Nanotechnology-based drug formulation and delivery systems for skin medical aesthetic dermatology: mechanisms, applications, and safety
Wang L., Yu D.
Narrative Review on Skin Aging, published in Front Pharmacol (2026) — 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
- Front Pharmacol (2026)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 42064808
- PMCID
- PMC13125078
- DOI
- 10.3389/fphar.2026.1804123
Abstract (original English)
Medical aesthetic dermatology is expanding rapidly in response to increasing demand for minimally invasive interventions and advanced topical therapies. The clinical performance of conventional dermatological formulations is frequently limited by inadequate skin penetration, poor stability of active ingredients, rapid degradation, and dose-related adverse effects. Nanotechnology-based drug formulation and delivery systems offer a translational solution to these challenges by enabling targeted, controlled, and sustained delivery of bioactive compounds to specific skin layers and appendages. Nanoscale carriers-including lipid-based systems, polymeric nanoparticles, nanoemulsions, and inorganic or hybrid nanomaterials-enhance dermal and follicular deposition, improve physicochemical stability, and modulate release kinetics of therapeutic and cosmeceutical agents. These mechanisms have facilitated improved outcomes across key aesthetic indications, including skin rejuvenation, pigmentary disorders, acne, hair restoration, and injectable aesthetic interventions. Emerging clinical and preclinical evidence suggests improved local efficacy and potentially reduced irritation and systemic exposure compared with conventional formulations, although further well-controlled clinical studies are required to confirm these benefits. Safety, toxicological behavior, and regulatory considerations
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.
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