| Literature DB >> 29936382 |
Xin Ji1, Qiao Tang1, Peng Pang2, Jianping Wu3, Thomas Brett Kirk3, Jiake Xu4, Dong Ma5, Wei Xue6.
Abstract
Antitumor efficacy of ursolic acid (UA) is seriously limited due to its low hydrophilicity and needy bioavailability. To overcome these obstacles, chemosensitive polyspermine (CPSP) conjugated with UA and folic acid (FA) as a novel targeted prodrug was designed and successfully synthesized in this investigation. This prodrug not only showed high aqueous solubility, GSH-triggered degradation and good biocompatibility, but also exhibited better inhibition effect on the tumor cells proliferation in comparison with free UA. FA-CPSP-UA could down-regulate the generation of GSH and manifest excellent ability in enhancing antitumor efficacy. In addition, FA-CPSP-UA could inhibit the expression of MMP-9, which led to restricting MCF-7 cells migration. Taken together, the results indicated that FA-CPSP-UA, as a carrier, can efficiently deliver UA to folate receptor positive cancer cells and improve tumor therapy of UA by Chemosensitive effect.Entities:
Keywords: Cancer therapy; Chemosensitivity; Polymeric prodrug; Targeted delivery; Ursolic acid
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Year: 2018 PMID: 29936382 DOI: 10.1016/j.colsurfb.2018.06.029
Source DB: PubMed Journal: Colloids Surf B Biointerfaces ISSN: 0927-7765 Impact factor: 5.268