Directed self-assembly of microscale hydrogels by electrostatic interaction

被引:82
|
作者
Han, Yu Long [1 ,2 ]
Yang, Yanshen [1 ,2 ]
Liu, Shaobao [2 ]
Wu, Jinhui [3 ]
Chen, Yongmei [2 ,4 ]
Lu, Tian Jian [2 ]
Xu, Feng [1 ,2 ]
机构
[1] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Key Lab Biomed Informat Engn, Minist Educ, Xian 710049, Peoples R China
[2] Xi An Jiao Tong Univ, Bioinspired Engn & Biomech Ctr, Xian 710049, Peoples R China
[3] Nanjing Univ, State Key Lab Pharmaceut Biotechnol, Nanjing 210093, Jiangsu, Peoples R China
[4] Xi An Jiao Tong Univ, Sch Sci, Dept Chem, MOE Key Lab Nonequilibrium Synth & Modulat Conden, Xian 710049, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
PHOTODEGRADABLE HYDROGELS; ENDOTHELIAL-CELLS; ADHESION; MODEL;
D O I
10.1088/1758-5082/5/3/035004
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The unique benefit of electrostatic self-assembly of microscale components in solution is demonstrated for the first time. In particular, positive and negative treatment of poly(ethylene glycol) (PEG) facilitates a novel bottom-up assembly approach using electrostatic interaction from microgels with opposite charges. Fundamental investigations of electrostatic interaction of microgels reveal that the contact area of microgels determines the total energy of construct and thus the final patterns. The electrostatic self-assembly approach enables the fabrication of large and complex biological related structures (e.g., multi-layer spheroid) with accurate control. By the design of the microgels, the thickness and number of microgels in each layer can be controlled. Biological investigations of positive and negative treatments of PEG further prove the possibility of using this approach in tissue engineering, regenerative medicine and drug delivery.
引用
收藏
页数:10
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