Computing Trick Turns Low-Cost Into High-Performance Microscopes
Engineers at the California Institute of Technology (Caltech) have devised a method to convert a relatively inexpensive conventional microscope into a billion-pixel imaging system that significantly outperforms the best available standard microscope. Such a system could greatly improve the efficiency of digital pathology, in which specialists need to review large numbers of tissue samples. By making it possible to produce robust microscopes at low cost, the approach also has the potential to bring high-performance microscopy capabilities to medical clinics in developing countries.
"In my view, what we've come up with is very exciting because it changes the way we tackle high-performance microscopy," says Changhuei Yang, professor of electrical engineering, bioengineering and medical engineering at Caltech.
Yang is senior author on a paper that describes the new imaging strategy, which appears in the July 28 early online version of the journal Nature Photonics.
"We found a way to actually have the best of both worlds," says Guoan Zheng, lead author on the new paper and the initiator of this new microscopy approach from Yang's lab. "We used a computational approach to bypass the limitations of the optics. The optical performance of the objective lens is rendered almost irrelevant, as we can improve the resolution and correct for aberrations computationally."
Indeed, using the new approach, the researchers were able to improve the resolution of a conventional 2X objective lens to the level of a 20X objective lens. Therefore, the new system combines the field-of-view advantage of a 2X lens with the resolution advantage of a 20X lens. The final images produced by the new system contain 100 times more information than those produced by conventional microscope platforms. And building upon a conventional microscope, the new system costs only about $200 to implement.
"One big advantage of this new approach is the hardware compatibility," Zheng says, "You only need to add an LED array to an existing microscope. No other hardware modification is needed. The rest of the job is done by the computer."
The new system acquires about 150 low-resolution images of a sample. Each image corresponds to one LED element in the LED array. Therefore, in the various images, light coming from known different directions illuminates the sample. A novel computational approach, termed Fourier ptychographic microscopy (FPM), is then used to stitch together these low-resolution images to form the high-resolution intensity and phase information of the sample—a much more complete picture of the entire light field of the sample.
Yang explains that when we look at light from an object, we are only able to sense variations in intensity. But light varies in terms of both its intensity and its phase, which is related to the angle at which light is traveling.
The researchers say that the new method could have wide applications not only in digital pathology but also in everything from hematology to wafer inspection to forensic photography. Zheng says the strategy could also be extended to other imaging methodologies, such as X-ray imaging and electron microscopy. -- by Kimm Fesenmaier, CalTech
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