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基于分子印迹的纸质微流控可穿戴传感器实时分析汗液生物标志物

Molecularly Imprinted Wearable Sensor with Paper Microfluidics for Real-Time Sweat Biomarker Analysis.

机构信息

Department of Biomedical Engineering, Texas A&M University, College Station 77843, Texas, United States.

Department of Pediatrics-Nutrition, Baylor College of Medicine, Houston 77030, Texas, United States.

出版信息

ACS Appl Mater Interfaces. 2024 Sep 4;16(35):46113-46122. doi: 10.1021/acsami.4c10033. Epub 2024 Aug 23.

DOI:10.1021/acsami.4c10033
PMID:39178237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11378148/
Abstract

The urgent need for real-time and noninvasive monitoring of health-associated biochemical parameters has motivated the development of wearable sweat sensors. Existing electrochemical sensors show promise in real-time analysis of various chemical biomarkers. These sensors often rely on labels and redox probes to generate and amplify the signals for the detection and quantification of analytes with limited sensitivity. In this study, we introduce a molecularly imprinted polymer (MIP)-based biochemical sensor to quantify a molecular biomarker in sweat using electrochemical impedance spectroscopy, which eliminates the need for labels or redox probes. The molecularly imprinted biosensor can achieve sensitive and specific detection of cortisol at concentrations as low as 1 pM, 1000-fold lower than previously reported MIP cortisol sensors. We integrated multimodal electrochemical sensors with an iontophoresis sweat extraction module and paper microfluidics for real-time sweat analysis. Several parameters can be simultaneously quantified, including sweat volume, secretion rate, sodium ion, and cortisol concentration. Paper microfluidic modules not only quantify sweat volume and secretion rate but also facilitate continuous sweat analysis without user intervention. While we focus on cortisol sensing as a proof-of-concept, the molecularly imprinted wearable sensors can be extended to real-time detection of other biochemicals, such as protein biomarkers and therapeutic drugs.

摘要

实时、非侵入式监测与健康相关的生化参数的迫切需求,推动了可穿戴汗液传感器的发展。现有的电化学传感器在实时分析各种化学生物标志物方面显示出了前景。这些传感器通常依赖于标签和氧化还原探针来产生和放大信号,以检测和定量分析物,但其灵敏度有限。在这项研究中,我们引入了一种基于分子印迹聚合物(MIP)的生化传感器,使用电化学阻抗谱法对汗液中的分子生物标志物进行定量分析,无需使用标签或氧化还原探针。这种分子印迹生物传感器可以实现对皮质醇的敏感和特异性检测,其检测浓度低至 1 pM,比以前报道的 MIP 皮质醇传感器低 1000 倍。我们将多模态电化学传感器与离子电渗汗液提取模块和纸微流控技术集成在一起,用于实时汗液分析。可以同时定量多种参数,包括汗液体积、分泌率、钠离子和皮质醇浓度。纸微流控模块不仅可以定量汗液体积和分泌率,而且还可以在无需用户干预的情况下实现连续的汗液分析。虽然我们专注于皮质醇感测作为概念验证,但这种基于分子印迹的可穿戴传感器可以扩展到实时检测其他生化物质,如蛋白质生物标志物和治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/7d12bde32f73/am4c10033_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/95ee9a946fda/am4c10033_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/8619a7bafb66/am4c10033_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/cf162c3c7ab3/am4c10033_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/2f59842ad2ef/am4c10033_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/7d12bde32f73/am4c10033_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/95ee9a946fda/am4c10033_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/8619a7bafb66/am4c10033_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/cf162c3c7ab3/am4c10033_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/2f59842ad2ef/am4c10033_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a1/11378148/7d12bde32f73/am4c10033_0005.jpg

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