(30e) Gold Nanoparticles Anchored Onto Polymer Brushes As Robust Anti-Microbial Surfaces | AIChE

(30e) Gold Nanoparticles Anchored Onto Polymer Brushes As Robust Anti-Microbial Surfaces

Authors 

Kapil, N. - Presenter, University College London
Mohamed, H., University College London
Ali, S., University College Hospital
Coppens, M. O., University College London
Antimicrobial resistance (AMR) is the capability of microorganisms, including bacteria, viruses, and fungi to withstand the impact of antimicrobial drugs. This resistance reduces the effectiveness of conventional medications, leading to the spread of infections and impacting modern surgery, chemotherapy, and organ transplantations. According to the WHO reports, 1.29 million global deaths were caused by AMR and this is projected to rise to 10 million deaths by 2050 if no actions are taken.[1] There are several ways to address antimicrobial resistance such as development of new drugs, public education, and responsible use of antibiotics. Another strategy to tackle this challenge is designing antimicrobial surfaces that can inhibit the growth and survival of such microorganisms. These surfaces can be used as coatings on surgical trays, catheters, shower filters and surgical implants. The common materials utilised as antimicrobial surfaces include copper, silver, zinc, titanium dioxide and quaternary ammonium compounds (QACs). However, leaching of these metal ions into the environment and low antimicrobial efficacy are major drawbacks associated with these materials. In this context, ultra-small gold nanoparticles (<1 nm in diameter) have gained significant attention as antimicrobial agents because of their inertness and production of reactive oxygen species (ROS), which destroy the bacterial cell wall.[2]

This study focuses on the development of stable antimicrobial surfaces by utilising the antimicrobial properties of gold nanoparticles and bacteriostatic properties of polymer brushes. Atomically precise gold nanoparticles of size ~ 0.8 nm are synthesised using a one pot strategy, and are subsequently attached to the polymer brushes that are tethered onto membrane surfaces.[3] The bacteriostatic properties of polymer brushes can be tuned by varying the charge, hydrophilicity/hydrophobicity and functionalisation of the polymer chain.[4] The synthesised surfaces are characterised using multiple characterisation techniques including TEM, SEM, XPS, FT-IR ICP-OES, DR-UV/VIS and AFM. The stability of these surfaces is verified by performing different leaching tests replicating hospital settings. The antimicrobial efficacy of these surfaces is tested against Escherichia coli (E. coli), Pseudomonas aeruginosa (P. aeruginosa) and Staphylococcus aureus (S. aureus) bacteria. These bacterial strains are known for their increasing resistance to antibiotics and are frequent causes of infections in healthcare settings.[5] The developed surfaces exhibit a 99.9%, 99.5%, and 99.9% reduction in S. aureus, P. aeruginosa and E. coli, respectively, within two hours of contact time. Furthermore, the effect of the size of gold nanoparticles, gold loadings and oxidation state on the antimicrobial properties is demonstrated. This technique is highly versatile and promising as these materials can be grafted on variety of surfaces such as polymers, glass, mica, and silicon depending on the desired application. These synthesised antimicrobial surfaces demonstrate exceptionally high efficacy against bacteria, showcasing their potential for diverse biomedical applications including manufacturing water filters, coatings for surgical instruments, medical trays, and catheter.

[1] C. J. Murray, K. S. Ikuta, F. Sharara, L. Swetschinski, G. R. Aguilar, A. Gray, C. Han, C. Bisignano, P. Rao, E. Wool, The lancet 2022, 399, 629-655.

[2] K. Zheng, M. I. Setyawati, D. T. Leong, J. Xie, ACS nano 2017, 11, 6904-6910.

[3] N. Kapil, T. Weissenberger, F. Cardinale, P. Trogadas, T. A. Nijhuis, M. M. Nigra, M.-O. Coppens, Angew. Chem. Int. Ed. 2021, 60, 18185-18193.

[4] H. Mohamed, S. Hudziak, V. Arumuganathan, Z. Meng, M.-O. Coppens, Molecular Systems Design & Engineering 2020, 5, 1219-1229.

[5] G. Mancuso, A. Midiri, E. Gerace, C. Biondo, Pathogens 2021, 10, 1310.