Evidence map›Paper›PMID 30356945›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2018

A Broad-Spectrum ROS-Eliminating Material for Prevention of Inflammation and Drug-Induced Organ Toxicity.

Lanlan Li, Jiawei Guo, Yuquan Wang, Xiaoxing Xiong, Hui Tao, Jin Li, Yi Jia, Houyuan Hu, Jianxiang Zhang

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed, 157 citations in OpenAlex.

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  10. Pathophysiology-Directed Engineering of a Combination Nanoanalgesic for Neuropathic Pain.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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 3 institutions in 1 country.

Lanlan LiDepartment of Pharmaceutics College of Pharmacy Third Military Medical University Chongqing 400038 China.
Jiawei GuoDepartment of Pharmaceutics College of Pharmacy Third Military Medical University Chongqing 400038 China.
Yuquan WangDepartment of Cardiology Southwest Hospital Third Military Medical University Chongqing 400038 China.
Xiaoxing XiongDepartment of Neurosurgery Renmin Hospital of Wuhan University Wuhan 430060 China.
Hui TaoDepartment of Pharmaceutics College of Pharmacy Third Military Medical University Chongqing 400038 China.
Jin LiDepartment of Pharmaceutics College of Pharmacy Third Military Medical University Chongqing 400038 China.
Yi JiaDepartment of Pharmaceutics College of Pharmacy Third Military Medical University Chongqing 400038 China.
Houyuan HuDepartment of Cardiology Southwest Hospital Third Military Medical University Chongqing 400038 China.
Jianxiang ZhangDepartment of Pharmaceutics College of Pharmacy Third Military Medical University Chongqing 400038 China.ORCID 0000-0002-0984-2947
Army Medical University · CNNorth Sichuan Medical University · CNWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the great potential of numerous antioxidants for pharmacotherapy of diseases associated with inflammation and oxidative stress, many challenges remain for their clinical translation. Herein, a superoxidase dismutase/catalase-mimetic material based on Tempol and phenylboronic acid pinacol ester simultaneously conjugated β-cyclodextrin (abbreviated as TPCD), which is capable of eliminating a broad spectrum of reactive oxygen species (ROS), is reported. TPCD can be easily synthesized by sequentially conjugating two functional moieties onto a β-cyclodextrin scaffold. The thus developed pharmacologically active material may be easily produced into antioxidant and anti-inflammatory nanoparticles, with tunable size. TPCD nanoparticles (TPCD NP) effectively protect macrophages from oxidative stress-induced apoptosis in vitro. Consistently, TPCD NP shows superior efficacies in three murine models of inflammatory diseases, with respect to attenuating inflammatory responses and mitigating oxidative stress. TPCD NP can also protect mice from drug-induced organ toxicity. Besides the passive targeting effect, the broad spectrum ROS-scavenging capability contributes to the therapeutic benefits of TPCD NP. Importantly, in vitro and in vivo preliminary experiments demonstrate the good safety profile of TPCD NP. Consequently, TPCD in its native and nanoparticle forms can be further developed as efficacious and safe therapies for treatment of inflammation and oxidative stress-associated diseases.

Indexed as

antioxidantsinflammationnanoparticlesreactive oxygen speciestargeted therapy

Identifiers

PMID30356945
PMCPMC6193162
OpenAlexW2885799223

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.