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"Side Effects May Not Include..."

Clark School Shows In Vivo "Nanofactories" Can Make and Deliver Targeted Drugs

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FOR IMMEDIATE RELEASE  February 27, 2007

CONTACT:

Faye Levine
301 405 0379
flevine@umd.edu

Figure 1: Scanning Electron Microscope image of the magnetic nanofactories attached to targeted E. coli cells. Download hi-res image. Credit: Clark School of Engineering-University of Maryland
          

COLLEGE PARK, Md. - The list of side effects on your prescription bottle may one day be a lot shorter, according to researchers at the University of Maryland's A. James Clark School of Engineering.

That's because instead of taking a conventional medication, you may swallow tiny "nanofactories," biochemical machines that act like cells, first conceived of at the Clark School.

For example, these ingested nanofactories, using magnetism, could detect a bacterial infection, produce a medication using the body's own materials, and deliver a dose directly to the bacteria. The drug would do its work only at the infection site, and thus not cause the side effects that may arise when an antibiotic travels throughout the body in search of infections.

William Bentley, professor and chair of the Fischell Department of Bioengineering at the Clark School, and several graduate students including Rohan Fernandes, have developed this "magnetic nanofactory" concept and published their research in Metabolic Engineering in December of last year. Colleagues around the country voiced their support for the technology in Nature Nanotechnology last month.

"In the lab," Bentley says, "our group showed we can produce a tiny nanofactory and attach it to a target cell magnetically. The nanofactory then makes small molecules from surrounding materials and delivers the molecules - potentially drug molecules—to the targeted cell."

Besides drug molecules, the researchers showed that the nanofactory could produce signaling molecules that communicate with the target cell or block the target cell from communicating with other, similar cells (a process called "quorum sensing") and thus prevent infection. The researchers attached the nanofactories to E. coli cells, targeting them with the help of a mixture of iron particles and chitosan, a substance derived from the shells of crustaceans like crabs and shrimp. The nanofactories then produced a signaling molecule that could render the E. coli harmless. Nanofactories could be designed to produce the needed drug molecules over an extended period of time.

Now that the viability of nanofactories has been shown, researchers must overcome a few challenges before they can be used in humans. First, nanofactories must be cloaked so that the body does not react to them as a foreign substance and try to attack them. Another goal is to find a method to shut down the nanofactory once it has produced the needed substance—a type of off-switch that could be activated from outside the body. These and other topics are being investigated in the Fischell Department of Bioengineering.

NOTE TO EDITORS:
The Metabolic Engineering and Nature Nanotechnology articles can be made available upon request.

Bentley Research Group Webpage: www.bioe.umd.edu/~bentley

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