TY - JOUR
T1 - Overcoming the limitations of COVID-19 diagnostics with nanostructures, nucleic acid engineering, and additive manufacturing
AU - Li, Nantao
AU - Zhao, Bin
AU - Stavins, Robert
AU - Peinetti, Ana Sol
AU - Chauhan, Neha
AU - Bashir, Rashid
AU - Cunningham, Brian T
AU - King, William P
AU - Lu, Yi
AU - Wang, Xing
AU - Valera, Enrique
N1 - Funding Information:
The authors are grateful to the National Science Foundation (NSF) , the National Institutes of Health (NIH) , and the Defense Advanced Research Projects Agency (DARPA) for the financial support for research projects highlighted in this paper. Specifically, BTC, XW, NL, BZ, and NC are grateful for support from NSF RAPID ( 20-27778 ), NIH NIAAA ( AA029348 ), and NIH NIAID ( AI120683 , AI130562 ). XW is also grateful for the support from NIH NIDCR ( DE030852 ). NL received graduate fellowship support from the Dynamic Research Enterprise for Multidisciplinary Engineering Sciences (DREMES) at Zhejiang University and the University of Illinois at Urbana-Champaign, funded by Zhejiang University , supervised by BTC. BZ is grateful to the Woese Institute for Genomic Biology for financial support as an IGB Postdoctoral Fellow. RB and EV are grateful for support from NSF RAPID ( 20-28431 ). RB, WPK, and EV acknowledge support from the Foxconn Interconnect Technology sponsored Center for Networked Intelligent Components and Environments (C-NICE). ASP and YL are grateful for support from NSF RAPID ( CBET 20-29215 ). ASP also thanks the PEW Latin American Fellowship for the support. BTC, RB and EV received support from the Jump Applied Research through Community Health through Engineering and Simulation (ARCHES) endowment through the Health Care Engineering Systems Center at UIUC.
Publisher Copyright:
© 2021
PY - 2022/2
Y1 - 2022/2
N2 - The COVID-19 pandemic revealed fundamental limitations in the current model for infectious disease diagnosis and serology, based upon complex assay workflows, laboratory-based instrumentation, and expensive materials for managing samples and reagents. The lengthy time delays required to obtain test results, the high cost of gold-standard PCR tests, and poor sensitivity of rapid point-of-care tests contributed directly to society's inability to efficiently identify COVID-19-positive individuals for quarantine, which in turn continues to impact return to normal activities throughout the economy. Over the past year, enormous resources have been invested to develop more effective rapid tests and laboratory tests with greater throughput, yet the vast majority of engineering and chemistry approaches are merely incremental improvements to existing methods for nucleic acid amplification, lateral flow test strips, and enzymatic amplification assays for protein-based biomarkers. Meanwhile, widespread commercial availability of new test kits continues to be hampered by the cost and time required to develop single-use disposable microfluidic plastic cartridges manufactured by injection molding. Through development of novel technologies for sensitive, selective, rapid, and robust viral detection and more efficient approaches for scalable manufacturing of microfluidic devices, we can be much better prepared for future management of infectious pathogen outbreaks. Here, we describe how photonic metamaterials, graphene nanomaterials, designer DNA nanostructures, and polymers amenable to scalable additive manufacturing are being applied towards overcoming the fundamental limitations of currently dominant COVID-19 diagnostic approaches. In this paper, we review how several distinct classes of nanomaterials and nanochemistry enable simple assay workflows, high sensitivity, inexpensive instrumentation, point-of-care sample-to-answer virus diagnosis, and rapidly scaled manufacturing.
AB - The COVID-19 pandemic revealed fundamental limitations in the current model for infectious disease diagnosis and serology, based upon complex assay workflows, laboratory-based instrumentation, and expensive materials for managing samples and reagents. The lengthy time delays required to obtain test results, the high cost of gold-standard PCR tests, and poor sensitivity of rapid point-of-care tests contributed directly to society's inability to efficiently identify COVID-19-positive individuals for quarantine, which in turn continues to impact return to normal activities throughout the economy. Over the past year, enormous resources have been invested to develop more effective rapid tests and laboratory tests with greater throughput, yet the vast majority of engineering and chemistry approaches are merely incremental improvements to existing methods for nucleic acid amplification, lateral flow test strips, and enzymatic amplification assays for protein-based biomarkers. Meanwhile, widespread commercial availability of new test kits continues to be hampered by the cost and time required to develop single-use disposable microfluidic plastic cartridges manufactured by injection molding. Through development of novel technologies for sensitive, selective, rapid, and robust viral detection and more efficient approaches for scalable manufacturing of microfluidic devices, we can be much better prepared for future management of infectious pathogen outbreaks. Here, we describe how photonic metamaterials, graphene nanomaterials, designer DNA nanostructures, and polymers amenable to scalable additive manufacturing are being applied towards overcoming the fundamental limitations of currently dominant COVID-19 diagnostic approaches. In this paper, we review how several distinct classes of nanomaterials and nanochemistry enable simple assay workflows, high sensitivity, inexpensive instrumentation, point-of-care sample-to-answer virus diagnosis, and rapidly scaled manufacturing.
KW - Additive manufactured materials
KW - COVID-19 diagnostics
KW - Nanochemistry
KW - Nanomaterials
KW - Nanostructures
KW - Nucleic acid engineering
KW - Point-of-care diagnosis
KW - SARS-CoV-2
UR - http://www.scopus.com/inward/record.url?scp=85119444103&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85119444103&partnerID=8YFLogxK
U2 - 10.1016/j.cossms.2021.100966
DO - 10.1016/j.cossms.2021.100966
M3 - Article
C2 - 34840515
SN - 1359-0286
VL - 26
JO - Current Opinion in Solid State and Materials Science
JF - Current Opinion in Solid State and Materials Science
IS - 1
M1 - 100966
ER -