A portable microfluidic in vitro diagnostic device for rapid detection of procalcitonin

被引:0
作者
Yang, Yujing [1 ]
Dou, Xinyao [3 ]
Zhang, Taiyi [2 ]
Xu, Zhipeng [4 ]
Wang, Yanting [2 ]
Cai, Gaozhe [5 ]
Huang, Xiaowen [2 ]
Liu, Bo [1 ]
机构
[1] Xiangfu Lab, Jiashan 314100, Peoples R China
[2] Shandong First Med Univ & Shandong Acad Med Sci, Inst Brain Sci & Brain Inspired Res, Jinan 250000, Peoples R China
[3] UCL, Dept Neurosci Physiol & Pharmacol, London WC1E 6BT, England
[4] Univ Sheffield, Div Clin Med, Med Sch, Sch Med & Populat Hlth, Beech Hill Rd, Sheffield S102RX, England
[5] Shanghai Univ, Sch Microelect, Shanghai 201800, Peoples R China
来源
NANOTECHNOLOGY AND PRECISION ENGINEERING | 2025年 / 8卷 / 04期
基金
上海市科技启明星计划;
关键词
In vitro diagnostics; Microfluidics; Image analysis; Signal amplification; Procalcitonin; Biomarker; LINKED-IMMUNOSORBENT-ASSAY; PROTEIN BIOMARKERS; IMMUNOASSAY;
D O I
10.1063/5.0252263
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Rapid and sensitive detection of targeted biomarkers in trace samples is of great significance for early in vitro diagnosis of diseases. Microfluidic technology has competitive advantages in this field due to its low cost, high efficiency, and high portability; however, the analysis of results tends to rely on bulky and sophisticated instruments, and this limits its applications. In this work, we developed a Raspberry Pi camera-based biomarker detection device based on microfluidic technology and digital image colorimetry. For highly sensitive biomarker detection on microfluidic chips, we propose a three-step signal-amplification colorimetric detection strategy consisting of: (1) the release of Ag+ ions from silver nanoparticles, (2) Ag+-inhibited urea hydrolysis colorimetry, and (3) microscopic lens magnification. For efficient evaluation of results, we employed an RGB image-processing system to quantitatively analyze color images captured by the Raspberry Pi camera. Further, we tested the functionality of the device with procalcitonin (PCT) in phosphate-buffered saline, plasma, and serum to simulate clinical situations. We determined the limit of detection as 1 ng/ml, and a good linear relationship was established between PCT concentration and color intensity within the detection range 1-10 ng/ml. Importantly, only a relatively short detection time (40 min) was required in all three environments. The results demonstrate the great potential of this device for biomarker detection and facilitating biomedical research.
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页数:9
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