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Encapsulation within nanoparticles, liposomes, self-emulsifying systems, and conjugation with targeting ligands such as folate and PEG significantly enhance the bioavailability, solubility, and targeted delivery of ginsenosides to tumor sites

Cell viability remained above 95% up to 100 nM but declined progressively at higher concentrations: 87 3% at 150 nM, 76 3.8% at 200 nM, 50 2.6% at 400 nM, and 22 2.6% at 1000 nM