This article is a slightly modified version of an article written by Matt Shipman, Research Lead in University Communications.
Professor Richard Spontak and his colleagues have developed two new types of elastomeric polymers with highly effective, broad-spectrum antimicrobial properties. This is the second of two articles describing the polymers. An article about the first type of polymer is here.
The second polymer possesses broad-spectrum antimicrobial properties, allowing it to kill a range of viruses and drug-resistant bacteria – including methicillin-resistant Staphylococcus aureus (MRSA) – in just minutes.
“We were exploring a different approach for creating antimicrobial materials when we observed some interesting behavior from this polymer and decided to explore its potential in greater depth,” says Spontak, who is also a professor in materials science and engineering and co-corresponding author of a paper describing the work. “And what we found is extremely promising as an alternate weapon to existing materials-related approaches in the fight against drug-resistant pathogens. This could be particularly useful in clinical settings – such as hospitals or doctor’s offices – as well as senior-living facilities, where pathogen transmission can have dire consequences.”
The polymer’s antimicrobial properties stem from its unique molecular architecture, which attracts water to a sequence of repeat units that are chemically modified (or functionalized) with sulfonic acid groups. Its name is abbreviated as TESETxx, where xx is a measure of the number of sulfonic acid groups that have been added to the core polymer structure.
“When microbes come into contact with the polymer, water on the surface of the microbes interacts with the sulfonic acid functional groups in the polymer – creating an acidic solution that quickly kills the bacteria,” says Dr. Reza Ghiladi, associate professor of chemistry at NC State and co-corresponding author of the paper. “These acidic solutions can be made more or less powerful by controlling the number of sulfonic acid functional groups in the polymer.”
The researchers tested the polymer against six types of bacteria, including three antibiotic-resistant strains: MRSA, vancomycin-resistant Enterococcus faecium, and carbapenem-resistant Acinetobacter baumannii. When 40% or more of the relevant polymer units contain sulfonic acid groups, the polymer killed 99.9999% of each strain of bacteria within five minutes.
In the figure, each graph represents the survival of (a) Gram-positive and (b) Gram-negative bacteria after exposure to a control (green), TESET26 (purple) and TESET52 (red) for 5 min. In (c), the survival of methicillin-susceptible S. aureus is presented for three TESET polymers varying in midblock sulfonation content (exposure times are included).
The researchers also tested the polymer against three viruses: an analog virus for rabies, a strain of influenza and a strain of human adenovirus.
“The polymer was able to fully destroy the influenza and the rabies analog within five minutes,” says Dr. Frank Scholle, associate professor of biological sciences and a co-author of the paper. “While the polymer with lower concentrations of the sulfonic acid groups had no practical effect against human adenovirus, it could destroy 99.997% of that virus at higher sulfonic acid levels.”
One concern of the researchers was that the polymer’s antimicrobial effect could progressively worsen over time, as sulfonic acid groups were neutralized when they interacted with positively charged ions (cations) in water. However, they found that the polymer could be fully “recharged” by exposing it to an acid solution.
“In laboratory settings, you could do this by dipping the polymer into a strong acid,” Ghiladi says. “But in other settings – such as a hospital room – you could simply spray the polymer surface with vinegar.”
This “recharging” process works because every time one of the negatively charged sulfonic acid groups combines with a cation in water – which can happen when the polymer comes into contact with microbes – the sulfonic acid group becomes electrically neutral. That makes the acid group ineffective against microbes. But when the neutralized polymer is subjected to acid, those functional groups can exchange bound cations with protons from the acid, making the sulfonic acid groups active again – and ready to kill microbial pathogens again.
“The work we’ve done here highlights a promising new approach to creating antimicrobial surfaces for use in the fight against drug-resistant pathogens – and hospital-acquired infections in particular,” Ghiladi says.
“Functional block polymers like this are highly versatile – usable as water-treatment media, soft actuators, solar cells and gas-separation membranes – and environmentally benign since they can be readily recycled and re-used,” Spontak adds. “These features make them particularly attractive for widespread use.
“And this work focused on only one polymer series manufactured by Kraton Polymers,” Spontak says. “We are very eager to see how we can further modify this and other polymers to retain such effective and fast-acting antimicrobial properties while improving other attributes that would be attractive for this and other applications.”
The paper, “Inherently self-sterilizing charged multiblock polymers that kill drug-resistant microbes in minutes,” appears in the journal Materials Horizons. First author of the paper is Bharadwaja S. T. Peddinti, a CBE Ph.D. student. The paper was co-authored by Mariana Vargas, a CBE undergraduate; and Dr. Steven Smith of The Procter & Gamble Company.
The work was supported by the NC State Nonwovens Institute. The researchers also received imaging assistance from the NC State Cellular and Molecular Imaging Facility, which is supported by the National Science Foundation under grant number DBI-1624613.