Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/81051
Title: Adsorption of hyaluronic acid on solid supports: Role of pH and surface chemistry in thin film self-assembly
Authors: Choi, Jae-Hyeok
Kim, Seong-Oh
Linardy, Eric
Dreaden, Erik C.
Zhdanov, Vladimir P.
Hammond, Paula T.
Cho, Nam-Joon
Keywords: Hyaluronic acid
Thin films
Adsorption kinetics
Quartz crystal microbalance
Atomic force microscopy
pH condition
Self-assembly
Issue Date: 2015
Source: Choi, J.-H., Kim, S.-O., Linardy, E., Dreaden, E. C., Zhdanov, V. P., Hammond, P. T., et al. (2015). Adsorption of hyaluronic acid on solid supports: Role of pH and surface chemistry in thin film self-assembly. Journal of Colloid and Interface Science, 448, 197-207.
Series/Report no.: Journal of Colloid and Interface Science
Abstract: Owing to its biocompatibility, resistance to biofouling, and desirable physicochemical and biological properties, hyaluronic acid (HA) has been widely used to modify the surface of various materials. The role of various physicochemical factors in HA adsorption remains, however, to be clarified. Herein, we employed quartz crystal microbalance with dissipation (QCM-D) in order to investigate HA adsorption at different pH conditions onto three substrates—silicon oxide, amine-terminated self-assembled monolayer (SAM) on gold, and carboxylic acid-terminated SAM on gold. The QCM-D experiments indicated specific pH conditions where either strong or weak HA adsorption occurs. The morphology of the adsorbed HA layers was investigated by atomic force microscopy (AFM), and we identified that strong HA adsorption produced a complete, homogenous and smooth HA layer, while weak HA adsorption resulted in rough and inhomogeneous HA layers. The observed specifics of the kinetics of HA adsorption, including a short initial linear phase and subsequent long non-linear phase, were described by using a mean-field kinetic model taking HA diffusion limitations and reconfiguration in the adsorbed state into account. The findings extend the physicochemical background of design strategies for improving the use of passive HA adsorption for surface modification applications.
URI: https://hdl.handle.net/10356/81051
http://hdl.handle.net/10220/40644
ISSN: 0021-9797
DOI: 10.1016/j.jcis.2015.01.060
Rights: © 2015 Elsevier Inc.
Fulltext Permission: none
Fulltext Availability: No Fulltext
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