TY - JOUR
T1 - Portable Pathogen Diagnostics Using Microfluidic Cartridges Made from Continuous Liquid Interface Production Additive Manufacturing
AU - Berger, Jacob
AU - Aydin, Mehmet Y.
AU - Stavins, Robert
AU - Heredia, John
AU - Mostafa, Ariana
AU - Ganguli, Anurup
AU - Valera, Enrique
AU - Bashir, Rashid
AU - King, William P.
N1 - Funding Information:
The authors gratefully acknowledge DARPA under cooperative agreement D19AC00012 for supporting J.B., M.Y.A., and R.S. Also, R.B. and E.V. acknowledge support for A.G. from NIH R21 AI146865A. We acknowledge partial support for A.M. by a cooperative agreement with Purdue University and the Agricultural Research Service of the United States Department of Agriculture (via sub-award 8000074077 to UIUC). Authors thank the staff at the Holonyak Micro and Nanotechnology Laboratory at UIUC for facilitating the research and the funding from University of Illinois. Authors thank the staff of the Biomedical Research Laboratory at Carle Hospital for facilitating the research. The following reagents were obtained through BEI Resources, NIAID, NIH: genomic DNA from Escherichia coli, Strain B6914-MS1, NR-3044; E. coli, Strain B6914-MS1, NR-6; genomic DNA from Staphylococcus aureus, Strain HFH-30106, NR-10320; Staphylococcus aureus, Strain HFH-30106, NR-10320; genomic DNA of Staphylococcus aureus, Strain MN8, HM-162D; Staphylococcus aureus, Strain MN8, HM-162D.
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/7/27
Y1 - 2021/7/27
N2 - Biomedical diagnostics based on microfluidic devices have the potential to significantly benefit human health; however, the manufacturing of microfluidic devices is a key limitation to their widespread adoption. Outbreaks of infectious disease continue to demonstrate the need for simple, sensitive, and translatable tests for point-of-care use. Additive manufacturing (AM) is an attractive alternative to conventional approaches for microfluidic device manufacturing based on injection molding; however, there is a need for development and validation of new AM process capabilities and materials that are compatible with microfluidic diagnostics. In this paper, we demonstrate the development and characterization of AM cartridges using continuous liquid interface production (CLIP) and investigate process characteristics and capabilities of the AM microfluidic device manufacturing. We find that CLIP accurately produces microfluidic channels as small as 400 μm and that it is possible to routinely produce fluid channels as small as 100 μm with high repeatability. We also developed a loop-mediated isothermal amplification (LAMP) assay for detection of E. coli from whole blood directly on the CLIP-based AM microfluidic cartridges, with a 50 cfu/μL limit of detection, validating the use of CLIP processes and materials for pathogen detection. The portable diagnostic platform presented in this paper could be used to investigate and validate other AM processes for microfluidic diagnostics and could be an important component of scaling up the diagnostics for current and future infectious diseases and pandemics.
AB - Biomedical diagnostics based on microfluidic devices have the potential to significantly benefit human health; however, the manufacturing of microfluidic devices is a key limitation to their widespread adoption. Outbreaks of infectious disease continue to demonstrate the need for simple, sensitive, and translatable tests for point-of-care use. Additive manufacturing (AM) is an attractive alternative to conventional approaches for microfluidic device manufacturing based on injection molding; however, there is a need for development and validation of new AM process capabilities and materials that are compatible with microfluidic diagnostics. In this paper, we demonstrate the development and characterization of AM cartridges using continuous liquid interface production (CLIP) and investigate process characteristics and capabilities of the AM microfluidic device manufacturing. We find that CLIP accurately produces microfluidic channels as small as 400 μm and that it is possible to routinely produce fluid channels as small as 100 μm with high repeatability. We also developed a loop-mediated isothermal amplification (LAMP) assay for detection of E. coli from whole blood directly on the CLIP-based AM microfluidic cartridges, with a 50 cfu/μL limit of detection, validating the use of CLIP processes and materials for pathogen detection. The portable diagnostic platform presented in this paper could be used to investigate and validate other AM processes for microfluidic diagnostics and could be an important component of scaling up the diagnostics for current and future infectious diseases and pandemics.
KW - Escherichia coli/genetics
KW - Humans
KW - Microfluidic Analytical Techniques
KW - Microfluidics
KW - Molecular Diagnostic Techniques
KW - Nucleic Acid Amplification Techniques
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U2 - 10.1021/acs.analchem.1c00654
DO - 10.1021/acs.analchem.1c00654
M3 - Article
C2 - 34251790
SN - 0003-2700
VL - 93
SP - 10048
EP - 10055
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 29
ER -