Evidence mapPaperPMID 42420710Full record

ReviewAdvances in experimental medicine and biology2026

Translational Nanomedicine and Delivery Tools for Cardiovascular Disease Therapy and Diagnostics.

Michael A Miller, Ryan M Williams

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Michael A MillerThe City College of New York, Department of Biomedical Engineering, New York, NY, USA.
Ryan M WilliamsThe City College of New York, Department of Biomedical Engineering, New York, NY, USA. ryan.williams@stonybrookmedicine.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular diseases are widespread causes of morbidity and mortality throughout the world. Nanomedicine is at the scale of biomolecular interfaces, the same scale as the development of plaques, thrombi, or misfolded proteins. A variety of nanomaterials, polymeric delivery tools, and engineered biologics have been developed to target and detect or treat the molecular causes of disease at the cellular level. In some cases, these nanostructures have been engineered to bypass immune recognition and deliver therapeutic cargoes. Targeted nanomaterial transport is also assistive technology for diagnostic imaging in cardiovascular disease. Selective localization of contrast agents for ultrasound, magnetic resonance, X-Ray, and optical imaging strategies enables disease-focused contrast. Continued nanomedicine research aims to produce highly specified and highly effective treatments for cardiovascular diseases, alongside enhancing point-of-care diagnostics. As these two sides of medicine progress, therapeutics and diagnostics meet at the nanoscale to create multifunctional image-enhancing and image-enhanced therapeutic tools against cardiovascular disease.

Indexed as

Cardiovascular AgentsCardiovascular DiseasesDrug Delivery SystemsNanomedicineTranslational Research, BiomedicalAnimalsContrast MediaHumansNanostructuresCardiovascular AgentsContrast MediaAtherosclerosisCardiovascular diseaseContrast agentsDrug deliveryGene therapyNanotechnology

Identifiers

PMID42420710

What Socratic holds

Textmetadata
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 Socratic graph.