Non-Covalent Self-Assembly and Covalent Polymerization Co-Contribute to Polydopamine Formation

被引:1860
作者
Hong, Seonki [1 ]
Na, Yun Suk [1 ]
Choi, Sunghwan [1 ]
Song, In Taek [1 ]
Kim, Woo Youn [1 ]
Lee, Haeshin [1 ,2 ,3 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem, Taejon 305701, South Korea
[2] Grad Sch Nanosci & Technol WCU, Taejon 305701, South Korea
[3] Korea Adv Inst Sci & Technol, KAIST Inst NanoCentury, Taejon 305701, South Korea
基金
新加坡国家研究基金会;
关键词
polydopamine; self-assembly; 5; 6-dihydroxyindole; melanin; cytotoxicity; DENSITY FUNCTIONALS; SURFACE-CHEMISTRY; DOPAMINE; NANOPARTICLES; IMMOBILIZATION; MOLECULES; FACILE; OXIDE; C-13;
D O I
10.1002/adfm.201201156
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Polydopamine is the first adhesive polymer that can functionalize surfaces made of virtually all material chemistries. The material-independent surface modification properties of polydopamine allow the functionalization of various types of medical and energy devices. However, the mechanism of dopamine polymerization has not yet been clearly demonstrated. Covalent oxidative polymerization via 5,6-dihydroxyindole (DHI), which is similar to the mechanism for synthetic melanin synthesis, has been the clue. Here, it is reported that a physical, self-assembled trimer of (dopamine)2/DHI exists in polydopamine, which has been known to be formed only by covalent polymerization. It is also found that the trimeric complex is tightly entrapped within polydopamine and barely escapes from the polydopamine complex. The result explains the previously reported in vitro and in vivo biocompatibility. The study reveals a different perspective of polydopamine formation, where it forms in part by the self-assembly of dopamine and DHI, providing a new clue toward understanding the structures of catecholamines such as melanin.
引用
收藏
页码:4711 / 4717
页数:7
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