A water-soluble poly(trisulfide) with antimicrobial activity

TY - UNPB

T1 - A water-soluble poly(trisulfide) with antimicrobial activity

AU - Pople, Jasmine M. M.

AU - Clarke, Ocean E.

AU - Dop, Romy A.

AU - Nicholls, Thomas P.

AU - Patel, Harshal D.

AU - Bloch, Witold M.

AU - Jia, Zhongfan

AU - Fraser-Miller, Sara J.

AU - Neill, Daniel R.

AU - Fothergill, Joanne L.

AU - Hasell, Tom

AU - Chalker, Justin M.

PY - 2025/9/2

Y1 - 2025/9/2

N2 - Antimicrobial resistance is a growing threat to human health and agriculture. Sulfur-containing compounds and elemental sulfur have a long history of use as antimicrobials, but challenges related to solubility and formulation have limited their broad application. Recent advances in sulfur polymer chemistry have enabled the development of novel sulfur-rich materials with antimicrobial activity. However, most of these materials are water-insoluble, limiting their use in biomedical and agricultural applications. Here, we report the synthesis of a linear poly(trisulfide) via photochemical ring-opening polymerization of a cyclic trisulfide monomer bearing a carboxylic acid. Deprotonation of the carboxylic acid renders the poly(trisulfide) fully water soluble, enabling minimum inhibitory concentration (MIC) assays to quantify its antimicrobial efficacy. The featured polymer exhibited potent antifungal activity against Candida albicans (MIC < 8 µg/mL) and stronger inhibition of the Gram-positive bacterium Staphylococcus aureus (MIC = 16 µg/mL) compared to the Gram-negative Escherichia coli (MIC > 512 µg/mL). This work demonstrates a simple and controllable synthesis of water-soluble poly(trisulfides) with antimicrobial activity, offering a new strategy to address antimicrobial resistance.

AB - Antimicrobial resistance is a growing threat to human health and agriculture. Sulfur-containing compounds and elemental sulfur have a long history of use as antimicrobials, but challenges related to solubility and formulation have limited their broad application. Recent advances in sulfur polymer chemistry have enabled the development of novel sulfur-rich materials with antimicrobial activity. However, most of these materials are water-insoluble, limiting their use in biomedical and agricultural applications. Here, we report the synthesis of a linear poly(trisulfide) via photochemical ring-opening polymerization of a cyclic trisulfide monomer bearing a carboxylic acid. Deprotonation of the carboxylic acid renders the poly(trisulfide) fully water soluble, enabling minimum inhibitory concentration (MIC) assays to quantify its antimicrobial efficacy. The featured polymer exhibited potent antifungal activity against Candida albicans (MIC < 8 µg/mL) and stronger inhibition of the Gram-positive bacterium Staphylococcus aureus (MIC = 16 µg/mL) compared to the Gram-negative Escherichia coli (MIC > 512 µg/mL). This work demonstrates a simple and controllable synthesis of water-soluble poly(trisulfides) with antimicrobial activity, offering a new strategy to address antimicrobial resistance.

U2 - 10.26434/chemrxiv-2025-p06vs

DO - 10.26434/chemrxiv-2025-p06vs

M3 - Preprint

BT - A water-soluble poly(trisulfide) with antimicrobial activity

PB - ChemRxiv

ER -