4.7 Article

A dry chemistry-based electrochemiluminescence device for point-of-care testing of alanine transaminase

Journal

TALANTA
Volume 256, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.talanta.2023.124287

Keywords

Automatic analyzer; Dry chemistry; Electrochemiluminescence; Point-of-care testing; Alanine transaminase detection

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Liver disease is a significant public health issue, especially in low- and middle-income countries. Detecting and diagnosing liver disease accurately is crucial, and alanine transaminase (ALT) is an important indicator. In this study, a dry chemistry-based electrochemiluminescence (DC-ECL) device was developed for point-of-care testing (POCT) of ALT, providing a reliable and automatic detection method. The results show that the device has a wide detection range, good linearity, and low detection limit, indicating its potential for development of similar POCT analyzers.
Liver disease causes serious public health problems because of its high prevalence, particularly affecting low- and middle-income countries. Alanine transaminase (ALT) is considered to be one of the most sensitive indicators for diagnosing liver disease. Although many strategies have been reported for ALT detection, few of them have solved the problem of automatic detection. In this work, for the first time, a dry chemistry-based electrochemiluminescence (DC-ECL) device is developed for point-of-care testing (POCT) of ALT, achieving real sampleto-answer detection. The proposed DC-ECL device consists of the following two components: (a) a DC-ECL chip consisting of the outer shell (including the top cap and pedestal) and detection layer (including the baseplate, electrode pad and carrier pad) and (b) an automatic ECL analyzer mainly including the data processing and instrument control unit, imaging detection unit, electrochemical reaction excitation unit, open detection window unit and rechargeable power supply. Under optimized conditions, the device had a wide detection range (0-1000 U/L), the ECL intensity linearly increased with ALT concentration (5-50 U/L) and logarithmic ALT concentration (50-1000 U/L), and the limit of detection was calculated to be 1.702 U/L. In addition, the DC-ECL device had the ability to measure ALT levels in human serum samples and showed acceptable selectivity, stability and repeatability. These results reveal that the DC-ECL device can overcome the disadvantages of traditional methods for ALT detection (such as high cost and requirement of professional technicians) and potentially opens the door to the development of similar POCT analyzers.

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