Biomimetic silk fibroin/alginate scaffolds incorporating ZnO nanoparticles and Citrus aurantium extract for epidermal differentiation of human adipose-derived stem cells.
Faghih M., Khavarpour M., Masoumi M., Esfahanian M.
Laboratory Study on Face & Skin, published in Tissue Cell (2025) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Laboratory Study
- Journal
- Tissue Cell (2025)
- Country
- Scotland
- Reported sample size
- —
- Source database
- PubMed
- PMID
- 41422574
- DOI
- 10.1016/j.tice.2025.103259
Abstract (original English)
Minerals and phytochemicals show great promise in regenerative medicine applications. This study aimed to develop and evaluate biomimetic silk fibroin/sodium alginate (SF/SA) scaffolds incorporating biosynthesized zinc oxide nanoparticles (ZnO NPs) and Citrus aurantium extract (HE) to enhance epidermal differentiation of human adipose-derived stem cells (h-ASCs). To this end, SF/SA scaffolds prepared at ratios of 1:2, 1:1, and 2:1 were structurally characterized to determine the optimal formulation. The 1:1 SF/SA scaffold demonstrated the most favorable physico-structural features, including high porosity (∼89 %), interconnected pores, and suitable mechanical strength (modulus ≈ 4.2 MPa; elongation ≈ 9 %). In the following, incorporation of ZnO NPs (1 mg/ml) further increased porosity (∼94 %) and surface roughness, improving cell attachment. Subsequent loading of HE (3 wt%) produced a denser but still interconnected matrix (porosity ∼96 %). The combined presence of ZnO NPs and HE enhanced cell adhesion and spreading, consistent with their uniform distribution within the scaffold. Gene expression analysis showed elevated levels of keratin 10 and keratin 14 during early culture (day 7), confirming initiation of epidermal differentiation, followed by a decreasing pattern of values toward day 14. Accordingly, the integration of biosynthesized ZnO NPs and Citrus aurantium extract wi
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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