Evidence map›Paper›PMID 39524922›Full record

ArticleInternational journal of nanomedicine2024

Temperature and Ultrasound-Responsive Nanoassemblies for Enhanced Organ Targeting and Reduced Cardiac Toxicity.

Mingzhou Jiang, Yiming Wang, Jinjin Zhang, Xi Fan, Milayi Jieensi, Fang Ding, Yiqing Wang, Xiaotian Sun

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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.

Mingzhou Jiang *Department of Cardiothoracic Surgery, Huashan Hospital of Fudan University, Shanghai, People's Republic of China.
Yiming Wang *Department of Cardiology, Huashan Hospital of Fudan University, Shanghai, People's Republic of China.
Jinjin Zhang *Department of Cardiology, Huashan Hospital of Fudan University, Shanghai, People's Republic of China.
Xi FanDepartment of Cardiothoracic Surgery, Huashan Hospital of Fudan University, Shanghai, People's Republic of China.
Milayi JieensiDepartment of Cardiothoracic Surgery, Huashan Hospital of Fudan University, Shanghai, People's Republic of China.
Fang DingDepartment of Cardiology, Huashan Hospital of Fudan University, Shanghai, People's Republic of China.
Yiqing WangDepartment of Cardiothoracic Surgery, Huashan Hospital of Fudan University, Shanghai, People's Republic of China.
Xiaotian SunDepartment of Cardiothoracic Surgery, Huashan Hospital of Fudan University, Shanghai, People's Republic of China.ORCID 0000-0003-3330-5460

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Biocompatible nanocarriers are widely employed as drug-delivery vehicles for treatment. Nevertheless, indiscriminate drug release, insufficient organ-specific targeting, and systemic toxicity hamper nanocarrier effectiveness. Stimuli-responsive nano-sized drug delivery systems (DDS) are an important strategy for enhancing drug delivery efficiency and reducing unexpected drug release. Methods: This study introduces a temperature- and ultrasound-responsive nano-DDS in which the copolymer p-(MEO Results: MPL-p exhibited excellent biocompatibility and rare drug release in circulation. When targeting delivery to the brain, ultrasound promoted the release of the loaded drugs in the brain without accumulation in other organs, avoiding the related adverse reactions, specifically those affecting the heart. Conclusion: This study established a novel temperature- and ultrasound-responsive DDS that reduced systemic adverse reactions compared with traditional DDS, especially in the heart, and demonstrated excellent organ delivery efficiency.

Indexed as

TemperatureAnimalsBrainDrug CarriersDrug Delivery SystemsDrug LiberationHeartHumansMagnetic Iron Oxide NanoparticlesMicePolyethylene GlycolsPolymersUltrasonic WavesDrug CarriersPolyethylene GlycolsPolymersdrug deliverymesoporous iron oxide nanoparticlessystemic toxicitytemperature- and ultrasound-responsive

Identifiers

PMID39524922
PMCPMC11550713

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Registered trials

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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.