Issue 15, 2024

Acoustofluidic-based microscopic examination for automated and point-of-care urinalysis

Abstract

Urinalysis is a heavily used diagnostic test in clinical laboratories; however, it is chronically held back by urine sediment microscopic examination. Current instruments are bulky and expensive to be widely adopted, making microscopic examination a procedure that still relies on manual operations and requires large time and labor costs. To improve the efficacy and automation of urinalysis, this study develops an acoustofluidic-based microscopic examination system. The system utilizes the combination of acoustofluidic manipulation and a passive hydrodynamic mechanism, and thus achieves a high throughput (1000 μL min−1) and a high concentration factor (95.2 ± 2.1 fold) simultaneously, fulfilling the demands for urine examination. The concentrated urine sample is automatically dispensed into a hemocytometer chamber and the images are then analyzed using a machine learning algorithm. The whole process is completed within 3 minutes with detection accuracies of erythrocytes and leukocytes of 94.6 ± 3.5% and 95.1 ± 1.8%, respectively. The examination outcome of urine samples from 50 volunteers by this device shows a correlation coefficient of 0.96 compared to manual microscopic examination. Our system offers a promising tool for automated urine microscopic examination, thus it has potential to save a large amount of time and labor in clinical laboratories, as well as to promote point-of-care urine testing applications in and beyond hospitals.

Graphical abstract: Acoustofluidic-based microscopic examination for automated and point-of-care urinalysis

Supplementary files

Article information

Article type
Paper
Submitted
10 May 2024
Accepted
10 Jun 2024
First published
13 Jun 2024

Lab Chip, 2024,24, 3679-3689

Acoustofluidic-based microscopic examination for automated and point-of-care urinalysis

X. He, F. Ren, Y. Wang, Z. Zhang, J. Zhou, J. Huang, S. Cao, J. Dong, R. Wang, M. Wu and J. Liu, Lab Chip, 2024, 24, 3679 DOI: 10.1039/D4LC00408F

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