Related Experiment Video
Updated: Jun 12, 2026

Preparation of Highly Porous Coordination Polymer Coatings on Macroporous Polymer Monoliths for Enhanced Enrichment of Phosphopeptides
Published on: July 14, 2015
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.
Abstract:
Amphotericin B has been an essential drug in the fight against leishmaniasis and fungal pathogens for decades, and has more recently gained attention for the very limited microbial resistance displayed against it. However, its toxicity has restricted its use to only the most severe cases of disease, and attempts to reduce these ill effects via formulation have had only minor success. Genetic engineering has allowed the development of superior amphotericin analogues, notably 16-descarboxyl-16-methyl amphotericin B (MeAmB), which shows a ten-fold reduction in toxicity in addition to a slight improvement in therapeutic activity. However, MeAmB is difficult to extract from its bacterial source and purify. Presented here is an alternative method of MeAmB purification. A biomimetic polymer with a high affinity for MeAmB was designed via computational modelling and synthesised. Prepared as a separation column, the polymer was able to retain the target MeAmB whilst allowing the removal of cell debris from the bacterial extract. Starting with a simple bacterial extract, the relatively simple process allowed the purification of an MeAmB salt complex at approximately 70% MeAmB, and likely higher purification from further extraction. The mean MeAmB recovery between the pre-purification extract sample and the final product was 81%. This is the first successful demonstration of extraction or purification of any amphotericin molecule with any polymeric material. The biomimetic polymer was additionally reusable and simple to fabricate, giving this technique significant advantages over traditional methods of extraction and purification of valuable compounds.
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.

