Fungal infections represent an increasing portion of the opportunistic
and hospital-acquired infections and are associated with high morbidi
ty and mortality. For years the field of antifungal chemotherapy was d
ominated by amphotericin B despite its severe adverse effects and trea
tment failures. Intensive efforts to limit the acute and chronic toxic
ity of the drug without attenuating its clinical efficacy and broad sp
ectrum of activity have led to the development of the newer lipid form
ulations of amphotericin B. Amphotericin B lipid complex is a promisin
g new formulation containing the active compound tightly packed in rib
bon-like lipid structures (7:3 DMPC/DMPG with amphotericin B 35 mol %)
. Numerous in vitro and animal studies have shown that ABLC has the sa
me spectrum of activity with amphotericin B-deoxycholate, with reduced
toxicity and improved pharmacokinetics and pharmacodynamics. Recently
completed human studies, including randomized controlled trials, clea
rly suggest that ABLC is at least as effective and much better tolerat
ed than conventional amphotericin B in the treatment of invasive candi
diasis, aspergillosis and other life-threatening fungal infections. Cu
rrently, the use of ABLC should be considered for patients refractory,
or intolerant to amphotericin B. The exact role of ABLC and the other
lipid formulations in the management of serious mycoses in selected p
atient populations should be clarified by further clinical trials and
cost-efficacy analyses.