Caltech bioengineers' vision produces "microscope on a chip"
July 29, 2008 -- Researchers at the California Institute of Technology (Pasadena, CA) have developed a high-resolution microscope they say can be mass produced for about $10. Small enough to fit on a fingertip, the device operates without lenses but boasts magnifying power equivalent to that of top-quality optical microscopes. And it requires only sunlight for illumination.
July 29, 2008 -- Researchers at the California Institute of Technology (Pasadena, CA) have developed a super-compact high-resolution microscope that they say can be mass produced for about $10. Small enough to fit on a fingertip, the device operates without lenses but boasts magnifying power equivalent to that of top-quality optical microscopes -- and it requires only sunlight for illumination.
The device promises to be of use in the field to analyze blood samples for malaria or check water supplies for giardia and other pathogens. "It could be put in a cell phone," said Changhuei Yang, assistant professor of electrical engineering and bioengineering, who developed it with the help of his Caltech colleagues. Yang and his colleagues described work leading to development of the device in an article in Laser Focus World in 2006.
The 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.
"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.
Fabrication is 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, 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 researchers' paper, "Lensless high-resolution on-chip optofluidic microscopes for Caenorhabditis elegans and cell imaging," was published yesterday, July 28, 2008, in the early online edition of the Proceedings of the National Academy of Sciences.