A two-minute assay for electronic quantification of antibodies in saliva enabled through a reusable microfluidic multi-frequency impedance cytometer and machine learning analysis

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Zhongtian Lin, Jianye Sui, Mehdi Javanmard
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引用次数: 2

Abstract

The use of saliva as a diagnostic fluid has always been appealing due to the ability for rapid and non-invasive sampling for monitoring health status and the onset and progression of disease and treatment progress. Saliva is rich in protein biomarkers and provides a wealth of information for diagnosis and prognosis of various disease conditions. Portable electronic tools which rapidly monitor protein biomarkers would facilitate point-of-care diagnosis and monitoring of various health conditions. For example, the detection of antibodies in saliva can enable rapid diagnosis and tracking disease pathogenesis of various auto-immune diseases like sepsis. Here, we present a novel method involving immuno-capture of proteins on antibody coated beads and electrical detection of dielectric properties of the beads. The changes in electrical properties of a bead when capturing proteins are extremely complex and difficult to model physically in an accurate manner. The ability to measure impedance of thousands of beads at multiple frequencies, however, allows for a data-driven approach for protein quantification. By moving from a physics driven approach to a data driven approach, we have developed, for the first time ever to the best of our knowledge, an electronic assay using a reusable microfluidic impedance cytometer chip in conjunction with supervised machine learning to quantifying immunoglobulins G (IgG) and immunoglobulins A (IgA) in saliva within two minutes.

Abstract Image

通过可重复使用的微流控多频阻抗细胞仪和机器学习分析,实现了唾液中抗体的两分钟电子定量分析
使用唾液作为诊断液一直很有吸引力,因为它能够进行快速和无创取样,以监测健康状况、疾病的发生和进展以及治疗进展。唾液富含蛋白质生物标志物,为各种疾病的诊断和预后提供了丰富的信息。快速监测蛋白质生物标志物的便携式电子工具将有助于即时诊断和监测各种健康状况。例如,唾液中抗体的检测可以快速诊断和追踪脓毒症等各种自身免疫性疾病的发病机制。在这里,我们提出了一种新的方法,包括免疫捕获抗体包被珠上的蛋白质和电检测珠的介电性质。当捕获蛋白质时,头部电学性质的变化非常复杂,很难以准确的方式进行物理建模。然而,在多个频率下测量数千个珠的阻抗的能力,允许数据驱动的蛋白质定量方法。通过从物理驱动方法转向数据驱动方法,据我们所知,我们首次开发了一种电子分析方法,使用可重复使用的微流控阻抗细胞仪芯片,结合监督机器学习,在两分钟内定量唾液中的免疫球蛋白G (IgG)和免疫球蛋白a (IgA)。
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来源期刊
Biomedical Microdevices
Biomedical Microdevices 工程技术-工程:生物医学
CiteScore
6.90
自引率
3.60%
发文量
32
审稿时长
6 months
期刊介绍: Biomedical Microdevices: BioMEMS and Biomedical Nanotechnology is an interdisciplinary periodical devoted to all aspects of research in the medical diagnostic and therapeutic applications of Micro-Electro-Mechanical Systems (BioMEMS) and nanotechnology for medicine and biology. General subjects of interest include the design, characterization, testing, modeling and clinical validation of microfabricated systems, and their integration on-chip and in larger functional units. The specific interests of the Journal include systems for neural stimulation and recording, bioseparation technologies such as nanofilters and electrophoretic equipment, miniaturized analytic and DNA identification systems, biosensors, and micro/nanotechnologies for cell and tissue research, tissue engineering, cell transplantation, and the controlled release of drugs and biological molecules. Contributions reporting on fundamental and applied investigations of the material science, biochemistry, and physics of biomedical microdevices and nanotechnology are encouraged. A non-exhaustive list of fields of interest includes: nanoparticle synthesis, characterization, and validation of therapeutic or imaging efficacy in animal models; biocompatibility; biochemical modification of microfabricated devices, with reference to non-specific protein adsorption, and the active immobilization and patterning of proteins on micro/nanofabricated surfaces; the dynamics of fluids in micro-and-nano-fabricated channels; the electromechanical and structural response of micro/nanofabricated systems; the interactions of microdevices with cells and tissues, including biocompatibility and biodegradation studies; variations in the characteristics of the systems as a function of the micro/nanofabrication parameters.
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