纳米医学
适体
药物输送
PEG比率
肝细胞癌
癌细胞
药理学
化学
药品
纳米载体
癌症研究
癌症
医学
体内
生物
生物技术
分子生物学
材料科学
纳米技术
内科学
纳米颗粒
经济
有机化学
财务
作者
Jianghong Lv,Tingting Meng,Yingping Zeng,Yu Tong,Lanxia Zhao,Jingwen Liu,Zhou Wentao,Pengbo Chen,Hong Yuan,Fuqiang Hu
标识
DOI:10.1021/acsbiomaterials.1c00357
摘要
Hepatocellular carcinoma (HCC) is known as the most common malignancy of the hepatobiliary system with a continued increase in incidence but limited therapeutic options. Nanomedicine has provided a promising strategy through engineered nanocarriers that are capable of targeting therapeutic agents specifically to tumor cells. In this research, two aptamer/peptide-modified lipid-based drug delivery systems (A54-PEG-SLN/OXA and A15-PEG-SLN/SAL) were developed as a sequential therapeutic strategy to conquer specific hepatocellular carcinoma. The nanomedicine A54-PEG-SLN/OXA was able to target specific hepatocellular carcinoma cell BEL-7402 and exhibited a strong targeting ability and antitumor efficiency both in vitro and in vivo. The A15-PEG-SLN/SAL could target and penetrate deeply to the spheroid composed of CD133+ cancer cells. In the study of developing a sequential therapeutic strategy, we demonstrated that A54-PEG-SLN/OXA could kill tumor cells and expose CD133+ cancer cells. After the administration of A15-PEG-SLN/SAL, the growth of the tumors was significantly inhibited. In conclusion, the aptamer/peptide-modified lipid-based drug delivery systems, A54-PEG-SLN/OXA and A15-PEG-SLN/SAL, could specifically target carcinoma cells and had an evident antitumor effect when administrated sequentially.
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