Calcium-Mediated Control of Polydopamine Film Oxidation and Iron Chelation

被引:33
|
作者
Klosterman, Luke [1 ]
Bettinger, Christopher J. [1 ,2 ]
机构
[1] Carnegie Mellon Univ, Dept Mat Sci & Engn, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Biomed Engn, Pittsburgh, PA 15213 USA
来源
基金
美国安德鲁·梅隆基金会;
关键词
polydopamine; melanin; thin film; metal cation; dopamine oxidation; RESONANCE RAMAN; AQUEOUS-SOLUTION; HYDROTHERMAL CARBONIZATION; MELANIN PRECURSORS; HYDROGEN-PEROXIDE; DOPAMINE; EUMELANIN; COATINGS; SPECTROSCOPY; COMPLEXES;
D O I
10.3390/ijms18010014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The facile preparation of conformal polydopamine (PDA) films on broad classes of materials has prompted extensive research into a wide variety of potential applications for PDA. The constituent molecular species in PDA exhibit diverse chemical moieties, and therefore highly variable properties of PDA-based devices may evolve with post-processing conditions. Here we report the use of redox-inactive cations for oxidative post-processing of deposited PDA films. PDA films incubated in alkaline CaCl2 solutions exhibit accelerated oxidative evolution in a dose-dependent manner. PDA films incubated in CaCl2 solutions exhibit 53% of the oxidative charge transfer compared to pristine PDA films. Carboxylic acid groups generated from the oxidation process lower the isoelectric point of PDA films from pH = 4.0 +/- 0.2 to pH = 3.1 +/- 0.3. PDA films exposed to CaCl2 solutions during post-processing also enhance Fe2+/Fe3+ chelation compared to pristine PDA films. These data illustrate that the molecular heterogeneity and non-equilibrium character of as-deposited PDA films afford control over the final composition by choosing post-processing conditions, but also demands forethought into how the performance of PDA-incorporated devices may change over time in salt solutions.
引用
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页数:14
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