Evidence map›Paper›PMID 42653552›Full record

ReviewMicromachines2026

Surface-Engineered Magnetic Nanoparticles in Skeletal Muscle Tissue Engineering: From Biological Interactions to Clinical Translation.

Md Imran Hossain, Sitansu Sekhar Nanda, Dong Kee Yi

Abstract readReview
In one paragraph

Review in Micromachines, 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

3 authors.

Md Imran HossainDeakin Institute for Frontier Materials, Faculty of Science, Engineering and Built Environment, Deakin University, Geelong, VIC 3216, Australia.ORCID 0000-0003-1611-3416
Sitansu Sekhar NandaDepartment of Chemistry, Myongji University, Yongin 17058, Republic of Korea.ORCID 0000-0002-7663-4830
Dong Kee YiDepartment of Chemistry, Myongji University, Yongin 17058, Republic of Korea.ORCID 0000-0003-2604-9323

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The repair and functional restoration of skeletal muscle tissue following trauma, degenerative disease, or volumetric muscle loss remains a significant unmet clinical challenge in tissue engineering, where the need to recapitulate the anisotropic architecture, mechanical compliance, and high metabolic demands of native muscle imposes stringent requirements on biomaterial design. Traditional cell culturing and scaffold fabrication strategies have proven insufficient to address these demands in isolation, particularly in integrating mechanical integrity, biochemical functionality, and biological activity within a single biomaterial system. Recent advances in material science have accelerated the evolution of skeletal muscle tissue engineering toward a more precise and technologically sophisticated discipline. In this context, surface-engineered magnetic nanoparticle (MNP) hybrids have emerged as a promising multifunctional platform, owing to their intrinsic biocompatibility, tunable physicochemical properties, and rapid, non-invasive responsiveness to external magnetic fields. These unique characteristics have enabled the development of magnetic force-based tissue engineering strategies, facilitating controlled myogenic cell organization, magnetically guided delivery of therapeutic agents and stem cells, enhanced muscle construct formation within responsive scaffolds, and real-time non-invasive monitoring of engineered systems via MRI. This review systematically synthesizes the recent advances in surface-engineered MNP platforms for skeletal muscle tissue engineering, covering organic and inorganic coating strategies, magnetically responsive scaffold integration, guided cell and drug delivery, and construct monitoring, whilst critically appraising the biocompatibility, biodistribution, and regulatory challenges that currently define the translational pathway for MNP-augmented skeletal muscle constructs.

Indexed as

magnetic drug deliverymagnetic hyperthermiamagnetic imagingmagnetic nanoparticlesskeletal muscle regenerationtissue engineering

Identifiers

PMID42653552
PMCPMC13515479

What OpenQuestion 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 OpenQuestion graph.