IN-VIVO ACTIVITY AND TOLERANCE OF CONVENTIONAL FORMULATION VERSUS FATEMULSION FORMULATION OF AMPHOTERICIN-B IN EXPERIMENTAL DISSEMINATED CANDIDIASIS IN NEUTROPENIC RABBITS
P. Chavanet et al., IN-VIVO ACTIVITY AND TOLERANCE OF CONVENTIONAL FORMULATION VERSUS FATEMULSION FORMULATION OF AMPHOTERICIN-B IN EXPERIMENTAL DISSEMINATED CANDIDIASIS IN NEUTROPENIC RABBITS, Journal of antimicrobial chemotherapy, 39(3), 1997, pp. 427-430
Amphotericin a can cause significant toxicity but this can be reduced
by direct dilution into a fat emulsion (Intralipid). To investigate th
e potential use of amphotericin B diluted in Intralipid, a study was m
ade of its activity in the treatment of subacute disseminated candidia
sis in persistently granulocytopenic rabbits, compared with the same d
ose of amphotericin B diluted in dextrose. Amphotericin-B-fat emulsion
was at least as effective as amphotericin-B-dextrose. Amphotericin-B-
fat emulsion was significantly more effective than amphotericin-B-dext
rose therapy in reducing candida colony counts in both kidney and live
r tissues (P < 0.05). Furthermore, amphotericin-B-fat emulsion was fou
nd less toxic on the renal function than conventional amphotericin B (
P < 0.05). From these experimental results, we conclude that amphoteri
cin-B-fat emulsion (Intralipid) was at least as effective and less tox
ic than conventional amphotericin B.