Evidence mapPaperPMID 41599391Full record

ReviewMolecules (Basel, Switzerland)2026

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

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

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Ellen Paim de Abreu PauloFaculty of Medicine, University of Sao Paulo (FMUSP), Sao Paulo 05403-000, Brazil.
Laertty Garcia de Sousa CabralFaculty of Medicine, University of Sao Paulo (FMUSP), Sao Paulo 05403-000, Brazil.ORCID 0000-0002-4586-2945
Jean-Luc PoyetINSERM UMRS1342-CNRS EMR8000, Institut de Recherche Saint-Louis, Hôpital Saint-Louis, 75010 Paris, France.ORCID 0000-0002-3747-255X
Durvanei Augusto MariaFaculty of Medicine, University of Sao Paulo (FMUSP), Sao Paulo 05403-000, Brazil.

Funding

CAPES-Foundation Coordination for the Improvement of Higher Education Personnel 88887.630761/2021-00
6 · The paper itself

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.

Indexed as

Antineoplastic AgentsLiposomesMelanomaNanotechnologySkin NeoplasmsAnimalsDrug Delivery SystemsHumansNanomedicineAntineoplastic AgentsLiposomesliposomal platformsmelanomananotechnologytargeted therapy

Identifiers

PMID41599391
PMCPMC12844216

What Socratic holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.