Em. Johnson et al., COMPARISON OF IN-VITRO ANTIFUNGAL ACTIVITIES OF FREE AND LIPOSOME-ENCAPSULATED NYSTATIN WITH THOSE OF 4 AMPHOTERICIN-B FORMULATIONS, Antimicrobial agents and chemotherapy, 42(6), 1998, pp. 1412-1416
The in vitro activity of a multilamellar liposomal formulation of nyst
atin (Nyotran) was compared with those of free nystatin and four pharm
aceutical preparations of amphotericin B. MICs for 200 isolates of two
Aspergillus spp,, seven Candida spp., and Cryptococcus neoformans wer
e determined by a broth microdilution adaptation of the method recomme
nded by the National Committee for Clinical Laboratory Standards. Mini
mum lethal concentrations (MLCs) of the six antifungal preparations we
re also determined, Both nystatin formulations possessed fungistatic a
nd fungicidal activities against the 10 species tested. Liposomal nyst
atin appeared to be as active as free nystatin, with MICs and MLCs tha
t were similar to, or lower than, those of the latter, Neither formula
tion of nystatin was as active as amphotericin B deoxycholate (Fungizo
ne) or amphotericin B lipid complex (Abelcet), but both were more effe
ctive than liposomal amphotericin B (AmBisome). Our results suggest th
at further evaluation of liposomal nystatin is justified.