Eleni Axioti
Enzymatic Synthesis of Functional PEGylated Adipate Copolymers
Axioti, Eleni; Dixon, Emily G.; Jepras, Thomas; Tin He, Fen; Hartman, Peter J.V.; Hopkins, Bradley; Di Bari, Vincenzo; Suksiriworapong, Jiraphong; Cuzzucoli Crucitti, Valentina; Galantini, Luciano; Francolini, Iolanda; Cavanagh, Robert J.; Taresco, Vincenzo
Authors
Emily G. Dixon
Thomas Jepras
Fen Tin He
Peter J.V. Hartman
Dr BRADLEY HOPKINS Bradley.Hopkins@nottingham.ac.uk
EPSRC DOCTORAL PRIZE FELLOW
Dr VINCENZO DI BARI Vincenzo.DiBari@nottingham.ac.uk
ASSISTANT PROFESSOR IN FOOD STRUCTURE
Jiraphong Suksiriworapong
Dr VALENTINA CUZZUCOLI CRUCITTI VALENTINA.CUZZUCOLICRUCITTI1@NOTTINGHAM.AC.UK
RESEARCH FELLOW
Luciano Galantini
Iolanda Francolini
Dr ROBERT CAVANAGH ROBERT.CAVANAGH1@NOTTINGHAM.AC.UK
RESEARCH FELLOW
Dr VINCENZO TARESCO VINCENZO.TARESCO@NOTTINGHAM.AC.UK
Assistant Professor
Abstract
Many new active pharmaceutical ingredients (APIs) demonstrate high hydrophobicity and low water-solubility issues. In this regard, polymeric nanoparticles (NPs) have been extensively used as drug delivery carriers for the encapsulation of such APIs. One commonly used polymer is polyethylene glycol (PEG), owing to its biocompatibility, high water solubility, and capacity to prolong the drug residence time. However, concerns have arisen regarding PEG's immunogenicity and limited biodegradability. In addition, inherent limitations, including limited chemical handles can restrict PEG's effectiveness in physiological conditions. For this reason, in the present study, we combine the advantages offered by PEG with the use of an enzymatic synthetic route to produce novel PEGylated polyesters. Furthermore, it has been proven that incorporation of hydrophobic diols into the PEGylated backbone influences NPs formation, stability, and drug encapsulation, despite high chemical similarity. As a preliminary result, samples containing PEG and 1,6-hexanediol in a 50 : 50 ratio (PEGA-Hex 50 %) and PEG and 2-hydroxyethyl disulfide in a 50 : 50 ratio (PEGA-SS 50 %) have proved to be the most promising candidates in this small library analysed. Both samples exhibited sufficient NPs stability, biocompatibility, and superior encapsulation efficiency compared to the other variants.
Citation
Axioti, E., Dixon, E. G., Jepras, T., Tin He, F., Hartman, P. J., Hopkins, B., Di Bari, V., Suksiriworapong, J., Cuzzucoli Crucitti, V., Galantini, L., Francolini, I., Cavanagh, R. J., & Taresco, V. (2025). Enzymatic Synthesis of Functional PEGylated Adipate Copolymers. ChemPlusChem, 90(5), Article e202400668. https://doi.org/10.1002/cplu.202400668
Journal Article Type | Article |
---|---|
Acceptance Date | Feb 24, 2025 |
Online Publication Date | Feb 28, 2025 |
Publication Date | 2025-05 |
Deposit Date | Mar 15, 2025 |
Publicly Available Date | Mar 18, 2025 |
Journal | ChemPlusChem |
Electronic ISSN | 2192-6506 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 90 |
Issue | 5 |
Article Number | e202400668 |
DOI | https://doi.org/10.1002/cplu.202400668 |
Public URL | https://nottingham-repository.worktribe.com/output/46582817 |
Publisher URL | https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cplu.202400668 |
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