Morpholino-terminated dendrimer shows enhanced tumor pH-triggered cellular uptake, prolonged circulation time, and low cytotoxicity

被引:12
|
作者
Guo, Leijia [1 ,2 ]
Wang, Chenhong [3 ]
Yang, Cuiping [3 ]
Wang, Xiuyan [1 ,2 ]
Zhang, Tianhong [3 ]
Zhang, Zhenqing [3 ]
Yan, Husheng [1 ,2 ]
Liu, Keliang [3 ]
机构
[1] Nankai Univ, Inst Polymer Chem, Minist Educ, Key Lab Funct Polymer Mat, Tianjin 300071, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China
[3] Beijing Inst Pharmacol & Toxicol, State Key Lab Toxicol & Med Countermeasures, Beijing 100850, Peoples R China
基金
中国国家自然科学基金;
关键词
Drug delivery; Dendrimer; PAMAM; pH-sensitive; Deep tumor penetration; GOLD NANOPARTICLES; POLYMERIC MICELLES; CHARGE; CANCER; PENETRATION; DELIVERY; BIODISTRIBUTION; NANOCARRIERS; FLUORESCENCE; ADSORPTION;
D O I
10.1016/j.polymer.2015.12.056
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Short circulation is a disadvantage of dendrimers as drug delivery carriers due to their small size. In this work, pH-sensitive morpholino-terminated generation 5 poly(amido amine) (PAMAM) is prepared. At neutral pH, the dendrimer has a hydrophilic neutral surface and thereby stealth property. Under tumor acidic environments, the dendrimer develops positive charges due to protonation of the morpholino groups, and cellular uptake of the dendrimer is subsequently enhanced. The dendrimer is predicted to penetrate deeper within the tumor due to its small size (similar to 9 nm), and thereby the pH-sensitive function can be efficiently achieved because the microenvironment in the deeper sites is more acidic. Moreover, the morpholino-terminated PAMAM exhibited longer in vivo circulation time compared to PAMAM and hydroxyl-terminated PAMAM, partly compensating for the disadvantage of short circulation of dendrimers. Furthermore, the morpholino-terminated PAMAM also showed lower cytotoxicity than PAMAM and hydroxyl-terminated PAMAM. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:189 / 197
页数:9
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