Evidence map›Paper›PMID 42482867›Full record

ArticleFrontiers in bioengineering and biotechnology2026

Dehydrated silk fibroin matrices as versatile delivery systems for extracellular vesicles.

Alp Sarisoy, Yong Xu, Stephan Rütten, Eva Miriam Buhl, Cecile Maire, Sandra Fuest, Ralf Smeets, Franz Lennard Ricklefs, Christian Apel

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 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

9 authors.

Alp SarisoyDepartment of Biohybrid & Medical Textiles (BioTex), Institute of Applied Medical Engineering, Uniklinik RWTH Aachen, Aachen, Germany.
Yong XuDepartment of Biohybrid & Medical Textiles (BioTex), Institute of Applied Medical Engineering, Uniklinik RWTH Aachen, Aachen, Germany.
Stephan RüttenElectron Microscopy Facility, Institute of Pathology, Uniklinik RWTH Aachen, Aachen, Germany.
Eva Miriam BuhlElectron Microscopy Facility, Institute of Pathology, Uniklinik RWTH Aachen, Aachen, Germany.
Cecile MaireDepartment of Neurosurgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Sandra FuestDepartment of Oral and Maxillofacial Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Ralf SmeetsDepartment of Oral and Maxillofacial Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Franz Lennard RicklefsDepartment of Neurosurgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Christian ApelDepartment of Biohybrid & Medical Textiles (BioTex), Institute of Applied Medical Engineering, Uniklinik RWTH Aachen, Aachen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles (EVs) have emerged as promising alternatives to cell-based therapies due to their low immunogenicity, ability to carry therapeutic cargo, and enhanced stability. However, rapid clearance from the bloodstream and phagocytic uptake by macrophages after systemic or local administration limit their therapeutic efficacy, highlighting the need for delivery systems that enable sustained and localized EV release. In this study, a natural protein silk fibroin (SF) was selected as a biomaterial carrier due to its tunable degradation kinetics and biocompatibility. SF was produced into nonwovens and films to investigate the effect of material structure on EV delivery in dehydrated SF matrices. A mild water vapor annealing approach was applied to tune structural stability and β-sheet formation while preserving EV integrity. Gingival fibroblast (GF)-derived EVs were successfully incorporated into nonwovens and films. EV-loaded nonwovens and films demonstrated distinct release characteristics over 14 days, with nonwovens providing a more controlled release and films showing delayed but accelerated release at later time points. EV morphology was preserved after release, and the EVs were notably internalized by human umbilical vein endothelial cells (HUVECs). Both EV-loaded materials enhanced the migration in a wound healing assay. These findings highlight the potential of dehydrated SF matrices as promising EV delivery systems for future regenerative medicine applications.

Indexed as

controlled releaseextracellular vesicle delivery systemsextracellular vesiclesfilmsnonwovenssilk fibroinwound healing

Identifiers

PMID42482867
PMCPMC13385103

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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.