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

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dc.contributor.authorAraújo-Silva, Henriquepor
dc.contributor.authorTeixeira, Patricia Vpor
dc.contributor.authorGomes, Andreia Cpor
dc.contributor.authorLúcio, M.por
dc.contributor.authorLopes, Carla Mpor
dc.date.accessioned2024-04-22T10:44:29Z-
dc.date.issued2023-
dc.identifier.issn0304-419X-
dc.identifier.urihttps://hdl.handle.net/1822/91170-
dc.description.abstractCancer 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.por
dc.description.sponsorshipThis work was supported by the Portuguese Foundation for Science and Technology (FCT) in the framework of the Strategic Funding UIDB/04650/2020 and UIDB/04050/2020 (CF-UM-UP and CBMA); UIDP/04378/2020 and UIDB/04378/2020 of the Research Unit on Applied Molecular Biosciences—UCIBIO and the project LA/P/0140/2020 of the Associate Laboratory Institute for Health and Bioeconomy—i4HB.por
dc.language.isoengpor
dc.publisherElsevier 1por
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04650%2F2020/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04050%2F2020/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F04378%2F2020/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04378%2F2020/PTpor
dc.rightsrestrictedAccesspor
dc.subjectHumanspor
dc.subjectDrug Delivery Systemspor
dc.subjectNeoplasmspor
dc.subjectLiquid Crystalspor
dc.subjectCancerpor
dc.subjectConventional therapiespor
dc.subjectCubosomespor
dc.subjectHexosomespor
dc.subjectLyotropic liquid crystalline (LLC) mesophasespor
dc.subjectSpongosomespor
dc.titleLyotropic liquid crystalline 2D and 3D mesophases: Advanced materials for multifunctional anticancer nanosystemspor
dc.typearticlepor
dc.peerreviewedyespor
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0304419X23001609por
oaire.citationIssue6por
oaire.citationVolume1878por
dc.identifier.eissn1879-2561-
dc.identifier.doi10.1016/j.bbcan.2023.189011por
dc.date.embargo10000-01-01-
dc.identifier.pmid37923232por
dc.subject.fosCiências Naturais::Outras Ciências Naturaispor
sdum.journalBiochimica et Biophysica Acta (BBA). Reviews on Cancerpor
oaire.versionCVoRpor
dc.subject.odsSaúde de qualidadepor
Aparece nas coleções:CBMA - Artigos/Papers

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