Researchers turn mobile phones into fluorescent microscopes

Wednesday, 02 December, 2009


Researchers at the University of California, Berkeley, are proving that a camera phone can capture far more than photos of people or pets at play. They have now developed a mobile phone microscope, or CellScope, that not only takes colour images of malaria parasites, but of tuberculosis bacteria labelled with fluorescent markers.

The prototype CellScope (described in the 22 July issue of the online journal PLoS ONE) moves a major step forward in taking clinical microscopy out of specialised laboratories and into field settings for disease screening and diagnoses.

“The same regions of the world that lack access to adequate health facilities are, paradoxically, well served by mobile phone networks,” said Dan Fletcher, UC Berkeley Associate Professor of Bioengineering and head of the research team developing the CellScope.

“We can take advantage of these mobile networks to bring low-cost, easy-to-use laboratory equipment out to more remote settings.”

The engineers attached compact microscope lenses to a holder fitted to a mobile phone. Using samples of infected blood and sputum, the researchers were able to use the camera phone to capture bright field images of Plasmodium falciparum, the parasite that causes malaria in humans, and sickle-shaped red blood cells. They were also able to take fluorescent images of Mycobacterium tuberculosis, the bacterial culprit that causes TB in humans. Moreover, the researchers showed that the TB bacteria could be automatically counted using image analysis software.

 

Figure 1: Mobile phone microscopy layout schematic, prototype and sample images.

(a) Mobile phone microscopy optical layout for fluorescence imaging. The same apparatus was used for brightfield imaging, with the filters and LED removed. Components only required for fluorescence imaging are indicated by ‘fluo’. Not to scale. (b) A current prototype, with filters and LED installed, capable of fluorescence imaging. The objective is not visible because it is contained within the optical tubing, and the sample is mounted adjacent to the metallic focusing knob. (c) Brightfield image of 6 µm fluorescent beads. (d) Fluorescent images of beads shown in (c). The field-of-view projected onto the camera phone CMOS is outlined. Scales bars are 10 µm. 

“The images can either be analysed on site or wirelessly transmitted to clinical centres for remote diagnosis,” said David Breslauer, co-lead author of the study and a graduate student in the UC San Francisco/UC Berkeley Bioengineering Graduate Group. “The system could be used to help provide early warning of outbreaks by shortening the time needed to screen, diagnose and treat infectious diseases.”

The engineers had previously shown that a portable microscope mounted on a mobile phone could be used for bright field microscopy, which uses simple white light - such as from a bulb or sunlight - to illuminate samples. The latest development adds to the repertoire fluorescent microscopy, in which a special dye emits a specific fluorescent wavelength to tag a target - such as a parasite, bacteria or cell - in the sample.

“Fluorescence microscopy requires more equipment - such as filters and special lighting - than a standard light microscope, which makes them more expensive,” said Fletcher. “In this paper we've shown that the whole fluorescence system can be constructed on a cell phone using the existing camera and relatively inexpensive components.”

The researchers used filters to block out background light and to restrict the light source, a simple light-emitting diode, to the 460 nm wavelength necessary to excite the green fluorescent dye in the TB-infected blood. Using an off-the-shelf phone with a 3.2 megapixel camera, they were able to achieve a spatial resolution of 1.2 µm. In comparison, a human red blood cell is about 7 µm in diameter.

 
Figure 2: Mobile phone microscopy images of diseased blood smears.

(a) Thick smear of Giemsa-stained malaria-infected blood. (b) Thin smear of Giemsa-stained malaria-infected blood. (c) Sickle-cell anaemia blood smear. White arrows point to two sickled red blood cells. Scale bars are 10 µm.

“LEDs are dramatically more powerful now than they were just a few years ago, and they are only getting better and cheaper,” said Fletcher. “We had to disabuse ourselves of the notion that we needed to spend many thousands on a mercury arc lamp and high-sensitivity camera to get a meaningful image. We found that a high-powered LED - which retails for just a few dollars - coupled with a typical camera phone could produce a clinical quality image sufficient for our goal of detecting in a field setting some of the most common diseases in the developing world.”

 
Figure 3: Fluorescence mobile phone microscopy images of tuberculosis in sputum.

(a) Fluorescence image of Auramine O-stained TB sputum sample. (b) Enlarged view of two tuberculosis bacilli from red-outlined area in (a). (c) Automated counting of fluorescently-labelled tuberculosis bacilli; counted bacilli are numbered and set to red in the image. Scale bars in (a) and (c) are 10 µm, scale bar in (b) is 1 µm.

The researchers pointed out that while fluorescent microscopes include additional parts, less training is needed to interpret fluorescent images. Instead of sorting out pathogens from normal cells in the images from standard light microscopes, health workers simply need to look for something the right size and shape to light up on the screen.

“Viewing fluorescent images is a bit like looking at stars at night,” said Breslauer. “The bright green fluorescent light stands out clearly from the dark background. It's this contrast in fluorescent imaging that allowed us to use standard computer algorithms to analyse the sample containing TB bacteria.”

Breslauer added that these software programs can be easily installed onto a typical mobile phone, turning the mobile phone into a self-contained field laboratory and a “good platform for epidemiological monitoring”.

While the CellScope is particularly valuable in resource-poor countries, Fletcher noted that it may have a place in any country's healthcare system, especially those plagued with cost overruns.

“A CellScope device with fluorescence could potentially be used by patients undergoing chemotherapy who need to get regular blood counts,” said Fletcher. “The patient could transmit from home the image or analysed data to a healthcare professional, reducing the number of clinic visits necessary.”

The CellScope developers have even been approached by experts in agriculture interested in using it to help diagnose diseases in crops. Instead of sending in a leaf sample to a laboratory for diagnosis, farmers could upload an image of the diseased leaf for analysis.

The researchers are currently developing more robust prototypes of the CellScope in preparation for further field testing.

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