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Published January 23, 2024 | Published
Journal Article

Low-Cost Biosensor Technologies for Rapid Detection of COVID-19 and Future Pandemics

Abstract

Many systems have been designed for the detection of SARS-CoV-2, which is the virus that causes COVID-19. SARS-CoV-2 is readily transmitted, resulting in the rapid spread of disease in human populations. Frequent testing at the point of care (POC) is a key aspect for controlling outbreaks caused by SARS-CoV-2 and other emerging pathogens, as the early identification of infected individuals can then be followed by appropriate measures of isolation or treatment, maximizing the chances of recovery and preventing infectious spread. Diagnostic tools used for high-frequency testing should be inexpensive, provide a rapid diagnostic response without sophisticated equipment, and be amenable to manufacturing on a large scale. The application of these devices should enable large-scale data collection, help control viral transmission, and prevent disease propagation. Here we review functional nanomaterial-based optical and electrochemical biosensors for accessible POC testing for COVID-19. These biosensors incorporate nanomaterials coupled with paper-based analytical devices and other inexpensive substrates, traditional lateral flow technology (antigen and antibody immunoassays), and innovative biosensing methods. We critically discuss the advantages and disadvantages of nanobiosensor-based approaches compared to widely used technologies such as PCR, ELISA, and LAMP. Moreover, we delineate the main technological, (bio)chemical, translational, and regulatory challenges associated with developing functional and reliable biosensors, which have prevented their translation into the clinic. Finally, we highlight how nanobiosensors, given their unique advantages over existing diagnostic tests, may help in future pandemics.

Copyright and License

© 2024 American Chemical Society.

Acknowledgement

Cesar de la Fuente-Nunez holds a Presidential Professorship at the University of Pennsylvania, is a recipient of the Langer Prize by the AIChE Foundation, and acknowledges funding from the Procter & Gamble Company, United Therapeutics, a BBRF Young Investigator Grant, and the Defense Threat Reduction Agency (DTRA; HDTRA11810041 and HDTRA1-21-1-0014). Research reported in this publication was supported by the Nemirovsky Prize, the National Institute of General Medical Sciences of the National Institutes of Health under award number R35GM138201, Penn Health-Tech Accelerator Award, the IADR Innovation in Oral Care Award, and by funds provided by the Dean’s Innovation Fund from the Perelman School of Medicine at the University of Pennsylvania. Heather Lukas and Wei Gao acknowledge the funding support from National Science Foundation Grant 2145802, Sloan Research Fellowship, and Merkin Institute for Translational Research at California Institute of Technology. We thank Dr. Karen Pepper for editing the manuscript and de la Fuente Lab members for insightful discussions. William Reis de Araujo acknowledges funding from Brazilian funding agencies CAPES, FAPESP (2022/03250-7, 2018/08782-1), and CNPq (438828/2018-6, 310282/2022-5) for supporting the research.

 

Additional details

Created:
January 12, 2024
Modified:
March 11, 2024