肽
药品
药物输送
体内
化学
结合
药理学
癌症研究
纳米技术
医学
材料科学
生物化学
生物
生物技术
数学
数学分析
作者
Qianqian Zhang,Peng Zhang,Shandong Jian,Jinting Li,Fengjiao Li,Xiaoliang Sun,Hongrui Li,Yang Zeng,Youlin Zeng,Songping Liang,Ping Chen,Zhonghua Liu
标识
DOI:10.1021/acs.molpharmaceut.0c00118
摘要
Employing a peptide-based nanoscale drug delivery system is an effective strategy to overcome the poor therapeutic outcomes of chemotherapeutic drugs. Here, we developed a self-assembling peptide-drug delivery system comprising a self-assembling anticancer peptide (R-lycosin-I), as revealed in our previous study, and 10-hydroxycamptothecin (HCPT) for cancer therapy. The results showed that peptide-drug conjugates (R-L-HCPT) could assemble into nanospheres of 40–60 nm in water. Compared with free HCPT, R-L-HCPT nanospheres not only inhibited tumor growth but also suppressed pulmonary metastatic nodules on B16–F10 cells in vivo. In summary, these results indicated that the self-assembling R-lycosin-I could provide a promising nanoscale platform for delivering small-molecule drugs. Moreover, our study might provide new opportunities for the development of a new class of functional peptide-drug-conjugated systems based on nanomaterials, which could synergistically enhance anticancer outcomes.
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