# Orange-Derived Extracellular Vesicles: Characterization and Therapeutic Applications in Normal and Diabetic Wound Healing in In Vivo Models

**Authors:** Chiara Gai, Margherita Alba Carlotta Pomatto, Federica Negro, Lucia Massari, Maria Chiara Deregibus, Massimo Cedrino, Cristina Grange, Alessandro Burello, Joanna Kopecka, Ivan Molineris, Anel Ordabayeva, Alessandro Damin, Federica Antico, Chiara Riganti, Vito Fanelli, Natasa Zarovni, Giovanni Camussi

PMC · DOI: 10.3390/cells15030244 · Cells · 2026-01-27

## TL;DR

Orange-derived extracellular vesicles (oEVs) can speed up wound healing in both healthy and diabetic mice, offering a promising and scalable alternative to human-derived vesicles.

## Contribution

The study demonstrates that plant-derived oEVs can be effectively purified using scalable methods and show therapeutic potential in wound healing.

## Key findings

- oEVs accelerated wound healing in both healthy and diabetic mice when combined with hydrogels.
- oEVs promoted cell migration, capillary-like structure formation, and antioxidant activity in vitro.
- TFF-purified oEVs retained the same physio-chemical and molecular properties as ultracentrifugation-derived oEVs.

## Abstract

What are the main findings?
Extracellular vesicles derived from orange juice (oEVs) accelerated wound healing in both healthy and diabetic mice when formulated with hydrogels.In vitro studies suggest that the regenerative properties of oEVs may be related to stimulation of cell migration, capillary-like structure formation, cell proliferation, and strong antioxidant activity against hyperglycemia and pro-inflammatory conditions.

Extracellular vesicles derived from orange juice (oEVs) accelerated wound healing in both healthy and diabetic mice when formulated with hydrogels.

In vitro studies suggest that the regenerative properties of oEVs may be related to stimulation of cell migration, capillary-like structure formation, cell proliferation, and strong antioxidant activity against hyperglycemia and pro-inflammatory conditions.

What are the implications of the main findings?
oEVs show potential as an alternative to human-derived EVs for regenerative medicine.oEVs could solve human EV limitations in scalability, variability, safety, and cost.

oEVs show potential as an alternative to human-derived EVs for regenerative medicine.

oEVs could solve human EV limitations in scalability, variability, safety, and cost.

Extracellular vesicles (EVs) of human origin show promise for regenerative medicine and wound healing. However, they have limitations regarding scalability, variability, safety, and costs. Plant-derived EVs may represent a valid alternative. This study investigated the regenerative potential of EVs extracted from orange juice (oEVs). oEVs obtained by standard ultracentrifugation were compared with oEVs purified by tangential flow filtration (TFF), a scalable technique suitable for large-scale and regulatory-compliant manufacturing. Comparisons included size, morphology, pH, Zeta potential, protein and RNA content, Raman spectroscopy, and proteomic, metabolomic, and RNA sequencing. The regenerative potential of oEVs was tested in vitro, with cell migration, endothelial tube formation, and proliferation assays performed. Antioxidant ability was tested on endothelial cells stressed by hyperglycemia or pro-inflammatory cytokine cocktails. Next, oEVs were formulated with different hydrogels and tested at different doses on skin ulcers on healthy and diabetic mice. TFF oEVs showed the same physio-chemical characteristics and a comparable molecular content as those isolated by ultracentrifugation, confirming the path to scalability. In vitro oEVs promoted cell migration, formation of capillary-like structures, cell proliferation, and strong antioxidant activity. Moreover, oEVs effectively accelerated in vivo wound closure in healthy and diabetic mice. Thus, oEVs may provide a useful and cost-effective ingredient for improved and effective wound treatment strategies.

## Linked entities

- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249), Diabetic (MESH:D003920), hyperglycemia (MESH:D006943), skin ulcers (MESH:D012883)
- **Chemicals:** oEVs (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12896877/full.md

## References

123 references — full list in the complete paper: https://tomesphere.com/paper/PMC12896877/full.md

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Source: https://tomesphere.com/paper/PMC12896877