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dc.contributor.authorVargas Requena, Claudia Lucia
dc.date.accessioned2025-12-08T16:46:13Z
dc.date.available2025-12-08T16:46:13Z
dc.date.issued2025-08-02es_MX
dc.identifier.urihttps://cathi.uacj.mx/20.500.11961/32092
dc.description.abstractLung cancer is the second most common type of cancer and the leading cause of cancer-related deaths worldwide. Some chemotherapeutic agents, such as curcumin and gemcitabine, have low bioavailability due to their hydrophobicity or the need for specialized transporters. Tis limits their cytotoxic potential against tumor cells but can be addressed through nanoencapsulation. Tis study evaluated the efects of nanometric encapsulation of curcumin and gemcitabine in chitosan, a biocompatible polymer, on the A549 lung cancer cell line and B16F10 murine melanoma cells. Te chemical properties of the synthesized nanoparticles were characterized using UV-vis spectroscopy, Fourier transform infrared (FTIR) spectroscopy, and scanning electron mi- croscopy (SEM). Te nanoparticles ranged in size from 180 to 197 nm, with a positive surface charge between 11.8 and 16.3 mV. Cytotoxicity assays were conducted on the A549 and B16F10 cell lines, along with morphological analyses of apoptosis and fow cytometry to assess cell death mechanisms. Compared to the free drugs, the nanometric encapsulation of curcumin and gemcitabine did not always enhance the cytotoxic efects, but it did induce pronounced apoptosis in the lung cancer cells. Tese fndings suggest that this approach could optimize drug delivery, reduce the required doses, and minimize side efects, thereby improving the overall efcacy of lung cancer treatment.es_MX
dc.description.urihttps://pmc.ncbi.nlm.nih.gov/articles/PMC12367379/#:~:text=Compared%20to%20the%20free%20drugs,in%20the%20lung%20cancer%20cells.es_MX
dc.language.isoenes_MX
dc.relation.ispartofProducto de investigación ICBes_MX
dc.relation.ispartofInstituto de Ciencias Biomédicases_MX
dc.subject.otherinfo:eu-repo/classification/cti/3es_MX
dc.titleEncapsulation of Curcumin and Gemcitabine: Cytotoxic Effect and Mechanisms of Death in Lung Canceres_MX
dc.typeArtículoes_MX
dcterms.thumbnailhttp://ri.uacj.mx/vufind/thumbnails/rupiicb.pnges_MX
dcrupi.institutoInstituto de Ciencias Biomédicases_MX
dcrupi.cosechableSies_MX
dcrupi.volumen2025es_MX
dcrupi.nopagina16es_MX
dc.identifier.doihttps://doi.org/10.1155/adpp/8816364es_MX
dc.journal.titleAdvances in Pharmacological and Pharmaceutical Scienceses_MX
dc.contributor.authorexternoZapata Benavides, Pablo
dc.contributor.coauthorexternoRodríguez Padilla, María Cristina
dcrupi.colaboracionextUniversidad Autónoma de Nuevo León, Méxicoes_MX
dcrupi.pronacesSaludes_MX


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