Biosensors; noninvasive method in detection of C-reactive protein (CRP)

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Hamidreza Hassanzadeh Khanmiri, Fatemeh Yazdanfar, Ahmad Mobed, Fatemeh Rezamohammadi, Mehrnoush Rahmani, Tannaz Haghgouei
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引用次数: 1

Abstract

Early diagnosis of C reactive protein (CRP) is critical to applying effective therapies for related diseases. Diagnostic technology in today's healthcare systems is mostly deployed in central laboratories, involves expensive and time-consuming processes, and is operated by specialized personnel. For example, the enzyme-linked immunosorbent assay (ELISA), considered the gold standard diagnostic method, is labor-intensive and requires complex procedures such as multiple washing and labeling steps. Due to these limitations of current diagnostic techniques, it is difficult for people to regularly monitor their health and ultimately the disease is more likely to be diagnosed at a later stage. The problem is exacerbated for economically disadvantaged people living in underdeveloped countries. To address these challenges in the traditional diagnostic field, point-of-care (POC) biosensors have emerged as a promising alternative. This allows patients to have their health checked regularly at or near their bedside without resorting to laboratory tests. Nanotechnology-based methods such as biosensors have been extensively researched and developed. Among biosensors, there are also label-free biosensors with high sensitivity that do not require complicated procedures and reduce test time. However, some drawbacks such as high cost, bulky size and need for trained personnel to operate have not been improved. In this review article, we provide an overview of routine methods in CRP diagnosis and then introduce biosensors as a modern, advanced alternative to older methods. Readers of this article can learn about biosensing and its benefits while being aware of the limitations of routine methods.

Graphical abstract

Abstract Image

生物传感器;检测C反应蛋白(CRP)的无创方法。
C反应蛋白(CRP)的早期诊断对于相关疾病的有效治疗至关重要。当今医疗系统中的诊断技术大多部署在中央实验室,涉及昂贵且耗时的过程,并由专业人员操作。例如,被认为是金标准诊断方法的酶联免疫吸附试验(ELISA)是劳动密集型的,需要复杂的程序,如多次洗涤和标记步骤。由于当前诊断技术的这些局限性,人们很难定期监测自己的健康状况,最终这种疾病更有可能在后期被诊断出来。对于生活在欠发达国家的经济弱势群体来说,这一问题更加严重。为了应对传统诊断领域的这些挑战,护理点(POC)生物传感器已成为一种很有前途的替代品。这使得患者可以在床边或床边附近定期进行健康检查,而无需进行实验室检测。基于纳米技术的方法,如生物传感器,已经得到了广泛的研究和开发。在生物传感器中,也有具有高灵敏度的无标签生物传感器,不需要复杂的程序并减少测试时间。然而,一些缺点,如高成本、体积庞大和需要训练有素的人员操作,并没有得到改善。在这篇综述文章中,我们概述了CRP诊断的常规方法,然后介绍了生物传感器作为一种现代、先进的替代方法。这篇文章的读者可以了解生物传感及其好处,同时了解常规方法的局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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