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Rapid colorimetric analysis of multiple microRNAs using encoded hydrogel microparticles. | LitMetric

Rapid colorimetric analysis of multiple microRNAs using encoded hydrogel microparticles.

Analyst

Department of Chemical and Biological Engineering, Korea University, Seoul, Republic of Korea.

Published: September 2021

AI Article Synopsis

  • MicroRNAs (miRNAs) are being researched as potential biomarkers for diagnosing serious diseases, with colorimetric bead-based assays becoming popular for their simplicity and affordability.
  • The encoded hydrogel microparticle-based colorimetric miRNA assay offers advantages like high sensitivity and capacity for multiple targets, though it has been limited by long reaction times.
  • This study introduces a rapid colorimetric assay that reduces reaction time by increasing enzyme binding and reaction temperature, maintaining sensitivity while allowing for effective multiplex miRNA detection.

Article Abstract

microRNAs (miRNAs) have attracted much attention as potential biomarkers for the diagnosis of various fatal diseases. With increasing interest in miRNA detection at practical sites, colorimetric bead-based assays have garnered much attention, because these allow for simple analysis with cheap and portable devices. Among them, the encoded hydrogel microparticle-based colorimetric miRNA assay is considered as one of the promising techniques, due to its strengths, such as large multiplex capacity, acceptable sensitivity, and simple analysis. However, it still imposes a limitation in terms of the assay time, particularly the colorimetric reaction time, which is too long, making the practical application of the assay difficult and undermining its detection accuracy. In this work, we present a rapid colorimetric assay based on encoded hydrogel microparticles, which exhibits a significant decrease in the colorimetric reaction time due to two factors: (1) an increase in the number of enzymes bound to hydrogel microparticles a post-synthesis functionalization method, and (2) an elevation in the enzyme reaction temperature during colorimetric labeling. We obtained a comparable sensitivity of the colorimetric assay with three different miRNA targets, even with a shortened colorimetric reaction time. Furthermore, we validated that our colorimetric detection method is suitable for multiplex miRNA detection, owing to its low cross-reactivity.

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Source
http://dx.doi.org/10.1039/d1an00622cDOI Listing

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