Insights into the Aggregation/Deposition and Structure of a Polydopamine Film

被引:323
作者
Ding, Yonghui [1 ]
Weng, Lu-Tao [2 ,3 ]
Yang, Meng [1 ]
Yang, Zhilu [4 ]
Lu, Xiong [4 ]
Huang, Nan [4 ]
Leng, Yang [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Mech & Aerosp Engn, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Mat Characterizat & Preparat Facil, Kowloon, Hong Kong, Peoples R China
[3] Hong Kong Univ Sci & Technol, Dept Chem & Biomol Engn, Kowloon, Hong Kong, Peoples R China
[4] Southwest Jiaotong Univ, Sch Mat Sci & Engn, Key Lab Adv Technol Mat, Chengdu 610031, Sichuan, Peoples R China
关键词
SYNTHETIC MELANINS; MASS-SPECTROMETRY; PLATELET-ADHESION; SURFACE-CHEMISTRY; 5,6-DIHYDROXYINDOLE; EUMELANINS;
D O I
10.1021/la5026608
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Surface-adherent polydopamine (PDA) films as multifunctional coatings can be easily deposited onto a wide range of materials through dopamine self-polymerization. However, a lack of in-depth understanding of PDA aggregation and deposition processes and definite structure elucidation of PDA make it challenging to tailor the surface characteristic and functionality of the PDA films. Herein, we demonstrate that the surface characteristics of the PDA films can be readily tuned by controlling the competitive interplay between PDA aggregation in solution and deposition on the substrate. Moreover, a structural investigation of the PDA films using analytical tools such as X-ray photoelectron spectroscopy (XPS), time-of-flight secondary ion mass spectrometry (ToF-SIMS), and matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) allows us to propose a new structure model for the PDA building block. The (DHI)(2)/PCA trimer complex, which consists of two 5,6-dihydroxyindole (DHI) units and one pyrrolecarboxylic acid (PCA) moiety, is definitely identified as a primary building block of PDA, and its formation is steered by covalent interactions in the initial stages of polymerization. In latter stages, the (DHI)(2)/PCA trimer complexes are further linked primarily through noncovalent interactions to build up the supramolecular structure of PDA. This study provides new insights into the mechanisms of PDA buildup.
引用
收藏
页码:12258 / 12269
页数:12
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