Evidence map›Paper›PMID 42394903›Full record

ArticleBioengineering & translational medicine2026

Shelf-stable, ready-to-use therapeutic patches: Dip-and-deliver solutions for personalized wound care.

Ameya P Chaudhari, Parmiss Khosravi, Zajeba Tabashsum, Hattie E Hensley, Claire J Wang, Emilie A Moses, Samantha Harris, Anthony Hazelton, Palas B Tiwade, Rachel VanKeulen-Miller and 4 more

Abstract read
In one paragraph

Article in Bioengineering & translational medicine, 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.

Ameya P ChaudhariDivision of Pharmacoengineering and Molecular Pharmaceutics Eshelman School of Pharmacy, University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.ORCID https://orcid.org/0000-0003-0456-5677
Parmiss KhosraviLampe Joint Department of Biomedical Engineering University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.
Zajeba TabashsumDepartment of Microbiology and Immunology University of North Carolina-Chapel Hill Chapel Hill North Carolina USA.
Hattie E HensleyLampe Joint Department of Biomedical Engineering University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.
Claire J WangDepartment of Chemistry University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.
Emilie A MosesDepartment of Chemistry University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.
Samantha HarrisDivision of Pharmacoengineering and Molecular Pharmaceutics Eshelman School of Pharmacy, University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.
Anthony HazeltonDepartment of Pharmacology School of Medicine, University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.
Palas B TiwadeDivision of Pharmacoengineering and Molecular Pharmaceutics Eshelman School of Pharmacy, University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.
Rachel VanKeulen-MillerDepartment of Pharmacology School of Medicine, University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.
Owen S FentonDivision of Pharmacoengineering and Molecular Pharmaceutics Eshelman School of Pharmacy, University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.ORCID https://orcid.org/0000-0002-5585-9280
Sergei S SheikoDepartment of Chemistry University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.ORCID https://orcid.org/0000-0003-3672-1611
Sarah E RoweDepartment of Microbiology and Immunology University of North Carolina-Chapel Hill Chapel Hill North Carolina USA.
Juliane NguyenDivision of Pharmacoengineering and Molecular Pharmaceutics Eshelman School of Pharmacy, University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.ORCID https://orcid.org/0000-0002-8578-7396

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic wounds often require advanced dressing materials that can conform to complex skin movements and maintain therapeutic efficacy. Conventional dressings are typically non-adhesive and non-auxetic, necessitating external fixation and limiting their mechanical compatibility with natural tissue deformation. To overcome these challenges, we developed an auxetic skin mesh platform with instant adhesion, enabling improved mechanical conformity and ability to mimic skin movement. In this study, we developed a shelf-stable auxetic skin mesh capable of loading and releasing a broad range of therapeutics through a simple dip-and-deliver process. We compared air-dried and freeze-dried meshes against unprocessed controls to evaluate mechanical strength, adhesion, porosity, and drug-release performance. The platform effectively delivered diverse cargos, including lipid nanoparticles (LNPs), extracellular vesicles (EVs), proteins, small molecules, and FDA-approved drugs such as platelet-derived growth factor (PDGF-BB) and antibiotics, demonstrating controlled release and enhanced angiogenesis in a diabetic mouse model. These results highlight the mesh's versatility as a bioadhesive drug-delivery system with strong potential to improve wound healing outcomes.

Identifiers

PMID42394903
PMCPMC13327606

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.