Investigation of polydopamine coatings by X-ray Photoelectron Spectroscopy as an effective tool for improving biomolecule conjugation

被引:110
作者
Rella, Simona [1 ]
Mazzotta, Elisabetta [1 ,2 ]
Caroli, Antonio [1 ]
De Luca, Maria [1 ]
Bucci, Cecilia [1 ]
Malitesta, Cosimino [1 ]
机构
[1] Univ Salento, Dipartimento Sci & Tecnol Biol & Ambientali, Via Monteroni, I-73100 Lecce, Italy
[2] CNR, IFAC, Via Madonna Piano, I-50019 Sesto Fiorentino, FI, Italy
关键词
Polydopamine; Biomolecule immobilization; X-ray Photoelectron Spectroscopy (XPS); MULTIFUNCTIONAL COATINGS; CELL-ADHESION; THIN-FILMS; IMMOBILIZATION; FUNCTIONALIZATION; CHEMISTRY; DOPAMINE; SURFACES; MOLECULES;
D O I
10.1016/j.apsusc.2018.03.057
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Polydopamine (PDA) films have attracted a rapidly increasing research attention during the last years due to its simple and rapid deposition under alkaline conditions in substrate independent manner providing a universal coating for materials with different chemical and physical properties. Furthermore, this polymerized layer is enriched with functional groups that enable immobilization of primary amine or thiol-based biomolecules via a simple dipping process. Although these aspects justify PDA wide and successful application as a versatile coating for biomolecule immobilization, several aspects have not been deeply investigated leaving some key details unclear and thus limiting PDA practical applications. A number of approaches are commonly used for the growth of PDA, but the effect of deposition conditions on film properties, which in turn influence biomolecule immobilization has not been systematically investigated yet. In the present work, an extensive characterization by X-ray Photoelectron Spectroscopy (XPS) is performed on PDA coatings grown under different experimental conditions. Comparison of XPS data about elemental composition, distribution of functional groups and thickness of PDA coatings provided valuable information for identifying more suitable PDA coating for biomolecule anchoring, further explored by in vitro experiments. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:31 / 39
页数:9
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