Evidence map›Paper›PMID 36367231›Full record

ArticleACS nano2022

Rescuing Cardiac Cells and Improving Cardiac Function by Targeted Delivery of Oxygen-Releasing Nanoparticles after or Even before Acute Myocardial Infarction.

Ya Guan, Hong Niu, Jiaxing Wen, Yu Dang, Mohamed Zayed, Jianjun Guan

Abstract read
In one paragraph

Article in ACS nano, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

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  9. Targeted delivery of engineered adipose-derived stem cell secretome to promote cardiac repair after myocardial infarction.Journal of controlled release : official journal of the Controlled Release Society · 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

6 authors.

Ya GuanInstitute of Materials Science and Engineering, Washington University in St. Louis, St. Louis, Missouri 63130, United States.ORCID 0000-0002-6889-4966
Hong NiuDepartment of Mechanical Engineering and Materials Science, Washington University in St. Louis, St. Louis, Missouri 63130, United States.
Jiaxing WenInstitute of Materials Science and Engineering, Washington University in St. Louis, St. Louis, Missouri 63130, United States.ORCID 0000-0003-1749-7765
Yu DangInstitute of Materials Science and Engineering, Washington University in St. Louis, St. Louis, Missouri 63130, United States.
Mohamed ZayedDepartment of Surgery, Section of Vascular Surgery, Washington University in St. Louis, St. Louis, Missouri 63110, United States.
Jianjun GuanInstitute of Materials Science and Engineering, Washington University in St. Louis, St. Louis, Missouri 63130, United States.ORCID 0000-0002-1040-3386

Funding

Hydrogel encapsulation of a tissue repair protein to treat chronic woundsR01AG056919 · NIA · OHIO STATE UNIVERSITY · PI GUAN, JIANJUN, LI, HAICHANG · 2017 to 2021
$2.4M
Targeted delivery of a proangiogenic and promyogenic protein for regeneration of diabetic ischemic limbsR01HL164062 · NHLBI · WASHINGTON UNIVERSITY · PI GUAN, JIANJUN, ZHANG, FUZHONG · 2022 to 2025
$2.3M
Regulation of Endothelial Lipid Metabolism in the Setting of Diabetes and Critical Limb Ischemia to Prevent Surgical ComplicationsR01HL153262 · NHLBI · WASHINGTON UNIVERSITY · PI ZAYED, MOHAMED A. · 2021 to 2024
$2.1M
Preservation and Vascularization of Cardiac Extracellular Matrix after Myocardial InfarctionR01HL138175 · NHLBI · WASHINGTON UNIVERSITY · PI GUAN, JIANJUN · 2019 to 2022
$1.8M
Regenerative wound dressings for accelerating diabetic wound healingR01DK133949 · NIDDK · WASHINGTON UNIVERSITY · PI GUAN, JIANJUN · 2022 to 2025
$1.8M
Stem Cell Oxygenation and Ischemic Tissue RegenerationR01HL138353 · NHLBI · WASHINGTON UNIVERSITY · PI GUAN, JIANJUN · 2017 to 2020
$1.5M
CONTROL OF CARDIAC FIBROSIS TO PREVENT CARDIAC FUNCTION DETERIORATIONR01EB022018 · NIBIB · WASHINGTON UNIVERSITY · PI GUAN, JIANJUN · 2016 to 2018
$1.1M
NHLBI NIH HHS R01 HL138175NHLBI NIH HHS R01 HL138353NHLBI NIH HHS R01 HL153262NHLBI NIH HHS R01 HL164062NIA NIH HHS R01 AG056919NIBIB NIH HHS R01 EB022018NIDDK NIH HHS R01 DK133949
6 · The paper itself

Abstract

Myocardial infarction (MI) causes massive cell death due to restricted blood flow and oxygen deficiency. Rapid and sustained oxygen delivery following MI rescues cardiac cells and restores cardiac function. However, current oxygen-generating materials cannot be administered during acute MI stage without direct injection or suturing methods, both of which risk rupturing weakened heart tissue. Here, we present infarcted heart-targeting, oxygen-releasing nanoparticles capable of being delivered by intravenous injection at acute MI stage, and specifically accumulating in the infarcted heart. The nanoparticles can also be delivered before MI, then gather at the injured area after MI. We demonstrate that the nanoparticles, delivered either pre-MI or post-MI, enhance cardiac cell survival, stimulate angiogenesis, and suppress fibrosis without inducing substantial inflammation and reactive oxygen species overproduction. Our findings demonstrate that oxygen-delivering nanoparticles can provide a nonpharmacological solution to rescue the infarcted heart during acute MI and preserve heart function.

Indexed as

Myocardial InfarctionNanoparticlesHeartHumansOxygenReactive Oxygen SpeciesOxygenReactive Oxygen Speciesacute myocardial infarctioncontrolled release of oxygenmyocardial repairnanoparticlestargeted delivery

Identifiers

PMID36367231
PMCPMC9930176

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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.