AI Article Synopsis

  • Multifunctional nanocarriers, specifically PLGA nanospheres with encapsulated CuO-NPs, hold promise for enhancing cancer treatment through antitumor activity and improved imaging capabilities.
  • In vitro studies show that this delivery system enables controlled release of CuO-NPs, especially when stimulated by laser irradiation, facilitating localized treatment options.
  • The research demonstrates that the combination of photothermal therapy with laser-triggered drug release using these nanocarriers can effectively target and treat head and neck cancer cells.

Article Abstract

Multifunctional nanocarriers have attracted considerable interest in improving cancer treatment outcomes. Poly(lactide-co-glycolide) (PLGA) nanospheres encapsulating copper oxide nanoparticles (CuO-NPs) are characterized by antitumor activity and exhibit dual-modal contrast-enhancing capabilities. An in vitro evaluation demonstrates that this delivery system allows controlled and sustained release of CuO-NPs. To achieve localized release on demand, an external stimulation by laser irradiation is suggested. Furthermore, to enable simultaneous complementary photothermal therapy, polydopamine (PDA) coating for augmented laser absorption is proposed. To this aim, two formulations of CuO-NPs loaded nanospheres are prepared from PLGA polymers RG-504 H (H-PLGA) and RG-502 H (L-PLGA) as scaffolds for surface modification through in situ polymerization of dopamine and then PEGylation. The obtained CuO-NPs-based multifunctional nanocarriers are characterized, and photothermal effects are examined as a function of wavelength and time. The results show that 808 nm laser irradiation of the coated nanospheres yields maximal temperature elevation (T = 41°C) and stimulates copper release at a much faster rate compared to non-irradiated formulations. Laser-triggered CuO-NP release is mainly depended on the PLGA core, resulting in faster release with L-PLGA, which also yielded potent anti-tumor efficacy in head and neck cancer cell line (Cal-33). In conclusion, the suggested multifunctional nanoplatform offers the integrated benefits of diagnostic imaging and laser-induced drug release combined with thermal therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971204PMC
http://dx.doi.org/10.1080/14686996.2021.1883406DOI Listing

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