School of Biomedical Engineering, College of Chemistry and Environmental Engineering, The Institute for Advanced Study (IAS), Shenzhen University, Shenzhen, Guangdong, 518060, P. R. China.
Beijing Key Laboratory for Bioengineering and Sensing Technology, University of Science and Technology Beijing, Beijing, 100083, P. R. China.
Adv Sci (Weinh). 2024 Nov;11(42):e2406196. doi: 10.1002/advs.202406196. Epub 2024 Sep 19.
The colloidal gold nanoparticle (AuNP)-based colorimetric lateral flow assay (LFA) is one of the most promising analytical tools for point-of-care disease diagnosis. However, the low sensitivity and insufficient accuracy still limit its clinical application. In this work, a machine learning (ML)-optimized colorimetric LFA with ultrasound enrichment is developed to achieve the sensitive and accurate detection of tau proteins for early screening of Alzheimer's disease (AD). The LFA device is integrated with a portable ultrasonic actuator to rapidly enrich microparticles using ultrasound, which is essential for sample pre-enrichment to improve the sensitivity, followed by ML algorithms to classify and predict the enhanced colorimetric signals. The results of the undiluted serum sample testing show that the protocol enables efficient classification and accurate quantification of the AD biomarker tau protein concentration with an average classification accuracy of 98.11% and an average prediction accuracy of 99.99%, achieving a limit of detection (LOD) as sensitive as 10.30 pg mL. Further point-of-care testing (POCT) of human plasma samples demonstrates the potential use of LFA in clinical trials. Such a reliable lateral flow immunosensor with high precision and superb sensing performance is expected to put LFA in perspective as an AD clinical diagnostic platform.
基于胶体金纳米颗粒(AuNP)的比色侧流分析(LFA)是用于即时疾病诊断的最有前途的分析工具之一。然而,其低灵敏度和不足的准确性仍然限制了它的临床应用。在这项工作中,开发了一种机器学习(ML)优化的比色 LFA 与超声富集,以实现对 tau 蛋白的灵敏和准确检测,用于早期筛选阿尔茨海默病(AD)。LFA 设备与便携式超声换能器集成,可利用超声快速富集微粒,这对于样品预富集以提高灵敏度至关重要,然后是 ML 算法来分类和预测增强的比色信号。未稀释血清样本测试的结果表明,该方案能够有效地对 AD 生物标志物 tau 蛋白浓度进行分类和准确定量,平均分类准确率为 98.11%,平均预测准确率为 99.99%,检测限(LOD)低至 10.30 pg mL。对人血浆样本的进一步即时检测(POCT)证明了 LFA 在临床试验中的潜在用途。这种具有高精度和卓越传感性能的可靠侧向流动免疫传感器有望使 LFA 成为 AD 临床诊断平台。