Evidence map›Paper›PMID 42021559›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2026

Mechanically Spatio-Chimeric Fibrin Assembly Enables Vascular-Integrated Muscle Reconstruction for Volumetric Muscle Loss Repair.

Su Hyun Jung, Minjun Kim, Da-Yoon Kim, Min Kyu Kim, Sieun Lee, Yoonhee Jin, Joo H Kang

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 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

7 authors.

Su Hyun JungDepartment of Biomedical Engineering, College of Information and Biotechnology, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.ORCID https://orcid.org/0000-0002-9892-1400
Minjun KimDepartment of Physiology, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0009-0006-0900-2282
Da-Yoon KimDepartment of Biomedical Engineering, College of Information and Biotechnology, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Min Kyu KimDepartment of Biomedical Engineering, College of Information and Biotechnology, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Sieun LeeDepartment of Physiology, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, Republic of Korea.
Yoonhee JinDepartment of Physiology, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-1263-9405
Joo H KangDepartment of Biomedical Engineering, College of Information and Biotechnology, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.ORCID https://orcid.org/0000-0001-9636-3209

Funding

Korean Fund for Regenerative Medicine 22A0102L1-11National Research Foundation of Korea 2024-00344187National Research Foundation of Korea RS-2024-00399800National Research Foundation of Korea RS-2026-25469505UNIST Research Fund 1.260001.01Yonsei University College of Medicine 6-2021-0243YUCM and YUCD & UNIST Collaborative Project 6-2024-0202
6 · The paper itself

Abstract

Volumetric muscle loss (VML), a severe injury involving irreversible loss of both muscle tissue and vasculature, poses a major barrier to the development of clinically viable muscle grafts. Functional restoration requires engineered constructs capable of reconstructing both contractile and vascular components that can functionally integrate with the host vasculature. Here, we introduce SPARC (spatio-chimeric, plasma-based, anisotropic, and shear-responsive construct), a mechanically bimodal fibrin hydrogel engineered via shear-guided assembly of plasma fibrin to recreate the structural and mechanical heterogeneity of native muscle. Controlled microfluidic shear generates aligned fibrillar bundles and a spatially graded bimodal stiffness architecture, establishing stiff, bundle-dense regions that favor myogenic differentiation and compliant regions that promote endothelial morphogenesis. When co-cultured with myoblasts and endothelial cells, the resulting anisotropic matrix directs spatially organized myogenic maturation and endothelial morphogenesis. In vivo evaluation in a murine VML model shows that vascularized muscle SPARC grafts restore muscle architecture and function, promoting neovascularization, myofiber regeneration, and enhanced motor recovery. Through its spatially mechano-programmed design, SPARC enables coordinated myogenic and endothelial organization within a single construct, establishing a scalable biofabrication strategy for functional repair of extensive muscle defects.

Indexed as

FibrinMechanical PhenomenaMuscle, SkeletalAnimalsEndothelial CellsHumansHydrogelsMiceMyoblastsNeovascularization, PhysiologicTissue EngineeringTissue ScaffoldsFibrinHydrogelsanisotropic 3D muscle scaffoldsmechanically bimodal hydrogel systemsshear‐driven fibrin assemblyvascular‐integrated muscle graftvolumetric muscle loss repair

Identifiers

PMID42021559
PMCPMC13449102

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LicenceCC BY
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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.