ACS Nano. 2024 Oct 15;18(41):27933-27948. doi: 10.1021/acsnano.4c05153. Epub 2024 Oct 4.
Successful integration of point-of-care testing (POCT) into clinical settings requires improved assay sensitivity and precision to match laboratory standards. Here, we show how innovations in amplified biosensing, imaging, and data processing, coupled with deep learning, can help improve POCT. To demonstrate the performance of our approach, we present a rapid and cost-effective paper-based high-sensitivity vertical flow assay (hs-VFA) for quantitative measurement of cardiac troponin I (cTnI), a biomarker widely used for measuring acute cardiac damage and assessing cardiovascular risk. The hs-VFA includes a colorimetric paper-based sensor, a portable reader with time-lapse imaging, and computational algorithms for digital assay validation and outlier detection. Operating at the level of a rapid at-home test, the hs-VFA enabled the accurate quantification of cTnI using 50 μL of serum within 15 min per test and achieved a detection limit of 0.2 pg/mL, enabled by gold ion amplification chemistry and time-lapse imaging. It also achieved high precision with a coefficient of variation of <7% and a very large dynamic range, covering cTnI concentrations over 6 orders of magnitude, up to 100 ng/mL, satisfying clinical requirements. In blinded testing, this computational hs-VFA platform accurately quantified cTnI levels in patient samples and showed a strong correlation with the ground truth values obtained by a benchtop clinical analyzer. This nanoparticle amplification-based computational hs-VFA platform can democratize access to high-sensitivity point-of-care diagnostics and provide a cost-effective alternative to laboratory-based biomarker testing.
成功将即时检测(POCT)整合到临床环境中需要提高检测灵敏度和精密度,以达到实验室标准。在这里,我们展示了如何通过放大生物传感、成像和数据处理的创新,结合深度学习,来帮助改善 POCT。为了展示我们方法的性能,我们提出了一种快速且具有成本效益的基于纸的高灵敏度垂直流动分析(hs-VFA),用于定量测量心肌肌钙蛋白 I(cTnI),这是一种广泛用于测量急性心脏损伤和评估心血管风险的生物标志物。hs-VFA 包括一个比色基于纸的传感器、一个带有延时成像的便携式读取器,以及用于数字检测验证和异常值检测的计算算法。hs-VFA 可作为快速家庭检测使用,每个检测仅需 15 分钟即可使用 50 μL 血清准确地定量 cTnI,检测限为 0.2 pg/mL,这得益于金离子扩增化学和延时成像。它还具有高精度,变异系数 <7%,动态范围非常大,覆盖了 6 个数量级的 cTnI 浓度,高达 100ng/mL,满足临床需求。在盲测中,这个基于计算的 hs-VFA 平台准确地定量了患者样本中的 cTnI 水平,并与通过台式临床分析仪获得的真实值有很强的相关性。这个基于纳米颗粒放大的计算 hs-VFA 平台可以使高灵敏度即时诊断更容易获得,并提供了一种具有成本效益的替代实验室生物标志物检测的方法。