Aptamer and Peptide-Modified Lipid-Based Drug Delivery Systems in Application of Combined Sequential Therapy of Hepatocellular Carcinoma

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 财务 纳米颗粒 经济 有机化学
作者
Jianghong Lv,Tingting Meng,Yingping Zeng,Yu Tong,Lanxia Zhao,Jingwen Liu,Zhou Wentao,Pengbo Chen,Hong Yuan,Fuqiang Hu
出处
期刊:ACS Biomaterials Science & Engineering [American Chemical Society]
卷期号:7 (6): 2558-2568 被引量:15
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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