Zhu Jing, Yu Wenrou, Xiong Hongyuan, Xia Xuliang, Li Yunlong, Huang Yingzhou
Chongqing Key Laboratory of Interface Physics in Energy Conversion, College of Physics, Chongqing University, Chongqing 401331, China.
The Second Affiliated Hospital of Chengdu Medical College, China National Nuclear, Corporation 416 Hospital, Chengdu, Sichuan 610000, P. R. China.
ACS Sens. 2025 Aug 22;10(8):6123-6131. doi: 10.1021/acssensors.5c01745. Epub 2025 Jul 22.
Traditional wearable devices for sweat detection often face limitations such as low detection sensitivity, insufficient mechanical properties, and discomfort during use. To address these challenges, hydrogels are utilized as sensor patches to improve skin sensor contact and combined with surface enhanced Raman spectroscopy (SERS) to enable rapid and sensitive analysis of biomarkers in sweat. In this study, a mechanically flexible, rapid, and ultrasensitive wearable plasmonic double network (PDN) hydrogel sensor utilizing silver nanoparticles (AgNPs) in situ was developed to detect the SERS spectra of urea and uric acid in synthetic sweat. With the incorporation of poly(vinyl alcohol) (PVA), the PDN hydrogel can stretch repeatedly and even double in size, making it more suitable for wearable devices. The AgNPs were uniformly dispersed within the hydrogel, which reduced the dissociation of AgNPs and increased the sensitivity of SERS detection at 0.1 and 10 pM for 4-mercaptobenzoic acid (4-MBA) and 4-aminothiophene (4-ATP), respectively. In sweat analysis, the concentration reached 10 pM for urea and 1 nM for uric acid. The PDN hydrogel worked well at different pH levels to adapt to a complex sweat environment. Combined with the Raman characteristic vibration peak, the important analysis of the machine learning model demonstrated that urea and uric acid play important roles in the identification of biomarkers in sweat. The data illustrated that this PDN hydrogel facilitates the exploration of wearable sweat devices and has significant potential for clinical applications in the early diagnosis of diseases.
传统的用于汗液检测的可穿戴设备常常面临诸如检测灵敏度低、机械性能不足以及使用过程中不适感等限制。为应对这些挑战,水凝胶被用作传感器贴片以改善与皮肤传感器的接触,并与表面增强拉曼光谱(SERS)相结合,从而能够对汗液中的生物标志物进行快速且灵敏的分析。在本研究中,开发了一种机械柔性、快速且超灵敏的可穿戴等离子体双网络(PDN)水凝胶传感器,该传感器原位利用银纳米颗粒(AgNPs)来检测合成汗液中尿素和尿酸的SERS光谱。通过加入聚乙烯醇(PVA),PDN水凝胶能够反复拉伸,甚至尺寸翻倍,使其更适合用于可穿戴设备。AgNPs均匀分散在水凝胶中,这减少了AgNPs的解离,并分别提高了对4-巯基苯甲酸(4-MBA)和4-氨基噻吩(4-ATP)在0.1和10 pM时SERS检测的灵敏度。在汗液分析中,尿素浓度达到10 pM,尿酸浓度达到1 nM。PDN水凝胶在不同pH水平下均能良好工作,以适应复杂的汗液环境。结合拉曼特征振动峰,机器学习模型的重要分析表明尿素和尿酸在汗液生物标志物的识别中发挥着重要作用。数据表明,这种PDN水凝胶有助于可穿戴汗液设备的探索,并且在疾病早期诊断的临床应用中具有巨大潜力。