Electrospun Polyvinyl Alcohol/Polyethylene Oxide Loaded With Cisplatin as a Potential Candidate for Anticancer and

Mohamed Gaber1, El-Refaie Kenawy1, Hamed A Abosharaf2

  • 1Chemistry Department, Faculty of Science, Tanta University, Tanta, Egypt.

Chemistry & Biodiversity
|January 18, 2026
PubMed

Insights

This study developed a cisplatin-loaded nanofiber drug delivery system (PVA-PEO-CIS) that effectively inhibits cervical cancer cells (HeLa) and exhibits potent antibacterial properties. The novel nanofiber formulation shows reduced toxicity to normal cells compared to free cisplatin.

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Drug Delivery Systems

Background:

  • Developing novel drug delivery systems is crucial for enhancing cancer therapy and reducing side effects.
  • Cisplatin is a widely used chemotherapy drug, but its efficacy can be limited by toxicity and resistance.
  • Nanofiber-based drug delivery offers potential for controlled release and improved therapeutic outcomes.

Purpose of the Study:

  • To fabricate and characterize cisplatin-loaded polyvinyl alcohol/polyethylene oxide nanofibers (PVA-PEO-CIS).
  • To evaluate the anticancer efficacy of PVA-PEO-CIS against cervical cancer cells (HeLa).
  • To assess the antibacterial activity and cytotoxicity of the developed nanofiber system.

Main Methods:

  • Electrospinning was employed to synthesize PVA-PEO-CIS nanofibers.
  • Characterization of the nanofiber morphology and drug loading was performed.
  • In vitro anticancer assays using HeLa and normal WI-38 cells were conducted.
  • Antibacterial activity was tested against various bacterial strains.
  • In vitro drug release studies were performed.

Main Results:

  • PVA-PEO-CIS nanofibers demonstrated significant inhibition of HeLa cell growth with a lower IC50 (19.82 µg/mL) compared to free cisplatin (26.31 µg/mL).
  • The nanofiber formulation exhibited reduced toxicity towards normal WI-38 cells compared to free cisplatin.
  • Drug release studies showed approximately 50% cisplatin release within 8 hours.
  • PVA-PEO-CIS nanofibers displayed potent bactericidal effects against Escherichia coli, Klebsiella pneumoniae, and Staphylococcus aureus.

Conclusions:

  • PVA-PEO-CIS nanofibers represent a promising drug delivery system for enhanced anticancer therapy.
  • The developed system shows potential for reducing cisplatin-induced toxicity.
  • The potent antibacterial activity suggests dual applications in tumor therapy and infection control.
  • PVA-PEO-CIS holds potential as a candidate medication for various biological applications.