This is the authors' abstract. We don't add key points for this paper.
The escalating global burden of melanoma and non-melanoma skin malignancies necessitates advanced treatment strategies beyond conventional modalities. Current interventions, including wide local excision and systemic chemotherapy, frequently demonstrate suboptimal therapeutic indices characterized by non-specific cytotoxicity and frequent disease recurrence. Recent advances in nanoscale engineering have yielded multifunctional platforms employing metallic (Au, Ag) and ceramic (ZnO, SiO₂) nanoparticles that address these limitations through: (i) enhanced epidermal permeability and retention, (ii) spatiotemporal control of drug release. Particularly noteworthy are tumor-targeted formulations such as RGD-conjugated TiO₂ nanoparticles and cetuximab-functionalized liposomes, which demonstrate >50% improvement in tumor regression compared to conventional therapies in preclinical models. However, translational implementation confronts substantial barriers, including batch-to-batch variability in nanomanufacturing and undefined long-term biodistribution profiles. Emerging paradigms integrating CRISPR-based gene editing with stimuli-responsive nanocarriers present novel opportunities for personalized oncodermatology. This comprehensive analysis aims to delineate critical pathways for clinical adoption of nanotherapeutic interventions in cutaneous oncology.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Othman Othman (2025) studied this question.
Synapse has enriched 8 closely related papers on similar clinical questions. Consider them for comparative context: