Evidence map›Paper›PMID 30380644›Full record

ArticleSensors (Basel, Switzerland)2018

Time Sequential Single-Cell Patterning with High Efficiency and High Density.

Yang Liu, Dahai Ren, Xixin Ling, Weibin Liang, Jing Li, Zheng You, Yaxiaer Yalikun, Yo Tanaka

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
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  4. Image-Based Live Cell Sorting.Trends in biotechnology · 2021
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yang LiuState Key Laboratory of Precision Measurement Technology and Instruments, Tsinghua University, Beijing 100084, China. ly-15@tsinghua.org.cn.
Dahai RenState Key Laboratory of Precision Measurement Technology and Instruments, Tsinghua University, Beijing 100084, China. rendh@tsinghua.edu.cn.
Xixin LingState Key Laboratory of Precision Measurement Technology and Instruments, Tsinghua University, Beijing 100084, China. xixin.ling@ptpcapital.com.
Weibin LiangState Key Laboratory of Precision Measurement Technology and Instruments, Tsinghua University, Beijing 100084, China. liang-wb12@tsinghua.org.cn.
Jing LiState Key Laboratory of Precision Measurement Technology and Instruments, Tsinghua University, Beijing 100084, China. lijing18@mails.tsinghua.edu.cn.
Zheng YouState Key Laboratory of Precision Measurement Technology and Instruments, Tsinghua University, Beijing 100084, China. yz-dpi@tsinghua.edu.cn.
Yaxiaer YalikunCenter for Biosystems Dynamics Research (BDR), RIKEN, 1-3 Yamadaoka, Suita, Osaka 565-0871, Japan. yaxiaer.yalikun@riken.jp.ORCID 0000-0003-0569-6740
Yo TanakaCenter for Biosystems Dynamics Research (BDR), RIKEN, 1-3 Yamadaoka, Suita, Osaka 565-0871, Japan. yo.tanaka@riken.jp.ORCID 0000-0003-1034-5718

Funding

National Natural Science Foundation of China 61071002National Program for Significant Scientific Instruments Development of China 2011YQ030134
6 · The paper itself

Abstract

Single-cell capture plays an important role in single-cell manipulation and analysis. This paper presents a microfluidic device for deterministic single-cell trapping based on the hydrodynamic trapping mechanism. The device is composed of an S-shaped loop channel and thousands of aligned trap units. This arrayed structure enables each row of the device to be treated equally and independently, as it has row periodicity. A theoretical model was established and a simulation was conducted to optimize the key geometric parameters, and the performance was evaluated by conducting experiments on MCF-7 and Jurkat cells. The results showed improvements in single-cell trapping ability, including loading efficiency, capture speed, and the density of the patterned cells. The optimized device can achieve a capture efficiency of up to 100% and single-cell capture efficiency of up to 95%. This device offers 200 trap units in an area of 1 mm², which enables 100 single cells to be observed simultaneously using a microscope with a 20× objective lens. One thousand cells can be trapped sequentially within 2 min; this is faster than the values obtained with previously reported devices. Furthermore, the cells can also be recovered by reversely infusing solutions. The structure can be easily extended to a large scale, and a patterned array with 32,000 trap sites was accomplished on a single chip. This device can be a powerful tool for high-throughput single-cell analysis, cell heterogeneity investigation, and drug screening.

Indexed as

Computer SimulationHumansHydrodynamicsJurkat CellsLab-On-A-Chip DevicesMCF-7 CellsPressureSingle-Cell AnalysisTime Factorscell patterningcell trappinglab-on-a-chipmicrofluidicssingle-cell analysis

Identifiers

PMID30380644
PMCPMC6264106

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.