Self-assembled pH-responsive supramolecular hydrogel for hydrophobic drug delivery

被引:13
|
作者
Wang, Lin [1 ,2 ]
Shi, Xuefeng [1 ]
Zhang, Jian [3 ]
Zhu, Yuejun [3 ]
Wang, Jinben [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, CAS Key Lab Colloid Interface & Chem Thermodynam, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] CNOOC Res Inst Co Ltd, State Key Lab Offshore Oil Exploitat, Beijing 100028, Peoples R China
来源
RSC ADVANCES | 2018年 / 8卷 / 55期
关键词
SOL-GEL TRANSITION; GEMINI SURFACTANT; ANTICANCER DRUGS; RELEASE; CURCUMIN; DOXORUBICIN; NANOPARTICLES; VERSATILE; MICELLES; BEHAVIOR;
D O I
10.1039/c8ra06064a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, a novel supramolecular hydrogel system, abbreviated as AGC(16)/NTS, prepared by molecular self-assembly of cationic gemini surfactant 1,3-bis(N,N-dimethyl-N-cetylammonium)-2-propylacrylatedibromide (AGC(16)) and anionic aromatic compound trisodium 1,3,6-naphthalenetrisulfonate (NTS), was used to encapsulate hydrophobic model drug curcumin (Cur), constructing a pH-responsive drug delivery system. Cur was effectively encapsulated into the hydrophobic domains of AGC(16)/NTS through hydrophobic interaction, which was confirmed by H-1 NMR measurement. The effects of Cur on the mechanical strength, phase transition behaviour and morphology of AGC(16)/NTS were characterized by rheology and cryogenic scanning electron microscopy (cryo-SEM) methods. The pH-responsive release of Cur from AGC(16)/NTS was obtained and the release amount of Cur ascended with pH value decreasing from 7.4 to 3.0. The hydrodynamic sizes of the released Cur-aggregates determined by dynamic light scattering (DLS) were used to analyse the release process of Cur at different pH. The cell viability assay and cell imaging experiment demonstrated that Cur-loaded hydrogel has much higher cytotoxicity and better cell uptake compared to free Cur. Overall, the AGC(16)/NTS hydrogel is a prospective material for use in encapsulation and controlled-release of hydrophobic drug molecules.
引用
收藏
页码:31581 / 31587
页数:7
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