Evidence map›Paper›PMID 35404518›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

A Versatile, Incubator-Compatible, Monolithic GaN Photonic Chipscope for Label-Free Monitoring of Live Cell Activities.

Yong Hou, Jixiang Jing, Yumeng Luo, Feng Xu, Wenyan Xie, Linjie Ma, Xingyu Xia, Qiang Wei, Yuan Lin, Kwai Hei Li and 1 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. 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. Article
  3. 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

11 authors.

Yong HouDepartment of Electrical and Electronic Engineering, The University of Hong Kong, Hong Kong, China.
Jixiang JingDepartment of Electrical and Electronic Engineering, The University of Hong Kong, Hong Kong, China.
Yumeng LuoSchool of Microelectronics, Southern University of Science and Technology, Shenzhen, 518055, China.
Feng XuDepartment of Electrical and Electronic Engineering, The University of Hong Kong, Hong Kong, China.
Wenyan XieDepartment of Biotherapy, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, 610065, China.
Linjie MaDepartment of Electrical and Electronic Engineering, The University of Hong Kong, Hong Kong, China.
Xingyu XiaDepartment of Mechanical Engineering, The University of Hong Kong, Hong Kong, China.
Qiang WeiCollege of Polymer Science and Engineering, State Key Laboratory of Polymer Materials and Engineering, Sichuan University, Chengdu, 610065, China.
Yuan LinDepartment of Mechanical Engineering, The University of Hong Kong, Hong Kong, China.
Kwai Hei LiSchool of Microelectronics, Southern University of Science and Technology, Shenzhen, 518055, China.
Zhiqin ChuDepartment of Electrical and Electronic Engineering, The University of Hong Kong, Hong Kong, China.ORCID 0000-0003-4671-5434

Funding

Early Career Scheme 27202919HKSAR Research Grants CouncilHKU Seed Fund 202010160007HKU Seed Fund 202011159019Innovation and Technology Commission of the Hong Kong SAR GovernmentNational Natural Science Foundation of China 11872325National Natural Science Foundation of China 12074170National Natural Science Foundation of China 62004088Platform Projects of the Innovation and Technology Support Program ITS/293/19FPResearch Grants Council GRF/17210520Research Grants Council GRF/17210618Research Grants Council GRF/17257016Small Equipment Grant 102009812
6 · The paper itself

Abstract

The ability to quantitatively monitor various cellular activities is critical for understanding their biological functions and the therapeutic response of cells to drugs. Unfortunately, existing approaches such as fluorescent staining and impedance-based methods are often hindered by their multiple time-consuming preparation steps, sophisticated labeling procedures, and complicated apparatus. The cost-effective, monolithic gallium nitride (GaN) photonic chip has been demonstrated as an ultrasensitive and ultracompact optical refractometer in a previous work, but it has never been applied to cell studies. Here, for the first time, the so-called GaN chipscope is proposed to quantitatively monitor the progression of different intracellular processes in a label-free manner. Specifically, the GaN-based monolithic chip enables not only a photoelectric readout of cellular/subcellular refractive index changes but also the direct imaging of cellular/subcellular ultrastructural features using a customized differential interference contrast (DIC) microscope. The miniaturized chipscope adopts an ultracompact design, which can be readily mounted with conventional cell culture dishes and placed inside standard cell incubators for real-time observation of cell activities. As a proof-of-concept demonstration, its applications are explored in 1) cell adhesion dynamics monitoring, 2) drug screening, and 3) cell differentiation studies, highlighting its potential in broad fundamental cell biology studies as well as in clinical applications.

Indexed as

GalliumCell AdhesionIncubatorsRefractometryGalliumgallium nitridechipscopegallium nitride (GaN)label-free sensingliving cell activitiesmonolithic integration

Identifiers

PMID35404518
PMCPMC9189681

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.