A smartphone-based multichannel magnetoelastic immunosensor for acute aortic dissection supplementary diagnosis.

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL Talanta Pub Date : 2025-01-01 Epub Date: 2024-09-18 DOI:10.1016/j.talanta.2024.126915
Yunmei Cao, Qiannan Wang, Mengshu Han, Yunxuan Zhang, Zhongyun Yuan, Kai Zhuo, Hongpeng Zhang, Zhijin Xing, Hu Jin, Chun Zhao
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Abstract

Some biomarkers of acute aortic dissection (AAD) can be used for the potential supplementary diagnosis of AAD, such as C-reactive protein (CRP), smooth muscle myosin heavy chain (SmMHC), and D-dimer (D-D). However, the current measurement methods for common markers primarily rely on sophisticated instruments. The operation process is complicated, and the reagents used are expensive. To provide chronic disease monitoring and home self-examination services for potential AAD patients in real time, we developed a smartphone-based multichannel magnetoelastic (ME) immunosensing device to detect protein levels. Our immunosensor reduced the aforementioned restrictions and demonstrated excellent performance for the supplementary diagnosis of AAD. In this paper, we successfully combined the intelligent terminal with the hardware system to sample the resonance frequency shift (RFS) on the multichannel ME immunosensor. According to the target detection objects with their respective antibodies in the immune binding response, multiple experiments were conducted to detect multiple groups of samples, and we found that a CRP concentration, a SmMHC concentration, and a D-D concentration in the range of 0.1-100μg/mL, 1-4ng/mL, and 0.25-5μg/mL were linearly proportional to the RFS of the ME immunosensor, respectively. For CRP, SmMHC, and D-D, the sensitivities were 13.37Hz/μg∙mL-1, 155.19Hz/ng∙mL-1, and 332.72Hz/μg∙mL-1, respectively, and the detection limits were 2.634×10-3μg/mL, 1.155×10-2ng/mL, and 3.687×10-3μg/mL, respectively. The experiments demonstrated that the accuracy and stability of our device were comparable to those of the vector network analyzer (VNA, Calibration instrument).

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用于急性主动脉夹层辅助诊断的基于智能手机的多通道磁弹性免疫传感器。
急性主动脉夹层(AAD)的一些生物标志物可用于 AAD 的潜在辅助诊断,如 C 反应蛋白(CRP)、平滑肌肌球蛋白重链(SmMHC)和 D-二聚体(D-D)。然而,目前常见标记物的测量方法主要依赖于精密仪器。操作过程复杂,所用试剂昂贵。为了向潜在的 AAD 患者提供实时的慢性病监测和家庭自检服务,我们开发了一种基于智能手机的多通道磁弹性(ME)免疫传感设备来检测蛋白质水平。我们的免疫传感器减少了上述限制,在辅助诊断 AAD 方面表现出卓越的性能。在本文中,我们成功地将智能终端与硬件系统相结合,对多通道磁弹性(ME)免疫传感器的共振频率偏移(RFS)进行了采样。根据目标检测对象与各自抗体的免疫结合反应,我们对多组样品进行了多次检测实验,发现CRP浓度、SmMHC浓度和D-D浓度在0.1-100μg/mL、1-4ng/mL和0.25-5μg/mL范围内分别与ME免疫传感器的RFS成线性关系。CRP、SmMHC和D-D的灵敏度分别为13.37Hz/μg∙mL-1、155.19Hz/ng∙mL-1和332.72Hz/μg∙mL-1,检测限分别为2.634×10-3μg/mL、1.155×10-2ng/mL和3.687×10-3μg/mL。实验结果表明,我们装置的准确性和稳定性与矢量网络分析仪(VNA,校准仪器)相当。
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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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