Polyenes - Ampho-terrible Toxicity

- Mechanism: Bind to ergosterol in the fungal cell membrane, forming pores that lead to leakage of intracellular contents and cell death.
| Drug | Spectrum of Activity | Clinical Use | Key Toxicity |
|---|---|---|---|
| Amphotericin B | Broad: Candida, Aspergillus, Cryptococcus, endemic mycoses. (Resistant: C. lusitaniae) | Severe, systemic mycoses. | 📌 Ampho-terrible: Nephrotoxicity, infusion reactions (fever, chills - "shake & bake"), electrolyte wasting (↓K⁺, ↓Mg²⁺). |
| Nystatin | Narrower; primarily Candida species. | Topical for oropharyngeal/cutaneous candidiasis ("swish and swallow/spit"). | Too toxic for systemic use; minimal side effects with topical/oral use. |
Azoles - Conazoles Get Confusing

Inhibit ergosterol synthesis by blocking fungal cytochrome P450 enzyme 14α-demethylase. Generally fungistatic.
| Drug | Candida | C. krusei/glabrata | Aspergillus | Cryptococcus | Zygomycetes | Endemic Mycoses |
|---|---|---|---|---|---|---|
| Fluconazole | ++ | - | - | + | - | ++ (Coccidio) |
| Itraconazole | + | - | +/- | + | - | ++ |
| Voriconazole | ++ | + | ++ | + | - | + |
| Posaconazole | ++ | + | + | + | + | + |
📌 Mnemonic: For Candida/Crypto? Fluconazole. Aspergillus? Voriconazole. Zygomycetes? Posaconazole.
Echinocandins - Fungins Finish Walls
📌 "-fungin" drugs finish fungal cell walls.
- Agents: Caspofungin, Micafungin, Anidulafungin.
- Mechanism: Inhibit cell wall synthesis by blocking $β(1,3)$-D-glucan synthase.
- Spectrum of Activity:
- Excellent vs.: Most Candida (including fluconazole-resistant C. glabrata/krusei) and Aspergillus.
- Ineffective vs.: Cryptococcus, Zygomycetes, and dimorphic fungi.
-D-glucan synthase inhibition in the fungal cell wall)
⭐ Administered only IV, these large lipopeptide molecules are favored for critically ill patients with invasive candidiasis due to their potent efficacy and excellent safety profile.
Miscellaneous Antifungals - The Odd Ones Out
| Agent | Mechanism | Spectrum | Key Use |
|---|---|---|---|
| Flucytosine (5-FC) | Inhibits DNA/RNA synthesis | Cryptococcus, Candida | Systemic mycoses |
| Griseofulvin | Disrupts mitotic spindle | Dermatophytes | Tinea capitis |
| Terbinafine | Inhibits squalene epoxidase | Dermatophytes | Onychomycosis |
High‑Yield Points - ⚡ Biggest Takeaways
- Amphotericin B has the broadest spectrum of activity, covering most clinically relevant yeasts, molds (including Mucorales), and endemic fungi.
- Voriconazole is the drug of choice for invasive Aspergillosis; it also provides excellent coverage for most Candida species.
- Echinocandins are highly active against Candida (including azole-resistant C. glabrata) and Aspergillus but have no activity against Cryptococcus.
- Fluconazole has a narrow spectrum, excellent for C. albicans and Cryptococcus maintenance, but misses molds and C. krusei.
- Itraconazole is the treatment of choice for non-severe, non-meningeal endemic mycoses like Histoplasmosis and Blastomycosis.
- Flucytosine is always used in combination, typically with Amphotericin B for cryptococcal meningitis.
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