Issue 23, 2022

Aldehyde-functional thermoresponsive diblock copolymer worm gels exhibit strong mucoadhesion

Abstract

A series of thermoresponsive diblock copolymer worm gels is prepared via reversible addition–fragmentation chain transfer (RAFT) aqueous dispersion polymerization of 2-hydroxypropyl methacrylate using a water-soluble methacrylic precursor bearing pendent cis-diol groups. Selective oxidation using an aqueous solution of sodium periodate affords the corresponding aldehyde-functional worm gels. The aldehyde groups are located within the steric stabilizer chains and the aldehyde content can be adjusted by varying the periodate/cis-diol molar ratio. These aldehyde-functional worm gels are evaluated in terms of their mucoadhesion performance with the aid of a fluorescence microscopy-based assay. Using porcine urinary bladder mucosa as a model substrate, we demonstrate that these worm gels offer a comparable degree of mucoadhesion to that afforded by chitosan, which is widely regarded to be a ‘gold standard’ positive control in this context. The optimum degree of aldehyde functionality is approximately 30%: lower degrees of functionalization lead to weaker mucoadhesion, whereas higher values compromise the desirable thermoresponsive behavior of these worm gels.

Graphical abstract: Aldehyde-functional thermoresponsive diblock copolymer worm gels exhibit strong mucoadhesion

Supplementary files

Article information

Article type
Edge Article
Submitted
11 Apr 2022
Accepted
17 May 2022
First published
26 May 2022
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2022,13, 6888-6898

Aldehyde-functional thermoresponsive diblock copolymer worm gels exhibit strong mucoadhesion

E. E. Brotherton, T. J. Neal, D. B. Kaldybekov, M. J. Smallridge, Vitaliy V. Khutoryanskiy and S. P. Armes, Chem. Sci., 2022, 13, 6888 DOI: 10.1039/D2SC02074B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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