Abstract
Annonaceous acetogenins (ACGs) are one of the most active constituents isolated from Annona species with potent antitumor activity. However, the poor solubility and severe side effect greatly limit their use in clinic. In this study, folic acid (FA) modified annonaceous acetogenins nanosuspensions (FA-PEG-ACGs-NSps) had been successfully prepared using DSPE-PEG-FA and soybean lecithin (SPC) as stabilizers. The resultant FA-PEG-ACGs-NSps had a mean particle size of 119.7 nm, a zeta potential of –23.0 mV and a high drug payload of 49.68%. The obtained ACGs-NSps had a good stability in various physiological media, and showed sustained drug release. Compared to common ACGs nanoparticles (PEG-ACGs-NSps), FA-PEG-ACGs-NSps showed significantly enhanced in vitro cytotoxicity against folate receptor-positive HeLa cell lines (IC50, 0.483 lg/mL vs. 0.915 lg/mL, p
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Li, H., Li, Y., Ao, H., Bi, D., Han, M., Guo, Y., & Wang, X. (2018). Folate-targeting annonaceous acetogenins nanosuspensions: Significantly enhanced antitumor efficacy in hela tumor-bearing mice. Drug Delivery, 25(1), 880–887. https://doi.org/10.1080/10717544.2018.1455761
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