Evidence map›Paper›PMID 28442910›Full record

ArticleInternational journal of nanomedicine2017

Targeted delivery of thymosin beta 4 to the injured myocardium using CREKA-conjugated nanoparticles.

Zheyong Huang, Yanan Song, Zhiqing Pang, Bo Zhang, Hongbo Yang, Hongtao Shi, Jing Chen, Hui Gong, Juying Qian, Junbo Ge

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 41 citations in OpenAlex.

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  10. Dendritic Self-assembled Structures from Therapeutic Charged Pentapeptides.Langmuir : the ACS journal of surfaces and colloids · 2022
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  16. Frontiers in cardiovascular medicine · 2021
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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

10 authors at 2 institutions in 2 countries.

Zheyong HuangShanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University.
Yanan SongShanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University.
Zhiqing PangSchool of Pharmacy, Fudan University, Key Laboratory of Smart Drug Delivery, Ministry of Education, Shanghai.
Bo ZhangInstitute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan, Hubei.
Hongbo YangShanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University.
Hongtao ShiShanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University.
Jing ChenShanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University.
Hui GongShanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University.
Juying QianShanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University.
Junbo GeShanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University.
Fudan University · CNWuhan Union Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThymosin beta 4 (Tβ4) has multiple beneficial facets for myocardial injury, but its efficiency is limited by the low local concentration within the infarct. Here, we established a Tβ4 delivery system for cardiac repair based on the interaction between the abundant fibrin in the infarct zone and the fibrin-targeting moiety clot-binding peptide cysteine-arginine-glutamic acid-lysine-alanine (CREKA). METHODS AND

resultsCREKA and Tβ4 were conjugated to nanoparticles (CNP-Tβ4). In vitro binding test revealed that CNP-Tβ4 had a significant binding ability to the surface of fibrin clots when compared to the control clots (NP-Tβ4). Based on the validation of fibrin expression in the early stage of ischemia injury, CNP-Tβ4 was intravenously administered to mice with acute myocardial ischemia-reperfusion injury. CNP-Tβ4 revealed a stronger fibrin-targeting ability than the NP-Tβ4 group and accumulated mainly in the infarcted area and colocalized with fibrin. Subsequently, treatment with CNP-Tβ4 resulted in a better therapeutic effect.

conclusionCRKEA modification favored Tβ4 accumulation and retention in the infarcted region, leading to augmented functional benefits. Fibrin-targeting delivery system represents a generalizable platform technology for regenerative medicine.

Indexed as

AnimalsDrug Delivery SystemsFibrinMaleMice, Inbred BALB CMolecular Targeted TherapyMyocardial Reperfusion InjuryMyocardiumNanoparticlesOligopeptidesRegenerative MedicineSignal TransductionThymosinThymosin beta(4)Tissue Distributioncysteinyl-arginyl-glutamyl-lysyl-alanylFibrinOligopeptidesThymosinThymosin beta(4)cardiovascularCREKAfibrinischemia reperfusiontargeting deliverythymosin beta 4

Identifiers

PMID28442910
PMCPMC5396927
OpenAlexW2606562166

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.