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Amphotericin B intralipid formulation: stability and particle size

J Y Ranchère1, J F Latour, C Fuhrmann

  • 1Department of Anesthesiology, Cancer Center Léon Bérard, Lyon, France.

Insights

Intralipid deoxycholate amphotericin B is not a stable formulation for treating fungal infections. This in-vitro study found precipitate and particle size increases, indicating potential risks with this amphotericin B delivery system.

Area of Science:

  • Mycology
  • Pharmacology
  • Pharmaceutical Technology

Background:

  • Amphotericin B is a critical antifungal agent for systemic infections.
  • Its clinical utility is often limited by significant toxicity.
  • Intralipid formulations are explored to improve drug delivery and reduce toxicity.

Purpose of the Study:

  • To evaluate the in-vitro compatibility and stability of deoxycholate amphotericin B when formulated with Intralipid.
  • To assess the physical characteristics of Intralipid deoxycholate amphotericin B solutions.

Main Methods:

  • In-vitro assessment of deoxycholate amphotericin B solutions.
  • Two dilution methods were used: deoxycholate amphotericin B in 5% dextrose and Intralipid, or deoxycholate amphotericin B in Intralipid alone.
  • Solution stability and particle size were analyzed.

Main Results:

  • Deoxycholate amphotericin B solutions in Intralipid exhibited instability.
  • A clear yellow precipitate formed in the tested formulations.
  • Significant increases in particle size (1.5-4-fold) were observed.

Conclusions:

  • Intralipid deoxycholate amphotericin B is not a stable or recommended formulation.
  • The observed instability and particle aggregation suggest potential risks for routine administration.
  • Further research into safer amphotericin B delivery systems is warranted.

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