Effect of Multilayer Termination on Nonspecific Protein Adsorption and Antifouling Activity of Alginate-Based Layer-by-Layer Coatings

Langmuir ◽  
2021 ◽  
Author(s):  
Thuvarakhan Gnanasampanthan ◽  
Cindy D. Beyer ◽  
Wenfa Yu ◽  
Jana F. Karthäuser ◽  
Robin Wanka ◽  
...  
Materials ◽  
2021 ◽  
Vol 14 (24) ◽  
pp. 7629
Author(s):  
Tomasz Kruk ◽  
Monika Bzowska ◽  
Alicja Hinz ◽  
Michał Szuwarzyński ◽  
Krzysztof Szczepanowicz

Control of nonspecific/specific protein adsorption is the main goal in the design of novel biomaterials, implants, drug delivery systems, and sensors. The specific functionalization of biomaterials can be achieved by proper surface modification. One of the important strategies is covering the materials with functional coatings. Therefore, our work aimed to functionalize multilayer coating to control nonspecific/specific protein adsorption. The polyelectrolyte coating was formed using a layer-by-layer technique (LbL) with biocompatible polyelectrolytes poly-L-lysine hydrobromide (PLL) and poly-L-glutamic acid (PGA). Nonspecific protein adsorption was minimized/eliminated by pegylation of multilayer films, which was achieved by adsorption of pegylated polycations (PLL-g-PEG). The influence of poly (ethylene glycol) chain length on eliminating nonspecific protein adsorption was confirmed. Moreover, to achieve specific protein adsorption, the multilayer film was also functionalized by immobilization of antibodies via a streptavidin bridge. The functional coatings were tested, and the adsorption of the following proteins confirmed the ability to control nonspecific/specific adsorption: human serum albumin (HSA), fibrinogen (FIB), fetal bovine serum (FBS), carcinoembryonic antigen human (CEA) monitored by quartz crystal microbalance with dissipation (QCM-D). AFM imaging of unmodified and modified multilayer surfaces was also performed. Functional multilayer films are believed to have the potential as a novel platform for biotechnological applications, such as biosensors and nanocarriers for drug delivery systems.


2017 ◽  
Vol 95 ◽  
pp. 195-206 ◽  
Author(s):  
A. Osypova ◽  
C.-A. Fustin ◽  
C.-M. Pradier ◽  
J. Landoulsi ◽  
S. Demoustier-Champagne

2015 ◽  
Vol 117 ◽  
pp. 384-391 ◽  
Author(s):  
Jinmei Wang ◽  
Hong Sun ◽  
Junjie Li ◽  
Dianyu Dong ◽  
Yabin Zhang ◽  
...  

Lab on a Chip ◽  
2005 ◽  
Vol 5 (10) ◽  
pp. 1005 ◽  
Author(s):  
Bo Huang ◽  
Hongkai Wu ◽  
Samuel Kim ◽  
Richard N. Zare

Langmuir ◽  
2017 ◽  
Vol 33 (42) ◽  
pp. 11264-11269 ◽  
Author(s):  
Priyesh Jain ◽  
Hsiang-Chieh Hung ◽  
Xiaojie Lin ◽  
Jinrong Ma ◽  
Peng Zhang ◽  
...  

2004 ◽  
Vol 845 ◽  
Author(s):  
Michela Ombelli ◽  
Lauren B. Costello ◽  
Qing Cheng Meng ◽  
Russell J. Composto ◽  
David M. Eckmann

ABSTRACTThe initial response of blood exposed to an artificial surface is the adsorption of blood proteins that triggers a number of biological reactions such as inflammation and blood coagulation. Competitive protein adsorption plays a key role in the hemocompatibility of the surface. The synthesis of nonfouling surfaces is therefore one of the major prerequisites for devices for biomedical applications. Polysaccharides are the main components of the endothelial cell glycocalyx and have the ability to reduce nonspecific protein adsorption and cell adhesion and, therefore, are generally coupled with a wide variety of surfaces to improve their biocompatibility. We have developed a procedure for covalently binding dextran and sodium hyaluronate (HA) on silicon wafers and we have been able to achieve a high level of control over the surface properties of the coatings. In the present research effort we focus on a detailed investigation of competitive bovine serum albumin (BSA) and bovine fibrinogen (Fg) adsorption on dextran- and HA-modified silicon surfaces. Polysaccharide based biomimetic layers preferentially adsorb BSA and, in general, strongly suppress protein adsorption with respect to bare silicon and APTES-activated silicon surfaces used as control.


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