Label-free in-vivo classification and tracking of red blood cells and platelets using Dynamic-YOLOv4 network

Author:

Guan Caizhong12ORCID,He Bin1ORCID,Zhang Hongting3ORCID,Yang Shangpan1ORCID,Xu Yang1ORCID,Xiong Honglian1ORCID,Zeng Yaguang1ORCID,Wang Mingyi1ORCID,Wei Xunbin4567ORCID

Affiliation:

1. Guangdong-Hong Kong-Macao Joint Laboratory for Intelligent, Micro-Nano Optoelectronic Technology, School of Physics and Optoelectronic Engineering, Foshan University, Foshan 528225, P. R. China

2. Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, P. R. China

3. The Second Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin 150001, P. R. China

4. Peking University Cancer Hospital & Institute, Beijing 100142, P. R. China

5. Biomedical Engineering Department, Peking University, Beijing 100081, P. R. China

6. Institute of Medical Technology, Peking University Health Science Center, Beijing 100191, P. R. China

7. International Cancer Institute, Peking University, Beijing 100191, P. R. China

Abstract

In-vivo flow cytometry is a noninvasive real-time diagnostic technique that facilitates continuous monitoring of cells without perturbing their natural biological environment, which renders it a valuable tool for both scientific research and clinical applications. However, the conventional approach for improving classification accuracy often involves labeling cells with fluorescence, which can lead to potential phototoxicity. This study proposes a label-free in-vivo flow cytometry technique, called dynamic YOLOv4 (D-YOLOv4), which improves classification accuracy by integrating absorption intensity fluctuation modulation (AIFM) into YOLOv4 to demodulate the temporal features of moving red blood cells (RBCs) and platelets. Using zebrafish as an experimental model, the D-YOLOv4 method achieved average precisions (APs) of 0.90 for RBCs and 0.64 for thrombocytes (similar to platelets in mammals), resulting in an overall AP of 0.77. These scores notably surpass those attained by alternative network models, thereby demonstrating that the combination of physical models with neural networks provides an innovative approach toward developing label-free in-vivo flow cytometry, which holds promise for diverse in-vivo cell classification applications.

Funder

the Special Fund for Research on National Major Research Instruments of China

the National Natural Science Foundation of China

the Research Fund of Guangdong-Hong Kong-Macao Joint Laboratory for Intelligent Micro-Nano Optoelectronic Technology

Special Fund for Science and Technology Innovation Cultivation of Guangdong University Students

Publisher

World Scientific Pub Co Pte Ltd

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