Jiehua Zhou, Liye Mei, Mingjie Yu, Xiao Ma, Dan Hou, Zhuo Yin, Xun Liu, Yan Ding, Kaining Yang, Ruidong Xiao, Xiandan Yuan, Yueyun Weng, Mengping Long, Taobo Hu, Jinxuan Hou, Yu Xu, Liang Tao, Sisi Mei, Hui Shen, Yaxiaer Yalikun, Fuling Zhou, Liang Wang, Du Wang, Sheng Liu, Cheng Lei
{"title":"Imaging flow cytometry with a real-time throughput beyond 1,000,000 events per second","authors":"Jiehua Zhou, Liye Mei, Mingjie Yu, Xiao Ma, Dan Hou, Zhuo Yin, Xun Liu, Yan Ding, Kaining Yang, Ruidong Xiao, Xiandan Yuan, Yueyun Weng, Mengping Long, Taobo Hu, Jinxuan Hou, Yu Xu, Liang Tao, Sisi Mei, Hui Shen, Yaxiaer Yalikun, Fuling Zhou, Liang Wang, Du Wang, Sheng Liu, Cheng Lei","doi":"10.1038/s41377-025-01754-9","DOIUrl":null,"url":null,"abstract":"<p>Imaging flow cytometry (IFC) combines the imaging capabilities of microscopy with the high throughput of flow cytometry, offering a promising solution for high-precision and high-throughput cell analysis in fields such as biomedicine, green energy, and environmental monitoring. However, due to limitations in imaging framerate and real-time data processing, the real-time throughput of existing IFC systems has been restricted to approximately 1000-10,000 events per second (eps), which is insufficient for large-scale cell analysis. In this work, we demonstrate IFC with real-time throughput exceeding 1,000,000 eps by integrating optical time-stretch (OTS) imaging, microfluidic-based cell manipulation, and online image processing. Cells flowing at speeds up to 15 m/s are clearly imaged with a spatial resolution of 780 nm, and images of each individual cell are captured, stored, and analyzed. The capabilities and performance of our system are validated through the identification of malignancies in clinical colorectal samples. This work sets a new record for throughput in imaging flow cytometry, and we believe it has the potential to revolutionize cell analysis by enabling highly efficient, accurate, and intelligent measurement.</p><figure></figure>","PeriodicalId":18069,"journal":{"name":"Light-Science & Applications","volume":"41 1","pages":""},"PeriodicalIF":20.6000,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Light-Science & Applications","FirstCategoryId":"1089","ListUrlMain":"https://doi.org/10.1038/s41377-025-01754-9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OPTICS","Score":null,"Total":0}
引用次数: 0
Abstract
Imaging flow cytometry (IFC) combines the imaging capabilities of microscopy with the high throughput of flow cytometry, offering a promising solution for high-precision and high-throughput cell analysis in fields such as biomedicine, green energy, and environmental monitoring. However, due to limitations in imaging framerate and real-time data processing, the real-time throughput of existing IFC systems has been restricted to approximately 1000-10,000 events per second (eps), which is insufficient for large-scale cell analysis. In this work, we demonstrate IFC with real-time throughput exceeding 1,000,000 eps by integrating optical time-stretch (OTS) imaging, microfluidic-based cell manipulation, and online image processing. Cells flowing at speeds up to 15 m/s are clearly imaged with a spatial resolution of 780 nm, and images of each individual cell are captured, stored, and analyzed. The capabilities and performance of our system are validated through the identification of malignancies in clinical colorectal samples. This work sets a new record for throughput in imaging flow cytometry, and we believe it has the potential to revolutionize cell analysis by enabling highly efficient, accurate, and intelligent measurement.