Beijing Key Laboratory of Lignocellulosic Chemistry, Engineering Research Center of Forestry Biomass Materials and Bioenergy (Ministry of Education), Beijing Forestry University, Beijing 100083, China
hejing2008@sina.com
收稿:2019-12-18,
修回:2020-2-7,
录用:2020-2-10,
网络首发:2020-04-22,
纸质出版:2020-08
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Wang, Y. S.; Li, G. L.; Zhu, S. B.; Jing, F. C.; Liu, R. D.; Li, S. S.; He, J.; Lei, J. D. A self-assembled nanoparticle platform based on amphiphilic oleanolic acid polyprodrug for cancer therapy. Chinese J. Polym. Sci. 2020, 38, 819–829
Ying-Sa Wang, Gui-Liang Li, Shang-Bin Zhu, et al. A Self-assembled Nanoparticle Platform Based on Amphiphilic Oleanolic Acid Polyprodrug for Cancer Therapy[J]. Chinese Journal of Polymer Science, 2020, 38(8): 819-829.
Wang, Y. S.; Li, G. L.; Zhu, S. B.; Jing, F. C.; Liu, R. D.; Li, S. S.; He, J.; Lei, J. D. A self-assembled nanoparticle platform based on amphiphilic oleanolic acid polyprodrug for cancer therapy. Chinese J. Polym. Sci. 2020, 38, 819–829 DOI: 10.1007/s10118-020-2401-2.
Ying-Sa Wang, Gui-Liang Li, Shang-Bin Zhu, et al. A Self-assembled Nanoparticle Platform Based on Amphiphilic Oleanolic Acid Polyprodrug for Cancer Therapy[J]. Chinese Journal of Polymer Science, 2020, 38(8): 819-829. DOI: 10.1007/s10118-020-2401-2.
Oleanolic acid (OA) is a pentacyclic triterpenoid compound with extensive biological effects
such as anti-inflammatory and anticancer activities. However
the application of OA in chemotherapy is hampered by its poor solubility and severe adverse effects. To solve the problems
we developed a self-assembled nanoparticle platform based on amphiphilic oleanolic acid polyprodrug
poly[oligo(ethylene glycol) methyl ether methacrylate]-
b
-poly(oleanolic acid methacrylate) (POEGMA-
b
-POAMA)
encapsulating 10-hydroxycamptothecin (HCPT) to achieve efficient cancer therapy. The polyprodrug was prepared
via
reversible addition-fragmentation chain transfer polymerization (RAFT)
and could self-assemble to prepare POEGMA-
b
-POAMA/HCPT nanoparticles (NPs). The obtained nanoparticles exhibited appropriate particle size
excellent drug stability
good drug loading capacity
and high drug loading efficiency.
In vitro
drug release indicated that the drug release was prolonged to 132 h. The POEGMA-
b
-POAMA/HCPT NPs enhanced cell cytotoxicity in 4T1 cells and MCF-7 cells and could be efficiently uptaken by 4T1 cells. Furthermore
in vivo
antitumor efficiency showed that the POEGMA-
b
-POAMA/HCPT NPs had great antitumor efficiency with considerably low adverse effects in the treatment of the 4T1 mouse breast tumor xenograft tumor. Therefore
POEGMA-
b
-POAMA/HCPT NPs provide great potential as a platform for drug delivery applications.
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