白桦酸
明胶
化学
体内
生物利用度
细胞毒性
生物相容性
纳米颗粒
药理学
材料科学
纳米技术
生物化学
体外
有机化学
医学
生物
生物技术
遗传学
作者
Shuting Lu,Xiaocheng Fan,Henan Wang,Yuliang Zhao,Wancheng Zhao,Mengzhu Li,Rongyao Lv,Ting Wang,Tiedong Sun
标识
DOI:10.1021/acsabm.9b01204
摘要
Betulinic acid (BA) is a natural antitumor agent and has biological activity against multiple human tumor cell lines with low cytotoxicity to normal cells, while the high hydrophobicity and the short half-life of this compound limit its clinical application. Here, gelatin-based dual-targeted nanoparticles of BA are promising to solve this problem. Hydrophobic BA is loaded in cyclodextrin to increase its solubility and prolong the circulation time in vivo. The nanoscale drug delivery systems can further enhance the bioavailability and the antitumor effect of BA and are passively targeted to the tumor tissue sites by enhanced permeability and retention effect. The RGD sequence of gelatin specifically recognizes tumor cells and brings agents into tumor cells. The nanoparticles were characterized by transmission electron microscopy, Fourier transform infrared, nuclear magnetic resonance, etc. In addition, we observed antitumor activity of the nanoparticles using both cell-based assays and mouse xenograft tumors, which proved that betulinic acid/gelatin-γ-cyclodextrin nanoparticles had a better tumor inhibition effect than betulinic acid/γ-cyclodextrin inclusion compound.
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