Development of IoT-Based Impedometric Biosensor for Point-of-Care Monitoring of Bone Loss

被引:26
作者
Afsarimanes, Nasrin [1 ]
Alahi, Md Eshrat E. [1 ]
Mukhopadhyay, Subhas Chandra [1 ]
Kruger, Marlena [2 ]
机构
[1] Macquarie Univ, Sch Engn, Sydney, NSW 2109, Australia
[2] Massey Univ, Sch Food & Nutr, Palmerston North 4474, New Zealand
关键词
Point-of-care (PoC) testing; bone turnover markers; interdigital sensor; molecular imprinting polymer (MIP); Internet of Things (IoT); ON-A-CHIP; ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY; ULTRASENSITIVE MULTIPLEXED DETECTION; SENSOR; TECHNOLOGY; SYSTEM;
D O I
10.1109/JETCAS.2018.2819204
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Early detection of disease is essential for an efficient treatment. Bone loss can be detected and monitored by regular measurement of serum or urine C-terminal telopeptide of type 1 collagen (CTx-1). Therefore, rapid, portable, and low-cost point-of-care devices are highly desirable. In this paper, we have reported an Internet of Things (IoT)-based selective, sensitive, quick, and inexpensive device for the quantification of CTx-1 levels in serum. A capacitive interdigital sensor was coated with artificial antibodies, prepared by molecular imprinting technology. Electrochemical impedance spectroscopy was used to evaluate the resistive and capacitive properties of the sample solutions. A microcontroller-based system was developed for the measurement of the level of CTx-1 in serum and for data transmission to an IoT-based cloud server. The data can be provided to the medical practitioner and a detailed investigation can start for early detection and treatment. The developed sensing system responded linearly in a range of 0.1 to 2.5 ppb, which covers the normal reference range of CTx-1 in serum, with a limit of detection of 0.09 ppb. The results demonstrated that the proposed portable biosensing system could provide a rapid, simple, and selective approach for CTx-1 measurement in serum. Sheep serum samples were tested using the proposed system and the validation of the results was done using an enzyme-linked immunosorbent assay kit.
引用
收藏
页码:211 / 220
页数:10
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