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A siRNA-induced peptide co-assembly system as a peptide-based siRNA nanocarrier for cancer therapy†
Materials Horizons ( IF 12.2 ) Pub Date : 2018-06-06 00:00:00 , DOI: 10.1039/c8mh00392k
Wenjun Li 1, 2, 3, 4, 5 , Dongyuan Wang 1, 2, 3, 4, 5 , Xiaodong Shi 1, 2, 3, 4, 5 , Jingxu Li 1, 2, 3, 4, 5 , Yue Ma 1, 2, 3, 4, 5 , Yanding Wang 1, 2, 3, 4, 5 , Tingting Li 3, 4, 5, 6 , Jianing Zhang 1, 2, 3, 4, 5 , Rongtong Zhao 1, 2, 3, 4, 5 , Zhiqiang Yu 5, 7, 8, 9, 10 , Feng Yin 1, 2, 3, 4, 5 , Zigang Li 1, 2, 3, 4, 5
Affiliation  

Herein, we report a unique siRNA-induced peptide co-assembly nanocarrier, which could efficiently co-assemble upon the addition of siRNA, forming nanospheres with high biocompatibility and transfection efficiency both in vitro and in vivo. In a tumor xenograft nude mouse model, these siRNA–peptide nanospheres inhibited tumor volume growth by >60%.

中文翻译:

siRNA诱导的肽共组装系统,作为基于肽的siRNA纳米载体,用于癌症治疗

在本文中,我们报道了同时具有高生物相容性和转染效率的唯一siRNA诱导肽共组装纳米载体,当加入的siRNA可能有效共组装,形成纳米球在体外体内。在肿瘤异种移植裸鼠模型中,这些siRNA-肽纳米球将肿瘤体积的生长抑制了60%以上。
更新日期:2018-06-06
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