3D-printed capillaric ELISA-on-a-chip with aliquoting

被引:32
作者
Parandakh, Azim [1 ,2 ]
Ymbern, Oriol [1 ,2 ]
Jogia, William [1 ,2 ]
Renault, Johan [1 ,2 ]
Ng, Andy [1 ,2 ]
Juncker, David [1 ,2 ]
机构
[1] McGill Univ, Biomed Engn Dept, 740 Dr Penfield Ave, Montreal, PQ H3A 0G1, Canada
[2] McGill Univ, McGill Genome Ctr, Montreal, PQ, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
POINT; ASSAY; MICROFLUIDICS; IMMUNOASSAY; DIAGNOSTICS;
D O I
10.1039/d2lc00878e
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sandwich immunoassays such as the enzyme-linked immunosorbent assay (ELISA) have been miniaturized and performed in a lab-on-a-chip format, but the execution of the multiple assay steps typically requires a computer or complex peripherals. Recently, an ELISA for detecting antibodies was encoded structurally in a chip thanks to the microfluidic chain reaction (Yafia et al. Nature, 2022, 605, 464-469), but the need for precise pipetting and intolerance to commonly used surfactant concentrations limit the potential for broader adoption. Here, we introduce the ELISA-on-a-chip with aliquoting functionality that simplifies chip loading and pipetting, accommodates higher surfactant concentrations, includes barrier channels that delay the contact between solutions and prevent undesired mixing, and that executed a quantitative, high-sensitivity assay for the SARS-CoV-2 nucleocapsid protein in 4x-diluted saliva. Upon loading the chip using disposable pipettes, capillary flow draws each reagent and the sample into a separate volumetric measuring reservoir for detection antibody (70 mu L), enzyme conjugate (50 mu L), substrate (80 mu L), and sample (210 mu L), and splits washing buffer into 4 different reservoirs of 40, 40, 60, and 20 mu L. The excess volume is autonomously drained via a structurally encoded capillaric aliquoting circuit, creating aliquots with an accuracy of >93%. Next, the user click-connects the assay module, comprising a nitrocellulose membrane with immobilized capture antibodies and a capillary pump, to the chip which triggers the step-by-step, timed flow of all aliquoted solutions to complete the assay in 1.5 h. A colored precipitate forming a line on a nitrocellulose strip serves as an assay readout, and upon digitization, yielded a binding curve with a limit of detection of 54 and 91 pg mL(-1) for buffer and diluted saliva respectively, vastly outperforming rapid tests. The ELISA chip is 3D-printed, modular, adaptable to other targets and assays, and could be used to automate ELISA in the lab; or as a diagnostic test at the point of care with the convenience and form factor of rapid tests while preserving the protocol and performance of central laboratory ELISA.
引用
收藏
页码:1547 / 1560
页数:15
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