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Multifunctional lipid nanocarriers: advancing topical skin cancer treatment.

Created on 23 Aug 2026

Authors

Lívia Vieira Depieri, Milena Finazzi Morais, Lorena Amorim Tiritan, Lara Marques Amaral, Letícia Maria da Silva Fernandes, Maria Vitória Lopes Badra Bentley

Published in

Expert opinion on drug delivery. Aug 22, 2026. Epub Aug 22, 2026.

Abstract

Skin cancer is among the most prevalent cancers worldwide and represents a substantial clinical and economic burden. Although topical therapy offers localized treatment and reduced systemic toxicity, its effectiveness is often limited by poor skin penetration, inadequate drug retention, and the complexity of the tumor microenvironment. These limitations have driven the development of multifunctional lipid nanocarriers that integrate therapeutic and delivery strategies within a single platform, offering opportunities to simultaneously address biological barriers and therapeutic targets and improve topical skin cancer treatment.
This review discusses advances in multifunctional lipid nanocarriers for topical skin cancer treatment, focusing on surface functionalization, stimulus-responsive systems, combination therapies, theranostic platforms, and physical delivery-assisted approaches. PubMed, Scopus, and Web of Science were searched through July 2026 without an initial date restriction. The biological rationale and potential of these strategies to improve drug delivery, tumor selectivity, and therapeutic efficacy are discussed.
Multifunctional lipid nanocarriers offer a versatile platform for addressing limitations of conventional skin cancer therapies. Integrating complementary functionalities can enhance therapeutic performance by targeting multiple biological and delivery-related barriers. Future progress will rely on identifying combinations that provide meaningful therapeutic advantages while remaining compatible with manufacturing, regulatory, and clinical requirements.

PMID:
42632072
Bibliographic data and abstract were imported from PubMed on 23 Aug 2026.

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