Parandakh Azim, Ymbern Oriol, Jogia William, Renault Johan, Ng Andy, Juncker David
Biomedical Engineering Department, McGill University, 740 Dr. Penfield Ave, Montreal, QC, H3A 0G1, Canada.
McGill Genome Centre, McGill University, Montreal, QC, Canada.
Lab Chip. 2023 Mar 14;23(6):1547-1560. doi: 10.1039/d2lc00878e.
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 , 2022, , 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 4×-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 μL), enzyme conjugate (50 μL), substrate (80 μL), and sample (210 μL), and splits washing buffer into 4 different reservoirs of 40, 40, 60, and 20 μL. The excess volume is autonomously drained 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 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.
诸如酶联免疫吸附测定(ELISA)之类的夹心免疫测定法已被微型化,并以芯片实验室的形式进行,但多个测定步骤的执行通常需要计算机或复杂的外围设备。最近,由于微流控链反应(Yafia,2022,,464 - 469),一种用于检测抗体的ELISA在芯片中进行了结构编码,但精确移液的需求以及对常用表面活性剂浓度的不耐受限制了其更广泛应用的潜力。在此,我们介绍一种具有等分功能的芯片上ELISA,它简化了芯片加载和移液操作,能适应更高的表面活性剂浓度,包括可延迟溶液接触并防止不必要混合的屏障通道,并且能对4倍稀释唾液中的SARS-CoV-2核衣壳蛋白进行定量、高灵敏度测定。使用一次性移液器加载芯片后,毛细流动将每种试剂和样品吸入单独的体积测量储液器中,用于检测抗体(70 μL)、酶偶联物(50 μL)、底物(80 μL)和样品(210 μL),并将洗涤缓冲液分成4个不同的储液器,体积分别为40、40、60和20 μL。多余的体积通过一个结构编码的毛细等分电路自动排出,产生准确度>93%的等分试样。接下来,用户通过点击连接测定模块,该模块包括带有固定捕获抗体的硝酸纤维素膜和一个毛细泵,连接到芯片上,这会触发所有等分溶液按步骤、定时流动,在1.5小时内完成测定。在硝酸纤维素条上形成一条线的有色沉淀物用作测定读数,数字化后,缓冲液和稀释唾液的结合曲线检测限分别为54和91 pg/mL,大大优于快速检测。ELISA芯片是3D打印的、模块化的,可适应其他目标和测定,可用于在实验室中实现ELISA自动化;或作为即时护理诊断测试,兼具快速检测的便利性和外形尺寸,同时保留中心实验室ELISA的方案和性能。