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Making better biosensors with electron density waves

Date:
October 29, 2010
Source:
Optical Society of America
Summary:
An emerging field with the tongue-twisting name of "optofluidic plasmonics" promises a new way to detect and analyze biological molecules for drug discovery, medical diagnostics, and the detection of biochemical weapons. Researchers have succeeded in merging a microfluidics system with plasmonics -- sometimes called "light on a wire" -- onto a single platform. Plasmonics is based on electron waves on a metal surface excited by incoming light waves.

An emerging field with the tongue-twisting name of "optofluidic plasmonics" promises a new way to detect and analyze biological molecules for drug discovery, medical diagnostics, and the detection of biochemical weapons. Investigators at the University of California, San Diego led by Yeshaiahu Fainman have succeeded in merging a microfluidics system with plasmonics -- sometimes called "light on a wire" -- onto a single platform. Plasmonics is based on electron waves on a metal surface excited by incoming light waves.

According to Fainman, tapping the potential of plasmonics for biomolecule detection systems has been a challenge, because localized optical field scales are usually much larger than the molecules in question. In order to make a useful optical biosensor, he says, "We need to increase the interaction cross-section by finding ways to localize optical interrogation fields ideally to the scales comparable to those of biomolecules." Since that is not currently possible, he and his team used an approach of integrating microfluidics and plasmonics on single chips, allowing fluid to ferry the molecules into the cross-section of the optical field.

Fainman expects the system to be particularly useful in studying large arrays of protein-protein interactions for identifying potential drugs that bind to specific target molecules, which may lead to earlier cancer diagnoses and faster discovery of new drugs. Unlike most current methods, optical detection does not require labeling of molecules with fluorescent or radioactive entities -- labels often hinder interaction by covering up or blocking binding surfaces.

The new platform also carries the advantage of being high throughput and multiplexed, offering researchers an opportunity to examine thousands of arrayed compounds simultaneously, which, he says, "biologists and physicians get very excited about."

The presentation, "Optofluidic Nano-Plasmonics for Biochemical Sensing," took place on Oct. 26 at the Frontiers in Optics (FiO) 2010/Laser Science XXVI -- the 94th annual meeting of the Optical Society (OSA), which was held together with the annual meeting of the American Physical Society (APS) Division of Laser Science at the Rochester Riverside Convention Center in Rochester, N.Y., from Oct. 24-28.


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The above story is based on materials provided by Optical Society of America. Note: Materials may be edited for content and length.


Cite This Page:

Optical Society of America. "Making better biosensors with electron density waves." ScienceDaily. ScienceDaily, 29 October 2010. <www.sciencedaily.com/releases/2010/10/101020195414.htm>.
Optical Society of America. (2010, October 29). Making better biosensors with electron density waves. ScienceDaily. Retrieved July 28, 2014 from www.sciencedaily.com/releases/2010/10/101020195414.htm
Optical Society of America. "Making better biosensors with electron density waves." ScienceDaily. www.sciencedaily.com/releases/2010/10/101020195414.htm (accessed July 28, 2014).

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