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Light-activated antimicrobial surface that also works in the dark: World's first

Date:
March 24, 2014
Source:
University College London
Summary:
A new antibacterial material that has potential for cutting hospital acquired infections has been developed by scientists. The combination of two simple dyes with nanoscopic particles of gold is deadly to bacteria when activated by light -- even under modest indoor lighting. And in a first for this type of substance, it also shows impressive antibacterial properties in total darkness.

The combination of two simple dyes with nanoscopic particles of gold is deadly to bacteria when activated by light - even under modest indoor lighting. And in a first for this type of substance, it also shows impressive antibacterial properties in total darkness.
Credit: Image courtesy of University College London

Researchers at UCL have developed a new antibacterial material which has potential for cutting hospital acquired infections. The combination of two simple dyes with nanoscopic particles of gold is deadly to bacteria when activated by light -- even under modest indoor lighting. And in a first for this type of substance, it also shows impressive antibacterial properties in total darkness.

The research, from by Sacha Noimark and Ivan Parkin (both UCL Chemistry) and Elaine Allan (UCL Eastman Dental Institute), is published today in the journal Chemical Science.

Hospital-acquired infections are a major issue for modern medicine, with pathogens like methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium difficile (C. diff) getting extensive publicity. Although medical establishments have stringent cleaning policies, insist on frequent hand-washing by staff, and have powerful drugs at their disposal, it is difficult to eliminate these infections unless you can make the hospital environment more hostile to microbes. Surfaces, such as door handles, medical equipment, keyboards, pens and so on are an easy route for germs to spread, even onto freshly-cleaned hands.

One possible solution to this is to develop alternative strategies such as antibacterial coatings that make surfaces less accommodating to germs. These surfaces are not like antibacterial fluids that just wash away -- the goal is to make a surface which is intrinsically deadly to harmful bacteria.

"There are certain dyes that are known to be harmful to bacteria when subjected to bright light," explains the study's corresponding author Ivan Parkin (Head of UCL Chemistry). "The light excites electrons in them, promoting the dye molecules to an excited triplet state and ultimately produces highly reactive oxygen radicals that damage bacteria cell walls. Our project tested new combinations of these dyes along with gold nanoparticles, and simplified ways of treating surfaces which could make the technology easier and cheaper to roll out."

The team, tested several different combinations of the dyes crystal violet (already used to treat staph infections), methylene blue and nanogold, deposited on the surface of silicone. This flexible rubbery substance is widely used as a sealant, a coating and to build medical apparatus such as tubes, catheters and gaskets, and can also be used as protective casings for things like keyboards and telephones.

While work to create antimicrobial surfaces in the past has often concentrated on complex ways of bonding dyes to the surface, this study took a simpler approach. The researchers used an organic solvent to swell the silicone, allowing the methylene blue and gold nanoparticles to diffuse through the polymer. They then dipped the silicone into a crystal violet solution to form a thin dye layer at the polymer surface.

In their tests, in which infected surfaces were subjected to light levels similar to those measured in hospital buildings, surfaces treated with a combination of crystal violet, methylene blue and nanogold showed the most potent bactericidal effect ever observed in such a surface. Moreover, the treatment did not significantly change the properties of the silicone (for instance, how water repellent it is), and the coating was not affected by rubbing with alcohol wipes, meaning it can stand up to the repeated cleaning that goes on in hospitals, without being worn off.

"Despite contaminating the surface with far more bacteria than you would ever see in a hospital setting, placed under a normal fluorescent light bulb, the entire sample was dead in three to six hours, depending on the type of bacteria," says the paper's lead author, Sacha Noimark. "That was an excellent result, but the bigger surprise was the sample which we left in the dark. That sample too showed significant reductions in bacterial load, albeit over longer timescales of about three to eighteen hours. The precise mechanism by which this dark-kill works is not yet clear, though."

This is the first time a light-activated antimicrobial surface has had any kind of effect in the dark. This, along with its unprecedented performance under hospital lighting conditions, and relatively simple and cost-effective manufacture, means that the technology is extremely promising for future applications.


Story Source:

The above story is based on materials provided by University College London. Note: Materials may be edited for content and length.


Journal Reference:

  1. Sacha Noimark, Elaine Allan, Ivan P Parkin. Light-Activated Antimicrobial Surfaces With Enhanced Efficacy Induced by a Dark-Activated Mechanism. Chemical Science, 2014; DOI: 10.1039/C3SC53186D

Cite This Page:

University College London. "Light-activated antimicrobial surface that also works in the dark: World's first." ScienceDaily. ScienceDaily, 24 March 2014. <www.sciencedaily.com/releases/2014/03/140324121457.htm>.
University College London. (2014, March 24). Light-activated antimicrobial surface that also works in the dark: World's first. ScienceDaily. Retrieved October 21, 2014 from www.sciencedaily.com/releases/2014/03/140324121457.htm
University College London. "Light-activated antimicrobial surface that also works in the dark: World's first." ScienceDaily. www.sciencedaily.com/releases/2014/03/140324121457.htm (accessed October 21, 2014).

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