Multifunctional nanoparticles self-assembled from polyethylenimine-based graft polymers as efficient anticancer drug delivery

被引:19
|
作者
Yan, Jianqin [1 ]
Su, Ting [1 ]
Cheng, Furong [1 ]
Cao, Jun [1 ]
Zhang, Hai [2 ]
He, Bin [1 ]
机构
[1] Sichuan Univ, Natl Engn Res Ctr Biomat, Chengdu 610064, Peoples R China
[2] Sichuan Univ, Coll Polymer Sci & Engn, Chengdu 610065, Peoples R China
关键词
Polyethyleneimine; pH-Sensitive; Hyaluronic acid; Active target; Drug delivery; HYALURONIC-ACID; DOXORUBICIN CONJUGATE; TARGETED DELIVERY; INTRACELLULAR DELIVERY; POLY(ETHYLENE GLYCOL); LIPID NANOPARTICLES; IN-VITRO; MICELLES; COPOLYMER; CD44;
D O I
10.1016/j.colsurfb.2017.02.030
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Multiple functionalization of nanoparticles has attracted great interest in drug delivery. In this paper, polymeric amphiphiles of polyethylenimine (PEI) conjugated with methoxy poly(ethylene glycol) aldehyde (mPEG-CHO), poly(epsilon caprolactone) aldehyde (PCL-CHO) and pyrene-1-carboxaldehyde (Py-CHO) were synthesized via Schiffs reaction. The conjugates self-assembled into nanoparticles with pH sensitivity to load anticancer drug doxorubicin (DOX), further coated with hyaluronic acid (HA) for tumor targeting. The mean size of nanoparticles was about 100 nm and the stability of the nanoparticles was well in aqueous solution. The nanoparticles coated with HA showed faster disassembly in acidic solution, resulting in faster drug release in the medium with pH 5.0 compared to uncoated nanoparticles. Moreover, the nanoparticles exhibited an endosomal escape function to accelerate the release of DOX in cancer cells, which led to low IC(50)s to kill breast cancer cells (4T1) and liver cancer cells (HepG2) in vitro. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:118 / 127
页数:10
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