# The expanding role of biocompatible hydrogels in plant-derived exosome-like nanovesicles for skin diseases: prospects and challenges

**Authors:** Sha Lv, Danyang Fan, Zhanhan Tang, Zhe Liu

PMC · DOI: 10.1080/07853890.2026.2643038 · Annals of Medicine · 2026-03-21

## TL;DR

This paper reviews how plant-derived nanovesicles combined with hydrogels can improve skin disease treatments, while highlighting challenges and future opportunities.

## Contribution

The paper systematically reviews the integration of plant-derived exosome-like nanovesicles with hydrogels for skin therapy, identifying key challenges and future directions.

## Key findings

- PDELNs in hydrogels show promise for treating inflammatory skin diseases and wound healing.
- Challenges include scalability, formulation stability, and skin penetration efficiency.
- Future research should focus on advanced technologies like phototherapy and microneedles.

## Abstract

Plant-derived exosome like nanovesicles known for their biocompatibility, minimal immunogenicity, and capacity to transport diverse therapeutic molecules, have emerged as effective carriers for targeted drug delivery. When integrated into hydrogels, these offer improved stability, prolonged release, and precise delivery to specific skin layers, thereby enhancing treatment outcomes.

We conducted structured search of the literature on plant-derived exosome-like nanovesicles (PDELNs) and hydrogel-based drug-delivery systems for skin applications. Relevant studies were identified from PubMed, ScienceDirect, and Google Scholar using keywords including plant-derived exosomes like nanovesicles, plant exosomes + skin, and plant exosomes + hydrogel. We selected Publications from 2010 to 2025 and focused on studies describing biological activity of plant-derived exosomes, as well as their therapeutic relevance for skin repair, regeneration, or wound healing. Research involving hydrogel formulations that incorporated plant-derived vesicles or comparable nano-carriers was also included. In vitro, in vivo (preclinical), and available clinical evidence were reviewed, while unrelated work (such as mammalian exosomes or non-skin studies) was excluded.

The combination of plant-derived exosomes like nanovesicles and hydrogels is potential therapeutic candidate in addressing various skin disorders, including inflammatory diseases, wound healing, and skin regeneration. However, challenges remain, including the scalability of exosome production, stability of formulations, and achieving effective skin penetration. Furthermore, regulatory considerations regarding the safety, toxicity, and long-term biocompatibility of these systems must be thoroughly evaluated. The review also emphasizes future research opportunities, the development of plant-derived exosomes like nanovesicles with higher therapeutic potential and the integration of advanced technologies like phototherapy and microneedles to further improve therapeutic efficacy.

The combination of PDELNs with hydrogel delivery systems have shown potential in preclinical models for the treatment of dermatological diseases, providing a novel strategy for skin care.

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, IVL (involucrin) [NCBI Gene 3713], CD63 (CD63 molecule) [NCBI Gene 967] {aka AD1, HOP-26, ME491, MLA1, OMA81H, Pltgp40}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, CD9 (CD9 molecule) [NCBI Gene 928] {aka BTCC-1, DRAP-27, MIC3, MRP-1, TSPAN-29, TSPAN29}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL22 (interleukin 22) [NCBI Gene 50616] {aka IL-21, IL-22, IL-D110, IL-TIF, ILTIF, TIFIL-23}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, FLG (filaggrin) [NCBI Gene 2312] {aka ATOD2, FLG-1, FLG1}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, CD81 (CD81 molecule) [NCBI Gene 975] {aka CVID6, S5.7, TAPA1, TSPAN28}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, ELN (elastin) [NCBI Gene 2006] {aka ADCL1, SVAS, WBS, WS}, TYR (tyrosinase) [NCBI Gene 7299] {aka ATN, CMM8, OCA1, OCA1A, OCAIA, SHEP3}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** fever (MESH:D005334), burn (MESH:D002056), dog-bite wounds (MESH:D004283), polycystic ovary syndrome (MESH:D011085), immune dysregulation (OMIM:614878), periodontitis (MESH:D010518), eczema (MESH:D004485), bronchopulmonary dysplasia (MESH:D001997), epidermal hyperplasia (MESH:D006965), squamous cell carcinoma (MESH:D002294), acanthosis (MESH:D000052), depigmenting skin disorder (MESH:D012871), acute ischemic stroke (MESH:D000083242), eosinophilic inflammation (MESH:D007249), cartilage defect (MESH:D002357), Melasma (MESH:D008548), myocardial infarction (MESH:D009203), erythema (MESH:D004890), macular holes (MESH:D012167), Vitiligo (MESH:D014820), melanoma (MESH:D008545), Acne vulgaris (MESH:D000152), water (MESH:D000069578), cutaneous (MESH:D018366), herpes simplex virus type 1 (HSV-1) infection (MESH:D006561), papules (MESH:D000169), autoimmune (MESH:D001327), SLE (MESH:D008180), pressure sores (MESH:D003668), skin ulcers (MESH:D012883), neurovascular abnormalities (MESH:D013901), inflammatory skin disorder (MESH:D012868), joint damage (MESH:D007592), AD (MESH:D003876), CLE (MESH:D008178), tissue injury (MESH:D017695), fibrosis (MESH:D005355), cancer (MESH:D009369), immune (MESH:D007154), cytotoxicity (MESH:D064420), Eczema herpeticum (MESH:D007617), type 1 diabetes (MESH:D003922), rash (MESH:D005076), PsA (MESH:D015535), inflammatory arthritis (MESH:D001168), corneal damage (MESH:D065306), dermatological diseases (MESH:D000168), spinal cord injury (MESH:D013119), diabetic (MESH:D003920), psoriasis (MESH:D011565), atherosclerosis (MESH:D050197), gastrointestinal health (MESH:D005767), colon cancer (MESH:D015179), oral mucositis (MESH:D013280), pancreatic cancer (MESH:D010190), basal cell carcinoma (MESH:D002280), Seborrheic dermatitis (MESH:D012628), Hyperpigmentation disorders (MESH:D017495), telangiectasia (MESH:D013684), Skin cancers (MESH:D012878)
- **Chemicals:** sucrose (MESH:D013395), flavonoid (MESH:D005419), alginate (MESH:D000464), melanin (MESH:D008543), steroid (MESH:D013256), metal (MESH:D008670), retinoids (MESH:D012176), water (MESH:D014867), EGCG (MESH:C045651), quercetin (MESH:D011794), ROS (MESH:D017382), sphingolipids (MESH:D013107), oil (MESH:D009821), PEG (MESH:D011092), petrolatum (MESH:D010577), chitosan (MESH:D048271), PLGA (MESH:D000077182), hyaluronic acid (MESH:D006820), iodixanol (MESH:C044834), silver (MESH:D012834), Lipids (MESH:D008055), polysaccharides (MESH:D011134), PNIPAAm (MESH:C052970), curcumin (MESH:D003474), MEMC (-), Polymer (MESH:D011108), oxygen (MESH:D010100)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Malassezia (genus) [taxon 55193], Homo sapiens (human, species) [taxon 9606], Panax ginseng (Asiatic ginseng, species) [taxon 4054], Zingiber officinale (ginger, species) [taxon 94328], Cutibacterium acnes (species) [taxon 1747], Mus musculus (house mouse, species) [taxon 10090], Catharanthus roseus (chatas, species) [taxon 4058], Rosa x damascena (damask rose, species) [taxon 3765]

## Full text

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## References

159 references — full list in the complete paper: https://tomesphere.com/paper/PMC13007457/full.md

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Source: https://tomesphere.com/paper/PMC13007457