Evidence map›Paper›PMID 37232858›Full record

ArticleBiosensors2023

Conductive Nanofibers-Enhanced Microfluidic Device for the Efficient Capture and Electrical Stimulation-Triggered Rapid Release of Circulating Tumor Cells.

Yisha Huang, Xilin Li, Jianwen Hou, Zhouying Luo, Guang Yang, Shaobing Zhou

Abstract read
In one paragraph

Article in Biosensors, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Liquid Biopsy in the Clinical Management of Cancers.International journal of molecular sciences · 2024
    Review
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

6 authors.

Yisha HuangInstitute of Biomedical Engineering, College of Medicine, Southwest Jiaotong University, Chengdu 610031, China.ORCID 0000-0003-3198-3006
Xilin LiSchool of Life Science and Engineering, Southwest Jiaotong University, Chengdu 610031, China.
Jianwen HouInstitute of Biomedical Engineering, College of Medicine, Southwest Jiaotong University, Chengdu 610031, China.
Zhouying LuoInstitute of Biomedical Engineering, College of Medicine, Southwest Jiaotong University, Chengdu 610031, China.
Guang YangInstitute of Biomedical Engineering, College of Medicine, Southwest Jiaotong University, Chengdu 610031, China.
Shaobing ZhouInstitute of Biomedical Engineering, College of Medicine, Southwest Jiaotong University, Chengdu 610031, China.

Funding

Fundamental Research Funds for the Central Universities 2682020ZT94Fundamental Research Funds for the Central Universities 2682022ZTPY040Fundamental Research Funds for the Central Universities 2682022ZTPY042National Natural Science Foundation of China 51703189National Natural Science Foundation of China 52273303Sichuan Science and Technology Program 2023NSFSC0323
6 · The paper itself

Abstract

The effective detection and release of circulating tumor cells (CTCs) are of great significance for cancer diagnosis and monitoring. The microfluidic technique has proved to be a promising method for CTCs isolation and subsequent analysis. However, complex micro-geometries or nanostructures were often constructed and functionalized to improve the capture efficiency, which limited the scale-up for high-throughput production and larger-scale clinical applications. Thus, we designed a simple conductive nanofiber chip (CNF-Chip)-embedded microfluidic device with a herringbone microchannel to achieve the efficient and specific capture and electrical stimulation-triggered rapid release of CTCs. Here, the most used epithelial cell adhesion molecule (EpCAM) was selected as the representative biomarker, and the EpCAM-positive cancer cells were mainly studied. Under the effects of the nanointerface formed by the nanofibers with a rough surface and the herringbone-based high-throughput microfluidic mixing, the local topographic interaction between target cells and nanofibrous substrate in the microfluidic was synergistically enhanced, and the capture efficiency for CTCs was further improved (more than 85%). After capture, the sensitive and rapid release of CTCs (release efficiency above 97%) could be conveniently achieved through the cleavage of the gold-sulfur bond by applying a low voltage (-1.2 V). The device was successfully used for the effective isolation of CTCs in clinical blood samples from cancer patients, indicating the great potential of this CNF-Chip-embedded microfluidic device in clinical applications.

Indexed as

Microfluidic Analytical TechniquesNanofibersNeoplastic Cells, CirculatingCell Line, TumorEpithelial Cell Adhesion MoleculeHumansLab-On-A-Chip DevicesMicrofluidicsEpithelial Cell Adhesion Moleculecirculating tumor cellsconductive nanofiberselectrochemical releaseelectrospinningmicrofluidics

Identifiers

PMID37232858
PMCPMC10216647

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.