Cancer cell membrane-coated upconversion nanoparticles/ZnxMn1-xS core-shell nanoparticles for targeted photodynamic and chemodynamic therapy of pancreatic cancer

被引:10
作者
Liu, Xiaoyan [1 ,2 ,3 ]
Chu, Zhaoyou [4 ,5 ]
Chen, Benjin [4 ,5 ]
Ma, Yan [5 ]
Xu, Lingling [5 ,6 ]
Qian, Haisheng [5 ,6 ]
Yu, Yue [1 ,2 ]
机构
[1] Shandong Univ, Cheeloo Coll Med, Jinan 250012, Shandong, Peoples R China
[2] Univ Sci & Technol China, Affiliated Hosp 1, Dept Gastroenterol, Div Life Sci & Med,USTC, Hefei 230001, Anhui, Peoples R China
[3] Anhui Med Univ, Luan Hosp, Luan Peoples Hosp, Dept Gastroenterol, Luan 237000, Anhui, Peoples R China
[4] Anhui Med Univ, Sch Basic Med Sci, Dept Pharmacol, Hefei 230032, Anhui, Peoples R China
[5] Anhui Med Univ, Anhui Prov Inst Translat Med, Sch Biomed Engn, Hefei 230032, Peoples R China
[6] Anhui Med Univ, Sch Biomed Engn, Hefei, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Upconversion nanoparticles; Chemodynamic therapy; Photodynamic therapy; Biomimetic nanoparticles; Pancreatic ductal adenocarcinomas; OXIDATIVE STRESS; CYTOTOXICITY; APOPTOSIS;
D O I
10.1016/j.mtbio.2023.100765
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Oxidative stress induced by reactive oxygen species (ROS) is promising treatment approach for pancreatic ductal adenocarcinoma (PDAC), which is typically insensitive to conventional chemotherapy. In this study, BxPC-3 pancreatic cancer cell membrane-coated upconversion nanoparticles/ZnxMn1-xS core-shell nanoparticles (abbreviated as BUC@ZMS) were developed for tumor-targeted cancer therapy via synergistically oxidative stress and overcoming glutathione (GSH) overexpression. Using a combination of photodynamic therapy (PDT) and chemodynamic therapy (CDT), the BUC@ZMS core-shell nanoparticles were able to elicit the death of pancreatic cancer cells through the high production of ROS. Additionally, the BUC@ZMS core-shell nanoparticles could deplete intracellular GSH and increase the sensitivity of tumor cells to oxidative stress. The in vivo results indicated that BUC@ZMS nanoparticles can accumulate specifically in tumor locations and suppress PDAC without generating obvious toxicity. Thus, it was determined that the as-prepared core-shell nanoparticles would be a viable treatment option for solid malignancies.
引用
收藏
页数:12
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