Super-sensitive bifunctional nanoprobe: Self-assembly of peptide-driven nanoparticles demonstrating tumor fluorescence imaging and therapy.
Super-sensitive bifunctional nanoprobe: Self-assembly of peptide-driven nanoparticles demonstrating tumor fluorescence imaging and therapy.
复制标题
超灵敏双功能纳米探针:肽驱动纳米颗粒的自组装展示肿瘤荧光成像和治疗
DOI:
10.1016/j.apsb.2021.07.020
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发表时间:
2022-03
影响因子:
14.5
通讯作者:
Wu, Guoqiu
中科院分区:
文献类型:
--
作者:
Xiao, Han;Zhang, Rui;Fan, Xiaobo;Jiang, Xinglu;Zou, Mingyuan;Yan, Xuejiao;Hao, Haiping;Wu, Guoqiu
关键词:
The development of nanomedicine has recently achieved several breakthroughs in the field of cancer treatment; however, biocompatibility and targeted penetration of these nanomaterials remain as limitations, which lead to serious side effects and significantly narrow the scope of their application. The self-assembly of intermediate filaments with arginine–glycine–aspartate (RGD) peptide (RGD-IFP) was triggered by the hydrophobic cationic molecule 7-amino actinomycin D (7-AAD) to synthesize a bifunctional nanoparticle that could serve as a fluorescent imaging probe to visualize tumor treatment. The designed RGD-IFP peptide possessed the ability to encapsulate 7-AAD molecules through the formation of hydrogen bonds and hydrophobic interactions by a one-step method. This fluorescent nanoprobe with RGD peptide could be targeted for delivery into tumor cells and released in acidic environments such as endosomes/lysosomes, ultimately inducing cytotoxicity by arresting tumor cell cycling with inserted DNA. It is noteworthy that the RGD-IFP/7-AAD nanoprobe tail-vein injection approach demonstrated not only high tumor-targeted imaging potential, but also potent antitumor therapeutic effects in vivo. The proposed strategy may be used in peptide-driven bifunctional nanoparticles for precise imaging and cancer therapy. Super-sensitive bifunctional nanoprobe that showed strong tumor-targeted imaging and antitumor therapeutic effects has been synthesized by one-step. This nanoparticle penetrated tumor cells to induce cell cycle arresting for cytotoxicity.
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