A smartphone-based colorimetric reader for bioanalytical applications using the screen-based bottom illumination provided by gadgets

• Published in: Biosensors & bioelectronics Vol. 67; pp. 248 - 255
• Main Authors: Vashist, Sandeep Kumar, van Oordt, Thomas, Schneider, E. Marion, Zengerle, Roland, von Stetten, Felix, Luong, John H.T.
• Format: Journal Article
• Language: English
• Published: England 15.05.2015
• Subjects: algorithms; Assaying; Assembly; Biosensing Techniques - instrumentation; biosensors; C-reactive protein; cameras; Colorimetry; Colorimetry - instrumentation; cost effectiveness; detection limit; diagnostic techniques; ELISA; enzyme-linked immunosorbent assay; Enzyme-Linked Immunosorbent Assay - instrumentation; Equipment Design; Equipment Failure Analysis; humans; Illumination; image analysis; lighting; Lighting - instrumentation; Mini; Mobile Applications; peroxidase; Proteins; Readers; Reproducibility of Results; Sensitivity and Specificity; Smartphone; Smartphones; Bicinchoninic acid protein assay; Immunoassay; Gadget; Smartphone-based colorimetric readout; Screen
• ISSN: 0956-5663; 1873-4235; 1873-4235
• DOI: 10.1016/j.bios.2014.08.027

A smartphone-based colorimetric reader (SBCR) was developed using a Samsung Galaxy SIII mini, a gadget (iPAD mini, iPAD4 or iPhone 5s), integrated with a custom-made dark hood and base holder assembly. The smartphone equipped with a back camera (5 megapixels resolution) was used for colorimetric imaging via the hood and base-holder assembly. A 96- or 24-well microtiter plate (MTP) was positioned on the gadget's screensaver that provides white light-based bottom illumination only in the specific regions corresponding to the bottom of MTP's wells. The pixel intensity of the captured images was determined by an image processing algorithm. The developed SBCR was evaluated and compared with a commercial MTP reader (MTPR) for three model assays: our recently developed human C-reactive protein sandwich enzyme-linked immunosorbent assay (ELISA), horseradish peroxidase direct ELISA, and bicinchoninic acid protein estimation assay. SBCR had the same precision, dynamic range, detection limit and sensitivity as MTPR for all three assays. With advanced microfabrication and data processing, SBCR will become more compact, lighter, inexpensive and enriched with more features. Therefore, SBCR with a remarkable computing power could be an ideal point-of-care (POC) colorimetric detection device for the next-generation of cost-effective POC diagnostics, immunoassays and diversified bioanalytical applications.