Simple manipulation of enzyme-linked immunosorbent assay (ELISA) using an automated microfluidic interface. Issue 18 (28th April 2022)

• Record Type: Journal Article
• Authors: Panraksa, Yosita; Jang, Ilhoon; Carrell, Cody S.; Amin, Anita G.; Chailapakul, Orawon; Chatterjee, Delphi; Henry, Charles S.
• Is Part Of: Analytical methods. Volume 14:Issue 18(2022)
• Page Start: 1774
• Page End: 1781
• Publication Date: 2022-04-28
• Subjects: Chemistry, Analytic -- Periodicals; Analytical biochemistry -- Periodicals; Chemical laboratories -- Standards -- Periodicals; 543.1905
• DOI: 10.1039/d2ay00326k
• Languages: English
• ISSNs: 1759-9660

Abstract

Abstract : ELISA on microfluidic interface device for lipoarabinomannan. Abstract : Among lateral flow immunoassay (LFIA) platforms, enzyme-based LFIAs provide signal amplification to improve sensitivity. However, most enzyme-based LFIAs require multiple timed steps, complicating their utility in point-of-care testing (POCT). Here, we report a microfluidic interface for LFIAs that automates sample, buffer, and reagent addition, greatly simplifying operation while achieving the high analytical stringency associated with more complex assays. The microfluidic interface also maintains the low cost and small footprint of standard LFIAs. The platform is fabricated from a combination of polyester film, double-sided adhesive tape, and nitrocellulose, and fits in the palm of your hand. All reagents are dried on the nitrocellulose to facilitate sequential reagent delivery, and the sample is used as the wash buffer to minimize steps. After the sample addition, a user simply waits 15 min for a colorimetric result. This manuscript discusses the development and optimization of the channel geometry to achieve a simple step enzyme amplified immunoassay. As a proof-of-concept target, we selected lipoarabinomannan (LAM), a WHO identified urinary biomarker of active tuberculosis, to demonstrate the device feasibility and reliability. The results revealed that the device successfully detected LAM in phosphate buffer (PBS) as well as spiked urine samples within 15 min after sample loading. The minimum concentration of color change was achieved at 25 ng mL −1 .