Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
Life Sciences Institute, University of Michigan, Ann Arbor, Michigan 48109, United States.
Anal Chem. 2023 Nov 21;95(46):17028-17036. doi: 10.1021/acs.analchem.3c03719. Epub 2023 Nov 9.
High-throughput screening (HTS) workflows are revolutionizing many fields, including drug discovery, reaction discovery and optimization, diagnostics, sensing, and enzyme engineering. Liquid chromatography (LC) is commonly deployed during HTS to reduce matrix effects, distinguish isomers, and preconcentrate prior to detection, but LC separation time often limits throughput. Although subsecond LC separations have been demonstrated, they are rarely utilized during HTS due to limitations associated with the speed of common autosamplers. In this work, these limits are overcome by utilizing droplet microfluidics for sample introduction. In the method, a train of samples segmented by air are continuously pumped into the inlet of an LC injection valve that is actuated once each sample fills the sample loop. Coupled with 2.1 mm diameter × 5 mm long columns packed with 2.7 μm superficially porous C18 particles operated at 5 mL/min, the injector enabled separation of 3 components at 1 s/sample and analysis of a 96-well plate in 1.6 min with <2% peak area relative standard deviation. Analyte-dependent carryover was minimized by including wash droplets composed of organic solvent in between sample droplets. High-throughput LC coupled with mass spectrometric detection using the segmented flow injector was applied to a screen of inhibitors of a cytochrome P450-catalyzed hydroxylation reaction. Measurements of the reaction substrate and product concentrations made using fast LC with the segmented flow injector correlated well with measurements made using a more conventional, 3 min LC method. These results demonstrate the potential for droplet microfluidics to be used for sample introduction during high-throughput LC analysis.
高通量筛选 (HTS) 工作流程正在彻底改变许多领域,包括药物发现、反应发现和优化、诊断、传感和酶工程。在 HTS 中,通常会部署液相色谱 (LC) 来减少基质效应、区分异构体并在检测前进行预浓缩,但是 LC 分离时间通常会限制通量。尽管已经证明了亚秒级的 LC 分离,但由于与常见自动进样器的速度相关的限制,它们在 HTS 中很少被利用。在这项工作中,通过利用液滴微流控技术进行样品引入来克服这些限制。在该方法中,通过空气分段的样品连续泵入 LC 进样阀的入口,该进样阀在每个样品充满样品环时被驱动一次。与 2.1mm 直径×5mm 长的柱联用,柱内填充 2.7μm 表面多孔 C18 颗粒,以 5mL/min 的流速运行,该注射器可在 1s/样品的条件下分离 3 种组分,并在 1.6min 内分析 96 孔板,相对标准偏差<2%。通过在样品液滴之间包含由有机溶剂组成的洗涤液滴,最小化了分析物依赖性的峰拖尾。高通量 LC 与使用分段流注射器的质谱检测相结合,应用于细胞色素 P450 催化的羟化反应抑制剂的筛选。使用分段流注射器进行快速 LC 测量的反应底物和产物浓度与使用更传统的 3 分钟 LC 方法测量的结果非常吻合。这些结果表明,液滴微流控技术有潜力用于高通量 LC 分析中的样品引入。