# Fermented Plant Extract-Loaded Collagen Scaffolds: Bioactive Hydrogels for Enhanced Wound Repair and Immune Modulation

**Authors:** Lesly Katleya Usme-Duque, Miguel A. Medina-Morales, María I. León-Campos, Marisol Cruz-Requena, Leopoldo J. Ríos-González, Rebeca Betancourt-Galindo, Jesús A. Claudio-Rizo

PMC · DOI: 10.3390/gels12020129 · Gels · 2026-02-01

## TL;DR

Collagen scaffolds loaded with fermented plant extracts improve wound healing and reduce inflammation by releasing bioactive compounds over time.

## Contribution

A novel collagen hydrogel system is developed for sustained delivery of fermented Flourensia cernua extract to enhance wound repair and immune modulation.

## Key findings

- Hydrogels with 14 wt.% extract showed sustained release and improved wound closure in vitro.
- Extract-loaded hydrogels reduced TNF-α secretion, indicating anti-inflammatory effects.
- Higher extract concentrations increased hydration and crosslinking density, affecting mechanical properties.

## Abstract

Fermented extracts of Flourensia cernua (F. cernua), enriched with bioactive polyphenols such as caffeic acid, apigenin, myricetin, and quercetin, exhibit strong potential to promote tissue regeneration. However, controlled delivery systems are required to enhance their bioavailability and therapeutic efficacy. In this study, F. cernua extracts (7–21 wt.%) were encapsulated in collagen hydrogels to develop bioactive matrices with sustained release properties. The hydrogel with 14 wt.% enabled sustained extract release from day 5 under physiological conditions and skin-mimicking pH (4.5). Increasing the extract concentration led to enhanced hydration behavior (>1400%) and crosslinking density (>45%), contributing to faster gelation. SEM analysis revealed fibrillar morphologies with amorphous globular domains whose prevalence increased with extract content and conferred improved thermal stability. Mechanical analysis indicated a decrease in matrix stiffness due to repulsive interactions between the extract components and the polymer network. Biodegradation studies showed slow hydrolytic and enzymatic degradation at skin pH in hydrogels containing 7 wt.% extract. All hydrogels demonstrated hemocompatibility, with no erythrocyte lysis. Moreover, hydrogels with 14 wt.% extract significantly enhanced the metabolic activity and proliferation of monocytes and fibroblasts, while 7 wt.% extract reduced TNF-α secretion, indicating anti-inflammatory potential. In vitro wound closure assays revealed 90% contraction within 10 days in fibroblast cultures exposed to 14 wt.% extract-loaded hydrogels. These results support the use of F. cernua-enriched collagen hydrogels as multifunctional scaffolds for wound healing and tissue regeneration.

## Linked entities

- **Chemicals:** caffeic acid (PubChem CID 689043), apigenin (PubChem CID 5280443), myricetin (PubChem CID 5281672), quercetin (PubChem CID 5280343)
- **Species:** Flourensia cernua (taxon 2604028)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}
- **Diseases:** respiratory diseases (MESH:D012140), fatigue (MESH:D005221), inflammation (MESH:D007249), injury to (MESH:D014947), cytotoxic (MESH:D064420), hemolytic damage (MESH:D000092582), Hemolysis (MESH:D006461), swelling (MESH:D004487), chronic (MESH:D002908), fungal (MESH:D009181), infected (MESH:D007239), cancer (MESH:D009369)
- **Chemicals:** myricetin (MESH:C040015), phenolic acids (MESH:C017616), ABTS (MESH:C002502), chitosan (MESH:D048271), formazan (MESH:D005562), terpenes (MESH:D013729), polypropylene (MESH:D011126), Gallic acid (MESH:D005707), apigenin (MESH:D047310), FDA (MESH:C018506), penicillin (MESH:D010406), oxygen (MESH:D010100), aluminum (MESH:D000535), Water (MESH:D014867), Polyphenol (MESH:D059808), hydrogen peroxide (MESH:D006861), silicon (MESH:D012825), ISO 10993-5 (-), AlCl3 (MESH:D000077410), F. (MESH:D005461), NaNO3 (MESH:C031618), trypan blue (MESH:D014343), magnesium (MESH:D008274), phenols (MESH:D010636), Flavonoid (MESH:D005419), 2,2-diphenyl-1-picrylhydrazyl (MESH:C004931), ethanol (MESH:D000431), Rhodamine B (MESH:C029773), polymer (MESH:D011108), ROS (MESH:D017382), calcium (MESH:D002118), streptomycin (MESH:D013307), flavonols (MESH:D044948), hydroxyl (MESH:D017665), ninhydrin (MESH:D009555), carbon (MESH:D002244), fluorescein (MESH:D019793), Tween 80 (MESH:D011136), flavones (MESH:D047309), HDI (MESH:C015262), mineral (MESH:D008903), polysaccharides (MESH:D011134), KCl (MESH:D011189), Nitrogen (MESH:D009584), polyurethane (MESH:D011140), H (MESH:D006859), hydroxybenzoic acids (MESH:D062385), MgSO4 (MESH:D008278), MTT (MESH:C070243), quercetin (MESH:D011794), isopropanol (MESH:D019840), caffeic acid (MESH:C040048), alcohols (MESH:D000438), urea (MESH:D014508)
- **Species:** Agave lechuguilla (species) [taxon 39513], Aspergillus niger (species) [taxon 5061], Homo sapiens (human, species) [taxon 9606], Flourensia cernua (species) [taxon 2604028]
- **Cell lines:** E50 — Rattus norvegicus (Rat), Transformed cell line (CVCL_C1LD), H-E100 — Homo sapiens (Human), Ovarian endometrioid adenocarcinoma, Cancer cell line (CVCL_B7S7), H-E150 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_B5UT), H — Rattus norvegicus (Rat), Adenocarcinoma of the rat prostate, Cancer cell line (CVCL_Y658), H-E50 — Mus musculus (Mouse), Hybridoma (CVCL_VI57)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12941376/full.md

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941376/full.md

## References

101 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941376/full.md

---
Source: https://tomesphere.com/paper/PMC12941376