared with equal dosages of conventional amphotericin B. A fi
nal judgement of the clinical efficacy and relative total cost of trea
tment with each individual formulation can only be made by direct comp
arative, clinical and pharmacoeconomic studies.