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Solution behavior and encapsulation properties of fatty acid–elastin-like polypeptide conjugates

Developing new biomaterials is an active research area owing to their applications in regenerative medicine, tissue engineering and drug delivery. Elastin-like polypeptides (ELPs) are good candidates for these applications because they are biosourced, biocompatible and biodegradable. With the aim of...

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Autores principales: Zhang, Tingting, Peruch, Frédéric, Weber, Amélie, Bathany, Katell, Fauquignon, Martin, Mutschler, Angela, Schatz, Christophe, Garbay, Bertrand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835928/
https://www.ncbi.nlm.nih.gov/pubmed/36712617
http://dx.doi.org/10.1039/d2ra06603c
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author Zhang, Tingting
Peruch, Frédéric
Weber, Amélie
Bathany, Katell
Fauquignon, Martin
Mutschler, Angela
Schatz, Christophe
Garbay, Bertrand
author_facet Zhang, Tingting
Peruch, Frédéric
Weber, Amélie
Bathany, Katell
Fauquignon, Martin
Mutschler, Angela
Schatz, Christophe
Garbay, Bertrand
author_sort Zhang, Tingting
collection PubMed
description Developing new biomaterials is an active research area owing to their applications in regenerative medicine, tissue engineering and drug delivery. Elastin-like polypeptides (ELPs) are good candidates for these applications because they are biosourced, biocompatible and biodegradable. With the aim of developing ELP-based micelles for drug delivery applications we have synthesized 15 acyl-ELP compounds by conjugating myristic, palmitic, stearic, oleic or linoleic acid to the N-terminus of three ELPs differing in molar mass. The ELP–fatty acid conjugates have interesting solution behavior. They form micelles at low temperatures and aggregate above the cloud point temperature (Tcp). The critical micelle concentration depends on the fatty acid nature while the micelle size is mainly determined by the ELP block length. We were able to show that ELPs were better hydrated in the micelles than in their individual state in solution. The micelles are stable in phosphate-buffered saline at temperatures below the Tcp, which can vary between 20 °C and 38 °C depending on the length or hydrophilicity of the ELP. Acyl-ELP micelles were loaded with the small hydrophobic molecule Nile red. The encapsulation efficiency and release kinetics showed that the best loading conditions were achieved with the largest ELP conjugated to stearic acid.
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spelling pubmed-98359282023-01-26 Solution behavior and encapsulation properties of fatty acid–elastin-like polypeptide conjugates Zhang, Tingting Peruch, Frédéric Weber, Amélie Bathany, Katell Fauquignon, Martin Mutschler, Angela Schatz, Christophe Garbay, Bertrand RSC Adv Chemistry Developing new biomaterials is an active research area owing to their applications in regenerative medicine, tissue engineering and drug delivery. Elastin-like polypeptides (ELPs) are good candidates for these applications because they are biosourced, biocompatible and biodegradable. With the aim of developing ELP-based micelles for drug delivery applications we have synthesized 15 acyl-ELP compounds by conjugating myristic, palmitic, stearic, oleic or linoleic acid to the N-terminus of three ELPs differing in molar mass. The ELP–fatty acid conjugates have interesting solution behavior. They form micelles at low temperatures and aggregate above the cloud point temperature (Tcp). The critical micelle concentration depends on the fatty acid nature while the micelle size is mainly determined by the ELP block length. We were able to show that ELPs were better hydrated in the micelles than in their individual state in solution. The micelles are stable in phosphate-buffered saline at temperatures below the Tcp, which can vary between 20 °C and 38 °C depending on the length or hydrophilicity of the ELP. Acyl-ELP micelles were loaded with the small hydrophobic molecule Nile red. The encapsulation efficiency and release kinetics showed that the best loading conditions were achieved with the largest ELP conjugated to stearic acid. The Royal Society of Chemistry 2023-01-12 /pmc/articles/PMC9835928/ /pubmed/36712617 http://dx.doi.org/10.1039/d2ra06603c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhang, Tingting
Peruch, Frédéric
Weber, Amélie
Bathany, Katell
Fauquignon, Martin
Mutschler, Angela
Schatz, Christophe
Garbay, Bertrand
Solution behavior and encapsulation properties of fatty acid–elastin-like polypeptide conjugates
title Solution behavior and encapsulation properties of fatty acid–elastin-like polypeptide conjugates
title_full Solution behavior and encapsulation properties of fatty acid–elastin-like polypeptide conjugates
title_fullStr Solution behavior and encapsulation properties of fatty acid–elastin-like polypeptide conjugates
title_full_unstemmed Solution behavior and encapsulation properties of fatty acid–elastin-like polypeptide conjugates
title_short Solution behavior and encapsulation properties of fatty acid–elastin-like polypeptide conjugates
title_sort solution behavior and encapsulation properties of fatty acid–elastin-like polypeptide conjugates
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835928/
https://www.ncbi.nlm.nih.gov/pubmed/36712617
http://dx.doi.org/10.1039/d2ra06603c
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