4.7 Article

Solvent selective membrane routing and microfluidic architecture towards centrifugal automation of customisable bead based immunoassays

Journal

SENSORS AND ACTUATORS B-CHEMICAL
Volume 356, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.131305

Keywords

Solvent-selective; Lipophilic membranes; Microfluidics; Lab-on-a-disc; Routing; Cervical Cancer; RAPID ELISA; Point of care

Funding

  1. Dublin City University
  2. Arizona State University

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The success of bioanalytical technologies deployed in decentralised settings relies on factors such as user-friendliness, ease-of-use, cost per-test (at low sample throughput), and adaptability to a wide range of analytes. The centrifugal microfluidic Lab-on-a-Disc (LoaD) platform, which can meet these criteria, faces challenges in implementing reliable flow routing and valving on a rapidly rotating cartridge. In this study, we demonstrate the automation of a bead-based Enzyme-Linked Immuno-Sorbent Assay (ELISA) using a novel membrane and centrifugal-stratification enabled router architecture. The assay is implemented in an entirely automated fashion using minimal instrumentation, showing the potential for customisation to specific targets.
The success of bioanalytical technologies deployed at decentralised settings is governed by various performance criteria such as user-friendliness, ease-of-use, cost per-test (at comparatively low sample throughput) and adaptability to a wide range of available analytes while performing with minimal instrumentation. The centrifugal microfluidic Lab-on-a-Disc (LoaD) platform is a highly customisable platform which can meet these criteria for decentralised testing. However, a key concern of LoaD systems is the difficulty in implementing reliable flow routing and valving on a rapidly rotating cartridge. To address this challenge, we demonstrate here, the microfluidic automation of a bead-based Enzyme-Linked Immuno-Sorbent Assays (ELISAs) through use of a novel solvent-selective membrane and centrifugal-stratification enabled router architecture. To rule out optical interference of the bead phase with the absorption measurements, we use these novel lipophilic membrane valves to route the reaction product of the ELISA from the bead-phase into a separate detection chamber. As a pilot application, we automate a Rapid Antigenic Protein in situ Display (RAPID) ELISA for detection of the E7 antibody biomarker, which is clinically relevant for HPV16 virus related cervical cancer, on a LoaD cartridge. Through combination of this membrane and routing technology with event-triggered valves, the assay is implemented in an entirely automated fashion using minimal instrumentation (low-cost spindle motor). Furthermore, our approach is highly flexible as the RAPID protocol can be customised to a specific target by functionalising the bead-based solid-phase with specific proteins.

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