Skin-on-chip: Quo vadis?
Ghiță-Răileanu M., Tihăuan BM., Lixandru-Petre IO., Gheorghiu GL., Pircalabioru GG., Cioca G.
Narrative Review on Face & Skin, Hip, published in APL Bioeng (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
- Narrative Review
- Journal
- APL Bioeng (2025)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 41127827
- PMCID
- PMC12539882
- DOI
- 10.1063/5.0268706
Abstract (original English)
There is a need for reconstructing the structural and functional complexity of human tissues such as skin to replace the animal models and provide accurate knowledge while solving ethical challenges in human medicine. Lately, microfluidics and tissue engineering have significantly advanced the development of 3D cell cultures and skin-on-chip (SoC), thus offering a cost-effective alternative to the generally used preclinical drug screening, toxicology applications, and cosmetic testing models. The current work presents a critical view on the SoC, from the fundamental concepts to the fabrication, applications, and commercialization. It comprehensively discusses the challenges faced by the 3D skin models and the perspectives of microphysiological skin platforms for preclinical pharmaceuticals and cosmeceuticals screening and disease research. It also highlights the technical and ethical requirements for successful SoC as physiological and pathological models applicable to personalized medicine. The SoC clinical and commercial translation depends on developing convergent biomanufacturing strategies and infrastructure focused on applications such as personalized skin disease models, skin grafts, and drug or cosmetics screening platforms.
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is a narrative review: it collects no new patient data and does not systematically appraise evidence quality.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
How we grade evidenceBrowse all related research
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