Hyaluronic acid-coated and Olaparib-loaded PEI - PLGA nanoparticles for the targeted therapy of triple negative breast cancer

被引:9
|
作者
Hu, Huiping [1 ,2 ]
Zhang, Yu [1 ,2 ]
Ji, Wenting [1 ]
Mei, Hao [1 ,2 ]
Wu, Tingting [1 ,2 ]
He, Zihao [1 ]
Wang, Kaiping [3 ]
Shi, Chen [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Pharm, Wuhan, Peoples R China
[2] Hubei Prov Clin Res Ctr Precis Med Crit Illness, Wuhan, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Med Coll Pharm, Hubei Key Lab Nat Med Chem & Resource Evaluat, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
Targeted delivery system; PEI-PLGA nanoparticles; hyaluronic acid; Olaparib; TNBC; DELIVERY; NANOTECHNOLOGY;
D O I
10.1080/02652048.2021.2014586
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Aim To prepare the hyaluronic acid-coated Olaparib-loaded PEI - PLGA nanoparticles (HA-Ola-PPNPs) and investigate their tumour-targeted anticancer effect. Methods The synthesis of HA-Ola-PPNPs was verified by DLS, TEM and SEM, followed was measured its cytotoxicity using CCK-8 assay. Confocal microscopy was used to observe the cellular uptake. Cell apoptosis was analysed by flow cytometry, biological SEM, and TEM. The expression of related proteins within the tumour site was investigated by immunostaining. Results The prepared HA-Ola-PPNPs showed a diameter of similar to 160 nm with a negatively charged surface (-16.9 +/- 2.7 mV) and sustained drug release behaviour. And the encapsulation efficiency of HA-Ola-PPNPs was 78.63 +/- 5.29%. HA-Ola-PPNPs exhibited efficient in vitro and in vivo antitumor activities. HA-Ola-PPNPs induced cell apoptosis by upregulating Bax, Cytochrome C, and Caspase 3, downregulating Bcl-2 in breast cancer-bearing mice. Conclusions According to the results, the Ola-loaded and HA-coated PEI - PLGA nanoparticles could be considered as a powerful tumour-targeted drug delivery system for TNBC treatment.
引用
收藏
页码:25 / 36
页数:12
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