兰州大学机构库 >化学化工学院
Open flow cytometer with the combination of 3D hydrodynamic single cell focusing and confocal laser-induced fluorescence detection
Wu, Chengxin1; Wei, Xing1; Men, Xue1; Xu, Yulong1; Bai, Junjie1; Wang, Yu1; Zhou, L(周雷)2; Yu, Yong-Liang1; Xu, Zhang-Run1; Chen, Ming-Li1; Wang, Jian-Hua1
2023-06-01
Source PublicationTALANTA   Impact Factor & Quartile
ISSN0039-9140
Volume258
AbstractFlow cytometry is among the most powerful tools for single-cell analysis, while the high cost and mechanical complexity of the commercial instrumentation limit the applications in personalized single-cell analysis. For this issue, we hereby construct an open and low-cost flow cytometer. It is highly compact to integrate the functions of (1) single cell aligning by a lab-made modularized 3D hydrodynamic focusing device, and (2) fluorescence detection of the single cells by a confocal laser-induced fluorescence (LIF) detector. The ceiling cost of the entire hardware for the LIF detection unit and 3D focusing device is $ 3200 and $ 400 respectively. A sheath flow velocity of 150 μL/min produces a focused sample stream of 17.6 μm × 14.6 μm at sample flow of 2 μL/min, based on the LIF response frequency and the laser beam spot diameter. The assay performance of the flow cytometer was evaluated by characterizing fluorescent microparticles and acridine orange (AO) stained HepG2 cells, producing throughputs of 40.5/s and 6.2/s respectively. Favorable assay precision and accuracy were demonstrated by the agreement of frequency histogram with imaging analysis, and good Gaussian-like distributions of fluorescent microparticles and AO-stained HepG2 cells. Practically, the flow cytometer was successfully applied for the evaluation of ROS generation in single HepG2 cells. © 2023 Elsevier B.V.
KeywordCells Cost benefit analysis Cytology Flow velocity Flowmeters Fluorescence Focusing Hydrodynamics Laser beams Laser optics Laser produced plasmas Acridine orange Cytometers Fluorescent microparticles Focusing device Hep-g2 cells High-throughput Laser induced fluorescence Sheath flows Single cells Single cells analysis
PublisherElsevier B.V.
DOI10.1016/j.talanta.2023.124424
Indexed ByEI
Language英语
EI Accession Number20231113736944
EI KeywordsFlow cytometry
EI Classification Number461.2 Biological Materials and Tissue Engineering ; 461.9 Biology ; 631 Fluid Flow ; 741.1 Light/Optics ; 741.3 Optical Devices and Systems ; 744.1 Lasers, General ; 744.8 Laser Beam Interactions ; 744.9 Laser Applications ; 911 Cost and Value Engineering ; Industrial Economics ; 912.2 Management ; 932.3 Plasma Physics ; 941.4 Optical Variables Measurements ; 943.1 Mechanical Instruments ; 943.2 Mechanical Variables Measurements
Original Document TypeJournal article (JA)
Citation statistics
Cited Times:1[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttps://ir.lzu.edu.cn/handle/262010/498568
Collection化学化工学院
Corresponding AuthorChen, Ming-Li; Wang, Jian-Hua
Affiliation
1.Research Center for Analytical Sciences, Department of Chemistry, College of Sciences, Northeastern University, Shenyang; 110819, China;
2.State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou; 730000, China
First Author AffilicationCollege of Chemistry and Chemical Engineering
Corresponding Author AffilicationCollege of Chemistry and Chemical Engineering
Recommended Citation
GB/T 7714
Wu, Chengxin,Wei, Xing,Men, Xue,et al. Open flow cytometer with the combination of 3D hydrodynamic single cell focusing and confocal laser-induced fluorescence detection[J]. TALANTA,2023,258.
APA Wu, Chengxin.,Wei, Xing.,Men, Xue.,Xu, Yulong.,Bai, Junjie.,...&Wang, Jian-Hua.(2023).Open flow cytometer with the combination of 3D hydrodynamic single cell focusing and confocal laser-induced fluorescence detection.TALANTA,258.
MLA Wu, Chengxin,et al."Open flow cytometer with the combination of 3D hydrodynamic single cell focusing and confocal laser-induced fluorescence detection".TALANTA 258(2023).
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