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Engineering viral genomics and nano-liposomes in microfluidic platforms for patient-specific analysis of SARS-CoV-2 variants

Satta, Sandro and Shahabipour, Fahimeh and Gao, Wei and Lentz, Steven R. and Perlman, Stanley and Ashammakhi, Nureddin and Hsiai, Tzung (2022) Engineering viral genomics and nano-liposomes in microfluidic platforms for patient-specific analysis of SARS-CoV-2 variants. Theranostics, 12 (10). pp. 4779-4790. ISSN 1838-7640. PMCID PMC9254234. doi:10.7150/thno.72339.

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New variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are continuing to spread globally, contributing to the persistence of the COVID-19 pandemic. Increasing resources have been focused on developing vaccines and therapeutics that target the Spike glycoprotein of SARS-CoV-2. Recent advances in microfluidics have the potential to recapitulate viral infection in the organ-specific platforms, known as organ-on-a-chip (OoC), in which binding of SARS-CoV-2 Spike protein to the angiotensin-converting enzyme 2 (ACE2) of the host cells occurs. As the COVID-19 pandemic lingers, there remains an unmet need to screen emerging mutations, to predict viral transmissibility and pathogenicity, and to assess the strength of neutralizing antibodies following vaccination or reinfection. Conventional detection of SARS-CoV-2 variants relies on two-dimensional (2-D) cell culture methods, whereas simulating the micro-environment requires three-dimensional (3-D) systems. To this end, analyzing SARS-CoV-2-mediated pathogenicity via microfluidic platforms minimizes the experimental cost, duration, and optimization needed for animal studies, and obviates the ethical concerns associated with the use of primates. In this context, this review highlights the state-of-the-art strategy to engineer the nano-liposomes that can be conjugated with SARS-CoV-2 Spike mutations or genomic sequences in the microfluidic platforms; thereby, allowing for screening the rising SARS-CoV-2 variants and predicting COVID-19-associated coagulation. Furthermore, introducing viral genomics to the patient-specific blood accelerates the discovery of therapeutic targets in the face of evolving viral variants, including B1.1.7 (Alpha), B.1.351 (Beta), B.1.617.2 (Delta), c.37 (Lambda), and B.1.1.529 (Omicron). Thus, engineering nano-liposomes to encapsulate SARS-CoV-2 viral genomic sequences enables rapid detection of SARS-CoV-2 variants in the long COVID-19 era.

Item Type:Article
Related URLs:
URLURL TypeDescription CentralArticle
Gao, Wei0000-0002-8503-4562
Hsiai, Tzung0000-0003-1734-0792
Additional Information:© 2022 The author(s). This is an open access article distributed under the terms of the Creative Commons Attribution License ( Received: 2022.02.23; Accepted: 2022.04.21; Published: 2022.06.06. The authors acknowledge that they have no competing interests. The authors also acknowledge funding sources from National Institutes of Health (1UG3TR003148, R01HL111437, R01HL129727), the American Heart Association (COVID-19 Rapid Response Award 20203858), California Institute for Regenerative Medicine (Grant Number DISC2COVID19-11838), UCLA David Geffen School of Medicine - Oversight COVID-19 Research Committee (OCRC) (Award Number: OCRC #45). The authors also acknowledge that some of the figures have been created or adapted using The authors have declared that no competing interest exists.
Funding AgencyGrant Number
American Heart AssociationCOVID-19 Rapid Response Award 20203858
California Institute for Regenerative Medicine (CIRM)DISC2COVID19-11838
UCLA Oversight COVID-19 Research CommitteeOCRC 45
Subject Keywords:Organ on-a-chip, microfluidics, viral genomics, mutations, variants of concerns, COVID-19, nano-liposomes
Issue or Number:10
PubMed Central ID:PMC9254234
Record Number:CaltechAUTHORS:20220810-254276000
Persistent URL:
Official Citation:Satta S, Shahabipour F, Gao W, Lentz SR, Perlman S, Ashammakhi N, Hsiai T. Engineering viral genomics and nano-liposomes in microfluidic platforms for patient-specific analysis of SARS-CoV-2 variants. Theranostics 2022; 12(10):4779-4790. doi:10.7150/thno.72339. Available from
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:116217
Deposited By: George Porter
Deposited On:11 Aug 2022 23:00
Last Modified:11 Aug 2022 23:00

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