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. 2015 Feb 3;32(1):40–45. doi: 10.5114/pdia.2014.40968

Table 1.

Amorolfine vs. ciclopirox lacquers: comparison of properties

Parameter Amorolfine Ciclopirox
Chemical structure Morpholine derivative – phenyl-morpholine Pyridine derivative – hydroxy pyridines
Transungual drug delivery system used in the lacquer Water-insoluble polymers Water-insoluble polymers, hydroxypropyl-chitosan (HPC)
Mechanism of action Inhibits sterol synthesis in fungal cell wall, depletion of ergosterol and accumulation of non-typical spherical sterols Decrease in activity of metal-dependent enzymes which affects ion transport through cytoplasmatic membranes
Antifungal activity Dermatophytes (Trichophyton spp., Microsporum spp., Epidermophyton spp.), yeasts (Candida spp., Cryptococcus spp., Malassezia spp.), molds (Alternaria spp., Hendersonula spp., Scopulariopsis spp.), other pathogenic fungi (Cladosporium, Coccidioides, Histioplasma, Sporothrix) Dermatophytes (Trichophyton spp., Microsporum spp., Epidermophyton floccosum), yeasts (Candida spp., Malassezia furfur, Cryptococcus neoformans, Sacchromyces cerevisiae), molds (Scopulariopsis brevicaulis, Aspergillus spp., Fusarium solani)
Antibacterial activity Only Actinomyces Gram-positive bacteria (Staphylococcus spp., Streptococcus spp.), Gram-negative bacteria (Escherichia spp., Proteus spp., Klebsiella spp., Salmonella spp., Shigella spp., Bacillus spp., Pseudomonas spp.), Mycoplasma
Anti-inflammatory activity None Present