A paper-in-polymer-pond (PiPP) hybrid microfluidic microplate for multiplexed ultrasensitive detection of cancer biomarkers.

Lab Chip

Department of Chemistry & Biochemistry, University of Texas at El Paso, 500 W University Ave, El Paso, TX, USA.

Published: October 2024

AI Article Synopsis

  • Conventional ELISA methods for detecting cancer biomarkers face challenges like long incubation times, high reagent requirements, and low sensitivity.
  • A new paper-in-polymer-pond (PiPP) hybrid microfluidic microplate has been developed to allow quick, cost-effective, and sensitive detection of disease biomarkers in under an hour without the need for sophisticated equipment.
  • The device achieves improved sensitivity and can be reused by replacing the paper layer, enabling better efficiency in reagent delivery and quantitative analysis using common imaging tools like scanners or smartphone cameras.

Article Abstract

Conventional affinity-based colorimetric enzyme-linked immunosorbent assay (ELISA) is one of the most widely used methods for the detection of biomarkers. However, rapid point-of-care (POC) detection of multiple cancer biomarkers by conventional ELISA is limited by long incubation time, large reagent volume, and costly instrumentation along with low sensitivity due to the nature of colorimetric methods. Herein, we have developed a reusable and cost-effective paper-in-polymer-pond (PiPP) hybrid microfluidic microplate for ultrasensitive and high-throughput multiplexed detection of disease biomarkers within an hour without using specialized instruments. A piece of pre-patterned chromatography paper placed in the PMMA polymer pond facilitates rapid protein immobilization to avoid intricate surface modifications of polymer and can be changed with a fresh paper layer to reuse the device. Reagents can be simply delivered from the top PMMA layer to multiple microwells in the middle PMMA layer flow-through microwells, thereby increasing the efficiency of washing and avoiding repeated manual pipetting or costly robots. Quantitative colorimetric analysis was achieved by calculating the brightness of images scanned by an office scanner or a smartphone camera. Sandwich-type immunoassay was performed in the PiPP hybrid device after the optimization of multiple assay conditions. Limits of detection of 0.32 ng mL for carcinoembryonic antigen (CEA) and 0.20 ng mL for prostate-specific antigen (PSA) were obtained, which were about 10-fold better than those of commercial ELISA kits. We envisage that this simple but versatile hybrid device can have broad applications in various bioassays in resource-limited settings.

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Source
http://dx.doi.org/10.1039/d4lc00485jDOI Listing

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