# PVA/Gelatin/Cnidium monnieri Composite Scaffolds for Atopic Dermatitis Skin Tissue Regeneration

**Authors:** Young Ho Seo, Sun Young Park, Sangmin Lee, Myunghoo Kim, Seon Beom Kim, Tae Hwan Oh

PMC · DOI: 10.3390/gels11020143 · 2025-02-18

## TL;DR

A new hydrogel scaffold combining PVA, gelatin, and Cnidium monnieri extract is developed to regenerate skin and reduce inflammation in atopic dermatitis.

## Contribution

A novel composite hydrogel scaffold is developed for atopic dermatitis treatment, combining PVA, gelatin, and Cnidium monnieri extract for tissue regeneration and inflammation suppression.

## Key findings

- The scaffold showed a highly porous structure that supports cell proliferation and controlled release of bioactives.
- Osthole and imperatorin from Cnidium monnieri were sustained in release and contributed to anti-inflammatory effects.
- The scaffold significantly suppressed IL-8 expression in HaCaT cells under inflammatory conditions.

## Abstract

Atopic dermatitis (AD) is a chronic inflammatory skin condition characterized by impaired barrier function and persistent inflammation, necessitating advanced therapeutic solutions. This study presents the development of a novel composite hydrogel scaffold composed of polyvinyl alcohol (PVA), gelatin, and Cnidium monnieri (CM) extract, designed to address the dual challenges of tissue regeneration and inflammation suppression. Fabricated via optimized freeze–thaw crosslinking and lyophilization, the scaffold exhibited a highly porous structure conducive to enhanced cell proliferation and controlled bioactive release. FT-IR analysis confirmed robust intermolecular interactions among PVA, gelatin, and CM bioactives, while SEM imaging revealed a well-developed porous network. The UPLC analysis demonstrated the sustained release of key CM compounds, such as osthole and imperatorin, which contributed to the scaffold’s anti-inflammatory properties. Biological assessments using HaCaT keratinocytes under inflammatory conditions induced by TNF-α and IFN-γ revealed improved cell viability and significant suppression of IL-8 expression, a critical marker in AD-related inflammation. These findings underscore the potential of the PVA/Gel/CM composite hydrogel as an advanced therapeutic platform for inflammatory skin disorders.

## Linked entities

- **Chemicals:** PVA (PubChem CID 11199), osthole (PubChem CID 10228), imperatorin (PubChem CID 10212), IL-8 (PubChem CID 169410440)
- **Diseases:** atopic dermatitis (MONDO:0004980)

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** skin condition (MESH:D012871), inflammatory skin disorders (MESH:D012868), AD (MESH:D003876), inflammation (MESH:D007249)
- **Cell lines:** HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11854940/full.md

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Source: https://tomesphere.com/paper/PMC11854940