Imaging-Guided Chemo-Photothermal Polydopamine Carbon Dots for EpCAM-Targeted Delivery toward Liver Tumor

被引:46
作者
Li, Zeyu [1 ]
Ni, Jiatong [1 ]
Liu, Liping [2 ]
Gu, Liyuan [3 ]
Wu, Zhiguang [4 ]
Li, Tianlong [4 ]
Ivanovich, Krasnyuk Ivan [4 ]
Zhao, Wancheng [1 ]
Sun, Tiedong [1 ]
Wang, Ting [1 ]
机构
[1] Northeast Forestry Univ, Coll Chem Chem Engn & Resource Utilizat, Engn Res Ctr Forest Biopreparat, Key Lab Forest Plant Ecol,Minist Educ, Harbin 150040, Peoples R China
[2] Harbin First Specialist Hosp, Harbin 150056, Peoples R China
[3] Henan Agr Univ, Coll Forestry, Zhengzhou 450002, Peoples R China
[4] Sechenov Univ, Inst Pharm, Moscow 119991, Russia
基金
中国国家自然科学基金;
关键词
polydopamine-based carbon dots; fluorescence imaging; cancer therapy; chemo-photothermal synergistic therapy; tumor-targeted delivery; imaging guiding; CELL ADHESION MOLECULE; DRUG-DELIVERY; CANCER; NANOPARTICLES; POPULATION; GRAPHENE; SYSTEM;
D O I
10.1021/acsami.1c05079
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We demonstrate a versatile nanoparticle with imaging-guided chemo-photothermal synergistic therapy and EpCAM-targeted delivery of liver tumor cells. EpCAM antibody (anti-EpCAM) and Pt(IV) were grafted onto the polydopamine carbon dots (PDA-CDs) by the amidation reaction. The EpCAM antibody of particles enables the targeted interaction with liver progenitor cells due to their overexpressed EpCAM protein. The tetravalent platinum prodrug [Pt(IV)] induces apoptosis with minimum toxic side effects through the interaction between cisplatin and tumor cell DNA. The nanoparticles displayed stable photothermal property and considerable anti-tumor therapeutic effect in vivo. Coupling with cellular imaging due to their fluorescence property, anti-EpCAM@PDA-CDs@Pt(IV) offers a convenient and effective platform for imaging-guided chemo-photothermal synergistic therapy toward liver cancers in the near future.
引用
收藏
页码:29340 / 29348
页数:9
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