Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/91170

TítuloLyotropic liquid crystalline 2D and 3D mesophases: Advanced materials for multifunctional anticancer nanosystems
Autor(es)Araújo-Silva, Henrique
Teixeira, Patricia V
Gomes, Andreia C
Lúcio, M.
Lopes, Carla M
Palavras-chaveHumans
Drug Delivery Systems
Neoplasms
Liquid Crystals
Cancer
Conventional therapies
Cubosomes
Hexosomes
Lyotropic liquid crystalline (LLC) mesophases
Spongosomes
Data2023
EditoraElsevier 1
RevistaBiochimica et Biophysica Acta (BBA). Reviews on Cancer
Resumo(s)Cancer remains a leading cause of mortality. Despite significant breakthroughs in conventional therapies, treatment is still far from ideal due to high toxicity in normal tissues and therapeutic inefficiency caused by short drug lifetime in the body and resistance mechanisms. Current research moves towards the development of multifunctional nanosystems for delivery of chemotherapeutic drugs, bioactives and/or radionuclides that can be combined with other therapeutic modalities, like gene therapy, or imaging to use in therapeutic screening and diagnosis. The preparation and characterization of Lyotropic Liquid Crystalline (LLC) mesophases self-assembled as 2D and 3D structures are addressed, with an emphasis on the unique properties of these nanoassemblies. A comprehensive review of LLC nanoassemblies is also presented, highlighting the most recent advances and their outstanding advantages as drug delivery systems, including tailoring strategies that can be used to overcome cancer challenges. Therapeutic agents loaded in LLC nanoassemblies offer qualitative and quantitative enhancements that are superior to conventional chemotherapy, particularly in terms of preferential accumulation at tumor sites and promoting enhanced cancer cell uptake, lowering tumor volume and weight, improving survival rates, and increasing the cytotoxicity of their loaded therapeutic agents. In terms of quantitative anticancer efficacy, loaded LLC nanoassemblies reduced the IC50 values from 1.4-fold against lung cancer cells to 125-fold against ovarian cancer cells.
TipoArtigo
URIhttps://hdl.handle.net/1822/91170
DOI10.1016/j.bbcan.2023.189011
ISSN0304-419X
e-ISSN1879-2561
Versão da editorahttps://www.sciencedirect.com/science/article/pii/S0304419X23001609
Arbitragem científicayes
AcessoAcesso restrito UMinho
Aparece nas coleções:CBMA - Artigos/Papers

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