Transforming Molecular Diagnostic Point of Care with Cell Phones

February 24, 2016
Transforming Molecular Diagnostic Point of Care with Cell Phones
Wells turn blue if a particular nucleic acid molecule is present. A cell-phone image of the wells can then undergo ratiometric spectral processing to provide a quantification of target molecules. [Ismagilov Lab]

Scientists at Caltech report that they have invented a new technique that can help bring emerging diagnostic capabilities out of laboratories and to the point of care. To address the need for a robust readout system for quantitative diagnostics, the researchers devised a novel visual readout method that uses analytical chemistries and image processing to provide unambiguous quantification of single nucleic acid molecules that can be performed by any cell phone camera.

The visual readout method is described and validated using RNA from the hepatitis C virus (HCV RNA) in a paper ("Reading Out Single-Molecule Digital RNA and DNA Isothermal Amplification in Nanoliter Volumes with Unmodified Camera Phones") in ACS Nano.

The work utilizes a microfluidic technology called SlipChip, which was invented several years ago in the lab of  Rustem Ismagilov, Ph.D., Caltech's Ethel Wilson Bowles and Robert Bowles Professor of Chemistry and Chemical Engineering and director of the Jacobs Institute for Molecular Engineering for Medicine. A SlipChip serves as a portable lab-on-a-chip and can be used to quantify concentrations of single molecules.

Each SlipChip encodes a complex program for isolating single molecules, such as DNA or RNA, along with chemical reactants in nanoliter-sized wells. The program also controls the complex reactions in each well: The chip consists of two plates that move—or "slip"—relative to one another, with each slip joining or separating the hundreds or even thousands of tiny wells, either bringing reactants and molecules into contact or isolating them. The architecture of the chip enables the user to have complete control over these chemical reactions and can prevent contamination.

The new visual readout method builds upon this SlipChip platform. Special indicator chemistries are integrated into the wells of the SlipChip device. After a nucleic acid amplification reaction wells change color depending on whether the reaction in it was positive or negative. For example, if a SlipChip is being used to count HCV RNA molecules in a sample, a well containing an RNA molecule that amplified during the reaction would turn blue; a well lacking an RNA molecule would remain purple.

To read the result, a user simply takes a picture of the entire SlipChip using any camera phone. Then the photo is processed using a ratiometric approach that transforms the colors detected by the camera's sensor into an unambiguous readout of positives and negatives.

Previous SlipChip technologies utilized a chemical that would fluoresce when a reaction took place within a well, but those readouts can be too subtle for detection by a common cell phone camera or can require specific lighting conditions, according to the researchers. The new method provides guidelines for selecting indicators that yield color changes compatible with the color sensitivities of phone cameras, and the ratiometric processing removes the need for a user to distinguish colors by sight.

"The readout process we developed can be used with any cell phone camera," says Jesus Rodriguez-Manzano, Ph.D., a postdoctoral scholar in chemical engineering and one of two first authors on the paper. "It is rapid, automated, and doesn't require counting or visual interpretation, so the results can be read by anyone—even users who are color blind or working under poor lighting conditions. This robustness makes our visual readout method appropriate for integration with devices used in any setting, including at the point of care in limited-resource settings. This is critical because the need for highly sensitive diagnostics is greatest in such regions."