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Updated: Jul 19, 2026

Broth Microdilution In Vitro Screening: An Easy and Fast Method to Detect New Antifungal Compounds
Published on: February 14, 2018
[Emerging azole antifungals]
Michel Wolff1, Lila Bouadma, Bruno Mourvillier
1Service de Réanimation Médicale et des Maladies Infectieuses, Hôpital Bichat-Claude-Bernard, AP-HP, France. michel.wolff@bch.aphp.fr
Abstract:
Azoles have maintained a key role in the treatment of invasive fungal infections which have a growing importance, especially in immunocompromised patients. Because of its good activity and safety, fluconazole has becoming the treatment of choice for invasive candidiasis, except those caused by Candida glabrata and C. krusei. In contrast, itraconazole which is active against Aspergillus sp has limited use for the treatment of invasive mould infections due to the high variability of its bioavailibility. Voriconazole is active against a broad range of fungal pathogens including Aspergillus sp and other molds, except Zygomycetes. Voriconazole is used as first-line therapy for invasive aspergillosis and for infections caused by Fusarium and Scedosporium. It is available in both oral and intravenous administration. Posaconazole has similar in vitro activity but currently only the oral form is available. Its main indication is refractory aspergillosis or intolerance to previous treatment. Posaconzole will be very useful for long-term therapy of zygomycetes infections.
Insights
Azole antifungals are crucial for invasive fungal infections in immunocompromised patients. Fluconazole is preferred for candidiasis, while voriconazole and posaconazole target molds like Aspergillus.
Area of Science:
- Medical Mycology
- Pharmacology
- Infectious Diseases
Context:
- Invasive fungal infections (IFIs) pose a significant threat, particularly to immunocompromised individuals.
- Azole antifungals are a cornerstone in managing IFIs due to their efficacy and safety profiles.
- The emergence of resistant fungal strains necessitates a thorough understanding of azole drug characteristics.
Purpose:
- To review the current role and applications of key azole antifungal agents in treating invasive fungal infections.
- To highlight the specific indications, strengths, and limitations of fluconazole, itraconazole, voriconazole, and posaconazole.
- To inform clinical decision-making regarding the optimal use of azoles based on pathogen and patient factors.
Summary:
- Fluconazole is the primary treatment for most invasive candidiasis, excluding infections by Candida glabrata and Candida krusei.
- Itraconazole's utility for invasive mold infections is limited by variable bioavailability, despite activity against Aspergillus species.
- Voriconazole offers broad-spectrum activity against molds, including Aspergillus, and is a first-line agent for invasive aspergillosis, Fusarium, and Scedosporium infections.
- Posaconazole, available orally, shows similar in vitro activity and is indicated for refractory aspergillosis, intolerance to other treatments, and potentially for zygomycetes infections.
Impact:
- Optimized selection of azole antifungals can improve patient outcomes and reduce treatment failures in invasive fungal infections.
- Understanding drug bioavailability and spectrum of activity is critical for effective antifungal stewardship.
- Further research into novel azole formulations and resistance mechanisms will enhance the management of life-threatening fungal diseases.
Related Concept Videos
Antifungal Agents
Fungal Group Zygomycota
Candidiasis
Antiprotozoal Agents
Fungal Phylum Ascomycota
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