细胞外小泡
计算机科学
微流控
吞吐量
胞外囊泡
可扩展性
工作流程
纳米技术
人工智能
微泡
材料科学
化学
生物
无线
数据库
小RNA
生物化学
基因
电信
细胞生物学
作者
Caroline Y. N. Nicoliche,Ricardo A. G. de Oliveira,Giulia S. da Silva,Larissa Fernanda Ferreira,Ian L. Rodrigues,Ronaldo C. Faria,A. Fazzio,Emanuel Carrilho,Letícia Gomes de Pontes,Gabriel R. Schleder,Renato S. Lima
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2020-06-29
卷期号:5 (7): 1864-1871
被引量:30
标识
DOI:10.1021/acssensors.0c00599
摘要
Extracellular vesicles (EVs) are a frontier class of circulating biomarkers for the diagnosis and prognosis of different diseases. These lipid structures afford various biomarkers such as the concentrations of the EVs (CV) themselves and carried proteins (CP). However, simple, high-throughput, and accurate determination of these targets remains a key challenge. Herein, we address the simultaneous monitoring of CV and CP from a single impedance spectrum without using recognizing elements by combining a multidimensional sensor and machine learning models. This multidetermination is essential for diagnostic accuracy because of the heterogeneous composition of EVs and their molecular cargoes both within the tumor itself and among patients. Pencil HB cores acting as electric double-layer capacitors were integrated into a scalable microfluidic device, whereas supervised models provided accurate predictions, even from a small number of training samples. User-friendly measurements were performed with sample-to-answer data processing on a smartphone. This new platform further showed the highest throughput when compared with the techniques described in the literature to quantify EVs biomarkers. Our results shed light on a method with the ability to determine multiple EVs biomarkers in a simple and fast way, providing a promising platform to translate biofluid-based diagnostics into clinical workflows.
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