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Updated: May 28, 2026

Anticancer Efficacy of Photodynamic Therapy with Lung Cancer-Targeted Nanoparticles
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Decreased lung carcinoma cell functions on select polymer nanometer surface features.

Lijuan Zhang1, Thomas J Webster

  • 1Department of Chemistry, School of Engineering, Brown University, Providence, Rhode Island 02912, USA.

Journal of Biomedical Materials Research. Part A
|October 12, 2011
PubMed
Summary

Biomaterial nanotopography influences lung cancer cell behavior. Poly-lactic-co-glycolic (PLGA) films with specific nanoscale features modulated cell adhesion, proliferation, and vascular endothelial growth factor (VEGF) synthesis, offering insights for regenerative medicine.

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Area of Science:

  • Biomaterials Science
  • Cancer Biology
  • Regenerative Medicine

Background:

  • Biomaterial nanotopographies can significantly influence various cell functions.
  • Understanding these interactions is crucial for developing advanced biomaterials.

Purpose of the Study:

  • To investigate the effect of poly-lactic-co-glycolic (PLGA) nanotopographies on lung epithelial carcinoma cell functions.
  • To analyze cell adhesion, proliferation, apoptosis, and vascular endothelial growth factor (VEGF) synthesis on PLGA films with defined surface features.

Main Methods:

  • Fabrication of PLGA films with nano-smooth, 23 nm, 300 nm, and 400 nm hemispherical nanotopographies using cast-molding and solvent evaporation.
  • Characterization of surface chemistry and topography using atomic force microscopy, electron spectroscopy for chemical analysis, and water contact angle measurements.

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  • Systematic evaluation of lung epithelial carcinoma cell adhesion, proliferation, apoptosis, and VEGF synthesis on the fabricated PLGA films.
  • Main Results:

    • Reduced lung epithelial carcinoma cell adhesion and proliferation were observed on nano-smooth and 400 nm PLGA surfaces.
    • Significantly decreased VEGF synthesis was noted on the 23 nm nanotopography compared to nano-smooth PLGA films.
    • Cell morphology varied across different nanotopographies, indicating topographical influence on cell behavior.

    Conclusions:

    • PLGA nanotopography plays a critical role in modulating lung carcinoma cell functions, including adhesion, proliferation, and VEGF secretion.
    • These findings provide foundational insights for designing PLGA-based biomaterials for applications in regenerative medicine and cancer therapy.
    • Tailoring nanotopography offers a potential strategy to control cancer cell behavior on biomaterials.