4.6 Article

Automated ELISA On-Chip for the Detection of Anti-SARS-CoV-2 Antibodies

Journal

SENSORS
Volume 21, Issue 20, Pages -

Publisher

MDPI
DOI: 10.3390/s21206785

Keywords

SARS-CoV-2; COVID-19; spike protein; ELISA; antibodies; serology; on-chip; automated; microfluidics

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The COVID-19 pandemic, with limited access to testing, has exacerbated the crisis, making reliable testing critical. Automated ELISA on-chip using microfluidic-based technologies is a promising alternative for detecting antibodies in COVID-19 patients and vaccinated individuals. Basic image analysis of photos taken with a smartphone can be a useful alternative in the absence of specialized equipment.
The COVID-19 pandemic has been the most critical public health issue in modern history due to its highly infectious and deathly potential, and the limited access to massive, low-cost, and reliable testing has significantly worsened the crisis. The recovery and the vaccination of millions of people against COVID-19 have made serological tests highly relevant to identify the presence and levels of SARS-CoV-2 antibodies. Due to its advantages, microfluidic-based technologies represent an attractive alternative to the conventional testing methodologies used for these purposes. In this work, we described the development of an automated ELISA on-chip capable of detecting anti-SARS-CoV-2 antibodies in serum samples from COVID-19 patients and vaccinated individuals. The colorimetric reactions were analyzed with a microplate reader. No statistically significant differences were observed when comparing the results of our automated ELISA on-chip against the ones obtained from a traditional ELISA on a microplate. Moreover, we demonstrated that it is possible to carry out the analysis of the colorimetric reaction by performing basic image analysis of photos taken with a smartphone, which constitutes a useful alternative when lacking specialized equipment or a laboratory setting. Our automated ELISA on-chip has the potential to be used in a clinical setting and mitigates some of the burden caused by testing deficiencies.

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