Philippa L. Jacob
Poly (glycerol adipate) (PGA) backbone modifications with a library of functional diols: Chemical and physical effects
Jacob, Philippa L.; Ruiz Cantu, Laura A.; Pearce, Amanda K.; He, Yinfeng; Lentz, Joachim C.; Moore, Jonathan C.; Machado, Fabricio; Rivers, Geoffrey; Apebende, Edward; Fernandez, Maria Romero; Francolini, Iolanda; Wildman, Ricky; Howdle, Steven M.; Taresco, Vincenzo
Authors
Laura A. Ruiz Cantu
Amanda K. Pearce
Dr YINFENG HE Yinfeng.He@nottingham.ac.uk
TRANSITIONAL ASSISTANT PROFESSOR
Joachim C. Lentz
Mr JONATHAN MOORE J.Moore@nottingham.ac.uk
RESEARCH FELLOW
Fabricio Machado
Dr GEOFFREY RIVERS GEOFFREY.RIVERS@NOTTINGHAM.AC.UK
Assistant Professor
Edward Apebende
Maria Romero Fernandez
Iolanda Francolini
Professor RICKY WILDMAN RICKY.WILDMAN@NOTTINGHAM.AC.UK
PROFESSOR OF MULTIPHASE FLOW AND MECHANICS
Professor STEVE HOWDLE STEVE.HOWDLE@NOTTINGHAM.AC.UK
PROFESSOR OF CHEMISTRY
Dr VINCENZO TARESCO VINCENZO.TARESCO@NOTTINGHAM.AC.UK
NOTTINGHAM RESEARCH FELLOW
Abstract
Enzymatically synthesised poly(glycerol adipate) (PGA) has shown a palette of key desirable properties required for a biomaterial to be considered a ‘versatile polymeric tool’ in the field of drug delivery. PGA and its variations can self-assemble into nanoparticles (NPs) and interact at different levels with small active molecules. PGA derivatives are usually obtained by functionalising the glyceryl side hydroxyl group present along the main polymer scaffold. However, if the synthetic pathways are not finely tuned, the self-assembling ability of these new polymeric modifications might be hampered by the poor amphiphilic balance. For this reason, we have designed a straightforward one-pot synthetic modification, using a small library of diols in combination with glycerol, aimed at altering the backbone of the polymer without affecting the hydrophilic glyceryl portion. The diols introduce additional functionality into the backbone of PGA alongside the secondary hydroxyl group already present. We have investigated how extra functionalities along the polymer backbone alter the final polymer reactivity as well the chemical and biological properties of the nanoparticles. In addition, with the intent to further improve the green credentials of the enzymatic synthesis, a solvent derived from renewable resources, (2-methyl tetrahydrofuran, 2-MeTHF) was employed for the synthesis of all the PGA-variants as a replacement for the more traditionally used and fossil-based tetrahydrofuran (THF). In vitro assays carried out to evaluate the potential of these novel materials for drug delivery applications demonstrated very low cytotoxicity characteristic against NIH 3T3 model cell line.
Citation
Jacob, P. L., Ruiz Cantu, L. A., Pearce, A. K., He, Y., Lentz, J. C., Moore, J. C., Machado, F., Rivers, G., Apebende, E., Fernandez, M. R., Francolini, I., Wildman, R., Howdle, S. M., & Taresco, V. (2021). Poly (glycerol adipate) (PGA) backbone modifications with a library of functional diols: Chemical and physical effects. Polymer, 228, Article 123912. https://doi.org/10.1016/j.polymer.2021.123912
Journal Article Type | Article |
---|---|
Acceptance Date | May 27, 2021 |
Online Publication Date | Jun 2, 2021 |
Publication Date | Jul 16, 2021 |
Deposit Date | Jun 3, 2021 |
Publicly Available Date | Jun 3, 2022 |
Journal | Polymer |
Print ISSN | 0032-3861 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 228 |
Article Number | 123912 |
DOI | https://doi.org/10.1016/j.polymer.2021.123912 |
Keywords | Polyglycerol adipate (PGA); Enzymatic polymerisation; Self-assembly |
Public URL | https://nottingham-repository.worktribe.com/output/5623788 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S0032386121005358?via%3Dihub |
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