Evidence map›Paper›PMID 41137637›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2026

Mesenchymal Stem Cell-Inspired Microneedle Platform for NIR-responsive Immunomodulation and Accelerated Chronic Wound Healing.

Chan Ho Moon, Hee Gyeong Ko, Hyun Lee, Seojoon Bang, Hyeong Seok Kang, Ju Yeong Gwon, Jong Hwa Seo, Nayoung Lee, So Won Jeon, Yun-A Kim and 12 more

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. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
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  7. Article
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  9. Review
  10. Article
  11. Microneedle-Assisted Cell Delivery and Therapy.Research (Washington, D.C.) · 2026
    Review
  12. Review
  13. 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

22 authors.

Chan Ho MoonDivision of Materials Science and Engineering, Hanyang University, Seoul, 04763, Republic of Korea.
Hee Gyeong KoDepartment of Biomedical-Chemical Engineering, The Catholic University of Korea, Bucheon, Gyeonggi-do, 14662, Republic of Korea.
Hyun LeeResearch Institute of Intelligent Manufacturing & Materials Technology, Korea Institute of Industrial Technology, Incheon, 21999, Republic of Korea.
Seojoon BangDivision of Materials Science and Engineering, Hanyang University, Seoul, 04763, Republic of Korea.
Hyeong Seok KangDivision of Materials Science and Engineering, Hanyang University, Seoul, 04763, Republic of Korea.
Ju Yeong GwonDepartment of Bioengineering, Hanyang University, Seoul, 04763, Republic of Korea.
Jong Hwa SeoDivision of Materials Science and Engineering, Hanyang University, Seoul, 04763, Republic of Korea.
Nayoung LeeDivision of Materials Science and Engineering, Hanyang University, Seoul, 04763, Republic of Korea.
So Won JeonDepartment of Biomedical-Chemical Engineering, The Catholic University of Korea, Bucheon, Gyeonggi-do, 14662, Republic of Korea.
Yun-A KimDepartment of Biomedical-Chemical Engineering, The Catholic University of Korea, Bucheon, Gyeonggi-do, 14662, Republic of Korea.
Jong Sang YoonDepartment of Biomedical-Chemical Engineering, The Catholic University of Korea, Bucheon, Gyeonggi-do, 14662, Republic of Korea.
Kyung-Yup ChaDepartment of Biomedical Engineering, Dongguk University, Seoul, 04620, Republic of Korea.
Min-Ho KangDepartment of Biomedical-Chemical Engineering, The Catholic University of Korea, Bucheon, Gyeonggi-do, 14662, Republic of Korea.
Dong Yun LeeDepartment of Bioengineering, Hanyang University, Seoul, 04763, Republic of Korea.
Soo-Hong LeeDepartment of Biomedical Engineering, Dongguk University, Seoul, 04620, Republic of Korea.
Gi Doo ChaDepartment of Systems Biotechnology, Chung-Ang University, Anseong-si, Gyeonggi-do, 17546, Republic of Korea.
Kisuk YangDivision of Bioengineering, College of Life Sciences and Bioengineering, Incheon National University, Incheon, 22012, Republic of Korea.
Donghyun LimDepartment of Bioengineering, Hanyang University, Seoul, 04763, Republic of Korea.
Heemin KangDepartment of Materials Science and Engineering, Korea University, Seoul, 02841, Republic of Korea.
Su Ryon ShinDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA, 02139, USA.
Han Young KimDepartment of Biomedical-Chemical Engineering, The Catholic University of Korea, Bucheon, Gyeonggi-do, 14662, Republic of Korea.ORCID 0000-0002-5585-9272
Hyun-Do JungDivision of Materials Science and Engineering, Hanyang University, Seoul, 04763, Republic of Korea.ORCID 0000-0001-8632-7431

Funding

Korea Health Industry Development Institute RS-2023-KH135936Korea Institute of Marine Science & Technology Promotion RS-2024-00405273Korean Fund for Regenerative Medicine KFRM24A0105L1National Research Foundation of Korea RS-2022-NR071672National Research Foundation of Korea RS-2024-00405381National Research Foundation of Korea RS-2025-00513935National Research Foundation of Korea RS-2025-00521275
6 · The paper itself

Abstract

Chronic diabetic wounds present substantial clinical challenges owing to sustained inflammation, compromised vascularization, and inadequate retention of therapeutic medications. Accordingly, motivated by mesenchymal stem cells (MSCs) that actively secrete bioactive exosomes in response to stimuli from the tissue microenvironment, a biomimetic microneedle (MN) platform (MSCi@MN) is created to address these challenges. The MSCi@MN exhibits a dual-compartment structure composed of MSC-derived extracellular nanovesicles (NV) conjugated with polydeoxyribonucleotide (PDRN; DNA), referred to as NV-DNA, encapsulated within dissolvable MN tips, and photothermal-responsive MXene nanoparticles (MX) incorporated into the base layer for targeted near-infrared (NIR)-activated drug delivery. Upon NIR irradiation, MSCi@MN quickly releases NV-DNA, effectively modifying the immune responses by facilitating anti-inflammatory M2 macrophage polarization and activating tolerogenic dendritic cells, thereby establishing a regenerative microenvironment. Transcriptomic research has verified that NV-DNA synergistically promotes angiogenesis, cellular proliferation, and extracellular matrix remodeling by activating complementary molecular pathways. In animal models of diabetes, MSCi@MNs markedly expedite wound repair, diminish inflammation, enhance angiogenesis, and restore skin appendages without systemic adverse effects. This MSC-inspired approach, which integrates biologically sensitive controlled release with robust immunoregenerative capabilities, has substantial potential for clinical use in chronic wound treatment and regenerative medicine.

Indexed as

ImmunomodulationInfrared RaysMesenchymal Stem CellsNeedlesWound HealingAnimalsDiabetes Mellitus, ExperimentalHumansMaleMiceNanoparticlesbioinspiredchronic wound healingmesenchymal stem cellmicroneedlenear‐infrared‐responsive

Identifiers

PMID41137637
PMCPMC12921356

What Socratic 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 Socratic graph.