A Hybrid Nanosystem for Prostate Cancer Therapy: Codelivery of Enzalutamide and Curcumin via Selenium-Embedded

Zahra Tavakoli1, Khosro Khajeh2, Bijan Ranjbar1,3

  • 1Department of Nanobiotechnology, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.

Chemistryopen
|March 10, 2026
PubMed

Insights

This study developed a dual-nanoparticle system combining selenium nanoparticles and enzalutamide within mesoporous silica nanoparticles for advanced prostate cancer therapy. The system demonstrated enhanced anticancer efficacy and targeted drug delivery, offering a promising new treatment strategy.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Oncology

Background:

  • Prostate cancer is a leading global cause of cancer deaths, necessitating improved therapeutic strategies.
  • Effective drug delivery systems are crucial for enhancing treatment efficacy and minimizing side effects.
  • Selenium nanoparticles and enzalutamide possess known anticancer properties relevant to prostate cancer treatment.

Purpose of the Study:

  • To co-encapsulate selenium nanoparticles and enzalutamide within mesoporous silica nanoparticles (MSNPs) for targeted prostate cancer therapy.
  • To evaluate the physicochemical properties and drug loading/release characteristics of the designed nanosystem.
  • To assess the in vitro anticancer efficacy and apoptotic effects of the dual-drug delivery system.

Main Methods:

  • MSNPs were synthesized using solvent extraction, characterized for surface area, pore volume, and pore size.
  • Enzalutamide was loaded into selenium-embedded MSNPs, and curcumin was encapsulated in chitosan nanoparticles.
  • Drug loading efficiency, pH-responsive drug release, and in vitro cytotoxicity (MTT assay) were evaluated.

Main Results:

  • Solvent-extracted MSNPs exhibited superior properties (surface area: 1017.4 m²/g, pore volume: 0.2531 cm³/g, pore size: ≈10 nm) compared to calcined MSNPs (pore size: ≈3 nm).
  • The enzalutamide-loaded MSNPs achieved a drug loading efficiency of 76.3 ± 0.5%, and chitosan nanoparticles showed high curcumin encapsulation efficiency (83.2 ± 0.7%).
  • The combined nanosystem demonstrated pH-responsive, gradual drug release and significantly enhanced time- and concentration-dependent anticancer effects, inducing apoptosis.

Conclusions:

  • The designed dual-nanoparticle system, co-delivering selenium and enzalutamide, shows significant potential for targeted prostate cancer therapy.
  • Curcumin plays a crucial role in augmenting the anticancer efficacy and apoptosis-inducing capabilities of the nanosystem.
  • This advanced drug delivery approach offers a promising strategy for overcoming limitations of current prostate cancer treatments.