The University of Southampton
University of Southampton Institutional Repository

Controllable hydrogen bonded self-association for the formation of multifunctional antimicrobial materials

Controllable hydrogen bonded self-association for the formation of multifunctional antimicrobial materials
Controllable hydrogen bonded self-association for the formation of multifunctional antimicrobial materials
SSAs are a class of supramolecular self-associating amphiphilic salt, the anionic component of which contains a covalently bound hydrogen bond donor–acceptor motif. This results in a monomeric unit which can adopt multiple hydrogen bonding modes simultaneously. Previous investigations have shown examples of SSAs to act as antimicrobial agents against clinically relevant methicillin-resistant Staphylococcus aureus (MRSA). Herein, we report an intrinsically fluorescent SSA which can self-associate producing dimers, spherical aggregates and hydrogels dependent on solvent environment, while retaining antimicrobial activity against both model Gram-positive (MRSA) and Gram-negative (Escherichia coli) bacteria. Finally, we demonstrate the SSA supramolecular hydrogel to tolerate the inclusion of the antibiotic ampicillin, leading to the enhanced inhibition of growth with both model bacteria, and derive initial molecular structure–physicochemical property–antimicrobial activity relationships.
2050-750X
4694-4700
White, Lisa J.
66137725-b91a-4157-ba97-56607f2dbadf
Boles, Jessica E.
13ce5778-19eb-4276-8328-d865a86f3c2c
Allen, Nyasha
340bcea8-ba6f-4500-b739-4d41b25bdcca
Alesbrook, Luke S.
2bf0d03e-2c96-49de-a390-5d6466cfeac7
Sutton, J. Mark
b6a22e5d-9ba1-454f-8153-8c5e26346300
Hind, Charlotte K.
fffbf552-21d9-41dd-9b0e-f75d71e2ab4e
Hilton, Kira L. F.
cc0687ab-e382-4117-9407-ab836b6f94e3
Blackholly, Laura R.
c8063cc4-ec80-40e7-bdd6-af1dd40c43c1
Ellaby, Rebecca J.
0b21ccab-3a2d-441f-bb52-d71c3f936ba9
Williams, George
26810522-92ef-4b61-a766-582bf15be280
Mulvihill, Daniel P.
702f83c0-c2e5-48f0-b745-62a7976a248d
Hiscock, Jennifer
030e8366-b001-41b9-ac1a-3bc400d9edc4
et al.
White, Lisa J.
66137725-b91a-4157-ba97-56607f2dbadf
Boles, Jessica E.
13ce5778-19eb-4276-8328-d865a86f3c2c
Allen, Nyasha
340bcea8-ba6f-4500-b739-4d41b25bdcca
Alesbrook, Luke S.
2bf0d03e-2c96-49de-a390-5d6466cfeac7
Sutton, J. Mark
b6a22e5d-9ba1-454f-8153-8c5e26346300
Hind, Charlotte K.
fffbf552-21d9-41dd-9b0e-f75d71e2ab4e
Hilton, Kira L. F.
cc0687ab-e382-4117-9407-ab836b6f94e3
Blackholly, Laura R.
c8063cc4-ec80-40e7-bdd6-af1dd40c43c1
Ellaby, Rebecca J.
0b21ccab-3a2d-441f-bb52-d71c3f936ba9
Williams, George
26810522-92ef-4b61-a766-582bf15be280
Mulvihill, Daniel P.
702f83c0-c2e5-48f0-b745-62a7976a248d
Hiscock, Jennifer
030e8366-b001-41b9-ac1a-3bc400d9edc4

White, Lisa J., Boles, Jessica E., Allen, Nyasha and Williams, George , et al. (2020) Controllable hydrogen bonded self-association for the formation of multifunctional antimicrobial materials. Journal of Materials Chemistry B, 2020 (8), 4694-4700. (doi:10.1039/D0TB00875C). (In Press)

Record type: Article

Abstract

SSAs are a class of supramolecular self-associating amphiphilic salt, the anionic component of which contains a covalently bound hydrogen bond donor–acceptor motif. This results in a monomeric unit which can adopt multiple hydrogen bonding modes simultaneously. Previous investigations have shown examples of SSAs to act as antimicrobial agents against clinically relevant methicillin-resistant Staphylococcus aureus (MRSA). Herein, we report an intrinsically fluorescent SSA which can self-associate producing dimers, spherical aggregates and hydrogels dependent on solvent environment, while retaining antimicrobial activity against both model Gram-positive (MRSA) and Gram-negative (Escherichia coli) bacteria. Finally, we demonstrate the SSA supramolecular hydrogel to tolerate the inclusion of the antibiotic ampicillin, leading to the enhanced inhibition of growth with both model bacteria, and derive initial molecular structure–physicochemical property–antimicrobial activity relationships.

This record has no associated files available for download.

More information

Accepted/In Press date: 4 May 2020
Additional Information: Funding for this research was provided by: Public Health England (PhD studentship for Jessica Boles) University of Kent (GCDC postdoctoral award George Williams) Royal Society (RGS\R2\180336)

Identifiers

Local EPrints ID: 475628
URI: http://eprints.soton.ac.uk/id/eprint/475628
ISSN: 2050-750X
PURE UUID: 469901fc-b5c3-441f-98b6-a4a4b9027219
ORCID for George Williams: ORCID iD orcid.org/0000-0001-6162-8895

Catalogue record

Date deposited: 22 Mar 2023 17:48
Last modified: 17 Mar 2024 04:17

Export record

Altmetrics

Contributors

Author: Lisa J. White
Author: Jessica E. Boles
Author: Nyasha Allen
Author: Luke S. Alesbrook
Author: J. Mark Sutton
Author: Charlotte K. Hind
Author: Kira L. F. Hilton
Author: Laura R. Blackholly
Author: Rebecca J. Ellaby
Author: George Williams ORCID iD
Author: Daniel P. Mulvihill
Author: Jennifer Hiscock
Corporate Author: et al.

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×