Evidence map›Paper›PMID 38023720›Full record

ArticleBioengineering & translational medicine2023

An AIE-active bacterial inhibitor and photosensitizer for selective imaging, killing, and photodynamic inactivation of bacteria over mammalian cells.

Fei Wang, Yupeng Shi, Po-Yu Ho, Engui Zhao, Chuen Kam, Qiang Zhang, Xin Zhao, Yue Pan, Sijie Chen

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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

9 authors at 4 institutions in 2 countries.

Fei WangSchool of Science Harbin Institute of Technology, Shenzhen, HIT Campus of University Town Shenzhen China.
Yupeng ShiMing Wai Lau Centre for Reparative Medicine Karolinska Institutet Hong Kong China.
Po-Yu HoMing Wai Lau Centre for Reparative Medicine Karolinska Institutet Hong Kong China.
Engui ZhaoSchool of Science Harbin Institute of Technology, Shenzhen, HIT Campus of University Town Shenzhen China.ORCID https://orcid.org/0000-0003-4953-0750
Chuen KamMing Wai Lau Centre for Reparative Medicine Karolinska Institutet Hong Kong China.
Qiang ZhangDepartment of Biomedical Engineering The Hong Kong Polytechnic University Hong Kong China.
Xin ZhaoDepartment of Biomedical Engineering The Hong Kong Polytechnic University Hong Kong China.ORCID https://orcid.org/0000-0002-9521-7768
Yue PanGuangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Guangdong-Hong Kong Joint Laboratory for RNA Medicine, Medical Research Center, Sun Yat-Sen Memorial Hospital Sun Yat-Sen University Guangzhou China.
Sijie ChenMing Wai Lau Centre for Reparative Medicine Karolinska Institutet Hong Kong China.ORCID https://orcid.org/0000-0001-5263-9189
Ming Wai Lau Centre for Reparative Medicine · HKHong Kong Polytechnic University · HKShenzhen Institute of Information Technology · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Photodynamic therapy is becoming increasingly popular for combat of bacteria. In the clinical photodynamic combat of bacteria, one critical issue is to avoid the potential damage to the host since the reactive oxygen species produced by photosensitizers are also harmful to mammalian cells. In this work, we report an aggregation-induced-emission-active bacterial inhibitor and photosensitizer, OEO-TPE-MEM (OTM), for the imaging, killing, and light-enhanced inactivation of bacteria. OTM could efficiently bind to and kill Gram-positive bacteria, while its affinity to Gram-negative bacteria is lower, and a higher OTM concentration is required for killing Gram-negative bacteria. OTM is also an efficient photosensitizer and could efficiently sensitize the production of reactive oxygen species, which enhances its killing effect on both Gram-positive and Gram-negative bacteria. More interestingly, OTM is very biocompatible with normal mammalian cells both in the dark and under light irradiation. OTM in mice models with bacteria-infected wounds could promote the healing of infected wounds without affecting their organs and blood parameters, which makes it an excellent candidate for clinical applications.

Indexed as

aggregation‐induced emissionbacterial inhibitorphotodynamic therapyphotosensitizerwound healing

Identifiers

PMID38023720
PMCPMC10658525
OpenAlexW4381273716

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.