Nanotechnology in Cutaneous Oncology: The Role of Liposomes in Targeted Melanoma Therapy

Melanoma is an aggressive skin cancer that continues to present major therapeutic difficulties. Although targeted drugs and immune checkpoint inhibitors have improved outcomes, resistance and treatment-related toxicity limit long-term benefit. In recent years, nanotechnology has been explored as a way to improve how drugs are delivered and to achieve greater tumor selectivity. Among available nanocarriers, liposomes have attracted particular interest. Built from lipid bilayers, they can carry both hydrophilic and hydrophobic molecules, and they are generally well tolerated. Importantly, their surface can be modified with polymers or targeting ligands to direct the carrier more selectively to melanoma cells. Experimental models show that liposomal drug formulations can increase concentrations in tumor tissue while limiting distribution to healthy organs. They have also been used successfully to combine different types of agents, chemotherapies, immunomodulators, and nucleic acids, within a single delivery system. These findings suggest genuine potential to address several of the shortcomings of conventional treatments. Although translation to the clinic is slowed by challenges such as formulation stability and large-scale production, liposomes represent an important step toward safer and more effective melanoma therapy within the broader field of oncologic nanotechnology.

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Publication Details

Journal
Molecules
Published
2026-01-19
DOI
https://doi.org/10.3390/molecules31020344
Primary Topic
Advancements in Transdermal Drug Delivery
Type
article
Field-Weighted Citation Impact
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article

Nanotechnology in Cutaneous Oncology: The Role of Liposomes in Targeted Melanoma Therapy

Ellen Paim de Abreu Paulo, Laertty Garcia de Sousa Cabral, Durvanei Augusto Maria, Jean-Luc Poyet
Molecules
Advancements in Transdermal Drug Delivery
article

Nanotechnology in Cutaneous Oncology: The Role of Liposomes in Targeted Melanoma Therapy

Ellen Paim de Abreu Paulo, Laertty Garcia de Sousa Cabral, Durvanei Augusto Maria, Jean-Luc Poyet
article en

Abstract

Melanoma is an aggressive skin cancer that continues to present major therapeutic difficulties. Although targeted drugs and immune checkpoint inhibitors have improved outcomes, resistance and treatment-related toxicity limit long-term benefit. In recent years, nanotechnology has been explored as a way to improve how drugs are delivered and to achieve greater tumor selectivity. Among available nanocarriers, liposomes have attracted particular interest. Built from lipid bilayers, they can carry both hydrophilic and hydrophobic molecules, and they are generally well tolerated. Importantly, their surface can be modified with polymers or targeting ligands to direct the carrier more selectively to melanoma cells. Experimental models show that liposomal drug formulations can increase concentrations in tumor tissue while limiting distribution to healthy organs. They have also been used successfully to combine different types of agents, chemotherapies, immunomodulators, and nucleic acids, within a single delivery system. These findings suggest genuine potential to address several of the shortcomings of conventional treatments. Although translation to the clinic is slowed by challenges such as formulation stability and large-scale production, liposomes represent an important step toward safer and more effective melanoma therapy within the broader field of oncologic nanotechnology.

MoleculesVol. 31(2)
Centre National de la Recherche Scientifique (FR), Inserm (FR), Universidade de São Paulo (BR), Centro Universitário das Faculdades Metropolitanas Unidas (BR), Université Paris Cité (FR), Instituto Butantan (BR), Hôpital Saint-Louis (FR)
Good health and well-being
Openalex Percentile: Top 83%
Advancements in Transdermal Drug Delivery
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Nanotechnology in Cutaneous Oncology: The Role of Liposomes in Targeted Melanoma Therapy — Ellen Paim de Abreu Paulo, Laertty Garcia de Sousa Cabral, et al. · Molecules (2026) | TGRS Research Map | TGRS