Design and fabrication of chitosan-based AIE active micelles for bioimaging and intelligent delivery of paclitaxel

被引:25
|
作者
Xu, Yang [1 ]
Liang, Na [2 ,3 ]
Liu, Jiyang [1 ]
Gong, Xianfeng [1 ]
Yan, Pengfei [1 ]
Sun, Shaoping [1 ,4 ]
机构
[1] Heilongjiang Univ, Sch Chem & Mat Sci, Key Lab Funct Inorgan Mat Chem, Minist Educ, Harbin 150080, Peoples R China
[2] Harbin Normal Univ, Coll Chem & Chem Engn, Harbin 150025, Peoples R China
[3] Harbin Normal Univ, Coll Chem & Chem Engn, 1,Shida Rd, Harbin 150025, Peoples R China
[4] Heilongjiang Univ, Sch Chem & Mat Sci, 74,Xuefu St, Harbin 150080, Peoples R China
基金
中国国家自然科学基金;
关键词
Polymeric micelles; Aggregation-induced emission (AIE); Bioimaging; Tumor targeting; pH responsive; AGGREGATION-INDUCED EMISSION; POLYMERIC MICELLES; DRUG-DELIVERY; HYALURONIC-ACID; NANOPARTICLES;
D O I
10.1016/j.carbpol.2022.119509
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this study, cetyl 4-formylbenzoate alkyl and 4-(2-hydroxyethoxy) benzophenonesalicylaldazide modified biotinylated chitosan (CS-BT-HBS-CB) featured with aggregation-induced emission (AIE) characteristic, active tumor-targeting ability and pH-responsive drug release property was designed and synthesized. The polymer was fabricated by introducing hydrophobic segment, tumor targeting ligand, acid-sensitive bond and AIE fluorophore to the backbone of chitosan. Due to its amphiphilicity, the polymer could self-assemble into micelles and encapsulate paclitaxel (PTX) to form PTX-loaded CS-BT-HBS-CB micelles. The mean size of the micelles was 167 nm, which was beneficial to the EPR effect. Moreover, with the help of above functional groups, the micelles exhibited excellent AIE effect, triggered drug release behavior by acidic condition, selective internalization by MCF-7 cells and excellent cellular imaging capability. In vivo studies revealed that the PTX-loaded CS-BT-HBS-CB micelles could enhance the antitumor efficacy with low systemic toxicity. This micellar system would be a potential candidate for cancer therapy and bioimaging.
引用
收藏
页数:12
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