Efficacy of ginsenoside Rg3 nanoparticles against Ehrlich solid tumor growth in mice

Mona A El-Banna1, Omnia M Hendawy2, Aziza A El-Nekeety3

  • 1Medical Biochemistry Department, National Research Centre, Dokki, Cairo, Egypt.

Insights

New ginsenoside Rg3 nanoparticles (Rg3-NPs) show enhanced antitumor effects against Ehrlich solid tumors (EST) in mice. These Rg3-NPs, formulated with whey protein isolates, maltodextrin, and gum Arabic, offer a promising therapeutic strategy for solid tumors.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Cancer Research

Background:

  • Solid tumors present significant clinical challenges due to poor surgical resectability and resistance to conventional therapies like radiation and chemotherapy.
  • Ginsenoside Rg3 is a known compound with potential antitumor properties, but its efficacy can be limited by formulation and delivery.
  • Developing novel drug delivery systems is crucial for improving the therapeutic outcomes of existing compounds against challenging cancers.

Purpose of the Study:

  • To fabricate ginsenoside Rg3 nanoparticles (Rg3-NPs) using whey protein isolates (WPI), maltodextrin (MD), and gum Arabic (GA).
  • To evaluate the in vivo antitumor efficacy of Rg3-NPs against Ehrlich solid tumors (EST) in a mouse model.
  • To compare the therapeutic effects of Rg3-NPs with native Rg3 and assess the dose-dependent response.

Main Methods:

  • Rg3-NPs were synthesized using WPI, MD, and GA, characterized for particle size and zeta potential.
  • Ehrlich solid tumors were induced in mice by injecting Ehrlich ascites cells.
  • Mice were treated with native Rg3 or varying doses of Rg3-NPs, and tumor growth, biochemical markers (AFP, Casp3, TNF-α, MMP-9, VEGF, MDA, SOD, GPx), and DNA damage were assessed.

Main Results:

  • Synthesized Rg3-NPs exhibited a spherical shape with an average particle size of 20 nm and a zeta potential of -5.58 mV.
  • Treatment with Rg3-NPs significantly reduced tumor weight and size compared to native Rg3.
  • Rg3-NPs demonstrated a dose-dependent improvement in biochemical parameters and reduced DNA damage, indicating enhanced antitumor activity and protective effects against EST.

Conclusions:

  • Fabrication of Rg3-NPs using WPI, MD, and GA significantly enhances the antitumor efficacy against Ehrlich solid tumors.
  • Rg3-NPs show superior therapeutic potential compared to native Rg3, likely due to improved delivery and possibly synergistic effects with the formulation components.
  • These findings suggest that Rg3-NPs represent a promising nanomedicine approach for managing solid tumors, warranting further investigation for clinical applications.

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