Light-activated nanoparticles prove effective against antibiotic-resistant 'superbugs'

January 18, 2016

In the ever-escalating evolutionary battle with drug-resistant bacteria, humans may soon have a leg up thanks to adaptive, light-activated nanotherapy developed by researchers at the University of Colorado Boulder.

Antibiotic-resistant bacteria such as Salmonella, E. Coli and Staphylococcus infect some 2 million people and kill at least 23,000 people in the United States each year. Efforts to thwart these so-called "superbugs" have consistently fallen short due to the bacteria's ability to rapidly adapt and develop immunity to common antibiotics such as penicillin.

New research from CU-Boulder, however, suggests that the solution to this big global problem might be to think small—very small.

In findings published today in the journal Nature Materials, researchers at the Department of Chemical and Biological Engineering and the BioFrontiers Institute describe new light-activated therapeutic nanoparticles known as "quantum dots." The dots, which are about 20,000 times smaller than a human hair and resemble the tiny semiconductors used in consumer electronics, successfully killed 92 percent of drug-resistant bacterial cells in a lab-grown culture.

"By shrinking these semiconductors down to the nanoscale, we're able to create highly specific interactions within the cellular environment that only target the infection," said Prashant Nagpal, an assistant professor in the Department of Chemical and Biological Engineering at CU-Boulder and a senior author of the study.

Previous research has shown that metal nanoparticles—created from gold and silver, among other metals—can be effective at combating antibiotic resistant infections, but can indiscriminately damage surrounding cells as well.

The quantum dots, however, can be tailored to particular infections thanks to their light-activated properties. The dots remain inactive in darkness, but can be activated on command by exposing them to light, allowing researchers to modify the wavelength in order to alter and kill the infected cells.

"While we can always count on these superbugs to adapt and fight the therapy, we can quickly tailor these to come up with a new therapy and therefore fight back faster in this evolutionary race," said Nagpal.

The specificity of this innovation may help reduce or eliminate the potential side effects of other treatment methods, as well as provide a path forward for future development and clinical trials.

"Antibiotics are not just a baseline treatment for bacterial infections, but HIV and cancer as well," said Anushree Chatterjee, an assistant professor in the Department of Chemical and Biological Engineering at CU-Boulder and a senior author of the study. "Failure to develop effective treatments for drug-resistant strains is not an option, and that's what this technology moves closer to solving."

Nagpal and Chatterjee are the co-founders of PRAAN Biosciences, Inc., a Boulder, Colorado-based startup that can sequence genetic profiles using just a single molecule, technology that may aid in the diagnosis and treatment of superbug strains. The authors have filed a patent on the new quantum dot technology.

Explore further: Why do some infections persist? Blame bacterial socialism, says new study

More information: Photoexcited Quantum Dots for Killing Multidrug-Resistant Bacteria, Nature Materials, DOI: 10.1038/nmat4542

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not rated yet Jan 19, 2016
Particles are called nano particles if they are 1 to 100 nm in size. A sugar molecules size is 1 nano-meter (nm) in size while water molecule is only 0.3 nm. These nano-particles have large surface area but very small weight( gravitational force is not important at nano-scale).A good example of nano-particles is milk, coffee or beer. These (milk, coffee or beer) are basically colloids. Colloids is a suspension of nano-particles in water. In the old days they call a suspension of nano-particles by the name of colloids. These colloids were investigated and studied very well. Look in the old publications in the J American Chemical Society or the journals of the Royal Society of Chemistry.

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