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

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,...

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Autores principales: Cowen, Todd, Walmsley, Simon, Karim, Kal, Haser, Resul, Caffrey, Patrick, Piletska, Elena, Rawlings, Bernard, Piletsky, Sergey A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377485/
https://www.ncbi.nlm.nih.gov/pubmed/37504161
http://dx.doi.org/10.3390/biomimetics8030273
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author Cowen, Todd
Walmsley, Simon
Karim, Kal
Haser, Resul
Caffrey, Patrick
Piletska, Elena
Rawlings, Bernard
Piletsky, Sergey A.
author_facet Cowen, Todd
Walmsley, Simon
Karim, Kal
Haser, Resul
Caffrey, Patrick
Piletska, Elena
Rawlings, Bernard
Piletsky, Sergey A.
author_sort Cowen, Todd
collection PubMed
description 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.
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spelling pubmed-103774852023-07-29 A Biomimetic Polymer for the Extraction and Purification of Superior Analogues of Amphotericin B Cowen, Todd Walmsley, Simon Karim, Kal Haser, Resul Caffrey, Patrick Piletska, Elena Rawlings, Bernard Piletsky, Sergey A. Biomimetics (Basel) Article 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. MDPI 2023-06-27 /pmc/articles/PMC10377485/ /pubmed/37504161 http://dx.doi.org/10.3390/biomimetics8030273 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cowen, Todd
Walmsley, Simon
Karim, Kal
Haser, Resul
Caffrey, Patrick
Piletska, Elena
Rawlings, Bernard
Piletsky, Sergey A.
A Biomimetic Polymer for the Extraction and Purification of Superior Analogues of Amphotericin B
title A Biomimetic Polymer for the Extraction and Purification of Superior Analogues of Amphotericin B
title_full A Biomimetic Polymer for the Extraction and Purification of Superior Analogues of Amphotericin B
title_fullStr A Biomimetic Polymer for the Extraction and Purification of Superior Analogues of Amphotericin B
title_full_unstemmed A Biomimetic Polymer for the Extraction and Purification of Superior Analogues of Amphotericin B
title_short A Biomimetic Polymer for the Extraction and Purification of Superior Analogues of Amphotericin B
title_sort biomimetic polymer for the extraction and purification of superior analogues of amphotericin b
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377485/
https://www.ncbi.nlm.nih.gov/pubmed/37504161
http://dx.doi.org/10.3390/biomimetics8030273
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