Evidence map›Paper›PMID 36014194›Full record

ArticleMicromachines2022

A Resistance-Based Microfluidic Chip for Deterministic Single Cell Trapping Followed by Immunofluorescence Staining.

Xiange Sun, Bowen Li, Wenman Li, Xiaodong Ren, Ning Su, Ruoxu Li, Jinmi Li, Qing Huang

Open access · goldAbstract read
In one paragraph

Article in Micromachines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 46% of its field
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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
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 at 1 institution in 1 country.

Xiange SunDepartment of Laboratory Medicine, Daping Hospital, Army Medical University, Chongqing 400042, China.
Bowen LiDepartment of Laboratory Medicine, Daping Hospital, Army Medical University, Chongqing 400042, China.
Wenman LiDepartment of Laboratory Medicine, Daping Hospital, Army Medical University, Chongqing 400042, China.
Xiaodong RenDepartment of Laboratory Medicine, Daping Hospital, Army Medical University, Chongqing 400042, China.
Ning SuDepartment of Laboratory Medicine, Daping Hospital, Army Medical University, Chongqing 400042, China.
Ruoxu LiDepartment of Laboratory Medicine, Daping Hospital, Army Medical University, Chongqing 400042, China.
Jinmi LiDepartment of Laboratory Medicine, Daping Hospital, Army Medical University, Chongqing 400042, China.
Qing HuangDepartment of Laboratory Medicine, Daping Hospital, Army Medical University, Chongqing 400042, China.ORCID 0000-0002-0140-8978
Army Medical University · CN

Funding

National Natural Science Foundation of China 82172370the Clinical Medical Research Talent Funding Project 2019XLC1010the Major Military Logistics Research Sub-Project AWS17J010 and 2018-KY-0083
6 · The paper itself

Abstract

Microchips are fundamental tools for single-cell analysis. Although various microfluidic methods have been developed for single-cell trapping and analysis, most microchips cannot trap single cells deterministically for further analysis. In this paper, we describe a novel resistance-based microfluidic chip to implement deterministic single-cell trapping followed by immunofluorescence staining based on the least flow resistance principle. The design of a large circular structure before the constriction and the serpentine structure of the main channel made the flow resistance of the main channel higher than that of the trapping channel. Since cells preferred to follow paths with lower flow resistance, this design directed cells into the capture sites and improved single-cell trapping efficiency. We optimized the geometric parameters using numerical simulations. Experiments using A549 and K562 cell lines demonstrated the capability of our chip with (82.7 ± 2.4)% and (84 ± 3.3)% single-cell trapping efficiency, respectively. In addition, cells were immobilized at capture sites by applying the pulling forces at the outlet, which reduced the cell movement and loss and facilitated tracking of the cell in real time during the multistep immunofluorescence staining procedure. Due to the simple operation, high-efficiency single-cell trapping and lower cell loss, the proposed chip is expected to be a potential analytical platform for single tumor cell heterogeneity studies and clinical diagnosis.

Indexed as

immunofluorescence stainingleast flow resistancemicrofluidic chipsingle-cell trapping

Identifiers

PMID36014194
PMCPMC9416254
OpenAlexW4290720654

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.