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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.
Abstract:
Solid tumors are fairly common and face many clinical difficulties since they are hardly surgically resectable and broadly do not respond to radiation and chemotherapy. The current study aimed to fabricate ginsenoside Rg3 nanoparticles (Rg3-NPs) and evaluate their antitumor effect against Ehrlich solid tumors (EST) in mice. Rg3-NPs were fabricated using whey protein isolates (WPI), maltodextrin (MD), and gum Arabic (GA). EST was developed by the injection of mice with Ehrlich ascites cells (2.5 × 106). The mice were divided into a control group, EST group, and the EST groups that were treated orally 2 weeks for with normal Rg3 (3 mg/kg b.w.), Rg3-NPs at a low dose (3 mg/kg b.w.), and Rg3-NPs at a high dose (6 mg/kg b.w.). Serum and solid tumors were collected for different assays. The results revealed that synthesized Rg3-NPs showed a spherical shape with an average particle size of 20 nm and zeta potential of -5.58 mV. The in vivo study revealed that EST mice showed a significant increase in AFP, Casp3, TNF-α, MMP-9, VEGF, MDA, and DNA damage accompanied by a significant decrease in SOD and GPx. Treatment with Rg3 or Rg3-NPs decreased the tumor weight and size and induced a significant improvement in all the biochemical parameters. Rg3-NPs were more effective than Rg3, and the improvement was dose-dependent. It could be concluded that fabrication of Rg3-NPs enhanced the protective effect against EST development which may be due to the synergistic effect of Rg3 and MD, GA, and WPI.
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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