Evidence map›Paper›PMID 35198963›Full record

ArticleMaterials today. Bio2022

Harnessing reactive oxygen/nitrogen species and inflammation: Nanodrugs for liver injury.

Min Liu, Qiong Huang, Yan Zhu, Li Chen, Yumei Li, Zhicheng Gong, Kelong Ai

Open access · goldAbstract read
In one paragraph

Article in Materials today. Bio, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 64 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

7 authors at 1 institution in 1 country.

Min LiuDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha, 410008, China.
Qiong HuangDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha, 410008, China.
Yan ZhuDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha, 410008, China.
Li ChenXiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410078, China.
Yumei LiDepartment of Assisted Reproduction, Xiangya Hospital, Central South University, Changsha, 410008, China.
Zhicheng GongDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha, 410008, China.
Kelong AiXiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410078, China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overall, 12% of the global population (800 million) suffers from liver disease, which causes 2 million deaths every year. Liver injury involving characteristic reactive oxygen/nitrogen species (RONS) and inflammation plays a key role in progression of liver disease. As a key metabolic organ of the human body, the liver is susceptible to injury from various sources, including COVID-19 infection. Owing to unique structural features and functions of the liver, most current antioxidants and anti-inflammatory drugs are limited against liver injury. However, the characteristics of the liver could be utilized in the development of nanodrugs to achieve specific enrichment in the liver and consequently targeted treatment. Nanodrugs have shown significant potential in eliminating RONS and regulating inflammation, presenting an attractive therapeutic tool for liver disease through controlling liver injury. Therefore, the main aim of the current review is to provide a comprehensive summary of the latest developments contributing to our understanding of the mechanisms underlying nanodrugs in the treatment of liver injury via harnessing RONS and inflammation. Meanwhile, the prospects of nanodrugs for liver injury therapy are systematically discussed, which provides a sound platform for novel therapeutic insights and inspiration for design of nanodrugs to treat liver disease.

Indexed as

Anti-inflammatoryLiver injuryNanocarriersNanozymeRONS-Scavenging

Identifiers

PMID35198963
PMCPMC8850330
OpenAlexW4210878941

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.