SKU: M035  / 
    CAS Number: 208538-73-2

    Micafungin Sodium

    $228.00 - $949.00

    Micafungin Sodium is the sodium salt of the semi-synthetic cyclic lipopeptide Micafungin.  Micafungin is an antifungal compound belonging to the antifungal class known as echinocandins.  It was reported in 1999 by Fujisawa (Japan).  It is synthesized from a fermentation product of Coleophoma empetri.  The sodium salt takes advantage of the aryl sulfate moiety providing improved water solubility and is the preferred formulation for in vitro studies.  

    Micafungin Sodium is soluble in ethanol, methanol, DMF or DMSO. Moderate water solubility.

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    Mechanism of Action Like all echinocandins, Micafungin inhibits β-(1,3)-D-glucan synthase which inhibits the synthesis of β-(1,3)-D-glucan, an essential component of the fungal cell wall.
    Spectrum Fungidical against most yeasts (Candida spp. )including those species resistant to fluconazole.  Fungistatic against Aspergillus spp.
    Microbiology Applications

    Micafungin is used for Candida causing candidemia, acute disseminated candidiasis.  It can also be used against Aspergillus and has been used in combination for aspergillosis studies.

    Broth dilution (BD) is the reference method for mold antifungal-susceptibility testing.  It involves serial two-fold dilutions of the antifungal in liquid medium inoculated with a standardized number of condia and incubated for a set period of time.  Clinical interpretive breakpoints (CBPs) for in vitro mold-susceptibility testing have not been established.  However, epidemiological-cutoff values (ECVs) can be used, defined as an MIC cut-off value that discriminates wild-type (WT) isolates from non-WT strains.  ECVs and WT MIC distributions are available for Aspergillus spp. and may help in detecting drug resistance (Powers-Fletcher et al, 2016).

    Echinocandins allow molds to germinate but inhibit growth at the tip of the emerging hyphae. This appears in culture microwell plates as compact, round “rosette” forms instead of extended hyphal growth. The lowest drug concentration that alters growth in this manner is referred to as the minimum effective concentration (MEC).

    Differences in methods between CLSI and EUCAST standards may impact MIC or MEC determination. Differences include glucose concentration, well shape, inoculum concentration and the fact that EUCAST has validated spectrometer readings for A. fumigatus.

    Disk diffusion testing of Candida spp. is available from CLSI  which provides zone diameters and interpretative criteria for common Candida spp. and Micafungin.

    In vitro activity of Micafungin against Candida spp. biofilms at different states of maturation (2, 6 and 24 h).  Clinical isolates (N=78)  growing as planktonic or sessile cells via broth microdilution methods were evaluated.  Findings confirm that Micafungin has high potential anti-Candida-biofilm activity but this effect does not comprise all Candida species and strains.  When growing as planktonic cells, strains were susceptible or intermediate.  However, for biofilms, Micafungin displays species- and strain-specific activity and the strongest antibiofilm activity is observed at early stages of biofilm formation (Prażyńska et al, 2018).

    Molecular Formula C56H71N9NaO23S
    References

     

    Powers-Fletcher MV, Kendall BA, Griffin AT, Hanson KE (2016)  Filamentous Fungi. Microbiol Spectr 4:10.1128

    Prażyńska M, Bogiel T and Gospodarek-Komkowska E (2018)  In vitro activity of Micafungin against biofilms of Candida albicansCandida glabrata, and Candida parapsilosis at different stages of maturation. Folia Microbiol 63:209–216

    Tomishima M. et al (1999)  FK463, a novel water-soluble echinocandin lipopeptide: Synthesis and antifungal activity. J. Antibiot. 52:674

    Wayne PA (2022)  Clinical and Laboratory Standards Institute.  Performance standards for antifungal susceptibility testing of yeasts.  3rd ed.  CLSI supplement M27M44S.

    Vehreschild J and Cornely AO (2006)  Micafungin Sodium, the second of the echinocandin class of antifungals: Theory and practice.  Future Microbiol. 1(2): 161–170