转移
阿霉素
癌症研究
纳米纤维
基质金属蛋白酶
药物输送
基质金属蛋白酶抑制剂
化学
药理学
癌症
医学
材料科学
化疗
纳米技术
内科学
生物化学
作者
Yujie Ji,Yanyu Xiao,Xu Liu,Jiayu He,Qian Chen,Weidong Li,Li Wu,Rui Chen,Jingjing Wang,Rongfeng Hu,Xudong Zhang,Zhen Gu,Zhipeng Chen
标识
DOI:10.1002/advs.201700867
摘要
Abstract Treatment of hepatocellular carcinoma (HCC) requires sustained suppression of tumor cell growth and metastasis for long‐term efficacy. However, traditional intratumoral drug delivery system always exhibits burst release with less therapeutic outcomes. Here, a new self‐assembling amphiphilic peptide drug conjugate (SAAPDC) is fabricated as a “two‐in‐one” nanofiber system comprising a hexapeptide as a matrix metalloproteinases (MMP) inhibitor and doxorubicin (DOX) for the treatment of HCC. The results indicate that doxorubicin‐conjugated peptide (DOX‐KGFRWR) self‐assembles to form long nanofibers showing sustained release property for inhibiting the enzymatic activities of MMP‐2 and MMP‐9. This nanofiber not only inhibits tumor growth in situ but also effectively prevents pulmonary metastasis in an SMMC7721 cell line–based mouse model. In summary, this hexapeptide‐based supermolecule system represents a promising nanoscale platform to sustain drug release with high loading capacity for intratumoral administration. Moreover, the delivery of chemotherapeutic drugs via drug‐bearing supramolecular MMP inhibitor nanofibers simultaneously inhibits metastasis and tumor growth to achieve synergistic effects for metastatic HCC therapy.
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