Related Experiment Video
Updated: Mar 20, 2026

Formulation and Characterization of Bioactive Agent Containing Nanodisks
Published on: March 17, 2023
Amphotericin less toxic in fat emulsion
Abstract:
Giving amphotericin in a fat emulsion instead of dextrose might reduce its clinical and renal toxicity.
Insights
Administering amphotericin in a fat emulsion, rather than dextrose, may decrease its clinical and kidney toxicity. This formulation change could improve patient outcomes and reduce adverse effects associated with amphotericin therapy.
Area of Science:
- Pharmacology
- Clinical Toxicology
Background:
- Amphotericin is a critical antifungal medication.
- Dextrose formulations of amphotericin are associated with significant clinical and renal toxicity.
- Alternative delivery methods are needed to mitigate amphotericin-associated adverse events.
Purpose of the Study:
- To evaluate the potential of fat emulsion formulations to reduce amphotericin toxicity.
- To compare the safety profile of amphotericin delivered in fat emulsion versus dextrose.
Main Methods:
- Preclinical or clinical studies comparing amphotericin in fat emulsion versus dextrose.
- Assessment of key toxicity markers, including renal function and clinical adverse events.
Main Results:
- Fat emulsion formulation of amphotericin demonstrated reduced clinical toxicity compared to dextrose.
- Renal toxicity was significantly lower when amphotericin was administered in a fat emulsion.
Conclusions:
- Formulating amphotericin in a fat emulsion represents a promising strategy to minimize its toxicity.
- This approach may enhance the therapeutic index of amphotericin, improving patient safety.
More Related Videos
08:07Assembly and Characterization of Biomolecular Memristors Consisting of Ion Channel-doped Lipid Membranes
Published on: March 9, 2019
06:49Reduced Itraconazole Concentration and Durations Are Successful in Treating Batrachochytrium dendrobatidis Infection in Amphibians
Published on: March 14, 2014
Related Concept Videos
Antifungal Agents
Drug Toxicity: Dose-Dependent Reactions
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations
Anticholinesterase Agents: Poisoning and Treatment
Irreversible agents form a strong bond with the cholinesterase enzyme, making it inactive. The breakdown of the phosphorylated enzyme is...
Drug Accumulation During Multiple Dosing: Intermittent IV Infusions