Evidence map›Paper›PMID 26657733›Full record

ArticleJournal of chromatographic science2016

A Rapidly Fabricated Microfluidic Chip for Cell Culture.

Rui Li, Xuefei Lv, Murtaza Hasan, Jiandong Xu, Yuanqing Xu, Xingjian Zhang, Kuiwei Qin, Jianshe Wang, Di Zhou, Yulin Deng

Abstract read
In one paragraph

Article in Journal of chromatographic science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. 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

10 authors.

Rui LiBeijing Key Laboratory of Bioseparation and Bioanalysis, Beijing Institute of Technology, Beijing 100081, China.
Xuefei LvBeijing Key Laboratory of Bioseparation and Bioanalysis, Beijing Institute of Technology, Beijing 100081, China.
Murtaza HasanDepartment of Materials Science and Engineering College of Engineering, Peking University, Beijing 100871, China.
Jiandong XuBeijing Key Laboratory of Bioseparation and Bioanalysis, Beijing Institute of Technology, Beijing 100081, China.
Yuanqing XuBeijing Key Laboratory of Bioseparation and Bioanalysis, Beijing Institute of Technology, Beijing 100081, China.
Xingjian ZhangBeijing Key Laboratory of Bioseparation and Bioanalysis, Beijing Institute of Technology, Beijing 100081, China.
Kuiwei QinBeijing Key Laboratory of Bioseparation and Bioanalysis, Beijing Institute of Technology, Beijing 100081, China.
Jianshe WangBeijing Key Laboratory of Bioseparation and Bioanalysis, Beijing Institute of Technology, Beijing 100081, China.
Di ZhouBeijing Key Laboratory of Bioseparation and Bioanalysis, Beijing Institute of Technology, Beijing 100081, China.
Yulin DengBeijing Key Laboratory of Bioseparation and Bioanalysis, Beijing Institute of Technology, Beijing 100081, China deng@bit.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microfluidic chips (μFC) are emerging as powerful tools in chemistry, biochemistry, nanotechnology and biotechnology. The microscale size, possibility of integration and high-throughput present huge technical potential to facilitate the research of cell behavior by creating in vivo-like microenvironments. Here, we have developed a new method for rapid fabrication of μFC with Norland Optical Adhesive 81 (NOA81) for multiple cell culture with high efficiency. The proposed method is more suitable for the early structure exploration stage of μFC than existing procedures since no templates are needed and fast fabrication methods are presented. Simple PDMS-NOA81-linked microvalves were embedded in the μFC to control or block the fluid flow effectively, which significantly broadened the applications of μFC. Various types of cells were integrated into the chip and normal viabilities were maintained up to 1 week. Besides, concentration gradient was generated to investigate the cells in the μFC responded to drug stimulation. The cells appeared different in terms of shape and proliferation that strongly demonstrated the potential application of our μFC in online drug delivery. The high biocompatibility of NOA81 and its facile fabrication (μFC) promise its use in various cell analyses, such as cell-cell interactions or tissue engineering.

Indexed as

Lab-On-A-Chip DevicesCell Line, TumorDimethylpolysiloxanesHumansbaysilonDimethylpolysiloxanes

Identifiers

PMID26657733
PMCPMC4885384

What OpenQuestion holds

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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.