Overcoming tumor resistance to cisplatin by cationic lipid-assisted prodrug nanoparticles

被引:50
|
作者
Cao, Zhi-Ting [1 ]
Chen, Zhi-Yao [2 ,3 ]
Sun, Chun Yang [2 ,3 ]
Li, Hong-Jun [2 ,3 ]
Wang, Hong-Xia [2 ,3 ]
Cheng, Qin-Qin [5 ]
Zuo, Zu-Qi [2 ,3 ]
Wang, Ji-Long [2 ,3 ]
Liu, Yang-Zhong [5 ]
Wang, Yu-Cai [2 ,3 ]
Wang, Jun [1 ,2 ,3 ,4 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230027, Anhui, Peoples R China
[2] Univ Sci & Technol China, Sch Life Sci, CAS Ctr Excellence Nanosci, Hefei 230027, Anhui, Peoples R China
[3] Univ Sci & Technol China, Med Ctr, Hefei 230027, Anhui, Peoples R China
[4] Univ Sci & Technol China, Innovat Ctr Cell Signaling Network, Hefei 230027, Anhui, Peoples R China
[5] Univ Sci & Technol China, Dept Chem, Hefei 230027, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Cisplatin resistance; Pt(IV) prodrug; Cationic nanoparticle; Lung cancer; POLYMERIC MICELLES NC-6004; COPPER TRANSPORTER CTR1; CANCER CELL-LINES; DRUG-DELIVERY; MULTIDRUG-RESISTANCE; TARGETED DELIVERY; RATIONAL DESIGN; SURFACE-CHARGE; PLATINUM DRUGS; PENETRATION;
D O I
10.1016/j.biomaterials.2016.04.001
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Chemotherapy resistance has become a major challenge in the clinical treatment of lung cancer which is the leading cancer type for the estimated deaths. Recent studies have shown that nanoparticles as drug carriers can raise intracellular drug concentration by achieving effectively cellular uptake and rapid drug release, and therefore reverse the acquired chemoresistance of tumors. In this context, nanoparticles-based chemotherapy represents a promising strategy for treating malignancies with chemoresistance. In the present study, we developed cationic lipid assisted nanoparticles (CLAN) to deliver polylactide-cisplatin prodrugs to drug resistant lung cancer cells. The nanoparticles were formulated through self assembly of a biodegradable poly(ethylene glycol)-block-poly(lactide) (PEG-PLA), a hydrophobic polylactide-cisplatin prodrug, and a cationic lipid. The cationic nanoparticles were proven to significantly improve cell uptake of cisplatin, leading to an increased DNA-Pt adduct and significantly promoted DNA damage in vitro. Moreover, our study reveals that cationic nanoparticles, although are slightly inferior in blood circulation and tumor accumulation, are more effective in blood vessel extravasation. The CLANs ultimately enhances the cellular drug availability and leads to the reversal of cisplatin resistance. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9 / 19
页数:11
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