Magnetically actuated cisplatin-loaded nanoparticle collectives enhance drug penetration for potentiated ovarian cancer chemotherapy

J Colloid Interface Sci. 2025 Jan 15;678(Pt A):108-118. doi: 10.1016/j.jcis.2024.08.160. Epub 2024 Aug 22.

Abstract

Chemotherapy is the main clinical treatment for ovarian cancer, but still faces challenges of low drug targeting efficiency and insufficient drug permeability. Drug-loaded nanoparticle collectives, which are actuated by magnetic field, could be targeted to a designated location and achieve targeted drug delivery. In this work, we report a strategy that utilizes magnetic mesoporous silica nanoparticles loaded with cis-diaminodichloroplatinum (Fe3O4@SiO2-CDDP) for targeted delivery of chemotherapeutic drugs and enhances penetration into deep tumors. The Fe3O4@SiO2-CDDP collectives actively moved to the target tumor site, and this movement was regulated by a magnetic actuation system. Under the action of a torque-force hybrid magnetic field (TFMF), Fe3O4@SiO2-CDDP could further penetrate into the interior of tumors and achieve pH-responsive drug release in the tumor environment. The feasibility of this strategy was verified in three-dimensional cell spheres in vitro and in a tumor-bearing mouse model in vivo. This magnetically actuated nanoparticle collectives enhanced drug penetration strategy provides a new paradigm for targeted drug delivery and potentiated tumor therapy.

Keywords: Drug delivery; Magnetic nanoparticles; Ovarian cancer; Tumor penetration.

MeSH terms

  • Animals
  • Antineoplastic Agents* / chemistry
  • Antineoplastic Agents* / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Cisplatin* / administration & dosage
  • Cisplatin* / chemistry
  • Cisplatin* / pharmacokinetics
  • Cisplatin* / pharmacology
  • Drug Carriers / chemistry
  • Drug Delivery Systems
  • Drug Liberation
  • Drug Screening Assays, Antitumor
  • Female
  • Humans
  • Magnetic Fields
  • Magnetite Nanoparticles / chemistry
  • Mice
  • Mice, Inbred BALB C
  • Nanoparticles / chemistry
  • Ovarian Neoplasms* / drug therapy
  • Ovarian Neoplasms* / pathology
  • Particle Size
  • Silicon Dioxide* / chemistry
  • Surface Properties

Substances

  • Cisplatin
  • Antineoplastic Agents
  • Silicon Dioxide
  • Magnetite Nanoparticles
  • Drug Carriers