Evidence mapPaperPMID 42232335Full record

ArticleRegenerative biomaterials2026

Integrated platform for EV separation and controlled release based on gelatin microspheres for diabetic wound treatment.

Yiqing Zhang, Qilin Huang, Hao Meng, Junli Chen, Yaying Hao, Xi Liu, Yangmengyuan Xu, Liqian Ma, Zhan Xu, Kui Ma and 4 more

Abstract read
In one paragraph

Article in Regenerative biomaterials, 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

14 authors.

Yiqing ZhangMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Qilin HuangMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Hao MengMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Junli ChenMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Yaying HaoMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Xi LiuMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Yangmengyuan XuMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Liqian MaMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Zhan XuMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Kui MaMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Wenzhi HuMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Xiaohua PanInstitute of Clinical Translation and Regenerative Medicine, The Second Affiliated Hospital of Shenzhen University, Shenzhen 518100, China.
Xiaobing FuMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.
Cuiping ZhangMedical Innovation Research Department, PLA General Hospital and PLA Medical College, Beijing 100048, China.ORCID https://orcid.org/0000-0003-0320-6226

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic wounds exhibit impaired healing owing to multiple pathological factors and current treatment options remain limited, underscoring the urgent need for novel therapeutic strategies. Extracellular vesicles (EVs) derived from mesenchymal stem cells (MSCs) are emerging as promising candidates for wound healing. However, the process from isolation to application of EVs is complex and time-consuming, which probably influences the activity and the therapeutic effects of EVs. To address these issues, we created the integrated platform for EV separation and controlled release. Gelatin microspheres (GMS) were prepared and functionalized with the variable domain of heavy-chain-only antibodies (GMS-VHH). GMS-VHH enabled the efficient capture of CD9-positive EVs in the culture supernatant of MSCs, forming EVs-loaded gelatin microspheres (GMS@EVs). The characterization of EVs demonstrated that the GMS-VHH isolation method outperformed traditional ultracentrifugation in terms of EV structural integrity. GMS@EVs exhibited excellent biocompatibility and promoted the proliferation of epidermal keratinocytes

Indexed as

diabetic wound healingextracellular vesiclesgelatin-microsphere

Identifiers

PMID42232335
PMCPMC13225271

What Socratic holds

Textmetadata
LicenceCC BY
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.