Molecules (Apr 2020)

Co-Loaded Curcumin and Methotrexate Nanocapsules Enhance Cytotoxicity against Non-Small-Cell Lung Cancer Cells

  • Loanda Aparecida Cabral Rudnik,
  • Paulo Vitor Farago,
  • Jane Manfron Budel,
  • Amanda Lyra,
  • Fernanda Malaquias Barboza,
  • Traudi Klein,
  • Carla Cristine Kanunfre,
  • Jessica Mendes Nadal,
  • Matheus Coelho Bandéca,
  • Vijayasankar Raman,
  • Andressa Novatski,
  • Alessandro Dourado Loguércio,
  • Sandra Maria Warumby Zanin

DOI
https://doi.org/10.3390/molecules25081913
Journal volume & issue
Vol. 25, no. 8
p. 1913

Abstract

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Background: As part of the efforts to find natural alternatives for cancer treatment and to overcome the barriers of cellular resistance to chemotherapeutic agents, polymeric nanocapsules containing curcumin and/or methotrexate were prepared by an interfacial deposition of preformed polymer method. Methods: Physicochemical properties, drug release experiments and in vitro cytotoxicity of these nanocapsules were performed against the Calu-3 lung cancer cell line. Results: The colloidal suspensions of nanocapsules showed suitable size (287 to 325 nm), negative charge (−33 to −41 mV) and high encapsulation efficiency (82.4 to 99.4%). Spherical particles at nanoscale dimensions were observed by scanning electron microscopy. X-ray diffraction analysis indicated that nanocapsules exhibited a non-crystalline pattern with a remarkable decrease of crystalline peaks of the raw materials. Fourier-transform infrared spectra demonstrated no chemical bond between the drug(s) and polymers. Drug release experiments evidenced a controlled release pattern with no burst effect for nanocapsules containing curcumin and/or methotrexate. The nanoformulation containing curcumin and methotrexate (NCUR/MTX-2) statistically decreased the cell viability of Calu-3. The fluorescence and morphological analyses presented a predominance of early apoptosis and late apoptosis as the main death mechanisms for Calu-3. Conclusions: Curcumin and methotrexate co-loaded nanocapsules can be further used as a novel therapeutic strategy for treating non-small-cell lung cancer.

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