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Improving design features and air bubble manipulation techniques for a single-step sandwich electrochemical ELISA incorporating commercial electrodes into capillary-flow driven immunoassay devices.
Kaewarsa, Phuritat; Schenkel, Melissa S; Rahn, Kira L; Laiwattanapaisal, Wanida; Henry, Charles S.
Affiliation
  • Kaewarsa P; Graduate Program in Clinical Biochemistry and Molecular Medicine, Department of Clinical Chemistry, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, 10330, Thailand.
  • Schenkel MS; Department of Chemistry, Colorado State, University, Fort Collins, Colorado, 80526, USA.
  • Rahn KL; Department of Chemistry, Colorado State, University, Fort Collins, Colorado, 80526, USA.
  • Laiwattanapaisal W; Biosensors and Bioanalytical Technology for Cell and Innovative Testing Research Unit, Department of Clinical Chemistry, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, 10330, Thailand.
  • Henry CS; Department of Chemistry, Colorado State, University, Fort Collins, Colorado, 80526, USA.
Analyst ; 149(7): 2034-2044, 2024 Mar 25.
Article in En | MEDLINE | ID: mdl-38407468
ABSTRACT
Integrating electrochemistry into capillary-flow driven immunoassay devices provides unique opportunities for quantitative point-of-care testing. Although custom electrodes can be inexpensive and are tunable, they require skilled fabrication. Here, we report the incorporation of a commercial electrode into a capillary-flow driven immunoassay (iceCaDI) device for a single end-user step sandwich electrochemical enzyme-linked immunosorbent assay (ELISA). The iceCaDI device is a pump-free portable microfluidic device with an integrated commercial screen-printed electrode and flow driven by capillary action. The iceCaDI device is composed of alternating polyester transparency film and double-sided adhesive film layers that are patterned with a laser cutter. This platform was designed to address known limitations of laminated device fabrication methods and operation. First, we developed a foldable laminated device fabrication using hinges for easy assembly and precise alignment. Second, reagent dispersing was achieved by incorporating a 1 mm wide arrow-shaped notch in the middle of the channel that trapped an air bubble and formed a baffle that facilitated reagent spreading to cover the detection area. Third, small vent holes were added to the top layer of the channels to prevent air bubbles from blocking flow. Finally, we fabricated a CRP immunosensor with a detection range of 0.625 to 10.0 µg mL-1 as a proof-of-concept to demonstrate an automatically driven sandwich electrochemical ELISA using the iceCaDI device. Three concentrations of CRP were successfully measured under flow conditions within 8 min. Our proposed device is a promising approach and a step forward in the development of point-of-care (POC) devices for techniques that traditionally require multiple user steps.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biosensing Techniques Language: En Journal: Analyst Year: 2024 Type: Article Affiliation country: Thailand

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biosensing Techniques Language: En Journal: Analyst Year: 2024 Type: Article Affiliation country: Thailand