This research explores the impact of metal-based nanoparticles on inflammation and oxidative stress in psoriasis, suggesting they may enhance treatment effectiveness.
Psoriasis is a chronic, immune-mediated inflammatory skin disorder characterized by excessive keratinocyte proliferation and the formation of erythematous, scaly plaques. Despite the availability of conventional therapies such as corticosteroids, vitamin D analogs, and systemic immunomodulators, their limited efficacy, adverse effects, and poor patient adherence highlight the need for innovative treatment approaches. Recent advances in nanotechnology, particularly the development of metal-based nanoparticles (MNPs), have opened new avenues for targeted and efficient psoriasis management. MNPs-including gold (AuNPs), silver (AgNPs), zinc oxide (ZnONPs), and titanium dioxide (TiO 2 NPs)-possess unique physicochemical features such as high surface-to-volume ratio and localized surface plasmon resonance (SPR), which enhance drug solubility, stability, and site-specific delivery. These nanoparticles can effectively penetrate psoriatic lesions, attenuate inflammation, regulate immune mediators, and reduce oxidative stress while minimizing systemic exposure. Furthermore, MNPs exhibit inherent anti-inflammatory, antioxidant, and antimicrobial activities, making them suitable candidates for topical formulations such as creams, gels, and nano-lotions. Although promising preclinical findings support their therapeutic potential, comprehensive clinical studies are still required to validate their safety, pharmacokinetics, and long-term outcomes. Overall, metal-based nanocarriers represent a transformative strategy for improving therapeutic precision and patient compliance in psoriasis management.
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Maheshwari et al. (2025) studied this question.
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