Evidence map›Paper›PMID 27486324›Full record

ArticleInternational journal of nanomedicine2016

Controlled release hydrogen sulfide delivery system based on mesoporous silica nanoparticles protects graft endothelium from ischemia-reperfusion injury.

Wenshuo Wang, Xiaotian Sun, Huili Zhang, Cheng Yang, Ye Liu, Wuli Yang, Changfa Guo, Chunsheng Wang

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Silica-Based Advanced Nanoparticles For Treating Ischemic Disease.Tissue engineering and regenerative medicine · 2023
    Review
  9. Review
  10. Review
  11. Unmet needs in glaucoma therapy: The potential role of hydrogen sulfide and its delivery strategies.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Smart HAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    Review
  19. Review
  20. 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

8 authors.

Wenshuo WangDepartment of Cardiac Surgery, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital.
Xiaotian SunDepartment of Cardiac Surgery, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital; Department of Cardiothoracic Surgery, Huashan Hospital, Fudan University.
Huili ZhangDepartment of Cardiology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University.
Cheng YangDepartment of Cardiac Surgery, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital.
Ye LiuState Key Laboratory of Molecular Engineering of Polymers; Department of Macromolecular Science, Fudan University, Shanghai, People's Republic of China.
Wuli YangState Key Laboratory of Molecular Engineering of Polymers; Department of Macromolecular Science, Fudan University, Shanghai, People's Republic of China.
Changfa GuoDepartment of Cardiac Surgery, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital.
Chunsheng WangDepartment of Cardiac Surgery, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hydrogen sulfide (H2S) functions as a protective gas transmitter in various physiological and pathological processes, but the lack of ideal donors severely hampers the clinical application of H2S. This study aims to construct a controlled release H2S donor and evaluate its protective effect on graft endothelium. Mesoporous silica nanoparticles (MSNs) were synthesized using the sol-gel method and loaded with diallyl trisulfide (DATS), an H2S-releasing agent named DATS-MSN. In vitro experiments showed that DATS-MSN could alleviate endothelial cell inflammation and enhance endothelial cell proliferation and migration. In vivo experiments demonstrated that the apoptosis of graft endothelium was mitigated in the presence of DATS-MSN. Our results indicated that DATS-MSN, releasing H2S in a controlled release fashion, could serve as an ideal H2S donor.

Indexed as

Allyl CompoundsAnimalsApoptosisCell DifferentiationCell ProliferationDelayed-Action PreparationsEndothelium, VascularFlow CytometryHumansHydrogen SulfideInflammationIn Situ Nick-End LabelingMembrane Potential, MitochondrialMice, Inbred BALB CNanomedicineNanoparticlesAllyl CompoundsDelayed-Action Preparationsdiallyl trisulfideHydrogen SulfideProtective AgentsSilicon DioxideSulfidescardiac allograft vasculopathycellular uptakeinflammatory responseproliferationrejection

Identifiers

PMID27486324
PMCPMC4957682

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.