A Biomimetic Polymer for the Extraction and Purification of Superior Analogues of Amphotericin B

Todd Cowen1, Simon Walmsley1, Kal Karim1

  • 1School of Chemistry, University of Leicester, Leicester LE1 7RH, UK.

Insights

A novel biomimetic polymer simplifies the purification of 16-descarboxyl-16-methyl amphotericin B (MeAmB), a less toxic antifungal drug. This advancement offers a more efficient method for obtaining MeAmB, improving its accessibility for treating severe fungal infections and leishmaniasis.

Area of Science:

  • Biochemistry
  • Polymer Science
  • Medicinal Chemistry

Background:

  • Amphotericin B is a crucial antifungal and anti-leishmaniasis drug, but its toxicity limits clinical application.
  • Genetic engineering yielded 16-descarboxyl-16-methyl amphotericin B (MeAmB) with reduced toxicity and improved efficacy.
  • Current MeAmB extraction and purification methods are challenging and inefficient.

Purpose of the Study:

  • To develop an alternative, efficient purification method for MeAmB.
  • To design and synthesize a biomimetic polymer with high affinity for MeAmB.
  • To demonstrate the polymer's efficacy in purifying MeAmB from bacterial extracts.

Main Methods:

  • Computational modeling was used to design a biomimetic polymer with MeAmB-binding affinity.
  • The synthesized polymer was fabricated into a separation column.
  • Bacterial extracts containing MeAmB were processed through the polymer column for purification.

Main Results:

  • The biomimetic polymer column successfully retained MeAmB while removing impurities.
  • Purification yielded an MeAmB salt complex with approximately 70% MeAmB purity.
  • Mean MeAmB recovery was 81%, demonstrating high efficiency.
  • This marks the first successful purification of any amphotericin using a polymeric material.

Conclusions:

  • A novel biomimetic polymer provides an effective and efficient method for MeAmB purification.
  • The polymer-based technique offers advantages over traditional purification methods, including reusability and ease of fabrication.
  • This advancement could improve the accessibility and clinical utility of less toxic amphotericin analogues.