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Bioingenieros de Caltech desarrollan "Microscopio en un Chip"

Caltech Bioengineers Develop "Microscope on a Chip"

PASADENA, Calif.--Researchers at the California Institute of Technology have turned science fiction into reality with their development of a super-compact high-resolution microscope, small enough to fit on a finger tip. This "microscopic microscope" operates without lenses but has the magnifying power of a top-quality optical microscope, can be used in the field to analyze blood samples for malaria or check water supplies for giardia and other pathogens, and can be mass-produced for around $10.

An on-chip implementation of the optofluidic microscope.

"The whole thing is truly compact--it could be put in a cell phone--and it can use just sunlight for illumination, which makes it very appealing for Third-World applications," says Changhuei Yang, assistant professor of electrical engineering and bioengineering at Caltech, who developed the device, dubbed an optofluidic microscope, along with his colleagues at Caltech.

The new instrument combines traditional computer-chip technology with microfluidics--the channeling of fluid flow at incredibly small scales. An entire optofluidic microscope chip is about the size of a quarter, although the part of the device that images objects is only the size of Washington's nose on that quarter.

"Our research is motivated by the fact that microscopes have been around since the 16th century, and yet their basic design has undergone very little change and has proven prohibitively expensive to miniaturize. Our new design operates on a different principle and allows us to do away with lenses and bulky optical elements," says Yang.

The fabrication of the microscopic chip is disarmingly simple. A layer of metal is coated onto a grid of charge-coupled device (CCD) sensor (the same sensors that are used in digital cameras). Then, a line of tiny holes, less than one-millionth of a meter in diameter, is punched into the metal, spaced five micrometers apart. Each hole corresponds to one pixel on the sensor array. A microfluidic channel, through which the liquid containing the sample to be analyzed will flow, is added on top of the metal and sensor array. The entire chip is illuminated from above; sunlight is sufficient.

When the sample is added, it flows--either by the simple force of gravity or drawn by an electric charge--horizontally across the line of holes in the metal. As cells or small organisms cross over the holes, one hole after another, the objects block the passage of light from above onto the sensor below. This produces a series of images, consisting of light and shadow, akin to the output of a pinhole camera.

Because the holes are slightly skewed, so that they create a diagonal line with respect to the direction of flow, the images overlap slightly. All of the images are then pieced together to create a surprisingly precise two-dimensional picture of the object.

Yang is now in discussion with biotech companies to mass-produce the chip. The platform into which the chip is integrated can vary depending upon the needs of the user. For example, health workers in rural areas could carry cheap, compact models to test individuals for malaria, and disposable versions could be carried into the battlefield. "We could build hundreds or thousands of optofluidic microscopes onto a single chip, which would allow many organisms to be imaged and analyzed at once," says Xiquan Cui, the lead graduate student on the project.

In the future, the microscope chips could be incorporated into devices that are implanted into the human body. "An implantable microscope analysis system can autonomously screen for and isolate rogue cancer cells in blood circulation, thus, providing important diagnostic information and helping arrest the spread of cancer," says Yang.

The paper, "Lensless high-resolution on-chip optofluidic microscopes for Caenorhabditis elegans and cell imaging," was published July 28 in the early online edition of the Proceedings of the National Academy of Sciences. Yang's coauthors are graduate students Xiquan Cui and Lap Man Lee; postdoctoral research associates Xin Heng and Weiwei Zhong; Paul W. Sternberg, the Thomas Hunt Morgan Professor of Biology and an Investigator with the Howard Hughes Medical Institute; and Demetri Psaltis, the Thomas G. Myers Professor of Electrical Engineering at Caltech.

The work was funded by DARPA's Center for Optofluidic Integration at Caltech, the Wallace Coulter Foundation, the National Science Foundation, and the National Institutes of Health.

### Contact: Kathy Svitil (626) 395-8022 ksvitil@caltech.edu

Credits: California Institute of Technology

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